Patent Application
20180148494
The invention features soluble fibroblast growth factor (FGF) decoy polypeptides and fusion polypeptides including an FGF decoy polypeptide and an aggrecan binding protein. The invention also features methods to prevent or treat skeletal growth retardation disorders, such as achondroplasia.
Fibroblast growth factor receptor 3 (FGFR3) is a member of the fibroblast growth factor (FGFR) family, in which there is high conservation of amino acid sequence between family members. Members of the FGFR family are differentiated by both ligand binding affinities and tissue distribution. A full-length FGFR polypeptide contains an extracellular domain, a single hydrophobic transmembrane domain, and a cytoplasmic tyrosine kinase domain. The extracellular domain (ECD) of FGFR polypeptides interacts with fibroblast growth factors (FGFs) to mediate downstream signaling. This signalling ultimately influences cellular differentiation. In particular, the FGFR3 protein plays a role in bone development by inhibiting chondrocyte proliferation at the growth plate and limiting bone elongation.
Gain-of-function point mutations in FGFR3 are known to cause several types of human skeletal growth retardation disorders, such as achondroplasia, severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), hypochondroplasia, thanatophoric dysplasia, and craniosynostosis. Achondroplasia is the most common form of short-limb dwarfism and is characterized by disproportionate shortness of limbs and relative macrocephaly. Approximately 97% of achondroplasia is caused by a single point mutation in the gene encoding FGFR3, in which a glycine residue is substituted with an arginine residue at position 380 of the FGFR3 gene. Following ligand binding, the mutation decreases the elimination of the receptor/ligand complex resulting in prolonged intracellular signaling. This prolonged FGFR3 signaling inhibits the proliferation and the differentiation of the cartilage growth plate, consequently impairing endochondral bone growth.
There exists a need for improved therapeutics that target dysfunctional FGFR3 for treating growth disorders, such achondroplasia.
The invention features improved sFGFR3 decoy polypeptides and methods of treatment using the same.
In a first aspect, the invention features a soluble Fibroblast Growth Factor (FGF) decoy polypeptide comprising a protein, said protein including an amino acid sequence including at least amino acid residues 1 to 310 or 1 to 323 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, wherein the variant has a sequence identity of at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 1 and specifically binds to an FGF (e.g., (FGF1), Fibroblast Growth Factor 2 (FGF2), Fibroblast Growth Factor 9 (FGF9), or Fibroblast Growth Factor (FGF 18)), in the presence or absence of a covalently linked heterologous polypeptide. When the heterologous polypeptide is present, it is generally present as a fusion protein that includes the aforementioned FGF binding moiety.
For example, the sFGF decoy polypeptide includes an amino acid sequence: (i) including at least amino acid residues 1 to 310 of the amino acid sequence of SEQ ID NO: 1, but not including at least amino acid residues 655 to 694 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, wherein the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 1; or (ii) including at least amino acid residues 1 to 357 of the amino acid sequence of SEQ ID NO: 2, but not including at least amino acid residues 703 to 741 of the amino acid sequence of SEQ ID NO: 2, or a variant of the amino acid sequence, wherein the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 2. Furthermore, the variant of (i) or (ii) specifically binds to an FGF (e.g., FGF1, FGF2, FGF9, or FGF 18). The fusion protein sFGF decoy polypeptide of the first aspect can also include an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 33, which is a fusion protein including an aggrecan-binding domain.
With respect to the fusion protein sFGF decoy polypeptide of the first aspect of the invention, the heterologous polypeptide can be an aggrecan-binding protein or fragment thereof. For example, the aggrecan-binding protein or fragment thereof can be selected from the group consisting of:
(a) a HPLN1 fragment including an amino acid sequence including at least amino acid residues 158 to 252, amino acid residues 259 to 349, or amino acid residues 158 to 349 of the amino acid sequence of SEQ ID NO: 3, or a variant of the amino acid sequence, in which the variant includes a sequence identity including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 3, and wherein the variant specifically binds to aggrecan;
(b) HPLN1 or a variant thereof, wherein the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 3, wherein the variant specifically binds to aggrecan;
(c) an antibody, an antibody derivative, or an antibody mimetic specific for aggrecan; or
(d) fibulin-1, borrelial aggrecan-binding protein (e.g., Borrelia glycosaminoglycan-binding protein (Bgp) and Borrelia burgdorferi high temperature requirement A (BbHtrA)), Cartilage oligomeric matrix protein/thrombospondin 5 (COMP/TSP5), or aggrecan-binding fragments thereof.
Alternatively, the heterologous polypeptide includes an Fc region.
In a second aspect, the invention features a soluble Fibroblast Growth Factor (sFGF) decoy polypeptide including an amino acid sequence: (i) including at least amino acid residues 1 to 310 or to 323 of the amino acid sequence of SEQ ID NO: 1, wherein the decoy polypeptide has a length of at least 311 amino acids, but not including at least amino acid residues 655 to 694 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 1; or (ii) including at least amino acid residues 1 to 357 of the amino acid sequence of SEQ ID NO: 2, but not including at least amino acid residues 703 to 741 of the amino acid sequence of SEQ ID NO: 2, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 2. In particular, the variant of (i) or (ii) specifically binds to an FGF (e.g., FGF1, FGF2, FGF9, or FGF 18).
In either the first or the second aspect of the invention, the fusion polypeptide or the sFGF decoy polypeptide can include:
(a) an amino acid sequence including amino acid residues 1 to 310 of the amino acid sequence of SEQ ID NO: 1, but not including amino acid residues 324 to 694 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) sequence identity to the amino acid sequence of SEQ ID NO: 1;
(b) an amino acid sequence including amino acid residues 1 to 357 of the amino acid sequence of SEQ ID NO: 2, but not including amino acid residues 371 to 741 of the amino acid sequence of SEQ ID NO:2, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 2;
(c) an amino acid sequence including amino acid residues 1 to 310 of the amino acid sequence of SEQ ID NO: 1, but not including amino acid residues 441 to 694 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 1;
(d) an amino acid sequence including amino acid residues 1 to 357 of the amino acid sequence of SEQ ID NO: 2, but not including amino acid residues 488 to 741 of the amino acid sequence of SEQ ID NO:2, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 2;
(e) an amino acid sequence including amino acid residues 1 to 310 of the amino acid sequence of SEQ ID NO: 1, but not including amino acid residues 549 to 694 of the amino acid sequence of SEQ ID NO: 1, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 1; or
(f) an amino acid sequence including amino acid residues 1 to 357 of the amino acid sequence of SEQ ID NO: 2, but not including amino acid residues 596 to 741 of the amino acid sequence of SEQ ID NO:2, or a variant of the amino acid sequence, in which the variant includes an amino acid sequence including at least 80% sequence identity to the amino acid sequence of SEQ ID NO: 2.
Furthermore, the variant of (a)-(f) specifically binds to an FGF (e.g., FGF1, FGF2, FGF9, or FGF 18).
Additionally, the sFGF decoy polypeptide can include (i) an amino acid sequence including amino acid residues 1 to 325 of the amino acid sequence of SEQ ID NO: 33, or (ii) an amino acid sequence including amino acid residues 1 to 338 of the amino acid sequence of SEQ ID NO: 33, or a variant of the amino acid sequence, in which the variant of (i) or (ii) includes an amino acid sequence including at least 80% sequence identity (e.g., at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity) to the amino acid sequence of SEQ ID NO: 33.
In another embodiment of the second aspect of the invention, the sFGF decoy polypeptide includes amino acids 1 to 310 of SEQ ID NO: 1 and also has a length of at least 311 amino acids.
In a third aspect, the invention features a nucleic acid encoding the fusion protein of the first aspect or the sFGF decoy polypeptide of the second aspect.
In a fourth aspect, the invention features a vector (e.g., a viral or other vector described herein) comprising the nucleic acid of the third aspect.
In a fifth aspect, the invention features a cell (such as a cell described herein) comprising the fusion protein of the first aspect , the sFGF decoy polypeptide of the second aspect, the nucleic acid of the third aspect, or the vector of the fourth aspect.
In a sixth aspect, the invention features the fusion protein of the first aspect, the sFGF decoy polypeptide of the second aspect, the nucleic acid of the third aspect, the vector of the fourth aspect or the cell of the fifth aspect for use as a medicament, in particular for use in the prevention or treatment of a skeletal growth retardation disorder, such as achondroplasia, in a subject in need thereof (e.g., a human). For instance, the skeletal growth retardation disorder is a FGFR3-related skeletal disease. The skeletal growth retardation disorder can be selected from the group consisting of achondroplasia, thanatophoric dysplasia type I (TDI), thanatophoric dysplasia type II (TDII), severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), hypochondroplasia, and a craniosynostosis syndrome. In particular, the skeletal growth retardation disorder is achondroplasia. Furthermore, the craniosynostosis syndrome is selected from the group consisting of Muenke syndrome, Crouzon syndrome, Apert syndrome, Jackson-Weiss syndrome, Pfeiffer syndrome, and Crouzonodermoskeletal syndrome.
The invention also features the fusion polypeptide of the first aspect or the sFGF decoy polypeptide of the second aspect formulated to provide about 0.0002 mg/kg/day to about 20 mg/kg/day of the fusion polypeptide or the sFGF decoy polypeptide to the subject in need thereof (e.g., a human). In particular, the fusion polypeptide or the sFGF decoy polypeptide are formulated to provide about 0.001 mg/kg/day to about 7 mg/kg/day of the fusion polypeptide or the sFGF decoy polypeptide to the subject in need thereof (e.g., a human).
In a seventh aspect, the invention features a method for monitoring the treatment of a skeletal growth retardation disorder including measuring body weight and/or skull size of a subject in need thereof (e.g., a human). In particular, body weight and/or skull size of the subject in need thereof (e.g., a human) are measured in response to administration of the fusion protein of the first aspect, the sFGF decoy polypeptide of the second aspect, the nucleic acid of the third aspect, the vector of the fourth aspect or the cell of the fifth aspect to the subject in need thereof (e.g., a human).
The invention also features a pharmaceutical composition including the fusion protein of the first aspect, the sFGF decoy polypeptide of the second aspect, the nucleic acid of the third aspect, the vector of the fourth aspect or the cell of the fifth aspect, and a pharmaceutically acceptable carrier for use in the prevention or treatment of a skeletal growth retardation disorder. The pharmaceutical composition can be formulated for subcutaneous, topical, oral, intranasal, intraocular, intravenous, or intramuscular administration. In particular, the pharmaceutical composition is formulated for subcutaneous administration.
Before the present invention is described in detail below, it is to be understood that this invention is not limited to the particular methodology, protocols and reagents described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.
Preferably, the terms used herein are defined as described in “A multilingual glossary of biotechnological terms: (IUPAC Recommendations)”, Leuenberger, H. G. W, Nagel, B. and Kölbl, H. eds. (1995), Helvetica Chimica Acta, CH-4010 Basel, Switzerland).
In the following, the elements of the invention will be described. These elements are listed with specific embodiments, however, it should be understood that they may be combined in any manner and in any number to create additional embodiments. The variously described examples and preferred embodiments should not be construed to limit the present invention to only the explicitly described embodiments. This description should be understood to support and encompass embodiments which combine the explicitly described embodiments with any number of the disclosed and/or preferred elements. Furthermore, any permutations and combinations of all described elements in this application should be considered disclosed by the description of the present application unless the context indicates otherwise.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising”, are to be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integer or step. As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural referents, unless the content clearly dictates otherwise.
The term “aggrecan” as used herein refers to a protein that in humans is encoded by the ACAN gene. It is also known as cartilage-specific proteoglycan core protein (CSPCP) and chondroitin sulfate proteoglycan 1. The gene is a member of the lectican (chondrotoitin sulfate proteoglycan) family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage. The protein is 2316 amino acids long and can be expressed in multiple isoforms fue to alternative splicing. The amino acid sequence can be obtained from the NCBI database (RefSeq accession number NP_001126).
An “aggrecan-binding protein” is a binding protein or fragment thereof that specifically binds to aggrecan, e.g., any protein or fragment thereof that interacts with the globular domain (G1, G2, or G3) of aggrecan. Exemplary aggrecan-binding proteins can include antibodies, fibulin-1, borrelial aggrecan-binding proteins (e.g., Borrelia glycosaminoglycan-binding protein (Bgp) and Borrelia burgdorferi high temperature requirement A (BbHtrA)), and cartilage oligomeric matrix protein/thrombospondin 5 (COMP/TSP5). For example, an aggrecan-binding protein may include human hyaluronan and proteoglycan link protein 1 (HPLN1) or fragments thereof. In particular, the HPLN1 fragment can include a cartilage link domain 1 (LK1; amino acids 158 to 252 of SEQ ID NO: 3), a cartilage link domain 2 (LK2; amino acids 259 to 349 of SEQ ID NO: 3), or both LK1 and LK2 domains (158 to 349 amino acids of SEQ ID NO: 3). Preferably, the HPLN1 fragment has an amino acid sequence excluding at least residues 53 to 140 of SEQ ID NO: 3, and/or excluding amino acids 1 to 140 or 1 to 157 of SEQ ID NO: 3. For example, an aggrecan-binding protein, such as HPLN1 or fragments thereof (e.g., amino acids 158 to 349 (LK1-LK2 domains) of SEQ ID NO: 3), may be fused to a sFGFR3 polypeptide fragment, such as a sFGFR3 polypeptide fragment including, e.g., amino acids 1 to 323 of SEQ ID NO: 1, in a sFGFR3 fusion polypeptide.
The term “binding protein” as used herein refers to proteins that specifically bind to another molecule. It is understood that the term includes fragments of the polypeptide so long as binding function is retained. Such binding proteins can include single binding domain proteins as well as multi-binding domain proteins. Multi-binding domain proteins include those proteins which contain two or more discreet and noncontiguous regions along the primary structure of the polypeptide which together contribute to the overall biding activity. A specific example of multi-binding domain proteins includes heavy and light antibody chains since the binding activity of each is derived from three noncontiguous complementarity determining regions. Binding proteins can be monomeric or multimeric species. Heteromeric binding proteins are a specific example of multimeric binding proteins which are composed of at least two different subunits which together exhibit binding activity toward a particular ligand. It is understood that when referring to multimeric binding proteins that the term includes fragments of the subunits so long as assembly of the polypeptides and binding function of the assembled complex is retained. Heteromeric binding proteins include, for example, antibodies and fragments thereof such as Fab and (Fab′)2 portions.
The term “biological activity of the parent polypeptide” refers to any activity or the parent polypeptide inside or outside a cell. For example, with respect to an aggrecan-binding protein, it is the ability to specifically bind aggrecan. With respect to the FGF decoy polypeptide, the term refers to (i) the capacity to specifically bind to FGF (e.g., FGF2); (ii) the capacity to reduce FGF intracellular signaling (e.g. Erk phosphorylation following FGFR3 receptor activation by its binding with FGFs); and/or (iii) the capacity to restore bone growth in vivo (e.g. in Fgfr3ach/+ mice).
The skilled in the art can easily determine whether a fragment or variant of a parent polypeptide is biologically active. It is noted that functional activation of the FGFR3 receptor may be readily assessed by the one skilled in the art according to known methods, as well as those described herein. Indeed, since activated FGFR3 receptor is phosphorylated on tyrosine residues located towards the cytoplasmic domain, i.e., on Tyr648 and Tyr647, functional activation of the FGFR3 receptor may for example be assessed by measuring its phosphorylation. For instance, analysis of ligand-induced phosphorylation of the FGFR3 receptor can be performed as described in Le Corre et al. (Org. Biomol. Chem., 8: 2164-2173, 2010). Alternatively, receptor phosphorylation in cells can be readily detected by immunocytochemistry, immunohistochemistry and/or flow cytometry using antibodies which specifically recognize this modification. For instance phosphorylation of FGFR3 on the Tyr648 and Tyr647 residues can be detected by immunocytochemistry, immunohistochemistry and/or flow cytometry using monoclonal or polyclonal antibodies directed against phosphorylated Tyr648 and Tyr647-FGFR3. Further, FGFR3, when associated with its ligand, mediates signaling by activating the ERK and p38 MAP kinase pathways, and the STAT pathway. Therefore, activation of FGFR3 receptor can also be assessed by determining the activation of these specific pathways as described by Horton et al. (Lancet, 370: 162-172, 2007).
The term “cell culture” refers to the process by which cells are grown under controlled conditions outside of their natural environment in or on a cell culture medium. The term “cell culture medium” refers to a liquid or gel for supporting the survival or growth of cells, especially cells as defined above, for example cells derived from multi-cellular eukaryotes, in particular animal cells. Such a medium comprises all nutrients required to support the survival or growth of such cells. The cell culture medium composition can be a dry powder composition, a liquid composition or a solid (e.g. gel or agar) composition. Suitable cell cultures and culturing techniques are well known in the art, see for example Peterson et al., Comp Immunol Microbiol Infect Dis. 1988; 11(2):93-8.
The term “codon-optimized” as used herein refers to the alteration of codons in the nucleic acid, in particular to reflect the typical codon usage of the host organism without altering the polypeptide encoded by the DNA. The host cell or host organism is preferably human. Codon-optimization can be performed by the skilled person without undue burden, e.g. by using online tools such as the JAVA Codon Adaption Tool (www.jcat.de) or Integrated DNA Technologies Tool (www.eu.idtdna.com/CodonOpt) by simply entering the nucleic acid sequence and the host organism for which the codons are to be optimized. The codon usage of different organisms is available in online databases, for example, on www.kazusa.or.jp/codon (to date 35,799 different organisms).
Optionally, the nucleic acid of the third aspect may be codon-optimized. With respect to the nucleic acid encoding for the fusion protein of the first aspect, only a part of the nucleic acid may be codon optimized, in particular one or more of the parts encoding for the detectable marker, the FGF decoy polypeptide, the peptide linker and/or the aggrecan-binding protein. With respect to the nucleic acid encoding for the FGF decoy polypeptide protein of the first aspect, only a part of the nucleic acid may be codon optimized, in particular one or more of the parts encoding for the detectable marker and/or the FGF decoy polypeptide. Preferably, the nucleic acid is codon-optimized to facilitate genetic manipulations by decreasing the GC content and/or for expression in a host cell.
The term “decoy” or “decoy receptor”, also known as “sink” or “trap”, refers to a receptor that binds a ligand, but is structurally incapable of signaling or presenting the agonist to signaling receptor complexes. A decoy acts as a molecular trap for the ligand, thereby preventing it from binding to its functional receptor. A decoy is preferably soluble. A decoy can be a sFGFR3 polypeptide or a fragment thereof as described herein.
The term “detectable label”, “marker” or “tag” as used herein refers to any kind of substance which is able to indicate the presence of another substance or complex of substances, in particular of the fusion protein of the first aspect or of the soluble FGF decoy polypetide of the second aspect. The detectable label can be a substance that is linked to or introduced in the substance to be detected. Preferred is a detectable label suitable for allowing for purification, quantification and/or in vivo detection. Examples of suitable labels include, but are not limited to, a fluorophore, a chromophore, a radiolabel, a metal colloid, an enzyme, or a chemiluminescent or bioluminescent molecule. In the context of the present invention suitable tags are preferably protein tags whose peptide sequences are genetically grafted into or onto a recombinant protein. Protein tags may e.g. encompass affinity tags, solubilization tags, chromatography tags, epitope tags, or fluorescence tags. Affinity tags are appended to proteins so that they can be purified from their crude biological source using an affinity technique. These include chitin binding protein (CBP), maltose binding protein (MBP), and glutathione-S-transferase (GST). The poly(His) tag is a widely used protein tag which binds to metal matrices. Solubilization tags are used, especially for recombinant proteins expressed in chaperone-deficient species to assist in the proper folding in proteins and keep them from precipitating. These include thioredoxin (TRX) and poly(NANP). Some affinity tags have a dual role as a solubilization agent, such as MBP, and GST. Chromatography tags are used to alter chromatographic properties of the protein to afford different resolution across a particular separation technique. Often, these consist of polyanionic amino acids, such as FLAG-tag. Epitope tags are short peptide sequences which are chosen because high-affinity antibodies can be reliably produced in many different species. These are usually derived from viral genes, which explain their high immunoreactivity. Epitope tags include V5-tag, Myc-tag, and HA-tag. These tags are particularly useful for western blotting, immunofluorescence and immunoprecipitation experiments, although they also find use in antibody purification. Fluorescence tags are used to give visual readout on a protein. GFP and its variants (e.g. mutant GFPs having a different fluorescent spectrum) and RFP and its variants (e.g., mutant RFPs having a different fluorescent spectrum) are the most commonly used fluorescence tags. More advanced applications of GFP/RFP include using it as a folding reporter (fluorescent if folded, colorless if not). Further examples of fluorophores include fluorescein, rhodamine, and sulfoindocyanine dye Cy5.
Preferred examples of a detectable label include but are not limited to AviTag (a peptide allowing biotinylation by the enzyme BirA and isolation by streptavidin (GLNDIFEAQKIEWHE, SEQ ID NO: 11)), Calmodulin-tag (a peptide bound by the protein calmodulin (KRRWKKNFIAVSAANRFKKISSSGAL, SEQ ID NO: 12)), polyglutamate tag (a peptide binding efficiently to anion-exchange resin such as Mono-Q (EEEEEE, SEQ ID NO: 13)), E-tag (a peptide recognized by an antibody (GAPVPYPDPLEPR, SEQ ID NO: 14)), FLAG-tag (a peptide recognized by an antibody (DYKDDDDK, SEQ ID NO: 15)), HA-tag (a peptide recognized by an antibody (YPYDVPDYA, SEQ ID NO: 16)), His-tag (5-10 histidines bound by a nickel or cobalt chelate (HHHHHH, SEQ ID NO: 17)), Myc-tag (a short peptide recognized by an antibody (EQKLISEEDL, SEQ ID NO: 18)), S-tag (KETAAAKFERQHMDS, SEQ ID NO: 19), SBP-tag (a peptide which binds to streptavidin (MDEKTTGWRGGHVVEGLAGELEQLRA RLEHHPQGQREP, SEQ ID NO: 20)), Softag 1 (for mammalian expression (SLAELLNAGLGGS, SEQ ID NO: 21)), Softag 3 (for prokaryotic expression (TQDPSRVG, SEQ ID NO: 22)), Strep-tag (a peptide which binds to streptavidin or the modified streptavidin called streptactin (Strep-tag II: WSHPQFEK, SEQ ID NO: 23)), TC tag (a tetracysteine tag that is recognized by FlAsH and ReAsH biarsenical compounds (CCPGCC, SEQ ID NO: 24)), V5 tag (a peptide recognized by an antibody (GKPIPNPLLGLDST, SEQ ID NO: 25)), VSV-tag (a peptide recognized by an antibody (YTDIEMNRLGK, SEQ ID NO: 26)), Xpress tag (DLYDDDDK, SEQ ID NO: 27), Isopeptag (a peptide which binds covalently to pilin-C protein (TDKDMTITFTNKKDAE, SEQ ID NO: 28)), SpyTag (a peptide which binds covalently to SpyCatcher protein (AHIVMVDAYKPTK, SEQ ID NO: 29)), BCCP (Biotin Carboxyl Carrier Protein, a protein domain biotinylated by BirA enabling recognition by streptavidin), Glutathione-S-transferase-tag (a protein which binds to immobilized glutathione), Green fluorescent protein-tag (a protein which is spontaneously fluorescent and can be bound by nanobodies), Maltose binding protein-tag (a protein which binds to amylose agarose), Nus-tag, Thioredoxin-tag, Fc-tag (derived from immunoglobulin Fc domain), Ty tag, Designed Intrinsically Disordered tags containing disorder promoting amino acids (P,E,S,T,A,Q,G; see Minde et al., Designing disorder: Tales of the unexpected tails. Intrinsically Disord. Proteins 1, e26790 1-5 (2013)).
The detectable label can be linked to the fusion protein via a cleavable sequence. Preferably, the sequence is recognizable and cleavable by a protease. The protease is preferably an enterokinase. In particular, it is preferred that the first (i.e., the N-terminal) residue of the cleavable sequence is not proline. The length of the cleavable sequence is preferably 2-20, 3-15 or 4-10 amino acids. An exemplary cleavable sequence is LVDQIPA (SEQ ID NO: 30). Preferably, the detectable label is at the N-terminus or at the C-terminus of the fusion protein of the first aspect, more preferably it is at the N-terminus. For example, the detectable label, such as a FLAG-tag (e.g., SEQ ID NO: 15) may be at the N-terminus of the sFGFR3 fusion polypeptide (see, e.g., amino acid residues 1 to 8 of SEQ ID NO: 4). Alternatively, the detectable label, such as a FLAG-tag (e.g., SEQ ID NO: 15), may be at the C-terminus of the sFGFR3 fusion polypeptide. Additionally, a detectable label, such as a FLAG-tag (e.g., SEQ ID NO: 15), may be at the N-terminus or at the C-terminus of a sFGFR3 polypeptide, e.g., sFGFR3_Del2 (amino acids 1 to 548 of SEQ ID NO: 1), sFGFR3_Del3 (amino acids 1 to 440 of SEQ ID NO: 1), and sFGFR3_Del4 (amino acids 1 to 323 of SEQ ID NO: 1).
The term “eukaryotic cell” is in particular a yeast or an animal cell. A yeast cell can be, in the broadest sense, any cell of a yeast organism, for example a cell from Kluyveromyces lactis, Kluyveromyces marxianus var. marxianus, Kluyveromyces thermotolerans, Candida utilis, Candida tropicalis, Candida albicans, Candida lipolytica and Candida versatilis, of the genus Pichia like Pichia stipidis, Piachia pastoris and Pichia sorbitophila, Cryptococcus, Debaromyces, Hansenula, Saccharomycecopsis, Saccharomycodes, Schizosaccharomyces, Wickerhamia, Debayomyces, Hanseniaspora, Kloeckera, Zygosaccharomyces, Ogataea, Kuraishia, Komagataella, Metschnikowia, Williopsis, Nakazawaea, Cryptococcus, Torulaspora, Bullera, Rhodotorula, Willopsis or Sporobolomyces. Preferably, though, the yeast cell is a Saccharomyces cell, in particular a Saccharomyces cerevisiae cell.
An animal cell may be a cell of a primate, mouse, rat, rabbit, dog, cat, hamster, cow, insect (e.g. Sf9 or Sf21) etc., preferably a human. Also, it may be a suspension or an adherent cell. A suspension cell is a cell that may naturally live in suspension (i.e. without being attached to a surface), or a cell that has been modified to be able to survive in suspension cultures, for example to be grown to higher densities than adherent conditions would allow. An adherent cell is a cell that requires a surface, such as tissue culture plastic or a microcarrier, which may be coated with extracellular matrix components (such as collagen and laminin) to increase adhesion properties and provide other signals needed for growth and differentiation. In one embodiment, the adherent cell is a monolayer cell. For example, the cell is selected from the group consisting of a hybridoma cell, a primary epithelial cell, an endothelial cell, a keratinocyte, a monocyte/macrophage, a lymphocyte, a hematopoietic stem cell, a fibroblast, a chondrocyte and a hepatocyte. More specifically, it may be selected from the group consisting of a CHO-K1 SV cell, a CHO DG44 cell, a CHO DP-12 cell, a CHO DHFR− cell, a CHO-GS cell, a BHK-21 cell, a HEK-293 embryonic kidney cell, a HeLa cervical epithelial cell, a PER-C6 retinal cell, an MDCK cell, an HDMEC cell, a HepG2 cell, an HL-60 cell, an HMEC-1 cell, a HUVEC cell, an HT1080 cell, a Jurkat cell, an MRC5 cell, a K562 cell, a HeLa cell, an NS0 cell, an Sp20 cell, a COS cell, and a VERO cell.
The term “extracellular domain” or “ECD” refers to the portion of a polypeptide (e.g., a FGFR3 polypeptide) that extends beyond the transmembrane domain into the extracellular space. As is described above, the ECD includes the IgG1 domain (aa 57-110), the IgG2 domain (aa 161-245), and the IgG3 domain (aa 268-357). An ECD of a FGFR3 may include a complete ECD (aa 57-110 of FGFR3) or may include a fragment of the ECD, such as an FGFR3 ECD that is lacking one or more amino acids present in the full length FGFR3 ECD. The ECD mediates binding of FGFRs to one or more FGFs. For instance, a soluble FGFR (e.g., sFGFR3) will include at least a portion of the ECD of the FGFR polypeptide. Exemplary ECDs of FGFR3 polypeptides may include, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, or 1 to 365 of SEQ ID NO: 1.
In the context of the invention, the term “FGFR3-related skeletal disease” is intended to mean a skeletal disease that is caused by an abnormal increased activation of FGFR3, in particular by expression of a gain-of-function mutant of the FGFR3 receptor. As used herein, the terms “gain-of-function FGFR3 receptor variant”, “gain-of-function mutant of the FGFR3” or “mutant FGFR3 displaying a prolonged activity” are used interchangeably and refer to a mutant of said receptor exhibiting a biological activity (i.e., triggering downstream signaling) which is higher than the biological activity of the corresponding wild-type receptor in the presence of FGF ligand. The FGFR3-related skeletal diseases are preferably FGFR3-related skeletal dysplasias and FGFR3-related craniosynostosis. The FGFR3-related skeletal dysplasias according to the invention may correspond to an inherited or to a sporadic disease. FGFR3-related skeletal dysplasias can include, but are not limited to, thanatophoric dysplasia type I, thanatophoric dysplasia type II, hypochondroplasia, achondroplasia and SADDAN (severe achondroplasia with developmental delay and acanthosis nigricans), Crouzon syndrome with acnthosis nigricans, Muenke syndrome, and CATSHL (camptodactyly, tall stature, scoliosis, and hearing loss).
For example, the FGFR3-related skeletal dysplasia is an achondroplasia caused by expression of the G380R gain-of-function mutant of the FGFR3 receptor. Alternatively, the FGFR3-related skeletal dysplasia is an achondroplasia caused by expression of the G375C, G346E, or S279C of the FGFR3 receptor. It is further noted that achondroplasia caused by another mutant of the FGFR3 receptor which would be identified in the future is also encompassed. The FGFR3-related skeletal dysplasia can also be a hypochondroplasia caused by expression of the N540K, K650N, K650Q, S84L, R200C, N262H, G268C, Y278C, V381E, gain-of-function mutant of the FGFR3 receptor. The FGFR3-related skeletal dysplasia can further be a thanatophoric dysplasia type I caused by expression of a gain-of-function mutant of the FGFR3 receptor chosen from the group consisting of R248C, S248C, G370C, S371C; Y373C, X807R, X807C, X807G, X807S, X807W and K650M FGFR3 receptors or a thanatophoric dysplasia type II caused by expression of the K650E gain-of-function mutant of the FGFR3 receptor. Additionally, the FGFR3-related skeletal dysplasia can be a severe achondroplasia with developmental delay and acanthosis nigricans caused by expression of the K650M gain-of-function mutant of the FGFR3 receptor.
The term “Fibroblast Growth Factor” or “FGF” refers to a member of the FGF family, which in humans comprises structurally related signaling molecules. The term preferably refers to any of FGF1, FGF2, FGF3, FGF4, FGF5, FGF6, FGF7, FGF8, FGF9, FGF10 and FGF18, which all bind fibroblast growth factor receptors (FGFRs). More preferably, it refers to at least FGF1, FGF2, FGF9 and/or FGF 18, which have been shown to bind FGFR3. Thus, the FGF referred to in all aspects and embodiments described herein is preferably FGF1, FGF2, FGF9 and/or FGF 18. Nevertheless, it must be borne in mind that other FGFs may also bind FGFR3 and are therefore also within the scope of the term FGF according to the invention.
A preferred FGF1 is human FGF1 having the amino acid sequence according to SEQ ID NO: 7. A preferred FGF2 is human FGF2 having the amino acid sequence according to SEQ ID NO: 8. A preferred FGF9 is human FGF9 having the amino acid sequence according to SEQ ID NO: 9. A preferred FGF18 is human FGF18 having the amino acid sequence according to SEQ ID NO: 10.
The term “Fibroblast Growth Factor Receptor 3”, “FGFR3” or “FGFR3 receptor”, as used herein, refers to any naturally occurring and functionally signalling FGFR3 polypeptide. In particular, FGFR3 refers to a polypeptide that specifically binds one or more FGFs (e.g., FGF1, FGF2, FGF9 and/or FGF 18). The human FGFR3 gene, which is located on the distal short arm of chromosome 4, encodes an 806 amino acid protein precursor (fibroblast growth factor receptor 3 isoform 1 precursor), which contains 19 exons. FGFRs (e.g., FGFR3) are tyrosine kinases spanning the cellular membrane, which are activated by binding of ligands of the FGF family of growth factors. FGFR3 and other FGFRs consist of three extracellular immunoglobulin-like domains of a membrane spanning domain and of two intracellular tyrosine kinase domains. FGFR3 can include all or fragment thereof and/or any mutation of a FGFR3 polypeptide, including soluble fragments of FGFR3, as well as polymorphic forms and splice variants. Mutations in the FGFR3 gene lead to craniosynostosis and multiple types of skeletal dysplasia, such as substitutions of a glycine residue at position 380 with an arginine residue (i.e., G380R). Alternative splicing occurs and additional variants have been described, including those utilizing alternate exon 8 rather than 9, but their full-length nature has not been determined. The FGFR3 receptor comprises an extracellular domain (amino acid residues 1 to 366), a transmembrane domain (amino acid residues 367 to 399) and an intracellular domain (amino acid residues 400 to 806). The extracellular domain comprises the IgG1 domain (amino acid residues 57 to 110), the IgG2 domain (amino acid residues 161 to 245) and the IgG3 domain (amino acid residues 268 to 357). The intracellular domain comprises two tyrosine kinase domains (amino acid residues 459 to 792). The naturally occurring human FGFR3 gene has a nucleotide sequence as shown in Genbank Accession number NM_000142.4 and the naturally occurring human FGFR3 protein has an amino acid sequence as shown in Genbank Accession number NP_000133, herein represented by SEQ ID NO: 6.
The term “fragment” is meant a portion of a polypeptide or nucleic acid molecule that contains, preferably, at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or more of the entire length of the reference nucleic acid molecule or polypeptide. A fragment may contain, e.g., 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 500, 600, 700, or more amino acid residues, up to the entire length of the reference polypeptide (e.g., FGFR3).
For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 50% (e.g., 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more) sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 50% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 55% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 60% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 65% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 70% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 75% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 80% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 85% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 90% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment may include any polypeptide having at least 95% sequence identity to a fragment of SEQ ID NO: 1, e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, or 1 to 680 of SEQ ID NO: 1. For example, a FGFR3 polypeptide fragment can include, e.g., amino acids 1 to 323 of SEQ ID NO: 1 (sFGFR3_Del4), amino acids 1 to 440 of SEQ ID NO: 1 (sFGFR3_Del3), or amino acids 1 to 548 of SEQ ID NO: 1 (sFGFR3_Del2). In an embodiment, a sFGFR3 polypeptide fragment consisting of amino acids 1 to 694 (sFGFR3_Del1) of SEQ ID NO: 1 is excluded as a soluble FGFR3 polypeptide within the scope of the invention.
The term “fusion protein” or “fusion polypeptide” relates to a protein comprising two or more polypeptides, preferably functional domains, derived from different proteins. The two or more polypeptides are linked directly or indirectly by peptide bonds. A fusion protein is generated by joining two or more nucleic acid sequences. This can be done recombinantly and also via nucleic acid synthesis. Translation of this fusion construct results in a single protein with the functional properties derived from the two or more polypeptides.
As used herein, the term “idiopathic skeletal growth retardation disorder” refers to a skeletal disease the cause of which is unknown and for which treatment with exogenous growth hormone (GH), e.g. recombinant human GH (rhGH), is ineffective.
The term “monitoring” as used herein refers to the accompaniment of a diagnosed skeletal growth retardation disorder during a treatment procedure or during a certain period of time, typically during at least 1 week, 2 weeks, 3 weeks, 4 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 1 year, 2 years, 3 years, 5 years, 10 years 15 years, or any other period of time. The term “accompaniment” means that states of and, in particular, changes of the state of the skeletal growth retardation disorder may be detected based on the body weight and/or skull length and/or width of the subject, particular based on changes therein in any type of periodical time segment, determined e.g., 1, 2, 3, 4 or more times per month or per year, or approximately every 1, 2, 3, 4, 5, 6, 7, 8, 12 or 16 weeks, over the course of the treatment. Body weight and/or skull size of the subject or changes thereof can also be determined at treatment specific events, e.g. before and/or after every treatment or drug/therapy administration.
The term “nucleic acid” or “nucleic acid molecule” is to be understood as a single or double-stranded oligo- or polymer of deoxyribonucleotide or ribonucleotide bases or both. Typically, a nucleic acid is formed through phosphodiester bonds between the individual nucleotide monomers. In the context of the present invention, the term nucleic acid includes but is not limited to ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) molecules. The depiction of a single strand of a nucleic acid also defines (at least partially) the sequence of the complementary strand. The nucleic acid may be single or double stranded, or may contain portions of both double and single stranded sequences. The nucleic acid may be obtained by biological, biochemical or chemical synthesis methods or any of the methods known in the art. As used herein, the term “nucleic acid” comprises the terms “polynucleotide” and “oligonucleotide”. In the context of the present invention, the term nucleic acid comprises in particular cDNA, recombinant DNA, and mRNA. The nucleic acid can also be an artificial nucleic acid. Artificial nucleic acids include polyamide or peptide nucleic acid (PNA), morpholino and locked nucleic acid (LNA), as well as glycol nucleic acid (GNA) and threose nucleic acid (TNA). Each of these is distinguished from naturally-occurring DNA or RNA by changes to the backbone of the molecule.
A “peptide linker”, “linker” or “splicer” in the context of the present invention refers to a peptide chain of between 1 and 100 amino acids. In preferred embodiments, a peptide linker according to the present invention has a minimum length of at least 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids. In further preferred embodiments, a peptide linker according to the present invention has a maximum length of 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 34, 33, 32, 31, 30, 29, 28, 27, 26, 25, 24, 23, 22, 21, or 20 amino acids. Preferred ranges are 5 to 25 and 10 to 20 amino acids in length. It is preferred that the peptide linker is a flexible peptide linker, i.e. provides flexibility among the two fusion protein members that are linked together. Such flexibility is generally increased if the amino acids are small and do not have bulky side chains that impede rotation or bending of the amino acid chain. Thus, preferably the peptide linker of the present invention has an increased content of small amino acids, in particular of glycins, alanines, serines, threonines, leucines and isoleucines. Preferably, at least 20%, 30%, 40%, 50%, 60% 70%, 80, 90% or more of the amino acids of the peptide linker are small amino acids.
For example, the amino acids of the linker are selected from glycines and serines, i.e., said linker is a poly-glycine or a poly-glycine/serine linker, wherein “poly” means a proportion of at least 50%, 60% 70%, 80, 90% or even 100% glycine and/or serine residues in the linker. In especially preferred embodiments, the above-indicated preferred minimum and maximum lengths of the peptide linker according to the present invention may be combined. In further preferred embodiments, the peptide linker of the present invention is non-immunogenic; in particularly preferred embodiments, the peptide linker is non-immunogenic in humans. For example, the sFGFR3 fusion polypeptide described herein (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33) can include a glycine and serine linker, such as the amino acid sequence SGSGSGSGSGSGSGS.
“Pharmaceutically” or “pharmaceutically acceptable” refers to molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to a mammal, especially a human, as appropriate. A pharmaceutically acceptable carrier or excipient refers to a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. The form of the pharmaceutical compositions, the route of administration, the dosage and the regimen naturally depend upon the condition to be treated, the severity of the illness, the age, weight, and sex of the subject, etc. The pharmaceutical compositions of the invention can be formulated for a topical, oral, intranasal, intraocular, intravenous, intramuscular or subcutaneous administration and the like.
The term “polypeptide” as used herein refers to any peptide-linked chain of amino acids, regardless of length or post-translational modification. A polypeptide usable in the present invention can be further modified by chemical modification. This means that a chemically modified polypeptide comprises other chemical groups than the naturally occurring amino acids. Examples of such other chemical groups include, without limitation, glycosylated amino acids and phosphorylated amino acids. Chemical modifications of a polypeptide may provide advantageous properties as compared to the parent polypeptide, e.g., one or more of enhanced stability, increased biological half-life, or increased water solubility. Chemical modifications applicable to a polypeptide of the invention include without limitation: PEGylation, glycosylation of non-glycosylated polypeptides, or the modification of the glycosylation pattern present in the polypeptide. Further exemplary modifications include: replacement(s) of an amino acid with a modified and/or unusual amino acid, e.g. a replacement of an amino acid with an unusual amino acid like Nle, Nva or Orn; modifications to the N-terminal and/or C-terminal ends of the peptides, such as, e.g., N-terminal acylation (preferably acetylation) or desamination, or modification of the C-terminal carboxyl group into an amide or an alcohol group; modifications at the amide bond between two amino acids: acylation (preferably acetylation) or alkylation (preferably methylation) at the nitrogen atom or the alpha carbon of the amide bond linking two amino acids; modifications at the alpha carbon of the amide bond linking two amino acids, such as, e.g., acylation (preferably acetylation) or alkylation (preferably methylation) at the alpha carbon of the amide bond linking two amino acids; chirality changes, such as, e.g., replacement of one or more naturally occurring amino acids (L enantiomer) with the corresponding D-enantiomers; retro-inversions in which one or more naturally-occurring amino acids (L-enantiomer) are replaced with the corresponding D-enantiomers, together with an inversion of the amino acid chain (from the C-terminal end to the N-terminal end); azapeptides, in which one or more alpha carbons are replaced with nitrogen atoms; and/or betapeptides, in which the amino group of one or more amino acid is bonded to the β carbon rather than the α carbon.
As used herein, “prevent”, “preventing” or “prevention” of a disease or disorder means preventing that such disease or disorder occurs in subject.
The term “prokaryotic cell” as used herein refers to any kind of bacterial organism suitable for application in recombinant DNA technology such as cloning or protein expression includes both Gram-negative and Gram-positive microorganisms. Suitable bacteria may be selected from e.g. Escherichia (in particular E. coli), Anabaena, Caulobacter, Gluconobacter, Rhodobacter, Pseudomonas, Paracoccus, Bacillus, Brevibacterium, Corynebacterium, Rhizobium (Sinorhizobium), Flavobacterium, Klebsiella, Enterobacter, Lactobacillus, Lactococcus, Methylobacterium, Propionibacterium, Staphylococcus or Streptomyces.
The term “skeletal growth retardation disorder”, as used herein, refers to a skeletal disease characterize by deformities and/or malformations of the bones. These disorders include, but are not limiting to, skeletal growth retardation disorders caused by growth plate (physeal) fractures, idiopathic skeletal growth retardation disorders and FGFR3-related skeletal diseases. For example, the skeletal growth retardation disorder may include a skeletal dysplasia, e.g., achondroplasia, homozygous achondroplasia, heterozygous achondroplasia, achondrogenesis, acrodysostosis, acromesomelic dysplasia, atelosteogenesis, camptomelic dysplasia, chondrodysplasia punctata, rhizomelic type of chondrodysplasia punctata, cleidocranial dysostosis, congenital short femur, craniosynostosis (e.g., Muenke syndrome, Crouzon syndrome, Apert syndrome, Jackson-Weiss syndrome, Pfeiffer syndrome, or Crouzonodermoskeletal syndrome), dactyly, brachydactyly, camptodactyly, polydactyly, syndactyly, diastrophic dysplasia, dwarfism, dyssegmental dysplasia, enchondromatosis, fibrochondrogenesis, fibrous dysplasia, hereditary multiple exostoses, hypochondroplasia, hypophosphatasia, hypophosphatemic rickets, Jaffe-Lichtenstein syndrome, Kniest dysplasia, Kniest syndrome, Langer-type mesomelic dysplasia, Marfan syndrome, McCune-Albright syndrome, micromelia, metaphyseal dysplasia, Jansen-type metaphyseal dysplasia, metatrophic dysplasia, Morquio syndrome, Nievergelt-type mesomelic dysplasia, neurofibromatosis (e.g., type 1, e.g., with bone manifestations or without bone manifestations; type 2; schwannomatosis; or any described herein), osteoarthritis, osteochondrodysplasia, osteogenesis imperfecta, perinatal lethal type of osteogenesis imperfecta, osteopetrosis, osteopoikilosis, peripheral dysostosis, Reinhardt syndrome, Roberts syndrome, Robinow syndrome, short-rib polydactyly syndromes, short stature, spondyloepiphyseal dysplasia congenita, spondyloepimetaphyseal dysplasia, or thanatophoric dysplasia. Accordingly, the invention provides for the treatment or prevention of symptoms of a skeletal growth retardation disorder, e.g., achondroplasia.
The term “soluble” as used herein indicates that the protein or polypeptide, in particular a receptor, is not directly bound to a cellular membrane, and is, accordingly, characterized by the absence or functional disruption of all or a substantial part of the transmembrane (i.e., lipophilic) domain, so that the soluble protein or polypeptide is devoid of any membrane anchoring function. The cytoplasmic domains may also be absent. In this respect, the transmembrane domain of FGFR3 extends from amino acid 367-399 of the wild-type sequence according to SEQ ID NO: 6 and the cytoplasmic domain of FGFR3 extends from amino acid 400-806 of the wild-type sequence according to SEQ ID NO: 6. The extracellular domain (ECD) of FGFR3 extends from amino acids 1 to 366 of the wild-type FGFR3 sequence according to SEQ ID NO: 6 or fragments thereof.
Exemplary sFGFR3 polypeptides can include, but are not limited to, at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, 1 to 680, or 1 to 690 of SEQ ID NO: 1. Additionally, sFGFR3 polypeptides can include any polypeptide having at least 50% (e.g., 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more) sequence identity to any of these sFGFR3 polypeptide fragments. For example, sFGFR3 polypeptides can include fragments of sFGFR3_Del1 (SEQ ID NO: 1). sFGFR3_Del1 (SEQ ID NO: 1) features a deletion of amino acids 311 to 422 of SEQ ID NO: 6. In particular, sFGFR3 polypeptides may include, e.g., amino acids 1 to 323 of SEQ ID NO: 1 (sFGFR3_Del4), amino acids 1 to 440 of SEQ ID NO: 1 (sFGFR3_Del3), or amino acids 1 to 548 of SEQ ID NO: 1 (sFGFR3_Del2). sFGFR3 polypeptides may also include a deletion of the N-terminus of the sFGFR3 polypeptide (e.g., amino acid residue 1 to 56 of SEQ ID NO: 1).
The term “soluble FGFR3 polypeptide” or “sFGFR3 polypeptide” as used herein refers to a FGFR3 polypeptide that is characterized by the absence or functional disruption of all or a substantial part of the transmembrane (i.e., lipophilic) domain and also does not contain any polypeptide portion that would anchor the FGFR3 polypeptide to a cell membrane. A sFGFR3 polypeptide is thus a non-membrane bound form of a FGFR3 polypeptide. In particular, the transmembrane domain of FGFR3 extends from amino acid residues 367 to 399 of the wild-type FGFR3 sequence (SEQ ID NO: 6). Thus the sFGFR3 polypeptide includes a deletion of amino acid residues 367 to 399 of the wild-type FGFR3 polypeptide sequence (SEQ ID NO: 6). The sFGFR3 polypeptide can further include deletions of the cytoplasmic domain of the wild-type FGFR3 polypeptide sequence (amino acid residues 400-806 of SEQ ID NO: 6). Additionally, the sFGFR3 can include deletions of the extracellular domain of the wild-type FGFR3 polypeptide sequence (amino acid residues 1 to 366 of SEQ ID NO: 6).
The term “specifically binds” as used herein refers to a binding reaction which is determinative of the presence of the herein defined binding partner (e.g., FGF or aggrecan) in a heterogeneous population of proteins and, in particular, cells, such as in an organism, preferably a human body. As such, the specified ligand binds to its defined binding partner and does not bind in a substantial amount to other molecules present in an organism, preferably human organism, and more preferably in extracellular fluids (e.g. interstitial fluid and plasma) or in/on the extracellular matrix, in particular the cartilage. Generally, a ligand that “specifically binds” a target molecule has an equilibrium dissociation constant KD is less than about 10−5 (e.g., 10−6, 10−7, 10−8, 10−9, 10−10, 10−11, and 10−12 or less) for that target molecule, preferably at room temperature (e.g., 20° C. to 25° C.). Methods of how to measure equilibrium dissociation constants are well known in the art. A preferred method uses a BiaCore® system. In particular with respect to a fragment and/or variant of a protein (such as an aggrecan-binding protein or FGFR3) that specifically binds another protein, specifically binds means that it has at least 10, 20, 30, 40, 50, 60, 70, 80, or 90% of the binding activity of the protein it is derived from (i.e., of the aggrecan-binding protein or FGFR3, respectively). For a suitable binding assay, see Example 1 (FGF/Aggrecan binding) and Example 4. Other proteins or fragments or variants thereof can be tested accordingly.
As used herein, the term “subject” or “patient” denotes a human or non-human mammal, such as a rodent, a feline, a canine, an equine, or a primate. Preferably, the subject is a human being, more preferably a child (i.e. in terms of the present invention a human that is still growing, particularly in height). It is noted that the cartilaginous matrix of the growth plate is less dense in a newborn or in a child than in an adult. Therefore, without wishing to be bound by theory, one can expect that the polypeptides of the invention will better penetrate said cartilaginous matrix in a newborn or a child. In one embodiment, the subject has been diagnosed as suffering from a skeletal growth retardation disorder as described herein, in particular an FGFR3-related skeletal disease.
As used herein, “treat”, “treating”, or “treatment” of a disease or disorder means accomplishing one or more of the following: (a) reducing the severity of the disorder; (b) limiting or preventing development of symptoms characteristic of the disorder(s) being treated; (c) inhibiting worsening of symptoms characteristic of the disorder(s) being treated; (d) limiting or preventing recurrence of the disorder(s) in an individual that have previously had the disorder(s); and (e) limiting or preventing recurrence of symptoms in individuals that were previously symptomatic for the disorder(s).
The above preferably applies to one or more symptoms of achondroplasia, which include: short stature, a long trunk, and shortened limbs, which are noticeable at birth; an adult height of between 42-56 inches; a head that is large and a forehead that is prominent; portions of the face can be underdeveloped; at birth, the legs appear straight, but as a child begins to walk, he or she develops a knock-knee or bowed-leg deformity; the hands and the feet appear large, but the fingers and toes are short and stubby; straightening of the arm at the elbow may be limited, but usually does not keep a patient from doing any specific activities; children may develop an excessive curve of the lower back and a waddling walking pattern; dental problems, e.g. from overcrowding of teeth; weight control problems; neurologic and respiratory problems; and/or fatigue, pain, and numbness in the: Lower back and/or spine.
The term “variant” is, with respect to polypeptides, to be understood as a polypeptide which differs in comparison to the polypeptide from which it is derived by one or more changes in the amino acid sequence. The polypeptide from which a protein variant is derived is also known as the parent polypeptide. Typically, a variant is constructed artificially, preferably by gene-technological means. Typically, the parent polypeptide is a wild-type protein or wild-type protein domain. The variants usable in the present invention may also be derived from homologs, orthologs, or paralogs of the parent polypeptide. The changes in the amino acid sequence may be amino acid exchanges, insertions, deletions, N-terminal truncations, or C-terminal truncations, or any combination of these changes, which may occur at one or several sites. In preferred embodiments, a variant usable in the invention exhibits a total number of up to 200 (up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, or 200) changes in the amino acid sequence (i.e. exchanges, insertions, deletions, N-terminal truncations, and/or C-terminal truncations). The amino acid exchanges may be conservative and/or non-conservative. In preferred embodiments, a variant usable in the present invention differs from the protein or domain from which it is derived by up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 amino acid exchanges, preferably conservative amino acid changes. Alternatively or additionally, a “variant” as used herein can be characterized by a certain degree of sequence identity to the parent polypeptide from which it is derived. More precisely, a protein variant in the context of the invention exhibits at least 80% sequence identity to its parent polypeptide. Preferably, the sequence identity of protein variants is over a continuous stretch of 20, 30, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 400, 500, 600 or more amino acids, more preferably over the entire length of the reference polypeptide (the parent polypeptide). The term “at least 80% sequence identity” is used throughout the specification with regard to polypeptide sequence comparisons. This expression preferably refers to a sequence identity of at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% to the respective reference polypeptide. Preferably, the polypeptide in question and the reference polypeptide exhibit the indicated sequence identity over a continuous stretch as specified above.
The sequence identity of a “variant” polypeptide of the invention can be determined over an identified range of an amino acid sequence of a sFGF decoy polypeptide of the invention (e.g., amino acids 1 to 310 of SEQ ID NO: 1) or with reference to the entire amino acid sequence of an identified sFGF decoy polypeptide (e.g., all of the amino acids of SEQ ID NO: 1). When determining the percent sequence identity for a variant polypeptide of the invention, the sequence alignment may omit any specifically excluded amino acid residues (e.g., amino acids 367 to 399 of SEQ ID NO: 6 or amino acids 324 to 694 of SEQ ID NO: 1). For example, for a variant polypeptide of a sFGF decoy polypeptide of the invention that exhibits at least 80% sequence identity to amino acids 1 to 310 of SEQ ID NO: 1, the sequence alignment for comparison may occur across only amino acids 1 to 310 or may take into account two or more identified ranges of amino acid sequences within the full length sFGF decoy polypeptide.
The term “variant” is, with respect to nucleic acids, to be understood as a polynucleotide which differs in comparison to the nucleic acid from which it is derived by one or more changes in the nucleotide sequence. The nucleic acid from which variant is derived is also known as the parent nucleic acid. Typically, a variant is constructed artificially, preferably by gene-technological means. Typically, the parent nucleic acid is a wild-type nucleic acid or part thereof. The variants usable in the present invention may also be derived from homologs, orthologs, or paralogs of the parent nucleic acid. The changes in the nucleotide sequence may be exchanges, insertions, deletions, 5′ truncations, or 3′ truncations, or any combination of these changes, which may occur at one or several sites. In preferred embodiments, a variant usable in the present invention exhibits a total number of up to 600 (up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 300, 400, 500 or 600) changes in the nucleotide sequence. The nucleotide exchanges may be lead to non-conservative and/or preferably conservative amino acid exchanges as set out above with respect to polypeptide variants. Alternatively or additionally, a “variant” as used herein can be characterized by a certain degree of sequence identity to the parent nucleic acid from which it is derived. More precisely, a nucleic acid variant in the context of the present invention exhibits at least 80% sequence identity to its parent nucleic acid. Preferably, the sequence identity of nucleic acid variants is over a continuous stretch of 20, 30, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 400, 500, 600 or more amino acids, more preferably over the entire length of the reference nucleic acid (the parent nucleic acid). The term “at least 80% sequence identity” is used throughout the specification also with regard to nucleic acid sequence comparisons. This term preferably refers to a sequence identity of at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% to the respective reference nucleic acid or to the respective reference nucleic acid. Preferably, the nucleic acid in question and the reference nucleic acid or exhibit the indicated sequence identity over a continuous stretch as specified above.
As used herein, the term “vector” refers to a protein or a polynucleotide or a mixture thereof which is capable of being introduced or of introducing the nucleic acid comprised therein into a cell. In the context of the present invention it is preferred that the nucleic acid of the third aspect is expressed within the cell upon introduction of the vector. Suitable vectors are known in the art and include, for example, plasmids, cosmids, artificial chromosomes (e.g. bacterial, yeast or human), bacteriophages, viral vectors (e.g. retroviruses, lentiviruses, adenoviruses, adeno-associated viruses or baculoviruses), or nano-engineered substances (e.g. ormosils). Required vector technologies are well known in the art (see e.g. Lodish et al., Molecular Cell Biology, W. H. Freeman; 6th edition, Jun. 15, 2007; or Green and Sambrook, Molecular Cloning—A Laboratory Manual, 2012 Cold Spring Harbor Laboratory Press).
We have discovered that polypeptide variants of soluble FGFR3 fibroblast growth factor receptor 3 (sFGFR3) may be used to treat or prevent skeletal growth retardation disorders, such as achondroplasia, in a subject in need thereof (e.g., a human, particularly an infant or a child). The invention provides sFGFR3 polypeptide variants including a fragment of the extracellular domain (ECD). In particular, sFGFR3 polypeptides of the invention include sFGFR3 deletion (Del) variants featuring a deletion of, e.g., amino acids 311 to 422 of SEQ ID NO: 6, to provide the following exemplary Del variants: sFGFR3_Del2 (amino acids 1 to 548 of SEQ ID NO: 1), sFGFR3_Del3 (amino acids 1 to 440 of SEQ ID NO: 1), and sFGFR3_Del4 (amino acids 1 to 323 of SEQ ID NO: 1). The invention also features fusion polypeptides including a sFGFR3 polypeptide fragment, such as a sFGFR3 polypeptide fragment including, e.g., amino acids 1 to 323 of SEQ ID NO: 1, fused to a heterologous polypeptide, such as an aggrecan-binding protein including human hyaluronan and proteoglycan link protein 1 (HPLN1) or fragments thereof (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)). Methods for administering sFGFR3 polypeptides (e.g., Del variants as described herein) and fusion polypeptides (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4)) to treat or prevent skeletal growth retardation disorders (e.g., achondroplasia) in a subject in need thereof (e.g., a human, particularly an infant or a child) are also described.
We have determined that smaller functional portions of sFGFR3 exhibit a similar mechanism of action relative to larger soluble FGFR3 fragments and full-length FGFR3 polypeptides while maintaining the capability of dimerization following fixation of free FGFs. Several FGFR3 polypeptide variants with shorter intra-cellular domains were designed. All variants bound human FGF2 with similar affinity relative to sFGFR3_Del1 (SEQ ID NO: 1). Therapeutic benefit was shown using even the shortest FGFR3 variant, sFGFR3_Del4 (amino acids 1 to 323 of SEQ ID NO: 1), which restored bone growth in transgenic Fgfr3ach/+ mice. Therapeutic efficacy in the treatment of achondroplasia was also observed when sFGFR3_Del4 was administered in a mouse model of this disease, thereby demonstrating the use of this FGFR3 fragment in treatment of growth disorders and for designing additional constructions, such as fusion proteins. The sFGFR3_Del4 construct was also used to validate the use of body weight and skull length monitoring as indexes of velocity of growth. Furthermore, the invention provides fusion proteins comprising the smaller functional portions of sFGFR3 and human hyaluronan and proteoglycan link protein 1 (HPLN1). These fusion proteins bind FGF, as well as aggrecan, and exhibit improved therapeutic benefit relative to previous sFGFR3 decoys.
The present disclosure is not limited to a particular Fibroblast Growth Factor Receptor 3 (FGFR3) polypeptide or nucleic acid encoding a FGFR3. FGFR3 polypeptides encompass members of the fibroblast growth factor receptor (FGFR) family that mediate binding to fibroblast growth factors (FGFs) (e.g., FGF1, FGF2, FGF3, FGF4, FGFS, FGF6, FGF7, FGF8, FGF9, FGF10, or FGF18) and play a role in bone development and maintenance. In particular, a FGFR3 polypeptide can bind to FGF1, FGF2, FGF9 and/or FGF 18.
An FGFR3 polypeptide can include a polypeptide having the amino acid sequence of any one of the known FGFR3 polypeptides or a fragment thereof. FGFR3 polypeptides can include naturally occuring isoforms, such as FGFR3 produced by alternative splicing of the Ig3 domain of FGFR3, in which the C-terminal half of Ig3 is encoded by two separate exons, exon 8 (isoform 1; FGFR3 IIIb) and exon 9 (isoform 3; FGFR3 IIIc). In particular, a FGFR3 polypeptide can include the FGFR3 IIIc-type ECD with the C-terminal Ig3 half encoded by exon 9 (Accession No. NP_000133), which corresponds to FGFR3 transcript variant 1(Accession No. NM_000142.4). A FGFR3 polypeptide can also include the FGFR3 IIIb-type ECD with the C-terminal half encoded by exon 8 (Accession No. NP_001156685), which corresponds to FGFR3 transcript variant 3 (Accession No. NM_001163213).
FGFR3 polypeptides may include not only the FGFR3 amino acid sequences described above, but any polypeptide having at least 50% (e.g., 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more) amino acid sequence identity to these FGFR3 polypeptides (e.g., SEQ ID NO: 6) or an amino acid fragment of these FGFR3 amino acid sequences (e.g., at least 50, 100, 150, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 550, 600, 650, 700, 750, or more amino acid residues of an FGFR3 amino acid sequence (e.g., SEQ ID NO: 6)). In addition to the exemplary FGFR3 polypeptides discussed above, this disclosure also provides any FGFR3 polypeptide comprising the identical or similar FGF binding affinity for treating skeletal growth retardation disorders (e.g., achondroplasia) in a patient, e.g., a human.
sFGFR3 polypeptides of the invention include soluble (e.g., non-membrane-bound) forms of any of the FGFR3s described herein. The present disclosure is not limited to a particular sFGFR3 and may include any sFGFR3 polypeptide that binds one or more FGFs (e.g., FGF1 (SEQ ID NO: 7), FGF2 (SEQ ID NO: 8), FGF9 (SEQ ID NO: 9), and/or FGF 18 (SEQ ID NO: 10)), and accordingly, may be used as a decoy receptor for one or more FGFs to treat skeletal growth retardation disorders, e.g., achondroplasia. The invention further includes nucleic acids encoding the sFGFR3 polypeptides described herein that may be used to treat the conditions described herein, e.g., achondroplasia, in a subject in need thereof, such as SEQ ID NO: 5. The sFGFR3 polypeptide can be, for example, fragments of FGFR3 isoform 2 lacking exons 8 and 9 encoding the C-terminal half of the IgG3 domain and exon 10 including the transmembrane domain (i.e., sFGFR3_Del1; SEQ ID NO: 1 and Accession No. NP_075254), corresponding to FGFR3 transcript variant 2 (Accession No. NM_022965). Compositions including sFGFR3 are further described in PCT publication Nos: WO 2014/111744 and WO 2014/111467, which are each incorporated herein by reference in their entirety.
For example, sFGFR3 polypeptides can include fragments of the amino acid sequence of FGFR3 isoform 2 (e.g., at least amino acids 1 to 300, 1 to 310, 1 to 320, 1 to 330, 1 to 340, 1 to 350, 1 to 360, 1 to 370, 1 to 380, 1 to 390, 1 to 400, 1 to 410, 1 to 420, 1 to 430, 1 to 440, 1 to 440, 1 to 450, 1 to 460, 1 to 470, 1 to 480, 1 to 490, 1 to 500, 1 to 510, 1 to 520, 1 to 530, 1 to 540, 1 to 550, 1 to 560, 1 to 570, 1 to 580, 1 to 590, 1 to 600, 1 to 610, 1 to 620, 1 to 630, 1 to 640, 1 to 650, 1 to 660, 1 to 670, 1 to 680, or 1 to 690 of SEQ ID NO: 1). In particular, sFGFR3 polypeptides may include, but are not limited to, amino acids 1 to 323 of SEQ ID NO: 1 (sFGFR3_Del4), amino acids 1 to 440 of SEQ ID NO: 1 (sFGFR3_Del3), or amino acids 1 to 548 of SEQ ID NO: 1 (sFGFR3_Del2).
sFGFR3 polypeptides and fragments thereof can also include an N-terminal signal peptide sequence. The N-terminal signal peptide is present on the synthesized protein when it is synthesized, but is typically cleaved from the sFGFR3 polypeptide upon export of the polypeptide from the cell. The sFGFR3 polypeptides and sFGFR3 fusion polypeptides of the invention include both secreted (i.e., lacking the N-terminal signal) and non-secreted (i.e., having the N-terminal signal) forms thereof. One skilled in the art will appreciate that the position of the N-terminal signal peptide will vary in different sFGFR3 polypeptides and may include, for example, the first 5, 8, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 27, 30, or more amino acid residues on the N-terminus of the polypeptide. For example, an exemplary signal peptide can include, but is not limited to, amino acids 1 to 22 of SEQ ID NO: 1. Additionally, sFGFR3 polypeptides and fusion polypeptides, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (corresponding to amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a FGFR3 fusion polypeptide (e.g., SEQ ID NO: 4 with or without amino acids 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33), can include deletions of the N-terminal amino acids, e.g., at least the amino acids 1 to 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 56 of SEQ ID NO: 1. One of skill in the art can predict the position of a signal sequence cleavage site, e.g., by an appropriate computer algorithm such as that described in Bendtsen et al. (J. Mol. Biol. 340(4):783-795, 2004) and available on the Web at www.cbs.dtu.dk/services/SignalP/.
sFGFR3 Fusion Polypeptides
sFGFR3 polypeptides of the invention can optionally be fused to a functional domain from a heterologous polypeptide (e.g., an aggrecan-binding protein) to provide a sFGFR3 fusion polypeptide, as described herein. In some sFGFR3 polypeptides, a flexible linker, may be included between the sFGFR3 polypeptide and the fusion polypeptide (e.g., an aggrecan-binding protein), such as a serine or glycine-rich sequence (e.g., a poly-glycine or a poly-glycine/serine linker). Further exemplary fusion proteins and linkers are described below.
For example, the sFGFR3 polypeptides described above, such as fragments of sFGFR3_Del1 (e.g., amino acids 1 to 323 of SEQ ID NO: 1 (sFGFR3_Del4), amino acids 1 to 440 of SEQ ID NO: 1 (sFGFR3_Del3), or amino acids 1 to 548 of SEQ ID NO: 1 (sFGFR3_Del2)), can be a fusion polypeptide including, e.g., an aggrecan-binding protein or any polypeptide that targets cartilage when administered to a subject (e.g., a human). In particular, any functional portion of a protein that binds to aggregan, e.g., any protein that interacts with the globular domain (G1, G2, or G3) of aggrecan, can be included in a sFGFR3 fusion polypeptide
Exemplary aggrecan-binding proteins that can be used to produce the SFGFR3 fusion polypeptides described herein include antibodies, fibulin-1, borrelial aggrecan-binding proteins (e.g., Borrelia glycosaminoglycan-binding protein (Bgp) and Borrelia burgdorferi high temperature requirement A (BbHtrA)), and cartilage oligomeric matrix protein/thrombospondin 5 (COMP/TSP5). For example, an aggrecan-binding protein may include human hyaluronan and proteoglycan link protein 1 (HPLN1) or fragments thereof. In particular, the HPLN1 fragment can include a cartilage link domain 1 (LK1; amino acids 158 to 252 of SEQ ID NO: 3), a cartilage link domain 2 (LK2; amino acids 259 to 349 of SEQ ID NO: 3), or both LK1 and LK2 domains (158 to 349 amino acids of SEQ ID NO: 3). Additional sFGFR3 fusion polypeptides may include any polypeptide that has at least 50% (e.g., 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%3 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more) amino acid sequence identity to the HPLN1 polypeptide (e.g., SEQ ID NO: 3) or an amino acid fragment thereof (e.g., at least 50, 100, 110, 120, 130, 140, 150, 150, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, or more amino acid residues of the entire length of the HPLN1 amino acid sequence (i.e., SEQ ID NO: 3)). For example, an aggrecan-binding protein or fragment thereof of a FGFR3 fusion polypeptide can include, e.g., both LK1 and LK2 domains (amino acids 158 to 349 of SEQ ID NO: 3), in combination with a sFGFR3 polypeptide or fragment thereof, such as amino acids 1 to 323 of SEQ ID NO: 1 (sFGFR3_Del4).
Additionally, the sFGFR3 polypeptides (e.g., sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4) can be a fusion polypeptide including, e.g., an Fc region of an immunoglobulin at the N-terminal or C-terminal domain. An immunoglobulin molecule has a structure that is well known in the art. It includes two light chains (˜23 kD each) and two heavy chains (˜50-70 kD each) joined by inter-chain disulfide bonds. Immunoglobulins are readily cleaved proteolytically (e.g., by papain cleavage) into Fab (containing the light chain and the VH and CH1 domains of the heavy chain) and Fc (containing the CH2 and CH3 domains of the heavy chain, along with adjoining sequences). Useful Fc fragments as described herein include the Fc fragment of any immunoglobulin molecule, including IgG, IgM, IgA, IgD, or IgE, and their various subclasses (e.g., IgG-1, IgG-2, IgG-3, IgG-4, IgA-1, IgA-2), from any mammal (e.g., human). For instance, the Fc fragment is human IgG-1. The Fc fragments of the invention may include, for example, the CH2 and CH3 domains of the heavy chain and any portion of the hinge region. The Fc region may optionally be glycosylated at any appropriate one or more amino acid residues known to those skilled in the art. An Fc fragment as described herein may have 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 50, or more additions, deletions, or substitutions relative to any of the Fc fragments described herein.
The sFGFR3 fusion polypeptides described herein may include a peptide linker region between the SFGFR3 polypeptide or fragment thereof and the heterologous polypeptide or fragment thereof (e.g., an aggrecan-binding protein or fragment thereof or an Fc region). The linker region may be of any sequence and length that allows the sALP to remain biologically active, e.g., not sterically hindered. Exemplary linker lengths are between 1 and 200 amino acid residues, e.g., 1-5, 6-10, 11-15, 16-20, 21-25, 26-30, 31-35, 36-40, 41-45, 46-50, 51-55, 56-60, 61-65, 66-70, 71-75, 76-80, 81-85, 86-90, 91-95, 96-100, 101-110, 111-120, 121-130, 131-140, 141-150, 151-160, 161-170, 171-180, 181-190, or 191-200 amino acid residues. For instance, linkers include or consist of flexible portions, e.g., regions without significant fixed secondary or tertiary structure. Preferred ranges are 5 to 25 and 10 to 20 amino acids in length. Such flexibility is generally increased if the amino acids are small and do not have bulky side chains that impede rotation or bending of the amino acid chain. Thus, preferably the peptide linker of the present invention has an increased content of small amino acids, in particular of glycines, alanines, serines, threonines, leucines and isoleucines.
Exemplary flexible linkers are glycine-rich linkers, e.g., containing at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or even 100% glycine residues. Linkers may also contain, e.g., serine-rich linkers, e.g., containing at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or even 100% serine residues. In some cases, the amino acid sequence of a linker consists only of glycine and serine residues. For example, the sFGFR3 fusion polypeptide (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33) can include a glycine and serine linker, such as the amino acid sequence SGSGSGSGSGSGSGS. A linker may optionally be glycosylated at any appropriate one or more amino acid residues. Additionally, a linker as described herein may include any other sequence or moiety, attached covalently or non-covalently. The linker may also be absent, in which the FGFR3 polypeptide and heterologous polypeptide (e.g., an aggrecan-binding protein or fragment thereof or Fc region) are fused together directly, with no intervening residues.
Additional amino acid residues can be introduced into the FGFR3 fusion polypeptide according to the cloning strategy used to produce the FGFR3 fusion polypeptides. For instance, the additional amino acid residues do not provide a portion of the FGFR3 transmembrane domain in order to maintain the polypeptide in a soluble form. Furthermore, any such additional amino acid residues, when incorporated into the FGFR3 polypeptide or fusion polypeptide of the invention, do not provide a cleavage site for endoproteases of the host cell. The likelihood that a designed sequence would be cleaved by the endoproteases of the host cell can be predicted as described, e.g., by Ikezawa (Biol. Pharm. Bull. 25:409-417, 2002).
The FGFR3 polypeptides and fusion polypeptides of the invention may be associated into dimers or tetramers. Additionally, the polypeptide or fusion polypeptide of the invention (e.g., a sFGFR3 polypeptide or fusion polypeptide) may be glycosylated or PEGylated.
Production of sFGFR3 Nucleic Acids and Polypeptides
Nucleic acids encoding sFGFR3 and sFGFR3 fusion polypeptides of the invention can be produced by any method known in the art. Typically, a nucleic acid encoding the desired fusion polypeptide is generated using molecular cloning methods, and is generally placed within a vector, such as a plasmid or virus. The vector is used to transform the nucleic acid into a host cell appropriate for the expression of the fusion polypeptide. Representative methods are disclosed, for example, in
Maniatis et al. (Cold Springs Harbor Laboratory, 1989). Many cell types can be used as appropriate host cells, although mammalian cells are preferable because they are able to confer appropriate post-translational modifications. Host cells of the present invention may include, e.g., Human Embryonic Kidney 293 (HEK 293) cells, Chinese Hamster Ovary (CHO) cell, L cell, C127 cell, 3T3 cell, BHK cell, COS-7 cell or any other suitable host cell known in the art. For example, the host cell is a HEK 293 cells. Alternatively, the host cell can be a CHO cell.
Provided herein are methods for treating a skeletal growth retardation disorder in a patient, such as a patient having achondroplasia (e.g., a human having achondroplasia). In particular, the patient may exhibit or may be likely to have one or more symptoms of a skeletal growth retardation disorder (e.g., achondroplasia). The method involves administering a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (corresponding to amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a FGFR3 fusion polypeptide (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33) to the patient (e.g., a human). For example, the patient exhibits signs or symptoms of a skeletal growth retardation disorder, such as those described herein (e.g., achondroplasia), e.g., prior to administration of the sFGFR3 polypeptide or FGFR3 fusion polypeptide. Treatment with a sFGFR3 polypeptide of the invention, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide of the invention (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33) can also occur after a patient (e.g., a human) has been diagnosed with a skeletal growth retardation disorder, such as those described herein (e.g., achondroplasia), or after a patient exhibits signs or symptoms of a skeletal growth retardation disorder, such as those described herein (e.g., achondroplasia). In particular, the patient is treated with sFGFR3_Del4-LK1-LK2.
Treatment with a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33) can result in an improvement in a symptom of a skeletal growth retardation disorder, e.g., achondroplasia. The methods can be used to treat symptoms associated with a skeletal growth retardation disorder, e.g., achondroplasia, such that there is reversal or a reduction in the severity of symptoms of the skeletal growth retardation disorder, e.g., achondroplasia.
Skeletal growth retardation disorders can be treated or prevented by administering a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide as described herein. In particular, the method involves administering a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) to a patient (e.g., a human). Skeletal growth retardation disorders that can be treated with the sFGFR3 polypeptides and sFGFR3 fusion polypeptides described herein are characterized by deformities and/or malformations of the bones and can include, but are not limited to, FGFR3-related skeletal diseases. In particular, the patient is treated with sFGFR3_Del4-LK1-LK2.
Administration of a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide as described herein (such as, e.g., sFGFR3_Del4-LK1-LK2) can treat a skeletal growth retardation disorder including, but not limited to, achondroplasia, achondrogenesis, acrodysostosis, acromesomelic dysplasia, atelosteogenesis, camptomelic dysplasia, chondrodysplasia punctata, rhizomelic type of chondrodysplasia punctata, cleidocranial dysostosis, congenital short femur, Crouzon syndrome, Apert syndrome, Jackson-Weiss syndrome, Pfeiffer syndrome, Crouzonodermoskeletal syndrome, dactyly, brachydactyly, camptodactyly, polydactyly, syndactyly, diastrophic dysplasia, dwarfism, dyssegmental dysplasia, enchondromatosis, fibrochondrogenesis, fibrous dysplasia, hereditary multiple exostoses, hypophosphatasia, hypophosphatemic rickets, Jaffe-Lichtenstein syndrome, Kniest dysplasia, Kniest syndrome, Langer-type mesomelic dysplasia, Marfan syndrome, McCune-Albright syndrome, micromelia, metaphyseal dysplasia, Jansen-type metaphyseal dysplasia, metatrophic dysplasia, Morquio syndrome, Nievergelt-type mesomelic dysplasia, neurofibromatosis (such as type 1 (e.g., with bone manifestations or without bone manifestations), type 2, or schwannomatosis), osteoarthritis, osteochondrodysplasia, osteogenesis imperfecta, perinatal lethal type of osteogenesis imperfecta, osteopetrosis, osteopoikilosis, peripheral dysostosis, Reinhardt syndrome, Roberts syndrome, Robinow syndrome, short-rib polydactyly syndromes, short stature, spondyloepiphyseal dysplasia congenita, or spondyloepimetaphyseal dysplasia. For instance, administration of the sFGFR3 polypeptides or sFGFR3 fusion polypeptide described herein may resolve and/or prevent symptoms associated with any of the aforementioned disorders.
The sFGFR3 polypeptides and sFGFR3 fusion polypeptides of the present invention can be used to treat symptoms associated with a skeletal growth retardation disorder, such as a FGFR3-related skeletal disease (e.g., achondroplasia). Non-limiting examples of symptoms of skeletal growth retardation disorders that may be treated, e.g., with a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide, include the following: short limbs and trunk, bowlegs, a waddling gait, skull malformations (e.g., a large head), cloverleaf skull, craniosynostosis (e.g., premature fusion of the bones in the skull), wormian bones (e.g., abnormal thread-like connections between the bones in the skull), anomalies of the hands and feet (e.g., polydactyly or extra fingers), “hitchhiker” thumbs and abnormal fingernails and toenails, and chest anomalies (e.g., pear-shaped chest or narrow thorax). Additional symptoms that can treated by administering sFGFR3 polypeptides and sFGFR3 fusion polypeptides can also include non-skeletal abnormalities in patients having skeletal growth retardation disorders, e.g., anomalies of the eyes, mouth, and ears, such as congenital cataracts, myopia, cleft palate, or deafness; brain malformations, such as hydrocephaly, porencephaly, hydranencephaly, or agenesis of the corpus callosum; heart defects, such as atrial septal defect, patent ductus arteriosus, or transposition of the great vessels; developmental delays; or mental retardation. Accordingly, adinistration of a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide, as described herein, may result in an improvement in one or more symptoms of a skeletal growth retardation disorder.
Any skeletal growth retardation disorder that is a FGFR3-related skeletal disease (e.g., caused by or associated with overactivation of FGFR3 as result of a gain-of-function FGFR3 mutation) can be treated by administering a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide as described herein to a patient (e.g., a human). For example, a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide can be administered to treat FGFR3-related diseases, such as skeletal dysplasias and FGFR3-related craniosynostosis. FGFR3-related skeletal diseases can include, but are not limited to, achondroplasia, thanatophoric dysplasia type I (TDI), thanatophoric dysplasia type II (TDII), severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), hypochondroplasia, and craniosynostosis (e.g., Muenke syndrome and Crouzon syndrome with acanthosis nigricans).
Patients (e.g., human patients) with mutations in the FGFR3 gene associated with different FGFR3-related skeletal disorders, such as achondroplasia, hypochondroplasia, SADDAN, TDI, and TDII, can also be treated with a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4, or a sFGFR3 fusion polypeptide, such as a fusion polypeptide including sFGFR3_Del4 and a fragment of an aggrecan-binding protein (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)).
For example, the sFGFR3 polypeptide or sFGFR3 fusion polypeptide can be administered to treat achondroplasia resulting from the G380R, G375C, G346E or S279C mutations of the FGFR3 gene. Administration of the sFGFR3 polypeptides and sFGFR3 fusion polypeptides may be used to treat the following exemplary FGFR3-related skeletal disorders: hypochondroplasia resulting from the G375C, G346E or S279C mutations of the FGFR3 gene; TDI resulting from the R248C, S248C, G3700, S3710, Y373C, X807R, X807C, X807G, X8075, X807W and K650M mutations of the FGFR3 gene; TDII resulting from the K650E mutation of the FGFR3 gene; and SADDAN resulting from the K650M mutation of the FGFR3 gene. Thus, a patient treated with the sFGFR3 polypeptides or sFGFR3 fusion polypeptides disclosed herein may have, e.g., a mutation in the FGFR3 gene.
Any of the aforementioned mutations in the FGFR3 gene (e.g., the G380R mutation of the FGFR3 gene) can be detected in a sample from the patient (e.g., a human with achondroplasia, hypochondroplasia, SADDAN, TDI, and TDII) prior to or after treatment (e.g., treatment with a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4, or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2). Additionally, the parents of the patient and/or fetal samples (e.g., fetal nucleic acid obtained from maternal blood, placental, or fetal samples) may be tested by methods known in the art for the mutation.
Achondroplasia is the most common cause of dwarfism in humans and can be treated or prevented by administering a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide as described herein. In particular, achondroplasia may be treated by administering a FGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively) or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) to a patient (e.g., a human). Administration of a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide, as described herein, may result in an improvement in symptoms including, but not limited to, growth retardation, skull deformities, orthodontic defects, cervical cord compression (with risk of death, e.g., from central apnea or seizures), spinal stenosis (e.g., leg and lower back pain), hydrocephalus (e.g., requiring cerebral shunt surgery), hearing loss due to chronic otitis, cardiovascular disease, neurological disease, respiratory problems, fatigue, pain, numbness in the lower back and/or spin, and obesity.
Patients treated using the sFGFR3 polypeptides or the sFGFR3 fusion polypeptides described herein may include, e.g., infants, children, and adults with achondroplasia. Infants are often diagnosed with achondroplasia at birth, and thus, treatment with a sFGFR3 polypeptide or sFGFR3 fusion protein, as described herein, may begin as early as possible in the patient's life, e.g., shortly after birth, or prior to birth (in utero).
Symptoms of achondroplasia in patients (e.g., humans) may also be monitored prior to or after a patient is treated with a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)). For instance, symptoms of achondroplasia may be monitored prior to treatment to assess the severity of achondroplasia and condition of the patient prior to performing the methods. The methods of the invention may include diagnosis of achondroplasia in a patient and monitoring the patient for changes in the symptoms of achondroplasia, such as changes in body weight, skull length and/or skull width of the patient based on changes monitored over a period of time, e.g., 1, 2, 3, 4 or more times per month or per year or approximately every 1, 2, 3, 4, 5, 6, 7, 8, 12 or 16 weeks over the course of treatment with the sFGFR3 polypeptide or the sFGFR3 fusion polypeptide of the present invention. Body weight and/or skull size of the patient or changes thereof can also be determined at treatment specific events, e.g. before and/or after administration of the sFGFR3 polypeptide or sFGFR3 fusion polypeptide as described herein. For example, body weight and/or skull size are measured in response to administration of the sFGFR3 polypeptide or sFGFR3 fusion polypeptide of the present invention.
Body weight can be measured simply be weighing the subject on a scale, preferably in a standardized manner, e.g. with the same (in particular for humans) or no clothes or at a certain time of the day, preferably in a fasting state (for example in the morning before breakfast is taken, or after at least 1, 2, 3, 4, 5 or more hours of fasting).
Skull size is preferably represented by length, height, width and/or circumference. Measurements can be taken by any known or self-devised standardized method. For a human subject, the measurement of skull circumference is preferred. It is usually taken with a flexible and non-stretchable material such as a tape, which is wrapped around the widest possible circumference of the head (though not around the ears or the facial area below and including the eyebrows), e.g. from the most prominent part of the forehead around to the widest part of the back of the head. Another preferred measurement for a human subject can determine the height of the skull, for example from the underside of the chin to the uppermost point of the head. For a rodent subject, the measurement of the length of the skull (e.g. tip of the nasal bone to back of the occipital bone) is preferred. Alternatively, also the width of the skull (e.g. widest points of the parietal bone) or the height of the skull (e.g. lowest point of the angular process of lower jaw to frontal bone) are preferred. Preferably, any measurement is taken more than once, e.g. at least 3 times, and the largest number us taken as the length, height, width and/or circumference.
A composition of the present invention (e.g., including a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) can be administered by a variety of methods known in the art. As will be appreciated by the skilled artisan, the route and/or mode of administration will vary depending upon the desired results. The route of administration can depend on a variety of factors, such as the environment and therapeutic goals. In particular, the sFGFR3 polypeptides and sFGFR3 fusion polypeptides described herein (e.g., sFGFR3_Del4-LK1-LK2) can be administered by any route known in the art, e.g., subcutaneous (e.g., by subcutaneous injection), intravenously, orally, nasally, intramuscularly, sublingually, intrathecally, or intradermally. By way of example, pharmaceutical compositions of the invention can be in the form of a liquid, solution, suspension, pill, capsule, tablet, gelcap, powder, gel, ointment, cream, nebulae, mist, atomized vapor, aerosol, or phytosome.
Dosage
Any amount of a pharmaceutical composition (e.g., including a sFGFR3 polypeptide, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) can be administered to a patient, such as a patient with a skeletal growth retardation disorder (e.g., a patient with achondroplasia). The dosages will depend on many factors including the mode of administration and the age of the patient. Typically, the amount of the composition (e.g., including a sFGFR3 polypeptide or a sFGFR3 fusion polypeptide) contained within a single dose will be an amount that is effective to treat a condition (e.g., achondroplasia) as described herein without inducing significant toxicity.
For example, the sFGFR3 polypeptides, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or sFGFR3 fusion polypeptides (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acids 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) described herein can be administered to patients (e.g., patients with achondroplasia) in individual doses ranging, e.g., from 0.0002 mg/kg to about 20 mg/kg (e.g., from 0.002 mg/kg to 20 mg/kg, from 0.01 mg/kg to 2 mg/kg, from 0.2 mg/kg to 20 mg/kg, from 0.01 mg/kg to 10 mg/kg, from 10 mg/kg to 100 mg/kg, from 0.1 mg/kg to 50 mg/kg, 0.5 mg/kg to 20 mg/kg, 1.0 mg/kg to 10 mg/kg, 1.5 mg/kg to 5 mg/kg, or 0.2 mg/kg to 3 mg/kg). In particular, the sFGFR3 polypeptide or sFGFR3 fusion polypeptides as described herein can be administered in individual doses of, e.g., 0.001 mg/kg to 7 mg/kg. These doses can be administered one or more times (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 or more times) per day, week, month, or year.
Exemplary doses of the sFGFR3 polypeptides of fragments thereof, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or sFGFR3 fusion polypeptides (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acids 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) include, e.g., 0.0002, 0.0005, 0.0010, 0.002, 0.005, 0.01, 0.02, 0.05, 0.1, 0.2, 0.5, 1, 2, 3, 2.5, 4, 5, 6, 7, 8, 9, 10, 15, or 20 mg/kg. For all dosages or ranges recited herein, the term “about” may be used to modify these dosages by ±10% of the recited values or range endpoints. In particular, sFGFR3 compositions in accordance with the present disclosure can be administered to patients in doses ranging from about 0.0002 mg/kg/day to about 20 mg/kg/day, about 0.02 mg/kg/day to about 15 mg/kg/day, or about 0.2 mg/kg/day to about 10 mg/kg/day (e.g., 0.75 mg/kg/day). For example, the sFGFR3 compositions can be administered to patients in a weekly dosage ranging, e.g., from about 0.0014 mg/kg/week to about 140 mg/kg/week, e.g., about 0.14 mg/kg/week to about 105 mg/kg/week, or, e.g., about 1.4 mg/kg/week to about 70 mg/kg/week (e.g., 5 mg/kg/week). The dosage will be adapted by the clinician in accordance with conventional factors such as the extent of the disease (e.g., achondroplasia) and different parameters from the patient (e.g., a patient with achondroplasia).
Dosages of compositions including sFGFR3 polypeptides, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or sFGFR3 fusion polypeptides (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acids 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) may be provided in either a single or multiple dosage regimens. Doses can be administered, e.g., hourly, bihourly, daily, bidaily, twice a week, three times a week, four times a week, five times a week, six times a week, weekly, biweekly, monthly, bimonthly, or yearly. Alternatively, doses can be administered, e.g., twice, three times, four times, five times, six times, seven times, eight times, nine times, 10 times, 11 times, or 12 times per day. In particular, the dosing regimen is twice weekly. For example, the sFGFR3 polypeptides or sFGFR3 fusion polypeptides described herein can be administered at a dosage of 2.5 mg/kg twice weekly. The duration of the dosing regimen can be, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 day(s), week(s), or month(s), or even for the remaining lifespan of the patient. The amount, frequency, and duration of dosage will be adapted by the clinician in accordance with conventional factors such as the extent of the disease and different parameters from the patient.
Preparations containing a sFGFR3 polypeptide (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, or amino acids 1 to 323 of SEQ ID NO: 1, respectively), or sFGFR3 fusion polypeptides (e.g., sFGFR3_Del4-LK1-LK2 (SEQ ID NO: 4 with or without amino acids 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33)) may be provided to patients in combination with pharmaceutically acceptable sterile aqueous or non-aqueous solvents, suspensions or emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oil, fish oil, and injectable organic esters. Aqueous carriers include water, water-alcohol solutions, emulsions or suspensions, including saline and buffered medical parenteral vehicles including sodium chloride solution, Ringer's dextrose solution, dextrose plus sodium chloride solution, Ringer's solution containing lactose, or fixed oils.
Intravenous vehicles may include fluid and nutrient replenishers, electrolyte replenishers, such as those based upon Ringer's dextrose, and the like. Pharmaceutically acceptable salts can be included therein, for example, mineral acid salts such as hydrochlorides, hydrobromides, phosphates, sulfates, and the like; and the salts of organic acids such as acetates, propionates, malonates, benzoates, and the like. Additionally, auxiliary substances, such as wetting or emulsifying agents, pH buffering substances, and the like, may be present in such vehicles. A thorough discussion of pharmaceutically acceptable carriers is available in Remington's Pharmaceutical Sciences (Mack Pub. Co., N.J. 1991).
Preferably, the pharmaceutical compositions contain vehicles which are pharmaceutically acceptable for a formulation capable of being injected. These may be in particular isotonic, sterile, saline solutions (monosodium or disodium phosphate, sodium, potassium, calcium or magnesium chloride and the like or mixtures of such salts), or dry, especially freeze-dried compositions which upon addition, depending on the case, of sterilized water or physiological saline, permit the constitution of injectable solutions. The doses used for the administration can be adapted as a function of various parameters, and in particular as a function of the mode of administration used, of the relevant pathology, or alternatively of the desired duration of treatment. For example, it is well within the skill of the art to start doses of the compound at levels lower than those required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved. However, the daily dosage of the products may be varied over a wide range from 0.01 to 1.000 mg per adult per day. Preferably, the compositions contain 0.01, 0.05, 0.1, 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100, 250 and 500 mg of the active ingredient for the symptomatic adjustment of the dosage to the subject to be treated. A medicament typically contains from about 0.01 mg to about 500 mg of the active ingredient, preferably from 1 mg to about 100 mg of the active ingredient. An effective amount of the drug is ordinarily supplied at a dosage level from 0.0002 mg/kg to about 20 mg/kg of body weight per day, especially from about 0.001 mg/kg to 7 mg/kg of body weight per day. To prepare pharmaceutical compositions, an effective amount of a polypeptide according to the invention may be dissolved or dispersed in a pharmaceutically acceptable carrier or aqueous medium.
The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions; formulations including sesame oil, peanut oil or aqueous propylene glycol; and sterile powders for the extemporaneous preparation of sterile injectable solutions or 20 dispersions. In all cases, the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. Solutions of the active compounds as free base or pharmacologically acceptable salts can be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.
The polypeptides and nucleic acids according to the invention can be formulated into a composition in a neutral or salt form. Pharmaceutically acceptable salts include the acid addition salts (formed with the free amino groups of the protein) and which are formed with inorganic acids such as,for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, histidine, procaine and the like. The carrier can also be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and 5 the like), suitable mixtures thereof, and vegetables oils. The proper fluidity can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminium monostearate and gelatin.
Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with several of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof. The preparation of more, or highly concentrated solutions for direct injection is also contemplated, where the use of DMSO as solvent is envisioned to result in extremely rapid penetration, delivering high concentrations of the active agents to a small tumor area. Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective. The formulations are easily administered in a variety of dosage forms, such as the type of injectable solutions described above, but drug release capsules and the like can also be employed. For parenteral administration in an aqueous solution, for example, the solution may be suitably buffered and the liquid diluent first rendered isotonic with sufficient saline or glucose. These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration. In this connection, sterile aqueous media which can be employed will be known to those of skill in the art in light of the present disclosure. For example, one dosage could be dissolved in 1 ml of isotonic NaCI solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion. Some variation in dosage will necessarily occur depending on the condition of the subject being treated. The person responsible for administration will, in any event, determine the appropriate dose for the subject.
Gene Therapy
The sFGFR3 polypeptides, such as sFGFR3_Del2, sFGFR3_Del3, and sFGFR3_Del4 (e.g., amino acids 1 to 548 of SEQ ID NO: 1, amino acids 1 to 440 of SEQ ID NO: 1, and amino acids 1 to 323 of SEQ ID NO: 1, respectively), or sFGFR3 fusion polypeptides such as sFGFR3_Del4-LK1-LK2 (e.g., SEQ ID NO: 4 with or without amino acid residues 1 to 8 of SEQ ID NO: 4 or SEQ ID NO: 33), could also be delivered through gene therapy, where an exogenous nucleic acid encoding the proteins is delivered to tissues of interest and expressed in vivo. Gene therapy methods are discussed, e.g., in Verme et al. (Nature 389:239-242, 1997), Yamamoto et al. (Molecular Therapy 17:S67-S68, 2009), and Yamamoto et al., (J. Bone Miner. Res. 26:135-142, 2011), each of which is hereby incorporated by reference. Both viral and non-viral vector systems can be used. The vectors may be, for example, plasmids, artificial chromosomes (e.g., bacterial, mammalian, or yeast artificial chromosomes), virus or phage vectors provided with an origin of replication, and optionally, a promoter for the expression of the nucleic acid encoding the viral polypeptide and optionally, a regulator of the promoter. The vectors may contain one or more selectable marker genes, for example, an ampicillin or kanamycin resistance gene in the case of a bacterial plasmid or a resistance gene for a fungal vector. Vectors may be used in in vitro, for example, for the production of DNA, RNA, or the viral polypeptide, or may be used to transfect or transform a host cell, for example, a mammalian host cell, e.g., for the production of the viral polypeptide encoded by the vector. The vectors may also be adapted to be used in vivo, for example, in a method of vaccination or gene therapy.
Examples of suitable viral vectors include, retroviral, lentiviral, adenoviral, adeno-associated viral, herpes viral, including herpes simplex viral, alpha-viral, pox viral, such as Canarypox and vaccinia-viral based systems. Gene transfer techniques using these viruses are known in the art. Retrovirus vectors, for example, may be used to stably integrate the nucleic acids of the invention into the host genome. Replication-defective adenovirus vectors by contrast remain episomal and therefore allow transient expression. Vectors capable of driving expression in insect cells (e.g., baculovirus vectors), in human cells, yeast, or in bacteria may be employed in order to produce quantities of the viral polypeptide(s) encoded by the nucleic acids of the invention, for example, for use in subunit vaccines or in immunoassays. In an additional example, a replication-deficient simian adenovirus vector may be used as a live vector. These viruses contain an El deletion and can be grown on cell lines that are transformed with an El gene. These vectors can be manipulated to insert a nucleic acid of the invention, such that the encoded viral polypeptide(s) may be expressed.
Promoters and other expression regulatory signals may be selected to be compatible with the host cell for which expression is designed. For example, mammalian promoters include the metallothionein promoter, which can be induced in response to heavy metals such as cadmium, and the 43-actin promoter. Viral promoters, such as the SV40 large T antigen promoter, human cytomegalovirus (CMV) immediate early (1E) promoter, rous sarcoma virus LTR promoter, adenovirus promoter, or a HPV promoter, particularly the HPV upstream regulatory region (URR) may also be used. All these promoters, as well as additional promoters, are well-described in the art.
The nucleic acid molecules described herein may also be administered using non-viral based systems. For example, these administration systems include microsphere encapsulation, poly(lactide-co-glycolide), nanoparticle, and liposome-based systems. Non-viral based systems also include techniques facilitating the delivery of “naked” polynucleotides (such as electroporation, “gene gun” delivery and various other techniques used for the introduction of polynucleotides).
The introduced polynucleotide can be stably or transiently maintained in the host cell. Stable maintenance typically requires that the introduced polynucleotide either contains an origin of replication compatible with the host cell or integrates into a replicon of the host cell such as an extrachromosomal replicon (e.g., a plasmid) or a nuclear or mitochondrial chromosome.
The invention is described by way of the following examples which are to be construed as merely illustrative and not limitative of the scope of the invention.
A diagram of the different domains of FGFR3, HPLN1 and a soluble FGFR3 (sFGFR3) is shown in
SEQ ID NO: 1 provides the amino acid sequence of sFGFR3 of PCT/EP2014/050800, SEQ ID NO: 2 the amino acid sequence of the same sFGFR3 but with the full Ig like C2 type domain 3, SEQ ID NO: 3 the amino acid sequence of HPLN1, SEQ ID NO: 4 the amino acid sequence of FLAG-sFGFR3_Del4-LK1-LK2 (see
The Del plasmids were obtained by site directed mutagenesis of the sFGFR3-pFLAG-CMV3 plasmid. The cDNA sequence for LK1-LK2 was optimized for Homo Sapiens while encoding for the original protein sequence (GeneOptimizer process, GeneArt). The synthesized fragment was subcloned into sFGFR3-pFLAG-CMV3 (Garcia, S. et al. 5, 203ra124 (2013)) using PmII and KpnI cloning sites. Plasmid DNA was purified from transformed bacteria and concentration determined by UV spectroscopy. Final constructs were verified by sequencing.
Recombinant proteins were produced by transient transfection using CaCl2 transfection reagent in HEK 293 cells. Each transfection was performed in a cell factory (High flask T600, Merck Millipore) with 80% confluent HEK 293 in 100 ml DMEM without phenol red (Life Technologies) supplemented with 2 mM glutamine (Life Technologies) and antibiotics (Life Technologies). CaCl2 (690 pi) and a pFLAG-sFGFR3 variant (240 μg) were resuspended with 6.27 ml H2O in 7.2 ml HBS, incubated 30 min at room temperature, and then incubated for 16 h onto the cells at 37° C. in 5% CO2. Medium was then replaced by 120 ml supplemented DMEM without phenol red. After 72 h, production medium was filtrated using 0.22 μm filters and concentrated on Amicon Ultra-15 60 kDa (Merck Millipore). Recombinant protein was then purified using an affinity column (ANTI-FLAG M2 Affinity Gel, Sigma Aldrich) according to the manufacturer's instructions. Protein amounts were measured by specific ELISA (R&D Systems) according to the manufacturer's instructions.
Fixed amounts of human FGF2, or human FGF9 (R&D Systems) were incubated for 2 h at 37° C. with increasing doses of each recombinant protein (0 to 250 ng/ml) in PBS 1% BSA. Specific commercial ELISA kits (R&D Systems; Clinisciences) were used to quantify remaining unbound FGFs. 1000 pg/ml or 1200 pg/ml were used for FGF2 and FGF9 respectively based on the sensitivity of the corresponding ELISA kits.
Aggrecan binding.
ELISA plate were coated with 10 μg/mL of Aggrecan (R&D systems #1220-PG-025) in a final volume of 50 μl per well and incubated overnight at room temperature. Plate were blocked with 300 μl of PBS 1% BSA per well during 1 h at room temperature. Different amount of protein (0 to 100 Ll) were incubated for 1 h at room temperature. Specific detection antibody against FGFR3 from an R&D system ELISA kit (#DYC766E) was used to detect recombinant protein fixed to aggrecan as recommended by the manufacturer.
The Principles of Laboratory Animal Care (NIH publication no. 85-23, revised 1985; http://grants1.nih.gov/grants/olaw/references/phspol.htm) and the European commission guidelines for the protection of animals used for scientific purposes (http://ec.europa.eu/environment/chemicals/lab_animals/legislation_en.htm) were followed at all times. All procedures were approved by the Institutional Ethic Committee for the use of Laboratory Animals (CIEPAL Azur) (approval #NCE-2012-52).
Experiments were performed on transgenic Fgfr3ach/+ animals in which expression of the mutant FGFR3 is driven by the Col2a1 promoter/enhancer (Naski et al., Development 125, 4977-4988, 1998). Mice were exposed to a 12 h light/dark cycle and had free access to standard laboratory food and water. Genotypes were verified by PCR of genomic DNA using the primers 5′-AGGTGGCCTTTGACACCTACCAGG-3′ (SEQ ID NO: 31) and 5′-TCTGTTGTGTTTCCTCCCTGTTGG-3′ (SEQ ID NO: 32), which amplify 360 bp of the FGFR3 transgene (Naski et al., supra).
Several doses of each recombinant protein were tested. At day 3, all newborn mice from a single litter received the same dose. Control litters received 10 μl of PBS containing 50% glycerol (vehicle). Thereafter, subcutaneous injections were done twice a week for three weeks, alternatively on the left and right sides of the back. Mice were observed daily with particular attention to locomotion and urination alterations. Breeding was set up to theoretically generate litters with half wild type and half heterozygous Fgfr3ach/+ mice. To avoid bias due to variations of phenotype penetrance, experiments were performed on at least 2 litters (one treated and one control) arising from the same breeders. No statistical difference between males and females has been observed; they were thus considered as one group for all analyses (Garcia, S. et al. Sci. Transl. Med. 5, 203ra124, 2013).
At day 22, all animals were sacrificed by lethal injection of pentobarbital. Gender was determined. All subsequent measurements and analyses were performed without knowing mice genotype to avoid any experimental bias. Genotyping were performed at the end of the study to reveal the correspondence of data with a specific genotype. Because achondroplasia is a disease with an important phenotypic variability, all animals were included in the study, to improve the power of the study. Animals dead before day 22 were used for the study of the impact of treatment on premature death and animals reaching day 22 were used for all the analyses. All experiments and data measurements were performed in a blinded manner at all times.
Following sacrifice at day 22, body weights were measured. Blood (500 μI) was harvested by cardiac puncture and 25 μl were mixed with 25 μl 0.5 M EDTA. Samples were analyzed without centrifugation for blood numeration (Hemavet 950FS, Mascot Hematology). Cadavers were carefully skinned and eviscerated and skeletal measurements (body and tail lengths) were obtained using an electronic digital calliper (Fisher Scientific). Total body length was measured from the nose to the end of the last caudal vertebra; tail was measured starting at the first caudal vertebra. Organs were harvested, weighed and stored in 10% formalin for further histological analysis using standard paraffin-embedded techniques. Organs were observed for macroscopic abnormalities such as modification of color or texture, presence of nodules.
To determine the PK/PD parameters of FLAG-sFGFR3 and FLAG-sFGFR3_Del4-LK1-LK2, 8 week-old WT mice received an intravenous or subcutaneous bolus of 50 mg/kg and 100 mg/kg of protein, respectively. At 15 min, 1 h, 3 h, 8 h, 24 h, and 48 h blood was harvested by retro-orbital puncture using heparin catheter (n=4). Concentration of the FLAG tagged protein was measured by anti FLAG ELISA (Sigma).
Statistical Analysis.
Statistical analyses were performed with GraphPad Prism 6.0 software. To determine the statistical tests to be used, necessary assumptions were verified. To verify normality and equal variance, an Agostino and Pearson omnibus normality test (alpha=0.05) and a Brown-Forsythe test (p<0.05) were performed, respectively. Because all skeletal measurements data sets (body weight, body length, tail length, cranium length, width, length/width) fulfilled normality and equal variance requirements, two-tailed Student's t test for comparisons of two independent groups were used in the different statistical analyses. Comparison of mortality data between treated and control groups was done using a Kruskal-Wallis test (p<0.05) with a Dunn's test. Comparison of blood numeration was done using a one-way ANOVA with a Dunnett's multiple comparison test (95% CI). For organ weight correlation analyses, Pearson or Spearman tests were used when data sets followed or not normal distribution, respectively multiple comparison test (alpha 0.05). To compare correlations, a Fisher r-to-z transformation was performed. Comparison of decoys binding to human and murine FGFs was done by linear regression.
Summary: All four sFGFR3_Del1, sFGFR3_Del2, sFGFR3_Del3 and sFGFR3_Del4 variants bind human FGF2 with similar affinity than the sFGFR3 full-length construct. sFGFR3_Del4 binds FGF9 with the same affinity as FLAG-sFGFR3.
All four variants were tested in vitro for their ability to bind human FGF2. Similar to the protocol used to validate the mechanism of action of the FLAG-sFGFR3 molecule; different amounts of FLAG-sFGFR3_Del were incubated with constant quantities of FGF2. All variants bind human FGF2 in a receptor-dose-dependent manner with a similar affinity than the initial FLAG-sFGFR3 protein (
Summary: Del4 is effective at restoring bone growth in transgenic Fgfr3ach/+ mice.
To evaluate FLAG-sFGFR3_Del4 for its therapeutic efficacy, 3 day-old animals received 2.5 mg/kg of protein twice per week for 3 weeks. Control groups received vehicle. Experiments were performed blinded. A total of 108 animals were included.
The biological effects of FLAG-sFGFR3_Del4 were evaluated following a 3-week-long injection regimen to 3 day-old neonate mice. All newborn male and female mice from one litter received the treatment twice per week over the course of 3 weeks: 2.5 mg/kg FLAG-sFGFR3_Del4, (n=74) or vehicle for control groups (n=52). The first observation was the significant reduction in mortality with treatment: mortality for vehicle-treated Fgfr3ach/+ mice was 63% compared with 40% in the treated group.
The velocity of growth was evaluated during the three-week treatment by monitoring cranium length and body weight on growing animals. Results show an improvement in growth velocity with the FLAG-sFGFR3_Del4 treatment (
At day 22, all surviving animals were sacrificed and their growth was evaluated as measurements of body weight, body length, and tail length. FLAG-sFGFR3_Del4 treatment had a positive effect on overall skeletal growth in similar range than FLAG-sFGFR3 treatment (
Summary: FLAG-sFGFR3_Del4-LK1-LK2 effectively binds FGF2 and aggrecan.
Prior to initiating in vivo studies, FLAG-sFGFR3_Del4-LK1-LK2 was evaluated for its ability to bind FGF2 and aggrecan. For this, different amounts of recombinant protein were incubated with constant quantities of FGF2. Our results show that FLAG-sFGFR3_Del4-LK1-LK2 binds human FGF2 with the same affinity as FLAG-sFGFR3 (
To verify aggrecan binding, different amounts of recombinant protein were incubated with a fixed amount of aggrecan. As seen in
Summary: FLAG-sFGFR3_Del4-LK1-LK2 is effective at restoring bone growth in Fgfr3ach/+ mice.
Comparison of the pharmacokinetic parameters between the initial full-length protein and the fusion protein was performed by the injection of a bolus of protein either by the intravenous or subcutaneous route. Results show that the FLAG-sFGFR3_Del4-LK1-LK2 protein had similar PK parameters with a blood half-life within the same range than that of FLAG-sFGFR3 (see Table 1). However, it has to be kept in mind that the fusion protein targets the cartilage and is therefore retained in this tissue, such that the half-life measured using blood would be expected to be much lower in comparison to FLAG-sFGFR3 which keeps circulating. In fact, in view of the computed instability index (II) (37.41 for FLAG-sFGFR3_Del4-LK1-LK2 classifying it as stable vs. 44.04 for FLAG-sFGFR3, classifying it as unstable), surprisingly indicating that FLAG-sFGFR3_Del4-LK1-LK2 is more stable than FLAG-sFGFR3, and in view of the similar half-life determined in blood, it must be assumed that the actual time for elimination of FLAG-sFGFR3_Del4-LK1-LK2 from the body is significantly longer than for FLAG-sFGFR3, which is highly advantageous since it may allow reducing the effective dosage and/or the frequency of administration.
The therapeutic potential of FLAG-sFGFR3_Del4-LK1-LK2 was evaluated by injecting subcutaneously 0.3 mg/kg of protein twice per week for 3 weeks starting at age day 3. Control groups received vehicle and experiments were performed blinded. A total of 102 animals were included.
FLAG-sFGFR3_Del4-LK1-LK2 treatment resulted in a significant reduction in mortality of transgenic animals, from 63% in the control group to 37.5% in the treated group. Velocity of growth was significantly improved by the FLAG-sFGFR3_Del4-LK1-LK2 treatment as seen in
Potential side effects were evaluated in liver, lung, heart, spleen and kidneys at the time of sacrifice. None of the 102 animals that received chronic subcutaneous injections of FLAG-sFGFR3_Del4-LK1-LK2 or vehicle presented macroscopic abnormalities. In all groups, organ weight changes correlated with changes in total body weight (Table 2), suggesting no direct effect of FLAG-sFGFR3_Del4-LK1-LK2 treatment on organ growth. Blood counts were normal for all animals in this study (Table 3).
This study shows that a fusion protein, containing portions of sFGFR3 and of HPLN1, can be used to restore endochondral bone growth in a murine model of achondroplasia.
We first validated that a decoy variant containing the extracellular portion and a very short portion of the intracellular domain of sFGFR3 was sufficient to cause effective FGF binding and engender in vivo efficacy restoring bone growth in mice carrying the G380R mutation.
The fusion protein has been designed to specifically target cartilage, thus increasing exposure of the target tissue, allowing decreasing a potential effective dose. Biodistribution studies suggest cartilage trapping with similar diffusion through body (PK/PD analysis). FLAG-sFGFR3_Del4-LK1-LK2 treatment is effective at restoring bone growth in the transgenic murine model. Similar to FLAG-sFGFR3, no apparent toxicity was associated with FLAG-sFGFR3_Del4-LK1-LK2 treatment, suggesting that this protein can be used as a therapeutic for achondroplasia and related disorders.
We have also validated the use of body weight and skull length and/or width monitoring to evaluate velocity of growth. While both approaches give similar results, it is technically easier to use body weight as an index of velocity as skull measurement on newborn animals may created unwanted side effects if not done properly.
In conclusion, it has been demonstrated that FLAG-sFGFR3_Del4-LK1-LK2 is a viable treatment option for achondroplasia and related disorders.
Further experiments were performed to generate sFGFR3 polypeptides (e.g., sFGFR3_Del4) and a sFGFR3 fusion polypeptide (e.g., sFGFR3_Del4-LK1-LK2) with a FLAG-tag in the C-terminal position. Recombinant proteins were produced by transient transfection using CaCl2 transfection reagent in FreeStyle™ 293FT cells (TheroFisher Scientific). The plasmid used was pBApo-EF1α-sFGFR3-FLAG plasmid for all variants (sFGFR3_Del1, sFGFR3_Del4, and sFGFR3_Del4-LK1-LK2). An Erlenmeyer flask (2000 ml) was seeded with 293FT cells at a concentration of 1.8×106 cells/ml. Cells were centrifuged for 5 minutes at room temperature prior to transfection, and then resuspended in 300 ml final volume of medium (FreeStyle™ 293 Expression Medium Life technologies). A solution including sFGFR3-FLAG (600 μg plasmid DNA) and 1.73 m of 2M CaCl2 was resuspended in 18 ml of 2× Hepes Buffered Saline (HBS) and then incubated for 30 min at room temperature. The mixture was then added to an erlenmeyer flask and 600 ml of fresh media was added after 4 hours. After 72 hours, the supernatant was purified using the Akta™ Flux 6 cross-flow filtration system with a combination of two different capsules: 1) the ULTA Prime GF capsule featuring a pleated glass microfibre depth filter with a 5 micron pore size rating and a filter surface area of 0.095 m2, and 2) the ULTA Pure HC capsule featuring a pleated polyethersulfone sterilizing grade membrane layer with a polyethersulfone prefilter with 0.6/0.2 micron pore size rating and a filter surface area of 0.1 m2 (GE Healthercare Life Sciences).
Stable cells lines were then generated by stable transfection of the GP2-293 packaging cell line using CaCl2 transfection (Clontech). The Del vectors were designed based on the transient transfection results obtained in 293FT cells to create stable cell lines that produce sFGFR3_Del1, sFGFR3_Del4, and sFGFR3_Del4-LK1-LK2. In particular, the plasmids included the signal peptide (MGAPACALALCVAVAIVAGASS) in the same as the previously designed N-terminal FLAG-sFGFR3 variants, the FLAG tag in the C terminal position, an EF1 a promoter instead of a CMV promoter, and a pBAbe backbone. Co-transfection of pVSVg and pBABE-EF1α Puro sFGFR3_Del1 Cter FLAG, pBABE-EF1α Puro sFGFR3_Del4-LK1-LK2 Cter FLAG, or pBABE-EF1 a Puro sFGFR3_Del4 Cter FLAG were performed according to the manufacturer's instructions.
The recombinant sFGFR3 polypeptides and fusion polypeptides were then purified using cross flow filtration system. The advantages of this technique are the elimination of contaminants without aggregation and the purified recombinant sFGFR3 polypeptide are produced under optimized conditions for IEX chromatography. The cross-flow filtration was performed using an Ultrafiltration Hollow Fiber Cartridge (Fiber: UFP-750C from GE Healthcare) at 10× concentration, followed by 3 times volume exchange in Tris 20 mM pH 7 for sFGFR3_Del1 and Tris 20 mM pH 8.5 for sFGFR3_Del4 and sFGFR3_Del4-LK1-LK2. Ion Exchange Chromatography (IEX) was then performed at pH 7 for sFGFR3_Del1 and at pH 8.5 for sFGFR3_Del4 and sFGFR3_Del4-LK1-LK2 using a Hi Prep Q FF 20 ml column (GE Healthcare Life Sciences). Aspiration and elution was performed at a rate of 5 ml/min. A volume fraction of 8 ml was added to the column, then the unbound sFGFR3 polypeptide was washed with a buffer including Tris 20 mM followed by a wash with Tris 20 mM, 1 M NaCl. Finally, size exclusion chromatography was performed using a HiLoad Superdex 200 prep grad (GE Healthcare), with 13 ml of the supernatant at a flow rate of 1 ml/min and an elution buffer of 20 mM Tris, 150 mM NaCl pH 7.4 for all recombinant sFGFR3 polypeptides and fusion polypeptides.
Western blots of the sFGFR3_Del1, sFGFR3_Del4, and sFGFR3_Del4-LK1-LK2 were performed using TBOLT™ 4-12% Bis-Tris Plus Gels (Life technologies) and an IBLOT® 2 Gel Transfer Device (Life Technologies) with a PVDF membrane stack. Sample preparation and migration were performed using the manufacturer's instructions. The transfer procedure was the P0 program of the iBlot® 2 Gel Transfer Device (i.e., 20V for 1 min, 23V for 4 min, and 25V for 2 min). After 30 minutes of blocking, incubation with anti-FLAG monoclonal M2 antibody (Sigma Aldrich) was performed for 1 hour. A C-DiGit Chemiluminescence Western Blot Scanner was then used for analysis with a standard ECL substrate (Licor).
When the FLAG tag of sFGFR3_Del1, sFGFR3_Del4, and sFGFR3_Del4-LK1-LK2 is in the N-terminal position followed by the signal peptide sequence, the sFGFR3 polypeptides and fusion polypeptide were not detectable via Western blot using the anti-FLAG monoclonal M2 antibody (
Treatment with sFGFR3_Del1 or sFGFR3_Del4-LK1-LK2 was performed in Fgfr3ach/+ mice as described in Garcia et al. (supra), which is incorporated herein by reference in its entirety. Mice were sacrificed at day 5 and day at day 22 after birth. The biobiodistribution of sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 in the growth plate of the mice and the effect of sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 on all bones, growth plate thickness, and the hypertrophic chondrocyte zone were determined over a three week period. The presence of the FLAG tagged polypeptides was determined in the growth plate. These results demonstrate that sFGFR3_Del4-LK1-LK2 is trapped faster within the growth plate (e.g., at day 5), which may be due to an aggrecan defect in Fgfr3ach/+ mice (
10B). There was also a greater accumulation of sFGFR3_Del1 at day 22 in Fgfr3ach/+ mice (
Skull measurements and x-ray radiography were also performed on wild-type mice and Fgfr3ach/+ mice after 5 days of treatment with sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 (Table 4;
Potency assays were performed to determine the effect of sFGFR3_Del1 (SEQ ID NO: 1) on Erk/P-Erk Intracellular signaling in ATDC5 chondrocyte cells. ATDC5 cells were plated at a density of 7.5×103 in 96-well plates and cultured for 24 hours in DMEM-F12/0.5% BSA (Life Technologies). Cells were then challenged for 24 hours with hFGF2 (100 pg/ml) in the presence of sFGFR3_Del1 (0 or 20 ng/ml). Intracellular signaling was evaluated with the ICW kit PhosphoPlus® p44/42 MAPK (Erk1/2)(Thr202/Tyr204) In-Cell Duet (ICW Compatible)-(cell signaling). After a 24 hour incubation, there was a decrease of Erk phosphorylation in ATDC5 cells incubated with sFGFR3_Del1 (SEQ ID NO: 1) and FGF decreased relative to ATDC5 cells incubated with sFGFR3_Del1 (SEQ ID NO: 1) or FGF alone (
The effect of different fractions of purified sFGFR3 polypeptide or sFGFR3 fusion polypeptide on cellular proliferation was determined in ATDC5 chondrocyte cells. Size-exclusion chromatography followed by western blot analysis was performed as described above to purify and identify fractions of sFGFR3_Del1 (
Behavioral studies were performed to characterize the long-term effects of sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 in the C57BL6/J mouse. sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 were each administered subcutaneously twice per week during the first 8 postnatal weeks, starting from postnatal day 3. There was three different groups (16 male mice per group) treated with sFGFR3_Del1, sFGFR3_Del4-LK1-LK2, or a vehicle at 2.5 mg/kg. Behavioral evaluation was conducted between postnatal weeks 10 and 14. The effects of sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2 on behavior, sensory capacities, motor capacities, psychological characteristics, and cognitive function were investigated.
These studies showed no indications of long term toxicity of treatment with sFGFR3_Del1 and sFGFR3_Del4-LK1-LK2. For the Irwin test, activity meter test, elevated plus-maze test, and forced swimming test, no changes in any group were observed. For odor discrimination, I observed a minor decrease with sFGFR3_Del4-LK1-LK2. Administration of sFGFR3_Del4-LK1-LK2 also appeared to result in a minor decrease of motor coordination during the accelerating rotarod test and a minor improvement of motor coordination and spatial memory during the Morris water maze test, which were not statistically different.
Pharmacokinetic studies were performed to determine the uptake of FGFR3_Del1 and sFGFR3_Del4-LK1-LK2 across the blood brain barrier in C57BL/6 mice. After intravenous (i.v.) bolus injection, brain tissue uptake of FGFR3_Del1 and sFGFR3_Del4-LK1-LK2 was measured at 4 time points (1 hour (h), 3 hours (h), 6 hours (h), and 24 hours (h)). FGFR3_Del1 and sFGFR3_Del4-LK1-LK2 were injected as radiolabeled tracer (125I-FGFR3_Del1 or 125I-sFGFR3_Del4-LK1-LK2) with 2.5 mg/kg unlabeled FGFR3_Del1 and sFGFR3_Del4-LK1-LK2. The injected dose of 125I-FGFR3_Del1 or 125I-sFGFR3_Del4-LK1-LK2 was about 10 μCi per animal, which corresponds to less than 0.1 mg/kg. After euthanizing the mice at 1 h, 3 h, 6 h or 24 h, the concentration of 125I-FGFR3_Del1 or 125I-sFGFR3_Del4-LK1-LK2 in organs and plasma was measured by liquid scintillation counting.
125I-FGFR3_Del1 or 125I-sFGFR3_Del4-LK1-LK2 concentrations were corrected for metabolism in plasma and in brain samples by measuring the fraction of trichloroacetic acid (TCA) precipitable material (e.g., intact tracer). The validity of the TCA correction was also confirmed by injecting samples on a size exclusion fast protein liquid chromatography (FPLC) column. The organ concentration of 125I-FGFR3_Del1 or 125I-sFGFR3Del4-LK1-LK2 was corrected for intravascular content (V0) by injecting radiolabeled albumin (3H-RSA) shortly before sacrificing the animal. The apparent organ volume of distribution of RSA represents V0. The dose of albumin was negligible (on the order of 1% of the physiological concentration). For all organs other than brain, the concentrations were calculated by subtracting the vascular content and taking into account the TCA precipitable fraction in plasma. However, no correction was made for the uptake of degraded material into these organs other than the brain because no TCA precipitation was performed.
The brain concentrations were calculated by the following formula: Cbrain(corr.)=[Vd(FGFR3_Del1)−V0]×Cplasma (terminal), in which Vd(FGFR3_Del1) is the volume of distribution of FGFR3_Del1 in brain (calculated as Cbrain/Cplasma), V0 is the volume of albumin distributed in the brain, and Cplasma(terminal) is the plasma concentration of FGFR3_Del1 at the terminal sampling time. Calculations for sFGFR3_Del4-LK1-LK2 were performed identically, and all concentrations were expressed as the percent of injected dose per gram or ml (% ID/g or % ID/mL), respectively, and the dose of the i.v. bolus equals 100%. If desired, these values may be converted to [mg/g] or [mg/mL] by multiplication with the injected dose: (body weight in g/1000 g)×2.5 mg. All body weights were in the range of 25 g-30 g.
There was no detectable brain uptake of 125I-FGFR3_Del1, as indicated by corrected brain concentrations (after correction for vascular content and degradation (TCA precipitability)), at any of the measured time points (1 h, 3 h, 6 h, or 24 h) (
Similar results were obtained for brain tissue uptake of 125I-sFGFR3_Del4-LK1-LK2. There was no detectable brain uptake of 125I-sFGFR3_Del4-LK1-LK2, as indicated by corrected brain concentrations (after correction for vascular content and degradation (TCA precipitability)), at any of the measured time points (1 h, 3 h, 6 h, or 24 h) (
In a non-compartmental analysis (NCA) of 125I-FGFR3_Del1 and 125I-sFGFR3_Del4-LK1-LK2 plasma concentrations with Phoenix WinNonlin, the area under the curve (AUC) of 125I-sFGFR3_Del4-LK1-LK2 was lower than the AUC of 125I-FGFR3_Del1 by a factor of 0.71 (
In conclusion, there is no measurable uptake of either FGFR3_Del1or sFGFR3_Del4-LK1-LK2 into brain tissue of mice at any of the time points analyzed in this study, at a dose of 2.5 mg/kg injected as an intravenous bolus. These results are based on the assumption that the 125I-FGFR3_Del1 and 125I-sFGFR3_Del4-LK1-LK2 (tracer-labeled proteins) behave similarly to unlabeled protein in brain tissue and plasma.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15290003.1 | Jan 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2016/000403 | 1/7/2016 | WO | 00 |
