Patent Application
20210371929
The present invention relates to a method for prediction of response to disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration comprising the use of a biomarker. Further, the present invention relates to a combination of biomarkers for use in a method for prediction of response to disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration, a computer device to perform a method according to the present invention and a device adapted for carrying out the inventive method.
Regenerative therapies for the repair of organic tissue, in particular of heart tissue, have been at the forefront of preclinical and clinical development in the last 17 years. In view of heart tissue, among the different approaches the direct application of bone marrow stem cells (BMSC) in heart tissue still has the most dedicated clinical developmental attention since the first-in-man application in 2001 and the initial promising clinical trials (Stamm C, Westphal B, Kleine H D, et al. Lancet. 2003; 361(9351):45-46; Tse H F, Kwong Y L, Chan J K, Lo G, Ho C L, Lau C P. Lancet 2003; 361(9351):47-9; Stamm C, Kleine H D, Choi Y H, et al. J Thorac Cardiovasc Surg 2007; 133(3):717-25). Yet, in these trials, clinically relevant improvements of LVEF (Left Ventricular Ejection Fraction) as well as non-responsive patients could be observed both in treatment and placebo groups (Timothy D H, Lem M, Jay H T, Circulation Research 2016; 119:404-406; Nasseri B A, Ebell W, Dandel M, et al. Eur Heart J. 2014, 35(19):1263-74; Bartunek J, Terzic A, Davison B A et al. Eur. Heart J. 2016 Dec. 23. pii: ehw543. doi: 10.1093/eurheartj/ehw543).
Hematopoietic stem cells (HCSs) are the stem cells that give rise to other blood cells. In vertebrates, the vast majority of hematopoiesis occurs in the bone marrow (BM) and is derived from a limited number of hematopoietic stem cells that are multipotent and capable of extensive self-renewal. The hematopoietic system has traditionally been considered unique among phenotypically characterized adult stem/progenitor cells (Slack J M. Science 2000; 287:1431-1433; Blau H M, Brazelton T R, Weimann J M. Cell 2001; 105:829-841; Korbling M, Estrov Z. New England Journal of Medicine 2003; 349:570-582) in that it is an organized, hierarchic system with multipotent, self-renewing stem cells at the top, lineage-committed progenitor cells in the middle, and lineage-restricted precursor cells, which give rise to terminally differentiated cells, at the bottom (Weissmann I L. Cell 2000; 100:157-168). However, disorders of clonal hematopoiesis have been described in hematological and cardiovascular disease patients and associated to congenital or somatic DNA mutations (Moehrle B M, Geiger H. Exp Hematol 2016; October; 44(10):895-901. doi: 10.2016/j.exphem.2016.06.253. Epub 2016 Jul. 8; Jaiswal S, Natarajan P, Silver A J et al. N Engl J Med 2017; Jul. 13; 377(2):111-121. doi: 10.1056/NEJMoa1701719. Epub 2017 Jun. 21.). The question arises, which mutations in stem congenital or somatic cell regulatory genes cause hematopoietic clonal advantage and impact cardiovascular pathology (Machiela M J, Chanock S J. Curr Opin Genet Dev 2017; February; 42:8-13. doi: 10.1016/j.gde.2016.12.002. Epub 2017 Jan. 6.).
One of the major genes associated with hematopoetic stem cell (HSC) proliferation disorders, such as myelodysplasia, erythrocytosis or leukemia by somatic mutation, is SH2B3 coding for the lymphocyte adapter protein (Lnk, LNK) adaptor protein (Elias H K, Bryder D, Park C Y. Semin Hematol 2017; January; 54(1):4-11. doi: 10.1053/j.seminhemato1.2016.11.002. Epub 2016 Nov. 20.). However, Lnk/SH2B3 expression regulation in human bone marrow (BM) and clonal blood stem and progenitor cells is largely unknown for cardiovascular regeneration (Steinhoff G, Nesteruk J, Wolfien M, Große J, Ruch U, Vasudevan P, Müller P. Adv Drug Deliv Rev 2017; Oct. 1; 120:2-24. doi: 10.1016/j.addr.2017.10.007. Epub 2017 Oct. 18; Zhu X, Fang J, Jiang D S, Zhang P, Zhao G N, Zhu X, Yang L, Wei X. 2-B3Hypertension 2015; September; 66(3):571-81. doi: 10.1161/HYPERTENSIONAHA.115.05183. Epub 2015 Jun. 22.).
Lnk/SH2B3 shares a pleckstrin homology domain, a Src homology 2 domain, and potential tyrosine phosphorylation sites with APS and SH-2B. It belongs to a family of adaptor proteins implicated in integration and regulation of multiple signaling events (Ahmed Z, Pillay T S. Biochem J 2003; 371:405-412., Huang X, Li Y, Tanaka K, Moore K G, Hayashi J I. Proc Natl Acad Sci USA 1995; 92:11618-11622; Takaki S, Watts J D, Forbush K A, Nguyen N T, Hayashi J, Alberola.IIa J, Aebersold R, Perlmutter R M. Biol Chem 1997; 272:14562-14570.) and has also been suggested to act as a negative regulator in the stem cell factor (SCF)/-c-Kit signaling pathway (Moehrle B M, Geiger H. Exp Hematol 2016; October; 44(10):895-901. doi: 10.1016/j.exphem.2016.06.253. Epub 2016 Jul. 8., Takaki S, Sauer K, Iritani B M, Chien S, Ebihara Y, Tsuji K, Takatsu K, Perlmutter R M. Immunity 2000; 13:599-609.). Lnk/SH2B3 has also been reported to play a critical role in maintaining the ability of HSCs to self-renew, in a study that based on BM c-Kit+/Sca-1+/Lineage (Lin)− (KSL) CD34− cells, which are a more immature HSC subpopulation than KSL CD34+ cells (Ema H, Sudo K, Seita J, Matsubara A, Morita Y, Osawa M, Takatsu K, Takaki S, Nakauchi H. Dev Cell 2005; 8:907-914.). Takaki et al. reported that Lnk/SH2B3 is expressed in hematopoietic cell lineages in mice, and BM cells of Lnk/SH2B3-deficient mice are competitively superior in hematopoietic population to those of WT mice (Takaki S, Morita H, Tezuka Y, Takatsu K. Lnk/SH2B3. J Exp Med 2002; 195:151-160.). They also clarified that not only HSC/hematopoietic progenitor cell (HPC) numbers but also the self-renewal capacity of some HSCs/HPCs were markedly increased in Lnk/SH2B3−/− mice (Ema H, Sudo K, Seita J, Matsubara A, Morita Y, Osawa M, Takatsu K, Takaki S, Nakauchi H. Dev Cell 2005; 8:907-914). In addition, they identified the functional domains of Lnk/SH2B3 and developed a dominant-negative Lnk/SH2B3 mutant that inhibits the functions of Lnk/SH2B3 endogenously expressed in the HSCs/HPCs and thereby potentiates the HPCs for engraftment (Takizawa H, Kubo-Akashi C, Nobuhisa I, Kwon S M, Iseki M, Taga T, Takatsu K, Takaki S.. Blood 2006; 107:2968-2975.).
The inventors have identified a method for prediction of response to disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration, comprising the determination of a biomarker. The present invention is thus directed to a method for prediction of response to cardiovascular regeneration comprising the determination of a biomarker, according to claim 1 of the present application. Further, the present invention relates to a combination of biomarkers for use in a method for prediction of response to the disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration, a computer device to perform such a method and a device adapted for carrying out the inventive method.
The present invention is thus directed to a method for prediction of response to disease therapy, in particular to cardiovascular regeneration, wherein the method comprises
The invention is further directed to a method for prediction of response to disease therapy, in particular to cardiovascular regeneration, wherein the method comprises
Preferably, the method of the present invention is an ex vivo I in vitro method. Moreover, it may comprise steps in addition to those explicitly mentioned above. For example, further steps may relate to sample pre-treatments or further evaluations or uses of the results obtained by the method. The method may be carried out manually or assisted by automation. Preferably, step (i) may in total or in part be assisted by automation, e.g. by a suitable robotic and sensory equipment. Steps (ii) and/or (iii) may be assisted by data processing units which carry out the respective comparisons and/or predictions.
The SH2B3 gene encodes a member of the SH2B adaptor family of proteins, which are involved in a range of signaling activities by growth factor and cytokine receptors. The encoded protein is a key negative regulator of cytokine signaling and plays a critical role in hematopoiesis. Mutations in this gene have been associated with susceptibility to celiac disease type 13 and susceptibility to insulin-dependent diabetes mellitus. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. SH2B3 is also identified under HGNC: 29605, Entrez Gene: 10019, Ensembl: ENSG00000111252, OMIM: 605093, UniProtKB: Q9UQQ2.
The term “predicting” as used herein means assessing the probability according to which a subject will benefit from disease therapy, in particular to tissue repair, preferably to cardiac repair, more preferably from cardiac stem cell therapy in that there is a functional improvement of the cardiovascular system as defined elsewhere herein in detail after the said cardiac therapy. Within the context of the present invention, the term cardiac repair and cardiac regeneration is used synonymously.
As will be understood by those skilled in the art, such an assessment is usually not intended to be correct for 100% of the subjects to be diagnosed. The term, however, requires that the assessment is correct for a statistically significant portion of the subjects (e.g. a cohort in a cohort study). Whether a portion is statistically significant can be determined without further ado by the person skilled in the art using various well known statistic evaluation tools, e.g., by determination of confidence intervals, p-value determination, Student's t-test, Mann-Whitney test etc. Details are found in Dowdy and Wearden, Statistics for Research, John Wiley & Sons, New York 1983. Preferred confidence intervals are at least 90%, at least 95%, at least 97%, at least 98% or at least 99%. The p-values are, preferably, 0.1, 0.05, 0.01, 0.005, or 0.0001.
The term “cardiovascular regeneration” as used herein includes the regeneration and/or treatment and/or improvement of diseases related to the cardiovascular system.
The term “biomarker” refers to molecules, the presence, absence or amount of which correlates with medical conditions or predispositions. Biomarkers may be any molecules and/or cells or subpopulations thereof, which occur in the subject. Typically, biomarkers are proteins, peptides, small molecules or nucleic acids, such as DNAs or RNAs, or cells and subpopulations thereof. In accordance with the present invention, the term preferably, refers to a gene and/or -gene expression, wherein the gene and/or -gene expression comprises a mutational variant. Such a gene and/or -gene expression may be analysed by sequencing of DNA and/or RNA. Analysing the gene and/or -gene expression might also include co-expression of a further gene and/or -gene expression. Such a determination of gene and/or -gene expression might be performed, e. g. in cardiomyocytes. According to a specific embodiment, the biomarker is selected from SH2B3-gene and/or -gene expression, wherein the SH2B3-gene and/or -gene expression comprises a mutational variant.
Determining the amount of a biomarker referred to in this specification relates to measuring the amount or concentration, preferably, semi-quantitatively or quantitatively. Measuring can be done directly or indirectly. Direct measuring relates to measuring the amount or concentration of the biomarker based on a signal which is obtained from the biomarker itself and the intensity of which directly correlates with the number of molecules of the biomarker present in the sample. Such a signal—sometimes referred to herein as intensity signal—may be obtained, e.g. by measuring an intensity value of a specific physical or chemical property of the biomarker. Indirect measuring includes measuring of a signal obtained from a secondary component (i.e. a component not being the biomarker itself) or a biological read out system, e.g. measurable cellular responses, ligands, labels, or enzymatic reaction products.
In accordance with the present invention, determining the amount of the biomarker can be achieved by all known means for determining the amount of a peptide, a protein, a small molecule, nucleic acids such as DNAs or RNAs or a cell or subpopulations thereof, in a sample. Said means comprise immunoassays and methods, which may utilize labelled molecules in various sandwich, competition, or other assay formats. Such assays are, preferably, based on detection agents such as antibodies, which specifically recognize the biomarker to be determined. The detection agents shall be either directly or indirectly capable of generating a signal indicating the presence or absence of the biomarker. Moreover, the signal strength can, preferably, be correlated directly or indirectly (e.g. reverse-proportional) to the amount of biomarker present in a sample. Further suitable methods comprise measuring a physical or chemical property specific for the biomarker such as its precise molecular mass or NMR spectrum. Said methods comprise, preferably, biosensors, optical devices coupled to immunoassays, FACS analysis, biochips, analytical devices such as mass-spectrometers, NMR-analysers, or chromatography devices. Further, methods include micro-plate ELISA-based methods, fully-automated or robotic immunoassays, enzymatic Cobalt binding assays, and latex agglutination assays.
Preferably, determining the amount of the biomarker comprises the steps of (a) contacting a cell capable of eliciting a cellular response the intensity of which is indicative of the amount of the biomarker with the said biomarker for an adequate period of time, (b) measuring the cellular response. For measuring cellular responses, the sample or processed sample is, preferably, added to a cell culture and an internal or external cellular response is measured. The cellular response may include the measurable expression of a reporter gene or the secretion of a substance, e.g. a peptide, polypeptide, or a small molecule. The expression or substance shall generate an intensity signal which correlates to the amount of the biomarker.
Also preferably, determining the amount of a biomarker comprises the step of measuring a specific intensity signal obtainable from the biomarker in the sample. As described above, such a signal may be the signal intensity observed at an m/z variable specific for the biomarker observed in mass spectra or an NMR spectrum specific for the biomarker.
The term “amount” as used herein encompasses the absolute amount of a biomarker, the relative amount or concentration of said biomarker as well as any value or parameter, which correlates thereto or can be derived therefrom. Such values or parameters comprise intensity signal values from all specific physical or chemical properties obtained from said peptides by direct measurements, e.g. intensity values in mass spectra or NMR spectra. Moreover, encompassed are all values or parameters which are obtained by indirect measurements specified elsewhere in this description, e.g. response levels determined from biological read out systems in response to the peptides or intensity signals obtained from specifically bound ligands. It is to be understood that values correlating to the aforementioned amounts or parameters can also be obtained by all standard mathematical operations and can be used without dimensions, e.g. in scoring systems as described elsewhere herein.
The term “comparing” as used herein encompasses comparing the amount of the biomarker comprised by the sample to be analysed with an amount of a suitable reference source specified elsewhere in this description. It is to be understood that comparing as used herein refers to a comparison of corresponding parameters or values, e.g., an absolute amount is compared to an absolute reference amount while a concentration is compared to a reference concentration or an intensity signal obtained from a test sample is compared to the same type of intensity signal of a reference sample. However, in accordance with the present invention it is also envisaged to calculate a value based on the measured amounts of the biomarkers. Said value is compared to reference intervals which have been derived from a multivariate discriminant analysis performed on amounts from a collective of subjects comprising pre-defined responders and non-responders to cardiac stem cell therapy. Further details may be found in the accompanying examples, below.
The comparison referred to in the method of the present invention may be carried out manually or computer assisted. For a computer assisted comparison, the value of the determined amount may be compared to values corresponding to suitable references which are stored in a database by a computer program. The computer program may further evaluate the result of the comparison, i.e. automatically provide the desired assessment in a suitable output format. Preferably, such an assessment is performed by machine learning (ML). Based on the comparison of the determined amounts and the reference, it is possible to predict a response to cardiac regeneration, e.g. a functional improvement of the heart after cardiac stem cell therapy. In particular, it shall be possible to predict whether there is a high probability (i.e. the subject will be a responder), a low probability (i.e. the subject will be a non-responder) or the subject is ambivalent. Therefore, the reference amount is to be chosen so that either a difference or a similarity in the compared amounts allows identifying those test subjects, which belong into the group of subjects exhibiting a symptom of acute inflammation having either an ischemic or non-ischemic cerebral damage. The method allows either excluding (rule-out) or identifying (rule-in) a subject as a subject suffering from (i) an ischemic cerebral damage or (ii) a non-ischemic cerebral damage.
The term “reference” as used herein refers to a value, threshold or interval based on amounts of the biomarker which allows for allocation of a subject into either the group of subjects which can be expected to benefit from the disease therapy, in particular from tissue repair, preferably from cardiac therapy, which can be expected not to benefit from the disease therapy, in particular from tissue repair, preferably from cardiac therapy, or those which are ambivalent.
Preferably, such a reference is a non-disease type or individual reference cell without somatic mutation gene and/or -gene expression. Even more preferably, such a reference is an SH2B3 non-disease type or individual reference cell without somatic mutation gene and/or -gene expression,
Such a reference can be a threshold amount, which separates these groups from each other. A suitable threshold amount separating the two groups can be calculated without further ado by the statistical tests referred to herein elsewhere based on amounts of the biomarkers from either a subject or group of subjects known to benefit from disease therapy, in particular to tissue repair, preferably to cardiac repair, or a subject or group of subjects known not to benefit from said therapy or those which are known to be ambivalent.
A reference can, in principle, also be calculated for a cohort of subjects as specified above based on the average or mean values for a given biomarker by applying standard statistically methods. In particular, accuracy and sensitivity of a test such as a method aiming to diagnose an event, or not, is best evaluated by its receiver-operating characteristics (ROC) (see especially Zweig 1993, Clin. Chem. 39:561-577). Accordingly, the reference to be used for the aforementioned method of the present invention may be generated by establishing a ROC for said cohort as described above and deriving a threshold amount therefrom. Dependent on a desired sensitivity and specificity for a diagnostic method, the ROC plot allows deriving suitable thresholds.
The term “sample” refers to a sample of a body fluid, and preferably, to a sample of (whole) blood, plasma or serum. The term, however, also encompasses all samples which are derived from the aforementioned whole blood, plasma or serum by, e.g. pre-treatment steps such as fractions of blood, plasma or serum obtained by, e.g. partial purification.
The term “subject” as used herein refers to an animal, preferably, a mammal and, most preferably, a human. The subject shall be in need of disease therapy, preferably of cardiac therapy. Preferably, a subject in need for cardiac therapy suffers from a cardiac disease such as heart failure or coronary artery disease, e.g. after myocardial infarction, and, more preferably, from heart failure.
The prediction made according to the method of the invention also allows for assessing whether the probability is high and, thus, it is expected that a functional improvement of the cardiac system in a subject occurs, or whether the probability is such that the therapy success is ambivalent or whether the probability is low and, thus, it is expected that a functional improvement of the cardiac system in a subject will not occur.
The present invention further relates to one or more biomarker/s selected from SH2B3-gene and/or -gene expression mutation variant and/or Lymphocyte adapter protein expression from SH2B3-gene and/or -gene expression mutation variant for use in a method for prediction of response to disease therapy, in particular from tissue repair, preferably for prediction of response to cardiovascular regeneration.
Also, the present invention is directed to a computer device comprising a processor and a memory encoding one or more machine learning (ML) models coupled to the processor, wherein said programs cause the processor to perform a method, said method comprising
(i) comparing the determined biomarker/s to a baseline value and/or a reference, preferably to a baseline value and/or a reference of SH2B3-gene and/or -gene expression without mutational variant,
(ii) predicting, based on the results of the comparison, whether a response to disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration, in the subject is to be expected, not expected or is ambivalent.
In addition, the present invention pertains to a device adapted for carrying out the inventive method, comprising
The term “device” as used herein relates to a system comprising the aforementioned units operatively linked to each other as to allow the diagnosis according to the methods of the invention. Preferred detection agents, which can be used for the analysing unit, are disclosed elsewhere herein. Preferred detection agents are antibodies or other proteins that specifically bind to the biomarker(s) and form detectable complexes. The analysing unit, preferably, comprises said detection agents in immobilized form on a solid support which is to be contacted to the sample comprising the biomarkers the amount of which is to be determined. Moreover, the analysing unit can also comprise a detector, which determines the amount of detection agent, which is specifically bound to the biomarker(s). The determined amount can be transmitted to the evaluation unit. Said evaluation unit comprises a data processing element, such as a computer, with an implemented algorithm for carrying out a comparison between the determined amount and a suitable reference. Suitable references can be derived from samples of subjects to be used for the generation of reference amounts as described elsewhere herein above. The results may be given as output of parametric diagnostic raw data, preferably, as absolute or relative amounts. It is to be understood that these data will need interpretation by the clinician. However, also envisaged are expert system devices wherein the output comprises processed diagnostic raw data the interpretation of which does not require a specialized clinician.
Further preferred embodiments of the invention are derived from the dependent claims together with the following description, whereby the patent claims of a certain category may be formed by dependent claims of a different category, and features of the different examples may be combined to new examples. It is to be understood that the definitions and explanations of the terms made above and below apply accordingly for all embodiments described in this specification and the accompanying claims. In the following, particular embodiments of the method of the present invention are specified further.
According to a preferred embodiment, the SH2B3-gene and/or -gene expression is a knock-out-gene and/or -gene expression variant. Preferably, such a knock-out-gene and/or -gene expression variant is a dominant negative SH2B31LNK− variant or LNK/SH2B3 deficient to inhibit the function of endogeneously expressed LNK/SH2B3.
Specifically, such a preferred variant is an SH2B3-gene and/or -gene expression variant that comprises at least one mutation of SH2B3-gene and/or -gene expression Variant 1 (Transcript: NM_005475.2) and/or SH2B3-gene and/or -gene expression Variant 2 (Transcript: NM_001291424.1), as depicted in
Preferably, the SH2B3-gene and/or -gene expression Variant 1 comprises a sequence selected from SEQ ID NO:1; the SH2B3-gene and/or -gene expression Variant 2 comprises a sequence selected from SEQ ID NO:2. While SEQ ID NO:2 lacks two alternate exons in the 5′ region, including a portion of the 5′ coding region, and initiates translation at an alternate start codon in an alternate exon, compared to SEQ ID NO:1. The encoded isoform 2 has a distinct N-terminus and is shorter than isoform 1.
By using the above SH2B3-gene or -gene expression mutational variant together with a further biomarker, in particular a biomarker selected from CD133 gene expression and/or CD133+/ml MNC cells in peripheral blood and/or CFU-Hill, the method according to the present invention is beneficially capable to increase sensitivity and specificity of prediction accuracy to more than about 60%.
A further preferred method uses analysis of LNK protein expression and function of an SH2B3-gene and/or -gene expression variant, thereby analysing inhibition and/or change of LNK function due to amino acid exchange or -deletion.
According to a specifically preferred embodiment, the method further uses one or more biomarker/s, wherein the further biomarkers is selected from the group of Angiogenic factor and/or Survival factor and/or Chemokine and/or circulation endothelial progenitor cells (EPC) and/or circulation endothelial cells (CEC) and/or circulating thrombocytes and/or circulating mononuclear cells and subpopulations, receptor/ligand expression on MNC subpopulations and/or whole genome sequence RNA.
According to a particularly preferred embodiment, the advantageous method further uses one or more biomarkers, wherein the further biomarker/s is/are selected from PLCG1, EPO, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB, VEGF, BEX3, Delta_CT_SH2B3, ZNF205, LTB, EMG1, CD34+ cells/ml PB, BAZ1A and/or CD133+ cells/ml PB.
Preferably, PLCG1, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB, BEX3, ZNF205, EMG1, BAZ1A and/or LTB is/are determined on an RNA level and/or EPO and/or VEGF is/are determined on a protein level.
Even more preferably, determination of EPO, VEGF, Delta_CT_SH2B3, CD34+ cells/ml PB and/or CD133+ cells/ml PB is conducted from preoperative samples.
According to an even more preferred embodiment the further biomarker/s is/are selected from PLCG1, EPO, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB and/or VEGF.
A combination of the above mentioned further biomarkers may be selected on an individual basis, depending on the disease type and/or disease state of the subject or patient, respectively. For example, a selection may encompass a combination of biomarkers including PLCG1, EPO, LPCAT2, GRB2, AP1B1, KLF8, MARK3 and/or VEGF (as depicted in
In addition to the above mentioned further biomarker/s, according to a next embodiment, for example, the Angiogenic factor is selected from VEGF, preferably from VEGF-B, and/or FGF, preferably from FGF-4, and/or HGF and/or Ang-1, the Survival factor is preferably selected from IGF-1 and the Chemokine is selected from IGF-2 and/or SDF-1.
It has been advantageously found in the studies underlying the present invention that analysing the amount of a combination of the biomarkers in a sample taken prior to cardiac therapy from a subject in need of said cardiac therapy, e.g. a subject suffering from heart failure, allows for predicting whether that subject will benefit from the therapy in that the cardiac regeneration or cardiovascular repair is improved after therapy. The techniques for measuring the amounts of the individual biomarkers are all well known in the art.
Beneficially, by implementing the method according to the present invention, sensitivity and specificity of prediction accuracy can be higher than about 90%, preferably higher than about 92%, more preferably higher than about 93%, most preferably higher than about 94%. Thus, the method of the present invention improves decision making of clinicians prior to the application of an expensive and cumbersome therapeutic measure such as cardiac therapy. Making the right decision, i.e. applying the therapy only if it is effective, will certainly also be beneficial for the individual patients and, in light of the cost consequences, for the public health system as such.
By using ML, the method is preferably further assisted since no individual comparisons must be carried out. Furthermore, the machine learning approach beneficially serves to balance and weighting the parameters such that reliability of the prediction can be further improved. Thus, an advantageous method of the present invention is preferably assisted by machine learning to facilitate and improve the overall prediction accuracy. In accordance with the present invention, the term “machine learning” relates to the study and construction of algorithms that can learn from and make predictions on data—the algorithms hereby overcome strictly static program instructions by making data-driven predictions or decisions through building a model from sample inputs.
In another embodiment of the method, such method further uses one or more biomarker/s, wherein the one or more biomarkers are selected from zinc finger protein ZDHHC2 and/or MYL4/ALC1 and/or INPP4B and/or RBM38 and/or CD133+ cells/m1 PB (peripheral blood) and/or CD34+ cells/ml PB and/or CD45+184+ cells/ml PB and/or CD45+ cell/ml PB and/or CD184+ cells/ml PB and/or MNC in PB and/or CFU-Hill of PB and/or RIOK3-gene expression in PB and/or ABCC13-gene expression in PB and/or COPS3-gene expression in PB and/or GUK1-gene expression in PB and/or AP3B1-gene expression in PB and/or TBC1D22B-gene expression in PB and/or RBM38-gene expression in PB and/or ZBTB33-gene expression in PB and/or AGO2-gene expression in PB.
In another preferred embodiment, the method is used for preoperative prediction of response to stem cell therapy and/or induction of angiogenesis response and/or tissue repair in the context of cardiovascular disease including myocardial infarction, stroke and peripheral ischemic vascular disease, heart disease and/or ischemic preconditioning. Such a therapy may include a treatment to use a cardiovascular implant or stent, a ventricular assist device (VAD), a pacemaker and/or an occluder or appropriate closure device. Also, such a therapy may include treatment of diabetes mellitus, tumor diseases, coeliakie, rheumatic diseases, infectious diseases, sepsis and/or hypertension. In particular, the method is used for preoperative prediction of improvement of left ventricular heart function, e. g. following deterioration of left ventricular ejection fraction (LVEF) after acute myocardial ST-segment elevations infarction (STEMI) and coronary artery 3-vessel disease sequentially treated by acute percutaneous coronary intervention (PCI) and secondary coronary artery bypass graft (CABG) revascularization and/or ischemia-reperfusion intervention.
In yet another preferred embodiment, the method for prediction of response to cardiac regeneration, in particular to stem cell therapy and/or induction of angiogenesis response and/or tissue repair in the context of cardiovascular disease uses a sample taken from a subject suffering from heart disease and/or arteriosclerosis. Such a sample may particularly be taken from a subject suffering from angina, acute myocardial injury, cellular necrosis, myocardium hypertrophy, heart failure, preferably ischemic heart failure, non-ischemic heart failure, myocarditis, atrial fibrillation, ventricular fibrillation and/or arteriosclerosis.
According to a preferred embodiment, the method comprises profiling of the results of the comparison of at least two, three, four, five, six or more time points. Advantageously, such time points comprise a sample taken preoperative and at days 1, 3, 10, 90, 180, and 730 post operation. By analysing the samples of at least two, three, four, five, six or more time points, specificity of prediction accuracy can be beneficially increased and even more.
A further embodiment of the beneficial method comprises the use of clinical diagnostic parameters. In particular, such parameters are selected from colony forming unit (CFU) Hill assay, Matrigel Plug assay, weight, and/or left ventricular end-systolic volume (LVESV).
According to a next preferred embodiment, the method is used for profiling of angiogenesis response.
Yet another preferred embodiment includes for the advantageous method to further comprise analysing an RNA and/or DNA and/or mRNA sequence and/or functional RNA such as microRNA and/or non-coding RNA and/or SNP comprising a diagnostic signature. Within the context of the invention, such a signature analysis of an RNA and/or DNA and/or SNP may be performed and/or supported by machine learning and/or pathway analysis. In the context of the present invention, pathway analysis is used to identify related RNA and/or DNA and/or SNP within a pathway or building pathway de novo from the RNA, DNA and/or SNP of interest.
Also, according to a further preferred embodiment, the advantageous method may comprise analysis of pharmacokinetic and pharmacogenetic data employing RNA and/or DNA sequencing analysis and/or network pathway analysis. Such pharmacokinetic data may be in particular obtained from subjects given medications from the group selected from a Statin, acetylsalicylic acid (ASS), a R-blocker, an angiotensin-converting-enzyme (ACE) inhibitor, an angiotensin II (ATII) receptor antagonist, an Aldosterone antagonist, a diuretic agent, a Ca-antagonist, an anti-Arrhythmic agent, Digitalis, Marcumar, and/or Nitrate.
A next preferred embodiment may additionally use analysis of phenotype of the subject, such as analysis of body weight.
According to an even further preferred embodiment, the method for prediction of cardiovascular repair comprises stem cell therapy to use transplantation of CD133 positive stem cells. Such a stem cell therapy may be optionally combined with CABG revascularization, used for induction of cardiac regeneration, and/or PCI. Though, a particularly preferred embodiment includes that cardiac stem cell therapy further comprises coronary artery bypass graft surgery.
Advantageously, cardiac regeneration and/or functional improvement of the heart after cardiac stem cell therapy are accompanied by an increase of LVEF of at least 5%.
The aforementioned inventive method is not restricted to be applied for human subjects only, but may also include animals. However, it is preferred for the method to be applied to human subject/s. In accordance with the invention, a sample of such a subject may be derived from blood, in particular peripheral blood, and/or a serum and/or a plasma sample and/or a tissue biopsy sample and/or a sample of circulating (stem) cells such as endothelial progenitor cells (EPC).
As depicted above, the present invention also pertains to one or more biomarker/s selected from SH2B3-gene and/or -gene expression mutation variant and/or Lymphocyte adapter protein expression from SH2B3-gene and/or -gene expression mutation variant for use in a method for prediction of response to disease therapy, in particular to tissue regeneration, preferably to cardiovascular regeneration.
According to a preferred embodiment, the biomarker is used in combination with one or more further biomarker/s, wherein the further biomarker is selected from the group of Angiogenic factor, Survival factor, Chemokine, circulating EPC, CEC, circulating thrombocytes, circulating mononuclear cells and subpopulations, receptor/ligand expression on MNC subpopulations and/or whole genomic sequence RNA.
According to a particularly preferred embodiment, the advantageous combination further uses one or more biomarkers, wherein the further biomarker/s is/are selected from PLCG1, EPO, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB, VEGF, BEX3, DeltaCTSH2B3, ZNF205, LTB, EMG1, CD34+ cells/ml PB, BAZ1A and/or CD133+ cells/ml PB.
Preferably, PLCG1, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB, BEX3, ZNF205, EMG1, BAZ1A and/or LTB is/are determined on an RNA level and/or EPO and/or VEGF is/are determined on a protein level.
Even more preferably, determination of EPO, VEGF, Delta_CT_SH2B3, CD34+ cells/ml PB and/or CD133+ cells/ml PB is conducted from preoperative samples.
According to an even more preferred embodiment the advantageous combination of further biomarker/s is/are selected from PLCG1, EPO, LPCAT2, GRB2, AP1B1, AFAP1, KLF8, MARK3, REX1BD, SACM1L, PDGFRB and/or VEGF.
A combination of those further biomarkers may be selected on an individual basis, depending on the disease type and/or disease state of the subject or patient, respectively. For example, a selection may encompass a combination of biomarkers including PLCG1, EPO, LPCAT2, GRB2, AP1B1, KLF8, MARK3 and/or VEGF (as depicted in
In addition to the above mentioned further biomarker/s, according to a next embodiment, for example, the Angiogenic factor is selected from VEGF and/or FGF, more preferably from VEGF-B and/or FGF-4, and/or HGF and/or Ang-1, the Survival factor is preferably selected from IGF-1 and the Chemokine is selected from IGF-2 and/or SDF-1.
Alternatively or additionally, such further biomarker/s comprise one or more biomarker/s selected from zinc finger protein ZDHHC2 and/or MYL4/ALC1 and/or INPP4B and/or RBM38, CD133+ cells/m1 PB and/or CD34+ cells/ml PB and/or CD45+184+ cells/ml PB and/orCD45+ cell/ml PB and/or CD184+ cells/ml PB and/or MNC in PB and/or CFU-Hill of PB and/or RIOK3-gene expression in PB and/or ABCC13-gene expression in PB and/or COPS3-gene expression in PB and/or GUK1-gene expression in PB and/or AP3B1-gene expression in PB and/or TBC1D22B-gene expression in PB and/or RBM38-gene expression in PB and/or ZBTB33-gene expression in PB and/or AGO2-gene expression in PB. Advantageously, the method is an ex vivo/in vitro method.
Preferably, the combination of such biomarkers is used in a method for prediction of response to disease therapy, in particular to tissue repair, preferably to cardiovascular regeneration, the method comprising
According to a preferred embodiment of the present invention, a combination of the above biomarkers are used in a method for prediction of response to cardiovascular regeneration, wherein the method further comprises analysis of clinical diagnostic data, and/or RNA and/or mRNA and/or functional RNA such as microRNA and/or non-coding RNA and/or SNP, and/or analysis of pharmacokinetic data, and/or analysis of phenotyping, e.g. body weight.
Yet more preferably, an advantageous method and/or an advantageous combination of the above biomarkers is/are used for preoperative prediction of response to stem cell therapy and wherein the stem cell therapy is accompanied by CABG.
The term “stem cell therapy” as used herein refers to all therapeutic approaches which comprise the transplantation of exogenous cardiomyocytes into the heart of a subject to be treated. Such cardiomyocytes may be generated by reprogramming non-cardiomyocyte progenitor cells into cardiomyocytes. Cells to be reprogrammed may be embryonic stem cells, induced pluripotent stem cells, multipotent cardiac progenitor cells, skeletal myoblasts or bone marrow derived stem cells. Moreover, mature cardiomyocytes may also be used, in particular, if stimulated to reenter into mitotic cell cycling. More preferably, the cardiac stem cell therapy according to the present invention comprises transplantation of CD133-positive cells, most preferably, CD133-positive bone marrow mononuclear cells. The cells may be transplanted as isolated single cells or in a preformed arrangement such as a tissue block formed by tissue engineering processes. Preferably, the cells are transplanted in accordance with the present invention by intramyocardial injection. Moreover, the term cardiac stem cell therapy may also encompass additional therapeutic measures such as drug treatments accompanying the transplantation process or other therapeutic measures such as surgery. Preferably, the cardiac stem cell therapy in accordance with the present invention further comprises coronary artery bypass graft surgery as described in the accompanying examples below.
The term “functional improvement of the heart” as used herein refers to a significant increase in the LVEF of the heart observed when comparing said LVEF before and after treatment of the subject. Preferably, a significant increase is an increase of 5% or more of LVEF observed after treatment. An increase of less than 5% is deemed to be insignificant. Further parameters which may be considered in addition for finding a functional improvement are a more than 10% decrease in perfusion defect size, a more than 10% decrease in left ventricle end systolic volume (LVESV) as quantified by MIBI SPECT and a more than 10% increase in peak systolic velocity measured by transthoracic echocardiogram.
Heart failure as used herein refers to any functional impairment of the heart including left-sided failures, right-sided failures or biventricular failures. Typically, the term heart failure as referred to herein is left-sided failure that results in reduced ejection fractions, e.g. a significantly reduced LVEF. Further symptoms of heart failure are well known to the clinician. Heart failure as referred to herein encompasses acute and chronic forms of heart failure and any stage of severity, e.g. for left-sided failures all stages according to the New York Heart Association (NYHA) classification system, NYHA I to IV.
The term “PLCG1” as used herein refers to a protein encoded by the corresponding gene and catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction plays an important role in the intracellular transduction of receptor-mediated tyrosine kinase activators. Two transcript variants encoding different isoforms have been found for this gene.
The term “LPCAT2” as used herein refers to a gene that encodes a member of the lysophospholipid acyltransferase family. The encoded protein may function in membrane biogenesis and production of platelet-activating factor in inflammatory cells. The enzyme may localize to the endoplasmic reticulum and the Golgi.
The term “GRB2” as used herein refers to Growth factor receptor-bound protein 2, also known as Grb2 and is an adaptor protein involved in signal transduction/cell communication. In humans, the GRB2 protein is encoded by the GRB2 gene. The protein encoded by this gene binds receptors such as the epidermal growth factor receptor and contains one SH2 domain and two SH3 domains.
The term “AP1B1” as used herein refers to AP-1 complex subunit beta-1 and is a protein that in humans is encoded by the AP1B1 gene. Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as one of the large subunits of this complex and is a member of the adaptin protein family.
The term “AFAP1” as used herein refers to Actin filament-associated protein 1 is a protein that in humans is encoded by the AFAP1 gene. The protein encoded by this gene is a Src binding partner. It may represent a potential modulator of actin filament integrity in response to cellular signals, and may function as an adaptor protein by linking Src family members and/or other signaling proteins to actin filaments. Two alternative transcripts encoding the same protein have been identified.
The term “KLF8” as used herein refers to Krueppel-like factor 8 and is a protein that in humans is encoded by the KLF8 gene. KLF8 belongs to the family of KLF protein. KLF8 is activated by KLF1 along with KLF3 while KLF3 represses KLF8.
The term “MARK3” as used herein refers to MAP/microtubule affinity-regulating kinase 3 and is an enzyme that in humans is encoded by the MARK3 gene. MARK3 has been shown to interact with stratifin.
The term “REX1BD” as used herein refers to ‘required for excision 1-B domain containing’ and is a protein coding gene. It interacts with 3-isobutyl-1-methyl-7H-xanthine, aflatoxin B1 and aflatoxin B2.
The term “SACM1L” as used herein refers to Staphylococcus aureus Cowan 1 phosphatidylinositide phosphatase and is an enzyme that in humans is encoded by the SACM1L gene.
The term “PDGFRB” as used herein refers to PDGFRB gene and encodes a typical receptor tyrosine kinase, which belongs to the type III tyrosine kinase receptor (RTK) family and is structurally characterized by five extracellular immunoglobulin-like domains, a single membrane-spanning helix domain, an intracellular juxtamembrane domain, a split tyrosine kinase domain and a carboxylic tail. Upon PDGF binding the dimerization of receptor releases the inhibitory conformations due to auto-phosphorylation of regulatory tyrosine residues in trans fashion. Tyrosine residues 857 and 751 are major phosphorylation sites for the activation of PDGFRβ.
The term “BEX3” as used herein refers to Brain Expressed X-Linked 3 and is a protein coding gene. Among its related pathways are p75 NTR receptor-mediated signalling and signalling by GPCR.
The term “ZNF205” as used herein refers to Zinc Finger Protein 205 and is a protein coding gene. Gene Ontology (GO) annotations related to this gene include nucleic acid binding and DNA-binding transcription factor activity.
The term “LTB” refers to Lymphotoxin Beta and is a protein coding gene. Among its related pathways are innate immune system and innate lymphoid cell differentiation pathways. Gene Ontology (GO) annotations related to this gene include signaling receptor binding and tumor necrosis factor receptor binding.
The term “EMG1” as used herein refers to EMG1 N1-Specific Pseudouridine Methyltransferase and is a protein coding gene. Among its related pathways are rRNA processing in the nucleus and cytosol and ribosome biogenesis in eukaryotes. Gene Ontology (GO) annotations related to this gene include methyltransferase activity.
The term “BAZ1A” as used herein refers to Bromodomain adjacent to Zinc Finger Domain 1A and is a component of the histone-fold protein CHRAC complex which facilitates nucleosome sliding by the ACF complex and enhances ACF-mediated chromatin assembly. The C-terminal regions of both CHRAC1 and POLE1 are required for these functions.
The term “vascular endothelial growth factor (VEGF)” as used herein refers to soluble polypeptide growth factor which stimulates angiogenesis, vasculogenesis and vascular permeability. It is produced by various cell types. There are five different VEGF polypeptides, VEGF-A, placenta growth factor (PGF), VEGF-B, VEGF-C, and VEGF-D. Preferably, the VEGF is selected from VEGF-B. In contrast to VEGF-A, VEGF-B plays a less pronounced role in the vascular system. Whereas VEGF-A is important for the formation of blood vessels, such as during development or in pathological conditions, VEGF-B seems to play a role only in the maintenance of newly formed blood vessels during pathological conditions. VEGF-B plays also an important role on several types of neurons. It is important for the protection of neurons in the retina and the cerebral cortex during stroke and of motoneurons during motor neuron diseases such as amyotrophic lateral sclerosis. VEGF-B exerts its effects via the FLT1 receptor (also known as Vascular Endothelial Growth Factor Receptor 1). VEGF-B has also been found to control endothelial uptake and transport of fatty acids in heart and skeletal muscle.
The term “Fibroblast growth factor (FGF)” as used herein refers to a family of growth factors, with members involved in angiogenesis, wound healing, embryonic development and various endocrine signaling pathways. Preferably, the FGF is selected from FGF-4. The term “FGF-4” as used herein refers to Fibroblast growth factor 4 protein that in humans is encoded by the FGF4-gene.
The term “HGF” as used herein refers to Hepatocyte growth factor (HGF) or scatter factor (SF), which is a paracrine cellular growth, motility and morphogenic factor. It is secreted by mesenchymal cells and targets and acts primarily upon epithelial cells and endothelial cells, but also acts on hematopoietic progenitor cells and T cells.
The term “Ang-1” as used herein refers to Angiopoietin 1, which is a type of Angiopoietin and is encoded by the gene ANGPT1. Angiopoietin is part of a family of vascular growth factors that play a role in embryonic and postnatal angiogenesis. Angiopoietin signaling most directly corresponds with angiogenesis, the process by which new arteries and veins form from preexisting blood vessels. Angiogenesis proceeds through sprouting, endothelial cell migration, proliferation, and vessel destabilization and stabilization. They are responsible for assembling and disassembling the endothelial lining of blood vessels. Angiopoietin Cytokines are involved with controlling microvascular permeability, vasodilation, and vasoconstriction by signaling smooth muscle cell surrounding vessels.
The term “Survival factor” as used herein encompasses a group of substances exhibiting anti-apoptotic effect.
The term “IGF-1” (Insulin like growth factor 1), also called Somatomedin C, refers to a protein that in humans is encoded by the IGF-1-gene. IGF-1 is a hormone similar in molecular structure to Insulin. It plays an important role in childhood growth and continues to have anabolic effects in adults. IGF-1 consists of 70 amino acids in a single chain with three intramolecular disulfide bridges. IGF-1 has a molecular weight of 7,649 Daltons.
The term “Chemokine” as used herein refers to a family of small cytokines or signaling proteins secreted by cells. Their name is derived from their ability to induce directed chemotaxis in nearby responsive cells; they are chemotactic cytokines.
Some chemokines are considered pro-inflammatory and can be induced during an immune response to recruit cells of the immune system to a site of infection, while others are considered homeostatic and are involved in controlling the migration of cells during normal processes of tissue maintenance or development. Chemokines are found in all vertebrates, some viruses and some bacteria, but none have been described for other invertebrates. Chemokines have been classified into four main subfamilies: CXC, CC, CX3C and XC. All of these proteins exert their biological effects by interacting with G protein-linked transmembrane receptors called chemokine receptors that are selectively found on the surfaces of their target cells.
The term “Erythropoietin (EPO)” as used herein refers to a soluble polypeptide being a cytokine. EPO is produced by kidney cells, typically, under hypoxic conditions. The term also encompasses variants of the human EPO polypeptides. Such variants have at least the same essential biological and immunological properties as the aforementioned EPO polypeptide. In particular, they share the same essential biological and immunological properties if they are detectable by the same specific assays referred to in this specification, e.g., by ELISA assays using polyclonal or monoclonal antibodies specifically recognizing the said EPO polypeptides. Moreover, it is to be understood that a variant as referred to in accordance with the present invention may have an amino acid sequence which differs due to at least one amino acid substitution, deletion and/or addition wherein the amino acid sequence of the variant is still, preferably, at least 50%, 60%, 70%, 80%, 85%, 90%, 92%, 95%, 97%, 98%, or 99% identical with the amino sequence of the specific IL-6. Variants may be allelic variants, splice variants or any other species specific homologs, paralogs, or orthologs. Moreover, the variants referred to herein include fragments of the specific EPO or the aforementioned types of variants as long as these fragments have the essential immunological and biological properties as referred to above. Such fragments may be, e.g., degradation products of EPO. Variants are deemed to share the same essential biological and immunological properties if they are detectable by the same specific assays referred to in this specification, e.g., by ELISA assays using polyclonal or monoclonal antibodies specifically recognizing the said EPO polypeptides. A preferred assay is described in the accompanying Examples. Further included are variants which differ due to posttranslational modifications such as phosphorylation or myristylation.
The term “SH2B adapter protein 3 (SH2B3)” as used herein refers to lymphocyte adapter protein (LNK). SH2B3 is a protein that in humans is encoded by the SH2B3-gene on chromosome 12. It is ubiquitously expressed in many tissues and cell types (Li Y, He X, Schembri-King J, Jakes S, Hayashi J, May 2000. Journal of Immunology. 164(10):5199-206).
The term “Interleukin-6 (IL-6)” as used herein refers to a soluble polypeptide being a pro-inflammatory cytokine and anti-inflammatory myokine. It is produced by T-cells and macrophages.
Preferably, IL-6 refers to human IL-6 as described, e. g., in Wong 1988, Behring Inst. Mitt 83: 40-47. More preferably, human IL-6 has an amino acid sequence as shown in Genbank accession number p05231.1, GI: 124347. The term also encompasses variants of the aforementioned human IL-6 polypeptides. Such variants have at least the same essential biological and immunological properties as the aforementioned IL-6 polypeptide.
In particular, they share the same essential biological and immunological properties if they are detectable by the same specific assays referred to in this specification, e.g., by ELISA assays using polyclonal or monoclonal antibodies specifically recognizing the said IL-6 polypeptides. Moreover, it is to be understood that a variant as referred to in accordance with the present invention may have an amino acid sequence which differs due to at least one amino acid substitution, deletion and/or addition wherein the amino acid sequence of the variant is still, preferably, at least 50%, 60%, 70%, 80%, 85%, 90%, 92%, 95%, 97%, 98%, or 99% identical with the amino sequence of the specific IL-6. Variants may be allelic variants, splice variants or any other species specific homologs, paralogs, or orthologs. Moreover, the variants referred to herein include fragments of the specific IL-6 or the aforementioned types of variants as long as these fragments have the essential immunological and biological properties as referred to above. Such fragments may be, e.g., degradation products of IL-6. Variants are deemed to share the same essential biological and immunological properties if they are detectable by the same specific assays referred to in this specification, e.g., by ELISA assays using polyclonal or monoclonal antibodies specifically recognizing the said IL-6 polypeptides. A preferred assay is described in the accompanying Examples. Further included are variants which differ due to posttranslational modifications such as phosphorylation or myristylation.
The term “insulin-like growth factor (IGF-2)” as used herein refers to one of three protein hormones that share structural similarity to insulin. IFG-2 is believed to be secreted by the liver and to circulate in the blood. It has growth-regulating, insulin-like and mitogenic activities. The growth factor has a major, but not absolute, dependence on somatotropin. It is believed to be a major fetal growth factor.
The term “stomal cell-derived factor 1 (SDF-1)”, also known as C-X-C motif chemokine 12 (CXCL12), is a chemokine protein that in humans is encoded by the CXCL12-gene on chromosome 10. It is ubiquitously expressed in many tissues and cell types. Stromal cell-derived factors 1-alpha and 1-beta are small cytokines that belong to the chemokine family, members of which activate leukocytes and are often induced by pro-inflammatory stimuli such as lipopolysaccharide, tumor necrosis factor (TNF), or 11_1. The chemokines are characterized by the presence of four conserved cysteines that form two disulfide bonds.
The term “zinc finger proteins (ZNFs)” as used herein refers to proteins and have a wide range of molecular functions. Given the wide variety of zinc-finger domains, ZNFs are able to interact with DNA, RNA, PAR (poly-ADP-ribose) and other proteins. Thus, ZNFs are involved in the regulation of several cellular processes. ZNFs are implicated in transcriptional regulation, ubiquitin-mediated protein degradation, signal transduction, actin targeting, DNA repair, cell migration, and numerous other processes. The term “ZDHHC2” as used herein refers to zinc fingers DHHC type.
The term “MYL4/ALC1” as used herein refers to Atrial Light Chain-1 (ALC-1), also known as Essential Light Chain. ALC-1 is a protein that in humans is encoded by the MYL4 gene.
The term “INPP4B” as used herein refers to Inositol polyphosphate 4-phosphatase II, which is a regulator of the phosphoinositide 3-kinase (PI3K) signaling pathway and is implicated as a tumor suppressor in epithelial carcinomas.
The term “RBM38” refers to RNA binding motif protein 38. RBM38, also named RNPC1, induces cell-cycle arrest in G1, at least in part, via binding to and stabilizing the mRNA of the cyclin-dependent kinase inhibitor p21.
The term “MNC” as used herein refers to mononuclear cells, which is any cell that has a single round nucleus; examples of a mononuclear cell are lymphocytes, monocytes, and dendritic cells. These cells are critical components of the immune system, which are involved in both humoral and cell-mediated immunity. MNCs are widely used product in research and clinical applications such as in microbiology, virology, oncology, vaccine development, transplant and regenerative biology, and toxicology.
The term “CFU-Hill” as used herein refers to an early outgrowth, formed by plating peripheral blood mononuclear cells on fibronectin-coated dishes, allowing adhesion and depleting non-adherent cells, and isolating discrete colonies.
The term “ABCC13” as used herein refers to ATP-binding cassette transporter sub-family C member 13, which is a protein that in humans is encoded by the ABCC13 gene.
The term “COPS3” as used herein refers to a protein that in human is encoded by the COPS3-gene. It encodes a subunit of the COP9 signalosome. The protein complex is supposed to exhibit isopeptidase activity. Among its related pathways are transcription-coupled nucleotide excision repair (TC-NER) and clathrin-mediated endocytosis. It is found in eukaryotic organisms including human.
The term “GUK1” as used herein refers to Guanylate kinase and is an enzyme that in humans is encoded by the GUK1 gene.
The term “AP3B1” as used herein refers to AP-3 complex subunit beta-1 which is a protein that in humans is encoded by the AP3B1 gene. This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin.
The term “TBC1D22B” as used herein refers to TBC1D22B (TBC1 Domain Family Member 22B), which is a protein coding gene and may act as a GTPase-activating protein for Rab (Ras-ralated protein) family protein(s). Gene Ontology (GO) annotations related to this gene include GTPase activator activity. A paralog of this gene is TBC1 D22A.
The term “ZBTB33” as used herein refers to Transcriptional regulator Kaiso, which is a protein that in humans is encoded by the ZBTB33-gene. This gene encodes a transcriptional regulator with bimodal DNA-binding specificity, which binds to methylated CGCG and also to the non-methylated consensus KAISO-binding site TCCTGCNA. The protein contains an N-terminal POZ/BTB domain and 3 C-terminal zinc finger motifs. It recruits the N-CoR repressor complex to promote histone deacetylation and the formation of repressive chromatin structures in target gene promoters. It may contribute to the repression of target genes of the Wnt (the term “Wnt” encompasses a diverse family of secreted lipid-modified signaling glycoproteins that are 350-400 amino acids in length) signaling pathway, and may also activate transcription of a subset of target genes by the recruitment of catenin delta-2 (CTNND2). Its interaction with catenin delta-1 (CTNND1) inhibits binding to both methylated and non-methylated DNA. It also interacts directly with the nuclear import receptor Importin-α2 (also known as karyopherin alpha2 or RAG cohort 1), which may mediate nuclear import of this protein. Alternatively spliced transcript variants encoding the same protein have been identified.
The term “AGO2” as used herein refers to a member of the Argonaute protein family which plays a central role in RNA silencing processes, as essential components of the RNA-induced silencing complex (RISC). Endonuclease activity and thus RNAi-dependent gene silencing exclusively belongs to AGO2. Considering the sequence conservation of PAZ and PIWI domains across the family, the uniqueness of AGO2 is presumed to arise from either the N-terminus or the spacing region linking PAZ and PIWI motifs.
Determining the amount of a biomarker may, preferably, comprise the steps of (a) contacting the biomarker with a specific ligand, (b) (optionally) removing non-bound ligand, (c) measuring the amount of bound ligand. The bound ligand will generate an intensity signal. Binding according to the present invention includes both covalent and non-covalent binding. A ligand according to the present invention can be any compound, e.g., a peptide, polypeptide, nucleic acid, or small molecule, binding to the peptide or polypeptide or protein or nucleic acid or cell described herein. Preferred ligands include antibodies, nucleic acids, peptides or polypeptides such as receptors or binding partners for the peptide or polypeptide and fragments thereof comprising the binding domains for the peptides, and aptamers, e.g. nucleic acid or peptide aptamers. Methods to prepare such ligands are well-known in the art. For example, identification and production of suitable antibodies or aptamers is also offered by commercial suppliers. The person skilled in the art is familiar with methods to develop derivatives of such ligands with higher affinity or specificity. For example, random mutations can be introduced into the nucleic acids, peptides or polypeptides. These derivatives can then be tested for binding according to screening procedures known in the art, e.g. phage display. Antibodies as referred to herein include both polyclonal and monoclonal antibodies, as well as fragments thereof, such as Fv, Fab and F(ab)2 fragments that are capable of binding antigen or hapten. The present invention also includes single chain antibodies and humanized hybrid antibodies wherein amino acid sequences of a non-human donor antibody exhibiting a desired antigen-specificity are combined with sequences of a human acceptor antibody. The donor sequences will usually include at least the antigen-binding amino acid residues of the donor but may comprise other structurally and/or functionally relevant amino acid residues of the donor antibody as well. Such hybrids can be prepared by several methods well known in the art. Preferably, the ligand or agent binds specifically to the peptide or polypeptide. Specific binding according to the present invention means that the ligand or agent should not bind substantially to (“cross-react” with) another peptide, polypeptide or substance present in the sample to be analysed. Preferably, the specifically bound peptide or polypeptide should be bound with at least 3 times higher, more preferably at least 10 times higher and even more preferably at least 50 times higher affinity than any other relevant peptide or polypeptide. Non-specific binding may be tolerable, if it can still be distinguished and measured unequivocally, e.g. according to its size on a Western Blot, or by its relatively higher abundance in the sample. Binding of the ligand can be measured by any method known in the art. Preferably, said method is semi-quantitative or quantitative. Further suitable techniques for the determination of a biomarker are described in the following.
First, binding of a ligand may be measured directly, e.g. by NMR or surface plasmon resonance. Second, if the ligand also serves as a substrate of an enzymatic activity of the biomarker of interest, an enzymatic reaction product may be measured (e.g. the amount of a protease can be measured by measuring the amount of cleaved substrate, e.g. on a Western Blot). Alternatively, the ligand may exhibit enzymatic properties itself and the “ligand/peptide or polypeptide” complex or the ligand which was bound by the biomarker, respectively, may be contacted with a suitable substrate allowing detection by the generation of an intensity signal. For measurement of enzymatic reaction products, preferably the amount of substrate is saturating. The substrate may also be labelled with a detectable label prior to the reaction. Preferably, the sample is contacted with the substrate for an adequate period of time. An adequate period of time refers to the time necessary for a detectable, preferably measurable, amount of product to be produced. Instead of measuring the amount of product, the time necessary for appearance of a given (e.g. detectable) amount of product can be measured. Third, the ligand may be coupled covalently or non-covalently to a label allowing detection and measurement of the ligand. Labelling may be done by direct or indirect methods. Direct labelling involves coupling of the label directly (covalently or non-covalently) to the ligand. Indirect labelling involves binding (covalently or non-covalently) of a secondary ligand to the first ligand. The secondary ligand should specifically bind to the first ligand. Said secondary ligand may be coupled with a suitable label and/or be the target (receptor) of tertiary ligand binding to the secondary ligand. The use of secondary, tertiary or even higher order ligands is often used to increase the signal. Suitable secondary and higher order ligands may include antibodies, secondary antibodies, and the well-known streptavidin-biotin system. The ligand or substrate may also be “tagged” with one or more tags as known in the art. Such tags may then be targets for higher order ligands. Suitable tags include biotin, digoxygenin, His-Tag, Glutathion-S-Transferase, FLAG, GFP, myc-tag, influenza A virus haemagglutinin (HA), maltose binding protein, and the like. In the case of a peptide or polypeptide, the tag is preferably at the N-terminus and/or C-terminus. Suitable labels are any labels detectable by an appropriate detection method. Typical labels include gold particles, latex beads, acridin ester, luminol, ruthenium, enzymatically active labels, radioactive labels, magnetic labels (“e.g. magnetic beads”, including paramagnetic and superparamagnetic labels), and fluorescent labels. Enzymatically active labels include e.g. horseradish peroxidase, alkaline phosphatase, beta-Galactosidase, Luciferase, and derivatives thereof. Suitable substrates for detection include di-amino-benzidine (DAB), 3,3′-5,5′-tetramethylbenzidine, NBT-BCIP (4-nitro blue tetrazolium chloride and 5-bromo-4-chloro-3-indolyl-phosphate. A suitable enzyme-substrate combination may result in a coloured reaction product, fluorescence or chemoluminescence, which can be measured according to methods known in the art (e.g. using a light-sensitive film or a suitable camera system). As for measuring the enzymatic reaction, the criteria given above apply analogously. Typical fluorescent labels include fluorescent proteins (such as GFP and its derivatives), Cy3, Cy5, Texas Red, Fluorescein, and the Alexa dyes. Further fluorescent labels are available e.g. from Molecular Probes (Oregon). Also the use of quantum dots as fluorescent labels is contemplated. Typical radioactive labels include 35S, 125I, 32P, 33P and the like. A radioactive label can be detected by any method known and appropriate, e.g. a light-sensitive film or a phosphor imager.
The amount of a biomarker may be, also preferably, determined as follows: (a) contacting a solid support comprising a ligand for the biomarker as specified above with a sample comprising the biomarker and (b) measuring the amount of biomarker which is bound to the support. The ligand, preferably chosen from the group consisting of nucleic acids, peptides, polypeptides, antibodies and aptamers, is preferably present on a solid support in immobilized form. Materials for manufacturing solid supports are well known in the art and include, inter alia, commercially available column materials, polystyrene beads, latex beads, magnetic beads, colloid metal particles, glass and/or silicon chips and surfaces, nitrocellulose strips, membranes, sheets, duracytes, wells and walls of reaction trays, plastic tubes etc. The ligand or agent may be bound to many different carriers. Examples of well-known carriers include glass, polystyrene, polyvinyl chloride, polypropylene, polyethylene, polycarbonate, dextran, nylon, amyloses, natural and modified celluloses, polyacrylamides, agaroses, and magnetite. The nature of the carrier can be either soluble or insoluble for the purposes of the invention. Suitable methods for fixing/immobilizing said ligand/s are well known and include, but are not limited to ionic, hydrophobic or covalent interactions and the like.
Suitable measurement methods according to the present invention also include fluorescence activated cell sorting (FACS) analysis, radioimmunoassay (RIA), enzyme-linked immunosorbent assay (ELISA), sandwich enzyme immune tests, electrochemiluminescence sandwich immunoassays (ECLIA), dissociation-enhanced lanthanide fluoro immuno assay (DELFIA), scintillation proximity assay (SPA) or solid phase immune tests. Further methods known in the art (such as gel electrophoresis, 2D gel electrophoresis, SDS polyacrylamid gel electrophoresis (SDS-PAGE), Western Blotting and mass spectrometry (MS) can be used alone or in combination with labelling or other detection methods as described above.
In order to carry out the method of the present invention, a kit is provided which is adapted for carrying out the inventive method, wherein the kit according to the present invention comprises detection agents for determining in a sample of said subject the amount of at least one of the above biomarkers. Such a kit advantageously allows for a straight forward conduction of the inventive method and/or measurement and/or determination of the biomarker/s according to the present invention.
The term “kit” as used herein refers to a collection of the aforementioned components, preferably, the components being provided separately or within a single container. The kit may also comprise instructions for carrying out the method of the present invention. These instructions may be in the form of a manual or may be provided by a computer program code which is capable of carrying out the comparisons referred to in the methods of the present invention and to establish a diagnosis accordingly when implemented on a computer or a data processing device. The computer program code may be provided on a data storage medium or device such as a storage medium (e.g. a Compact Disc, USB drives or external hard disks) or directly on a computer or data processing device. Moreover, the kit may, preferably, comprise standards for reference amounts as described elsewhere herein in detail.
Further characteristics of the present invention are derived from the examples in combination with the claims and the figures. Single features may be, in a particular embodiment, realised in combination with other features and do not limit the scope of protection of the present invention. The following description of the examples according to the invention may relate to the figures, whereby
The following examples shall merely illustrate the invention. They shall, whatsoever, not be construed as limiting the scope thereof.
Peripheral blood bone marrow response was studied by whole genome and circulating EPC analysis in the randomized phase 3 PERFECT trial biomarker subgroup at the Rostock trial site with complete available biobank, clinical (per protocol), and biomarker data (n=23) (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017 August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29.). CD133+ BMSC treated (n=13) and placebo controls (n=14) were equally distributed. In the biomarker patient cohort (n=23; Placebo/CD133+ 9/14) of the PERFECT trial we investigated systemic bone marrow stem cell response in peripheral blood in Responders (R) classified by ΔLVEF≥5% after 180 d (n=14; Placebo/CD133+ 7/7) and Non-responders (NR) classified by ΔLVEF<5% after 180 d (n=9; Placebo/CD133+ 5/4) in both treatment groups (intramyocardial Placebo vs. CD133+).
The R/NR gene expression and biomarker data of postischemic myocardial regeneration were compared to mouse Lnk/SH2B3 knockout deficient conditions studied in an experimental setting of myocardial infarction in Lnk−/− mice vs. Lnk+/+ wild type (WT) mice studied at different time points (day 0, 1, 3, 7, 14, 28) before and post-MI.
The PERFECT trial was a randomised, multicenter, placebo-controlled, double-blinded phase 3 study investigating the myocardial regeneration effects of intramyocardial CD133+ BMSC treatment in combination with coronary artery bypass graft (CABG) revascularization for post infarction myocardial ischemia (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017 August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29., Baughn L B, Meredith M M, Oseth L, Smolarek T A, Hirsch B. Cancer Genet. 2018 October; 226-227:30-35. doi: 10.1016/j.cancergen.2018.05.004. Epub 2018 Jun. 8.). A prespecified and post-hoc biomarker outcome analysis was published (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017; August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29.). Inclusion criteria of the PERFECT trial were (a) coronary artery disease after MI with the indication for CABG surgery, (b) reduced LVEF (25-50%) and (c) presence of a localized kinetic/hypokinetic/hypoperfused area of left ventricular (LV) myocardium defining the SC target area. Assessments were performed preoperative and at days 1, 3, 10, 90, 180, and 730 post operation.
RNAseq analysis and mRNA RT-PCR in PB: Analyses and examinations were performed before unblinding of the trial and under careful adherence to the protection of data privacy (pseudonyms).
RNA of frozen EDTA blood samples was isolated in a three step procedure: First, the GeneJET Stabilized and Fresh Whole Blood RNA Kit (Thermo Scientific) was used following manufacturer's instructions. Second, isolated RNA was precipitated with 2.5 volumes ethanol under high salt conditions (10% of 3 M sodium acetate, pH 5.2). After DNase digest (Thermo Scientific) the RNA was finally purified using Agencourt RNAClean XP beads (Beckman Coulter). Isolated RNA was analyzed on a Bionalyzer (Agilent) using RNA 6000 Nano Chips (Agilent). Quality controlled RNA was used to construct sequencing libraries using the Universal Plus mRNA—Seq Technology (Nugen) following manufacturer's instructions. Brief: mRNA was selected by oligo d(T) beads, reverse transcribed and Globin derived cDNA was cleaved by the Globin depletion module (Nugen). Quality controlled and quantified libraries were sequenced on a HiSeq1500 system (Illumina) in single-end mode (100 nt read length). For RNAseq data analysis, we performed adapter clipping and quality trimming procedures for data pre-processing and aligned the reads to the hg19 genome with the aid of kallisto. Differential expression analysis was performed using the likelihood ratio test of the sleuth package (genes with >2-fold change and a q value <0.05 are considered as significantly differentially expressed). The gene annotation, including functional annotation clustering and functional classification, was performed with Enrichr (Kuleshov, M. V. et al., Nucleic Acids Res. 2016, vol 44(W1), doi: 10.1093/nar/gkw377, Epub 2016 May 3).
Variant Calling from Transcriptomic Data
The previously preprocessed RNAseq datasets (preoperative and postoperative) have been aligned to the hg19 reference with Star (2-pass mode). The variant calling was applied by the Gatk toolkit (McKenna, A. et al., Genome Res. 2010, vol. 20(9): 1297-1303, doi: 10.1101/gr.107524.110) with specialized filters (e.g. variants are only considered, if they are confirmed with five independent reads). Variant annotation was done with reftools.
The Lnk/SH2B3−/− mouse strain was generated as described previously (Takaki S. et al., J. Exp. Med. 2002; 195:151-160). C57BL/6 mice (CLEA Japan, Tokyo, Japan) were used as WT control mice. GFP transgenic mice (GFP-Tg mice; C57BL/6TgN [act EGFP] Osb Y01) were mated with WT mice or Lnk/SH2B3−/− mice and generated WT/GFP mice or Lnk/SH2B3−/−/GFP mice, respectively, for BM transplantation (BMT) studies. All experimental procedures were conducted in accordance with the Japanese Physiological Society Guidelines for the Care and Use of Laboratory Animals and the study protocol was approved by the Ethics Committee in RIKEN Center for Developmental Biology.
Eight-week-old to twelve-week-old mice were anesthetized with an intraperitoneal injection of 400 mg/kg 2,2,2-tribromoethanol (Avertin; Sigma, St.Louis, Mo.). MI was induced by ligating left arterior descending (LAD) coronary artery as described previously (Fabregat A, Sidiropoulos K, Garapati P, et al. Nucleic Acids Res 2016, Jan. 4; 44 (D1):D481-7. doi: 10.1093/nar/gkv1351. Epub 2015 Dec. 9.).
At necropsy, hearts were embedded in O.C.T.™ Compound (Tissue-Tek®) followed by snap frozen in liquid nitrogen, and sectioned at 6 μm by a cryostat (Leica microsystems, Wetzlar, Germany). Total RNA for RT-PCR analysis was isolated by selective dissection of fibrosis and pen-infarction area in LV myocardium. For BrdU incorporation study, mice were injected 100 μL of 10 mg/mL BrdU solution (BD Pharmingen) intraperitoneally 16 hours before sacrifice.
Total RNA was obtained from mouse heart tissue at pre- and 3 days post MI using a TRIzol (Invitrogen) according to the manufacturer's instructions. The first-strand cDNA was synthesized using the PrimeScript RT reagent Kit (Takara Bio, Otsu, Japan) and amplified by AmpliTaq Gold DNA polymerase (Applied Biosystems, Foster City, Calif.). PCR was performed using a PCR thermal cycler (MJ Research PTC-225, Bio-Rad, Hercules, Calif.). The mouse Lnk/SH2B3 and β-actin were amplified by the following conditions: Lnk/SH2B3, 42 cycles of 94° C. for 30 seconds, 57° C. for 30 seconds, and 72° C. for 30 seconds, followed by a final hold at 72° C. for 5 minutes; β-actin, 35 cycles of 94° C. for 30 seconds, 57° C. for 30 seconds, and 72° C. for 30 seconds, followed by a final hold at 72° C. for 5 minutes. Subsequently, PCR products were visualized in 1.5% ethidium bromide-stained agarose gels with a 100-bp DNA Ladder (Invitrogen). Primer sequences are indicated in Supplemental Table 1S.
Total RNA was obtained from KSL cells using RNeasy Mini Kit (QIAGEN, Hilden, Germany) according to the manufacturer's procedure. After the first-strand cDNA was synthesized, real-time quantitative RT-PCR was performed with ABI Prism 7700 (Applied Biosystems) using SYBR Green Master Mix Reagent (Applied Biosystems). Primer sequences are indicated in Supplemental Table 1S.
The results were statistically analyzed using a software package (Statview 5.0, Abacus Concepts Inc, Berkeley, Calif.). All values were expressed as mean±standard deviation (mean±SD). The comparisons among more than three groups were made using the one-way analysis of variances (ANOVA) in Prism 4 (GraphPad Software, San Diego, Calif.). Post hoc analysis was performed by Tukey's multiple comparison test. Differences of P<0.05 were considered to denote statistical significance.
Data Analysis with Machine Learning
Identifying key features and classification of the comprehensive patient data was obtained by employing supervised and unsupervised ML algorithms (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017 August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29.). We preprocessed the data while removing features with low variance and high correlation for dimension reduction following best practices recommendations. We compared the following supervised algorithms: AdaBoost, Gradient Boosting (GB), Support Vector Machines (SVM) and Random Forest (RF) (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017 August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29.). We employed classifiers that are suitable for training on small data sets for a comparison of features given little training and chose the most appropriate algorithm according to accuracy and robustness towards overfitting (Al-Naqeb D. Scientifica (Cairo). 2016; 2016:2079704. doi: 10.1155/2016/2079704. Epub 2016 May 30.). Supervised ML models have been 10-fold cross-validated and 100 times repeated. We then applied feature selection for the AdaBoost, GB and RF classifiers to further reduce the number of features to <20. We employed t-distributed stochastic neighbor embedding (t-SNE) for unsupervised machine learning classification and nonlinear dimensionality reduction (Steinhoff G, Nesteruk J, Wolfien M, et al. EBioMedicine 2017 August; 22:208-224. doi: 10.1016/j.ebiom.2017.07.022. Epub 2017 Jul. 29.).
By the means of Systems Biology approaches, we aimed to uncover time-dependent expression response patterns among the investigated patient datasets. The identification of enriched signaling pathways was done by using the Reactome Functional Interaction (RFI) and the BisoGenenet Cytoscape applications, which were designed to find enhanced pathways and network patterns within curated and experimentally validated databases (Fabregat A, Sidiropoulos K, Garapati P, et al. Nucleic Acids Res 2016; Jan. 4; 44 D1:D481-7. doi: 10.1093/nar/gkv1351. Epub 2015 Dec. 9.). In addition, we subsequently used TiCoNE (Time Course Network Enricher) for the time course network enrichment analysis of the patient-specific expression data. The tool employs different mathematical algorithms to identify time patterns emerging in the expression data for a given interaction network by using the partitioning around medoids (PAM) and the Clustering for Large Applications (CLARA) algorithm, which are a specialized k-medoid clustering approaches. The error rates (FDR) and p-values have been computed by using globally permutations with 1000 iterations. The Pearson Product Moment Correlation (PPMC) has been used to compare the different clusters. The gene expression patterns within the motifs are considered to be common for p-values <0.05.
Weighted gene coexpression network analysis (WGCNA) was performed by applying the R package “WGCNA” to RNAseq data. We first constructed the topological overlap matrix (TOM) of all investigated transcripts (160.000) using the soft thresholding method. We calculated the eigenvalues of the transcripts and evaluated the adjacency based on distance. We subjected transcripts to hierarchical clustering (average linkage) and assigned transcripts with the dynamic hybrid method into groups. We computed the connectivity based on the interaction partners (k) and evaluated the gene significance, which represents the resulting module membership.
Peripheral blood (PB) whole genome expression and circulating endothelial progenitor cells (EPC) analysis were studied at day 0, 1, 3, 10 in the phase 3 PERFECT (CABG and CD133+BMSC or Placebo) trial biomarker subgroup (n=23) of responders (R, n=14; ΔLVEF+16% day 180/0) and non-responders (NR, n=9; ΔLVEF −1.1% day 180/0) and in independent center biomarker patient cohort (n=14).
Left ventricular functional recovery was accompanied by an increase in myocardial perfusion (R vs NR, p<0.05). Twenty biomarkers were identified for preoperative prediction of cardiac regeneration capacity (R/NR 95.6% accuracy, 91% AUC) in PB (
The invention illustratively described herein suitably may be practised in the absence of any element or elements, limitation or limitations which is/are not specifically disclosed herein. Thus, for example, in each instance herein any of the terms “comprising”, “consisting essentially of” and “consisting of” may be replaced with either of the other two terms. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.
All references cited in this specification are herewith incorporated by reference with respect to their entire disclosure content and the disclosure content specifically mentioned in this specification.
BAZ1A=Bromodomain adjacent to zinc finger domain protein 1A
BCIP=5-Bromo-4chloro-3-indolyl-phosphate
CEC=Circulating endothelial cells, CEC panel, CDs measured in PB
CFU=Colony-forming unit
CI=Confidence interval
Delta_CT_SH2B3 (ΔCT SH2B3)=normalized value of SH2B3 gene expression (normalisation vs. housekeeping gene Glycerine aldehyde-3-phosphate-dehydrogenase
EPC=Endothelial Progenitor Cells, EPC panel, CDs measured in PB
GRB2=Growth factor receptor-bound protein 2
HR=Hazard ratio
HIF=Hypoxia-Inducible Factor, transcription factor
IHG=Analysis performed in accordance with ISHAGE guidelines
ML=Machine learning
MNC=Mononuclear cells
PB=Peripheral blood
PBMNC=mononuclear cells isolated from peripheral blood
PPS=Group of patients for per-protocol set
SACM1 L=Staphylococcus aureus Cowan 1 phosphatidylinositide phosphatase
SAE=Serious adverse event
SAS=Group of patients for safety set
t-SNE=t-distributed stochastic neighbour embedding
VEGF rec=Vascular Endothelial Growth Factor Receptor
ZNF205=Zinc finger protein 205
Homo sapiens
Homo sapiens
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2018 125 324.9 | Oct 2018 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/077650 | 10/11/2019 | WO | 00 |
