Method for the detection, preparation and depletion of CD4+ t lymphocytes

Abstract

The present invention relates an in vitro method for detecting class II restricted CD4+ T cells in a sample. Herein a sample is contacted with an isolated complex of an MHC class II molecule and a peptide. This peptide comprises an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C or C-xx-[CST] motif. CD4+ T cells are detected by measuring the binding of the complex with cells in the sample, wherein the binding of the complex to a cell is indicative for the presence of CD4+ T cells in the sample. The present invention further relates to an isolated complex of an MHC Class II molecule and a peptide comprising an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C or C-xx-[CST] motif.

Description

REFERENCE TO SEQUENCE LISTING SUBMITTED ELECTRONICALLY

The content of the electronically submitted sequence listing (Name: 2752_0115_sequence_listing.txt; Size: 7,042 bytes; and Date of Creation: Jul. 9, 2019) filed with the application is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to synthetic peptides encompassing class II-restricted major histocompatibility complex (MHC) T cell epitopes containing a thioredox motif within flanking residues for the detection, preparation or depletion of CD4+ T lymphocytes in or from body fluids or culture medium.

BACKGROUND OF THE INVENTION

Lymphocytes play a central role in the elaboration of immune responses against foreign antigens and in the control of diseases. Such recruitment and activation of lymphocytes can be beneficial as in responses against infectious agents, or detrimental, such as exemplified by auto-immune diseases, responses to allergens and in graft rejection. There are therefore a large number of circumstances in which it would be advantageous to detect, enumerate, purify or deplete such lymphocytes. Current methods to achieve these goals are, however, unsatisfactory.

Lymphocytes are divided in several lineages and subsets according to the presence of surface molecule and function. Lymphocytes of the CD4 lineage are characterized by the presence of the CD4 molecule, a co-receptor associated with the antigen-specific T cell receptor (called CD3).

CD4+ T cells recognize antigens after their processing by antigen-presenting cells and presentation by class II major histocompatibility complexes (MHC class II). This results in the formation of an immune synapse through assembly of MHC class II determinants, antigen-derived peptides and the antigen-specific T cell receptor (TCR), a molecular complex which is stabilized by recruitment of the CD4+ molecule.

However, the recognition of a peptide-MHC class II complex by a TCR is of low affinity, namely several orders of magnitude lower than for the binding of an antibody to its epitope. This is due to the fact that the TCR contacts a linear sequence made of 9 amino acid residues bound to class II MHC cleft, together with residues pertaining to the MHC molecule itself, as opposed to the large area made by antibody and epitope binding. TCR low affinity results in inefficient detection, in particular in complex body fluids.

This has led to the development of methods in which peptide-MHC complexes are reconstituted using a soluble form of MHC. Usually, soluble MHC molecules are multimerized in the form of dimers, tetramers or pentamers. Numerous variants of these multimers have recently been described (Davis et al. (2011) Nature Rev. Immunol. 11, 551-558. However, although both the specificity and sensitivity of these multimers have been significantly increased, these detection tools still remain relatively inefficient under circumstances of low T cell frequency or when TCR affinity is a limiting factor, such as for T cells in naïve configuration.

MHC class II multimers for detecting T cell epitopes are reviewed in for example Nepom (2012) J. Immunol. 188, 2477-2482. This review also points to the limited affinity of MHC class II multimers for CD4+ cells, and the use of citrinullated amino acids to improve this affinity Wooldridge et al. (2009) Immunology 126, 147-164 discuss peptide-MHC complexes and the low affinity of epitope MHC complexes. An attempt to increase T cell epitope binding with MHC class II complexes, by introducing hydrophobic amino acids adjacent to the epitope sequence is described in WO97040852.

WO2008017517 describes peptides with a T cell epitope and a reductase motif sequence in the generation of a cytolytic T cell population. Carlier et al. (2012) PloS ONE 7(10), e45366, 1-14 disclose that the synapse formed between the MHC-peptide complex and cognate TCR is stabilized by this type of peptides. The experimental results herein demonstrate that the number and the duration of dimer formation between antigen presenting cells and CD4+ T cells increases when peptides are used which comprises a T cell epitope sequence and a redox motif sequence.

The contrast between the increasing need for methods to detect CD4+ T cells in areas as diverse as auto-immune diseases, cancer or evaluation of responses towards vaccination, to cite just a few, and the poor efficiency of available methods makes it an urgent need to improve such methods

SUMMARY OF THE INVENTION

The first aspect of the invention relates to in vitro methods for detecting class II restricted CD4+ T cells in a sample. These methods comprise the steps of:

• • providing a sample,
  • contacting the sample with an isolated complex of an MHC class II molecule and a peptide, the peptide comprising an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C [SEQ ID NO:11] or C-xx-[CST] [SEQ ID NO:12] motif,
  • detecting CD4+ T cells by measuring the binding of the complex with cells in the sample, wherein the binding of the complex to a cell is indicative for the presence of CD4+ T cells in the sample.

In specific embodiments the motif is CxxC [SEQ ID NO:13].

In specific embodiments the linker has a length of maximum 4 amino acids.

In other embodiments the peptide occurs in a non-covalent complex with the MHC class II molecule and has a length of between 12 and 20 amino acids.

The sample can be a blood sample, a tissue sample, such as synovial fluid from rheumatoid arthritis patients, pleural fluid of e.g. patients with infectious pneumonia or tuberculosis.

A sample can comprise different types of CD4+ T cells.

The CD4+ T cells to be detected in the sample can be one or more of naïve CD4+ T cells, antigen-exposed CD4+ T cells, Tregs, induced Tregs, CD4+ T cells obtained during therapy or during vaccination, or CD4+ T cells in tissues.

In particular embodiments, the complex is a fusion protein of the peptide and an MCH class II molecule.

In particular embodiments the MHC Class II molecule is present in a cell lysate, or in a purified fraction of the cell lysate. The MHC molecule can be obtained by recombinant expression.

Typically the epitope sequence in the peptide is identical to the sequence in the antigen. Alternatively, the MHC class II anchoring residues are modified compared to the epitope as occurring in the antigen to modulate the binding affinity of the peptide to the CD4+ T cells.

Different variations of complexes are envisaged such as MHC molecules in the complex as tetramers, dextramers, soluble complexes, complexes attached to an insoluble carrier or a substrate.

Embodiments of the methods of the invention further comprise the step of isolating the CD4+ T cells bound to the complex.

Embodiments of the methods of the invention further comprise the step of detecting or isolating subpopulations of detected CD4+ T cells.

Embodiments of the methods of the invention further comprising the step of detecting or isolating subpopulations of isolated CD4+ T cells.

Another aspect of the present invention relates to a composition comprising a an isolated complex of:

An MCH class II molecule and

a peptide comprising an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C [SEQ ID NO:11] or C-xx-[CST] [SEQ ID NO:12] motif

In typical embodiments the motif is CxxC [SEQ ID NO:13]. In other typical embodiments the linker has a length of at most 4 amino acids.

The complex between the peptide and the MHC molecule can be a non-covalently bound complex or can be a covalently bound complex.

The complex can also be a fusion protein of an MHC class II protein with said peptide. In typical embodiments, wherein the peptide occurs in a non-covalent complex or in a covalent complex, other than a fusion protein, the peptide has a length of between 12 and 20 amino acids.

The complex can be attached to a carrier, such as a bead or a plate.

A further aspect of the invention relates to the use of a peptide comprising a MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids, a sequence with a [CST]-xx-C [SEQ ID NO:11] or C-xx-[CST] [SEQ ID NO:12] motif, for increasing the binding affinity of a complex of an MHC II class II molecule and a peptide with a T cell epitope to an MHC class II restricted CD4+ T cell.

A yet further aspect of the invention relates to the use of a [CST]-xx-C [SEQ ID NO:11] or C-xx-[CST] [SEQ ID NO:12] motif for generating a peptide with a T cell epitope and said motif sequence for increasing the binding affinity of an isolated MHC II class II molecule/epitope complex to an MHCII class II restricted CD4+ T cell.

The methods of the present invention can be used, for example in the following applications:

• • detecting effector CD4+ T cells towards an autoimmune antigen for monitoring an auto immune disease treatment
  • detecting vaccine specific CD4+ T cells for monitoring vaccination efficacy
  • eliminating CD4+ T cells of a recipient prior to a transplantation.
  • enriching a population of CD4+ T cells prior to expanding said population of cells and optionally expanding the cells in the presence of the peptide
  • or isolating CD4+ T cells at different time points for identifying mutations in the TCR (T cell receptor)

The improved methods and compounds of the present invention find their application in e.g.:

(1) analytical purposes: detection of T cell precursor frequency before vaccination, evaluation of peptide binding affinity for MHC class II complexes, follow-up of specific T cells during the course of vaccination or under immunosuppressive therapy, identification of cells regardless of their biological activity, identification of cells implicated in the mechanism of disease, depletion of specific T cells, and detection of T cells in situ, such in organ biopsies;

(2) Preparative purposes: preparation of specific T cells for evaluation of function, preparation of T cells for culture and purification and TCR sequencing

(3) Quality control of cell populations aimed, for instance, at cell therapy;

(4) Therapeutic purposes, including depletion of specific CD4+ T cells before organ grafting.

The structure of MHC class II molecules allows peptides of up to 20 amino acids to be presented to T cells. The core sequence is usually made of 9 amino acids which are inserted into the MHC class II cleft. Flanking regions protrude at both the carboxy- and amino-terminal end of the epitope.

The WO2008017517 patent application describes the use of oxidoreductase motifs inserted into the flanking residues of class II-restricted epitopes for the therapy of a number of diseases. It is demonstrated that the oxidoreductase motif stabilizes the synapse formed between the MHC-peptide complex and cognate TCR, as reported in Carlier et al., PloS ONE 7(10): e45366 1-14. The increased synapse formation described therein is supported by experiments with purified APC and CD4+ T cells, which show an increase in number and duration of dimer formation between APC and CD4+ T cells, which results in an effect on various functional properties of CD4+ T cells. An effect on the binding affinity between APC and CD4+ is not discussed in the prior art.

We made the unexpected observation that addition of an oxidoreductase motif within flanking residues of class II epitopes, increases the binding affinity of MHC-epitope complexes with CD4+ T cells, also when the MCH molecules are used as isolated complexes. This allows using peptides with a T cell epitope sequence and a redox motif in the detection and preparation of antigen-specific CD4+ T cells and for all subsequent manipulation of such cells.

The methods and compositions of the present invention allow a specific and high affinity detection of CD4+ T cells.

This specificity and affinity allow more sensitive and specific diagnostic methods.

The specificity and affinity also allows the isolation of CD4+ T cells in higher numbers and higher purity.

The present invention allows detecting CD4+ T cells using isolated MHC class II molecules, outside the context of antigen presentation on intact living cells. The finding that specific and high affinity CD4+ T cell binding can be obtained in the absence of the various interactions that occur between APC and CD4+ T cells is a major finding of the present invention.

The methods of the present invention can be performed on tissues and body fluids, and partially purified fractions thereof.

The methods of the present invention can be performed on samples comprising different types of CD4+ cells and different types of T cells.

The affinity and specificity allows performing cell detection and isolation using a repertoire of techniques which is known for the detection of cell surface antigens using antibodies, or the detection of receptors using ligands. Examples hereof are the immobilisation and manipulation of the MCH-peptide complex on substrates or beads and the labelling of the complex with detectable groups, such as chromophoric groups or magnetic beads.

DETAILED DESCRIPTION

Definitions

The term “peptide” as used herein refers to a molecule comprising an amino acid sequence of connected by peptide bonds, but which can in a particular embodiment comprise non-amino acid structures (like for example a linking organic compound).

A peptide in the context of the present invention comprises at least an MHC class II T cell epitope sequence and a redox motif sequence. These two features are described and defined in further detail below.

In the methods and products of the present application such peptide occurs as a complex with an MHC class II molecule. This complex can be a non-covalent complex of peptide and MHC molecule, or a covalent complex by crosslinking functional groups of peptide and MHC molecule via e.g. SH, COOH, NH₂, or OH groups.

In the above complexes the peptide comprising the epitope (8, 9 or 10 amino acids) and the redox motif (4 amino acids) will typically have a length between 12, 13 or 14 amino acids and 16, 17 or 18 amino acids. Depending on the length of the linker and flanking residues the peptide can have a length up to 20, 21, 24, 25 or 30 amino acids.

A specific type of covalent complex is a fusion protein of a peptide with a MHC class II T cell epitope and a redox motif, and an MHC class II molecule (further referred to as “peptide-MHC fusion protein”).

Peptides according to the invention can contain any of the conventional 20 amino acids or modified versions thereof, or can contain non-naturally occurring amino-acids incorporated by chemical peptide synthesis or by chemical or enzymatic modification. Of particular interest are modified versions of cysteine with a thiol group such as mercaptovaline, homocysteine or other natural or non-natural amino acids with a thiol function.

“Oxidoreductase motif”, “redox motif”, “reductase motif” or “motif”, refers to a four amino acid sequence with the motif CxxC [SEQ ID NO:13] CxxS [SEQ ID NO:14], CxxT [SEQ ID NO:15], SxxC [SEQ ID NO:16], TxxC [SEQ ID NO:17]. These alternatives can be written as [C]-X(2)-[CS] [SEQ ID NO:18] or [CS]-X(2)-[C] [SEQ ID NO:19].

The term “epitope” refers to one or several portions (which may define a conformational epitope) of an antigenic protein which is/are specifically recognised and bound by an antibody or a portion thereof (Fab′, Fab2′, etc.) or a receptor presented at the cell surface of a B or T cell lymphocyte, and which is able, by said binding, to induce an immune response.

The term “T cell epitope” in the context of the present invention refers to a dominant, sub-dominant or minor T cell epitope, i.e. a part of an antigenic protein that is specifically recognised and bound by a receptor at the cell surface of a T lymphocyte. Whether an epitope is dominant, sub-dominant or minor depends on the immune reaction elicited against the epitope. Dominance depends on the frequency at which such epitopes are recognised by T cells and able to activate them, among all the possible T cell epitopes of a protein.

The term “MHC class II restricted T cell epitope” in the context of the present invention refers to a T cell epitope which is recognised by MHC class II molecules and consists of a sequence of +/−9 amino acids (8, 9 or 10 AA) which fit in the groove of the MHC II molecule. Within a peptide sequence representing a T cell epitope of 9 AA, the amino acids in the epitope are numbered P1 to P9, amino acids N-terminal of the epitope are numbered P−1, P−2 and so on, amino acids C terminal of the epitope are numbered P+1, P+2 and so on.

The term “antigen” as used herein refers to a structure of a macromolecule, typically protein (with or without polysaccharides) or made of proteic composition comprising one or more hapten (s) and comprising T cell epitopes. The term “antigenic protein” as used herein refers to a protein comprising one or more T cell epitopes. An auto-antigen or auto-antigenic protein as used herein refers to a human or animal protein present in the body, which elicits an immune response within the same human or animal body.

The term “food or pharmaceutical antigenic protein” refers to an antigenic protein naturally present in a food or pharmaceutical product, such as in a vaccine.

The term “natural”, when referring to a protein or peptide or a fragment thereof relates to the fact that the sequence is identical to a naturally occurring sequence. This term includes as well wild type sequences as polymorphism and mutants which occur in a population. In contrast therewith the term “artificial” refers to a sequence or peptide which as such does not occur in nature, as peptide or fragment of a protein sequence. Optionally, an artificial sequence is obtained from a natural sequence by limited modifications such as changing one or more amino acids within the naturally occurring sequence or by adding amino acids N- or C-terminally of a naturally occurring sequence.

The term “homologue” as used herein with reference to the epitopes used in the context of the invention, refer to molecules having at least 50%, at least 70%, at least 80%, at least 90%, at least 95% or at least 98% amino acid sequence identity with the naturally occurring epitope, thereby maintaining the ability of the epitope to bind an antibody or cell surface receptor of a B and/or T cell. Particular embodiments of homologues of an epitope correspond to the natural epitope modified in at most three, more particularly in at most 2, most particularly in one amino acid. Specific embodiments hereof are modified epitopes which have a higher binding affinity for CD4+ T cells compared to the unmodified epitope.

The term “derivative” as used herein with reference to the peptides of the invention refers to molecules which contain at least the peptide active portion (i.e. capable of detecting CD4+ T cell) and, in addition thereto comprises a portion which can have different purposes such as stabilising the peptides or altering the pharmacokinetic or pharmacodynamic properties of the peptide.

The term “immune disorders” or “immune diseases” refers to diseases wherein a reaction of the immune system is responsible for or sustains a malfunction or non-physiological situation in an organism. Included in immune disorders are, inter alia, allergic disorders and autoimmune diseases.

The terms “allergic diseases” or “allergic disorders” as used herein refer to diseases characterised by hypersensitivity reactions of the immune system to specific substances called allergens (such as pollen, stings, drugs, or food). Allergy is the ensemble of signs and symptoms observed whenever an atopic individual patient encounters an allergen to which he/she has been sensitised, which may result in the development of various diseases, in particular respiratory diseases and symptoms such as bronchial asthma. Various types of classifications exist and mostly allergic disorders have different names depending upon where in the mammalian body it occurs. “Hypersensitivity” is an undesirable (damaging, discomfort-producing and sometimes fatal) reaction produced in an individual upon exposure to an antigen to which it has become sensitised; “Immediate hypersensitivity” depends of the production of IgE antibodies and is therefore equivalent to allergy.

An “allergen” is defined as a substance, usually a macromolecule or a proteic composition which elicits the production of IgE antibodies in predisposed, particularly genetically disposed, individuals (atopics) patients. Similar definitions are presented in Liebers et al. (1996) Clin. Exp. Allergy 26, 494-516. Examples of allergens are airborne allergens, food allergens, venoms, mite allergens (e.g. Der p 1 and Der p 2).

The terms “autoimmune disease” or “autoimmune disorder” refer to diseases that result from an aberrant immune response of an organism against its own cells and tissues due to a failure of the organism to recognise its own constituent parts (down to the sub-molecular level) as “self”. The group of diseases can be divided in two categories, organ-specific and systemic diseases.

Examples of antigens involved in auto-immune diseases, known as autoantigens are thyroglobulin, thyroid peroxidase, TSH receptor, insulin (proinsulin), glutamic acid decarboxylase (GAD), tyrosine phosphatase IA-2, myelin oligodendrocyte protein, heat-shock protein HSP60.

Other antigens include “pathogen-associated antigens”, such as viruses, bacteria, mycobacteria or parasites with an intracellular life cycle, or viruses, bacteria and parasites with extracellular life cycle.

The term “allofactor” refers to a protein, peptide or factor (i.e., any molecule) displaying polymorphism when compared between 2 individuals of the same species, and, more in general, any protein, peptide or factor that is inducing an (alloreactive) immune response in the subject receiving the allofactor.

Examples of allofactors are proteins use in a replacement therapy for coagulation defects or fibrinolytic defects, including factor VIII, factor IX and staphylokinase; hormones such as growth hormone or insulin; cytokines and growth factors, such as interferon-alpha, interferon-gamma, GM-CSF and G-CSF; antibodies for the modulation of immune responses, including anti-IgE antibodies in allergic diseases, anti-CD3 and anti-CD4 antibodies in graft rejection and a variety of autoimmune diseases, anti-CD20 antibodies in non-Hodgkin lymphomas, erythropoietin in renal insufficiency.

The term “alloantigen” refers to an antigen generated by protein polymorphism in between 2 individuals of the same species. Examples thereof are MHC class I and/or class II molecules, minor histocompatibility antigens, and tissue-specific alloantigens.

The term “tumor-associated antigen” refers to any protein, peptide or antigen associated with (carried by, produced by, secreted by, etc) a tumor or tumor cell(s). Tumor-associated antigens may be (nearly) exclusively associated with a tumor or tumor cell(s) and not with healthy normal cells or may be overexpressed (e.g., 10 times, 100 times, 1000 times or more) in a tumor or tumor cell(s) compared to healthy normal cells. More particularly a tumor-associated antigen is an antigen capable of being presented (in processed form) by MHC determinants of the tumor cell. Hence, tumor-associated antigens are likely to be associated only with tumours or tumor cells expressing MHC molecules.

Examples are antigens from oncogenes such as MAGE identified in some melanomas; proto-oncogenes, such as cyclin D1 expressed on soft tissues carcinomas such as those of the kidney or parathyroid, as well as in multiple myeloma; virus-derived proteins, such as those from the Epstein-Barr virus in some carcinomas and in some Hodgkin-type lymphomas; surviving factors, which are anti-apoptotic factors such as survivin or bcl2; clonotypic determinants, such as idiotypic determinants derived from B cell receptor in follicular lymphomas or multiple myelomas or T cell receptor determinants in T cell malignancies.

The term “major histocompatibility antigen” refers to molecules belonging to the HLA system in man (H2 in the mouse), which are divided in two general classes. MHC class I molecules are made of a single polymorphic chain containing 3 domains (alpha 1, 2 and 3), which associates with beta 2 microglobulin at cell surface. Class I molecules are encoded by 3 loci, called A, B and C in humans. Such molecules present peptides to T lymphocytes of the CD8+ subset.

“Class II molecules” as occurring on cells are transmembrane proteins consisting of 2 polymorphic chains, each containing 2 chains (alpha 1 and 2, and beta 1 and 2). These class II molecules are encoded by 3 loci, DP, DQ and DR in man.

For the purpose of the present invention it is required and sufficient that the MCH molecule-T cell epitope complex can bind to a CD4+ T cell.

MHC molecules can be isolated from cells or produced in recombinant expression systems.

“Isolated” when referring to MHC class II proteins and complexes with peptides refers to compounds, obtained via recombinant processes or (partial) purification of cells, including lysates and fractions of lysates.

The term “minor histocompatibility antigen” refers to peptides that are derived from normal cellular proteins and are presented by MHC belonging to the class I and/or the class II complexes. Any genetic polymorphism that qualitatively or quantitatively affects the display of such peptides at the cell surface can give rise to a minor histocompatibility antigen.

“CD4+ T cells” are characterized by the surface expression of CD4 glycoprotein. CD4+ cells which are applicable in the context of the present invention include:

• • Tregs (regulatory T cells) which are involved in active suppression of inappropriate immune responses. These cells are CD4+, CD25+, FoxP3+ cells.
  • Induced Tregs such as Tr1 or Th3 CD4+ T cells, involved in suppression of inappropriate immune responses, said cells characterized by any combination of surface markers such as Lag3^hi and CD49b, intracellular IL-10 and TGF-beta, and granzyme B.
  • Naïve CD4+ T cells which express CD45A and CD197, have a low or intermediate expression of CD44, and a low cytokine production with no preferred pathway.
  • Polarised CD4+ cells which have a high CD44 expression and the production of a restricted set of cytokines.
  • Cytolytic CD4+ T cells (cCD4+ T cells) which have been characterised in detail in WO2009/101207 and are characterized by i.a. the absence of FoxP3 expression.

The term “viral vector protein” when used herein refers to any protein or peptide derived from a viral vector itself, and which is encoded by the backbone of the vector. It does not refer to the therapeutic protein itself which is cloned in the viral vector. In the exceptional event that a viral protein would be cloned in a viral vector, this protein still classifies as a therapeutic protein and not as a viral vector protein. Typically such viral vector proteins are antigenic and comprise one or more epitopes such as T-cell epitopes.

Examples of proteins encountered in the backbone of a vector are those obtained from RNA viruses such as gamma-retroviruses and lentiviruses and from DNA viruses such as adenoviruses, adeno-associated viruses, herpes viruses and poxviruses.

The term “alloreactivity” refers to an immune response that is directed towards allelic differences between the graft recipient and the donor. Alloreactivity applies to antibodies and to T cells. The present invention relies entirely on T cell alloreactivity, which is based on T cell recognition of alloantigens presented in the context of MHC determinants as peptide-MHC complexes.

“Complex” in the context of the present invention relates to an association of one or more MHC class II molecules with a peptide comprising an epitope. The association can be a non-covalent association by the spontaneous binding of the peptide with the MHC molecule via salt bridges, hydrogen bridges and hydrophobic contacts. The association can also be a covalent association via chemical crosslinking using crosslinking agents and bifunctional molecules.

In a specific type of complex the MCH class II molecule and the peptide is a recombinant fusion protein (a so called peptide-MHC fusion proteins).

“Motifs” of amino acid sequences are written herein according to the format of Prosite. The symbol X is used for a position where any amino acid is accepted.

Alternatives are indicated by listing the acceptable amino acids for a given position, between square brackets (′[ ]′). For example: [CST] stands for an amino acid selected from Cys, Ser or Thr. Amino acids which are excluded as alternatives are indicated by listing them between curly brackets (′{ }′). For example: {AM} stands for any amino acid except Ala and Met. The different elements in a motif are separated from each other by a hyphen -. Repetition of an identical element within a motif can be indicated by placing behind that element a numerical value or a numerical range between parentheses. For example: X(2) corresponds to X-X, X(2, 4) corresponds to X-X or X-X-X or X-X-X-X, A(3) corresponds to A-A-A.

The present invention is based upon the finding that a peptide, comprising a T cell epitope and a peptide sequence having reducing activity is capable of detecting CD4+ T cells.

Accordingly, in its broadest sense, the invention relates to methods and compositions of peptides which comprise at least one T-cell epitope of an antigen (self or non-self) with a potential to interact with a CD4+ T cell TCR, coupled to a peptide with a thioreductase sequence motif. The T cell epitope and the redox motif sequence are optionally separated by a linker sequence. In further optional embodiments the peptide additionally comprises additional “flanking” sequences.

Typical embodiments of peptides used in the methods and compositions of the invention can be schematically represented as Flanking sequence-Epitope-Linker-Motif-Flanking sequence or Flanking sequence-Motif-Linker-Epitope-Flanking, wherein “Epitope” represents a T-cell epitope of an antigen (self or non-self) with a potential to react with the TCR of CD4+ T lymphocytes, “Linker” represents an optional linker of between 0 and 7 amino acids, “Motif” represents a four amino acids oxidoreductase motif, and “Flanking sequence” optional additional amino acids. The reducing activity can be assayed for its ability to reduce a sulfhydryl group such as in the insulin solubility assay wherein the solubility of insulin is altered upon reduction, or with a fluorescence-labelled insulin. Alternatively, the reducing activity can be evaluated in a fluorometric assay in which a peptide is incubated with a oxidized substrate freeing fluorescence after being reduced. The peptide with the oxidoreductase may be coupled at the amino-terminus side of the T-cell epitope or at the carboxy-terminus of the T-cell epitope. Peptide fragments with reducing activity are encountered in thioreductases which are small disulfide reducing enzymes including glutaredoxins, nucleoredoxins, thioredoxins and other thiol/disulfide oxydoreductases (Holmgren (2000) Antioxid Redox Signal 2, 811-820; Jacquot et al. (2002) Biochem Pharm 64, 1065-1069). They are multifunctional, ubiquitous and found in many prokaryotes and eukaryotes. They exert reducing activity for disulfide bonds on proteins (such as enzymes) through redox active cysteines within conserved active domain consensus sequences: C-X(2)-C [SEQ ID NO:13], C-X(2)-S [SEQ ID NO:14], C-X(2)-T [SEQ ID NO:15], S-X(2)-C [SEQ ID NO:16], T-X(2)-C [SEQ ID NO:17] (Fomenko et al. (2003) Biochemistry 42, 11214-11225; Fomenko et al. (2002) Prot. Science 11: 2285-2296), in which X stands for any amino acid. Such domains are also found in larger proteins such as protein disulfide isomerase (PDI) and phosphoinositide-specific phospholipase C.

In order to have reducing activity, the cysteines present in the motif should not occur as part of a cystine disulfide bridge. Also methylated versions of cysteine are contemplated in the peptides used in the present invention.

As explained in detail further on, peptides can be made by chemical synthesis, which allows the incorporation of non-natural amino acids. Accordingly, in the motif of reducing compounds, C represents either cysteine or another amino acids with a thiol group such as mercaptovaline, homocysteine or other natural or non-natural amino acids with a thiol function. In order to have reducing activity, the cysteines present in the motif should not occur as part of a cystine disulfide bridge.

The amino acid X in the [CST]-X(2)-[CST] [SEQ ID NO:20] motif can be any natural amino acid, including S, C, or T or can be a non-natural amino acid. In particular embodiments X is an amino acid with a small side chain such as Gly, Ala, Ser or Thr. In further particular embodiments at least one X in the [CST]-X(2)-[CST] [SEQ ID NO:20] motif is His, Pro or Tyr. Other embodiments refer to peptides with the motif wherein one or both X are not cysteine. Other embodiments refer to peptides wherein cysteines do not occur as, two, three or four consecutive cysteine, such as for example in tetracysteine tags.

Further embodiments refer to peptides wherein the one or two cysteines of the[C]-X(2)-[CST] [SEQ ID NO:12] or [CST]-X(2)-[C] [SEQ ID NO:11] motif are the only cysteines in the non-epitope part of the peptide. More specifically the linker between the epitope and the motif does not contain a cysteine.

In certain embodiments wherein the epitope sequence itself comprises no cysteine residues, the one or two cysteines of the redox motif is/are the only cysteines in the peptide.

In the peptides comprising the motif described above as the reducing compound, the motif is located such that, when the epitope fits into the MHC groove, the motif remains outside of the MHC binding groove. The motif is placed either immediately adjacent to the epitope sequence within the peptide (i.e. there are no amino acids in-between the epitope sequence and the oxidoreductase motif (“linker of 0 amino acid”)) or is separated from the T cell epitope by a linker. More particularly, the linker comprises an amino acid sequence of 7 amino acids or less. Most particularly, the linker comprises 1, 2, 3, or 4 amino acids. Alternatively, a linker may comprise 5, 6, or 7 amino acids. When the motif sequence is adjacent to the epitope sequence this is indicated as position P−4 to P−1 or P+1 to P+4 compared to the epitope sequence. The peptides can further comprise additional short amino acid sequences N or C-terminally of the (artificial) sequence comprising the T cell epitope and the reducing compound (motif). Such an amino acid sequence is generally referred to herein as a ‘flanking sequence’. In further embodiments, a short amino acid sequence may be present N and/or C terminally of the reducing compound and/or epitope sequence in the peptide. More particularly a flanking sequence is a sequence of between 1 and 7 amino acids, most particularly a sequence of 2 amino acids.

As can be understood the length of a peptide in a non-covalent complex with an MHC molecule is at least 12-14 amino acids (8-10 AA epitope+4 AA redox motif). But the length increases with the presence of linker sequence (additional 7 AA) and a flanking sequence at one (additional 7 AA) or both (additional 14 AA) ends. Typically sequences are used with a length between 12 up to 20 or 25 amino acids.

In particular embodiments, the motif is located N-terminal from the epitope.

In other embodiments, a motif is located both N-terminal and C-terminal from the epitope.

In further particular embodiments, where the motif present in the peptide contains one cysteine, this cysteine is present in the motif in the position remote from the epitope, thus the motif occurs as C-X(2)-T [SEQ ID NO:15] or C-X(2)-S [SEQ ID NO:14] N-terminally of the epitope or occurs as T-X(2)-C [SEQ ID NO:17] or S-X(2)-C [SEQ ID NO:16] C-terminally of the epitope.

In certain embodiments of the present invention, peptides are provided comprising one epitope sequence and a motif sequence. In further particular embodiments, the motif occurs several times (1, 2 or even 3 times) in the peptide, for example as repeats of the motif which can be spaced from each other by one or more amino acids (e.g. CXXC X CXXC X CXXC [SEQ ID NO:21]), or as repeats which overlap with each other such as in the sequence CXXCXXCXXC [SEQ ID NO:22]. Alternatively, one or more motifs are provided at both the N and the C terminus of the T cell epitope sequence.

Accordingly, peptides comprise, in addition to a reducing compound, a T cell epitope derived from an antigen, typically an allergen or an auto-antigen, a pathogen-associated antigen, a viral vector antigen, a tumor-associated antigen, an allofactor or a alloantigen, depending on the application. As described below a T cell epitope in a protein sequence can be identified by functional assays and/or one or more in silico prediction assays. The amino acids in a T cell epitope sequence are numbered according to their position in the binding groove of the MHC proteins. In particular embodiments, the T-cell epitope present within the peptides of the invention consists of between 8 and 20 amino acids, yet more particularly of between 8 and 16 amino acids, yet most particularly consists of 8, 9, 10, 11, 12, 13, 14, 15 or 16 amino acids. In a more particular embodiment, the T cell epitope consists of a sequence of 8, 9, or 10 amino acids. The T cell epitope sequence is an epitope sequence which fits into the cleft of an MHC II protein, also known as an MHC class II restricted T cell epitope.

The T cell epitope of the peptides of the present invention can correspond either to a natural epitope sequence of a protein or can be a modified version thereof, provided the modified T cell epitope retains its ability to bind within the MHC cleft, similar to the natural T cell epitope sequence.

The modified T cell epitope can have the same binding affinity for the MHC protein as the natural epitope, but can also have a lower or higher affinity. In particular embodiments the binding affinity of the modified peptide is no less than 10-fold less than the original peptide, more particularly no less than 5 times less. It is a finding of the present invention that the peptides of the present invention have a stabilising effect on protein complexes formed between the pMHC and the complementary TCR. Accordingly, the stabilising effect of the peptide-MHC complex compensates for the lowered affinity of the modified epitope for the MHC molecule. An example hereof is the Ile28Asn substitution of Der p 2 peptide p21-35, which despite a lower affinity for the MHC II cleft, is capable of eliciting the same T cell response as the natural Der p 2 peptide p21-35.

As detailed above, in particular embodiments, the peptides of the present invention comprise a reducing motif as described herein linked to a T cell epitope sequence. According to a particular embodiment the peptides are peptides from proteins which do not comprise within their native natural sequence an amino acid sequence with redox properties in the vicinity (i.e. within a sequence of 11 amino acids N or C terminally) of the epitope of interest, more specifically which do not comprise in their native natural sequence a consensus sequence of thioredoxin, glutaredoxin or thioreductases or homologues thereof, in the vicinity of the epitope of interest.

The presence of a reductase motif in the vicinity of an epitope in an antigen protein is very rare. In some embodiments the peptide with the epitope and the motif is a fragment of a naturally occur protein. In most embodiments the peptide is an artificial peptide, wherein the sequence around the epitope has been modified to introduce at least the redox motif.

The identification of a suitable T cell epitope of an antigenic protein for use in the generation of peptides as described in the methods above is detailed below.

The identification and selection of a T-cell epitope from such antigenic proteins for use in the context of the present invention is known to a person skilled in the art.

Non-natural (or modified) T-cell epitopes can further optionally be tested on their binding affinity to MHC class II molecules. This can be performed in different ways. For instance, soluble HLA class II molecules are obtained by lysis of cells homozygous for a given class II molecule. The latter is purified by affinity chromatography. Soluble class II molecules are incubated with a biotin-labelled reference peptide produced according to its strong binding affinity for that class II molecule. Peptides to be assessed for class II binding are then incubated at different concentrations and their capacity to displace the reference peptide from its class II binding is calculated by addition of neutravidin. Methods can be found in for instance Texier et al. (2000) J. Immunol. 164, 3177-3184.

Additionally and/or alternatively, one or more in vitro algorithms can be used to identify a T cell epitope sequence within an antigenic protein. Suitable algorithms include, but are not limited to those found on the following websites:

• • antigen.i2r.a-star.edu.sg/predBalbc/;
  • imtech.res.in/raghava/mhcbn/;
  • syfpeithi.de/home.htm;
  • bs.informatik.uni-tuebingen.de/SVMHC;
  • bio.dfci.harvard.edu/Tools/antigenic.html;
  • jenner.ac.uk/MHCPred/.

More particularly, such algorithms allow the prediction within an antigenic protein of one or more nonapeptide sequences which will fit into the groove of an MHC II molecule.

Peptides and proteins can be generated using recombinant DNA techniques, in bacteria, yeast, insect cells, plant cells or mammalian cells. Peptides of limited length, can be prepared by chemical peptide synthesis, wherein peptides are prepared by coupling the different amino acids to each other. Chemical synthesis is particularly suitable for the inclusion of e.g. D-amino acids, amino acids with non-naturally occurring side chains or natural amino acids with modified side chains such as methylated cysteine.

Chemical peptide synthesis methods are well described and peptides can be ordered from companies such as Applied Biosystems and other companies. Peptide synthesis can be performed as either solid phase peptide synthesis (SPPS) or contrary to solution phase peptide synthesis. The best-known SPPS methods are t-Boc and Fmoc solid phase chemistry. During peptide synthesis several protecting groups are used. For example hydroxyl and carboxyl functionalities are protected by t-butyl group, Lysine and tryptophan are protected by t-Boc group, and asparagine, glutamine, cysteine and histidine are protected by trityl group, and arginine is protected by the pbf group. In particular embodiments, such protecting groups can be left on the peptide after synthesis.

Alternatively, the peptides, and especially fusion proteins of peptide and MHC molecule can be synthesized by using nucleic acid molecules which encode the peptides of this invention in an appropriate expression vector which include the encoding nucleotide sequences. Such DNA molecules may be readily prepared using an automated DNA synthesizer and the well-known codon-amino acid relationship of the genetic code. Such a DNA molecule also may be obtained as genomic DNA or as cDNA using oligonucleotide probes and conventional hybridization methodologies. Such DNA molecules may be incorporated into expression vectors, including plasmids, which are adapted for the expression of the DNA and production of the polypeptide in a suitable host such as bacterium, e.g. Escherichia coli, yeast cell, animal cell or plant cell.

The physical and chemical properties of a peptide of interest (e.g. solubility, stability) are examined to determine whether the peptide is/would be suitable for use for applications as defined for the present invention. Typically this is optimised by adjusting the sequence of the peptide. Optionally, the peptide can be modified after synthesis (chemical modifications e.g. adding/deleting functional groups) using techniques known in the art.

Peptides are loaded on class II MHC molecules. In one embodiment, cells presenting the relevant MHC class II molecule are incubated with the peptide. The cells are then used as such to bind the cognate TCR, either in soluble phase followed by facs analysis, or after insolubilisation on plates or on beads. These techniques are well described in the art. In an alternative embodiment, cells are lysed and the MHC class II molecules loaded with peptide are prepared by, for instance, chromatography. The pMHC complexes, with or without labelling, can then be used in soluble phase to interact with a population of CD4+ T cells, or insolubilized on plates or beads or any suitable solid-phase support for the detection of CD4+ T cells.

In another embodiment, MHC class II molecules are produced by cDNA technology using cell transfection or transduction. The cDNA construct can contain the full-length class II molecule with its intramembranous sequences for surface anchoring and use of cells as described above, or without the intramembranous sequence for secretion. Such secreted class II molecules can be purified and used as described above, in soluble forms or after insolubilisation on a solid surface such as plates or beads.

WO2011147894 discloses chimeric proteins of an alpha-chain and beta-chain of a MHC-class II protein, a linker and an epitope of interest, wherein the epitope is linked to the a-chain via the linker.

Basic leucine zippers, cysteine bridges (see e.g. WO2011101681), or chemical crosslinking can be used to connect the alpha and beta chain of the MHC molecules. Recombinant versions, lacking the transmembrane domains are also described in WO2011101681. Fusion proteins combining two MHC molecules are described, optionally as fusion protein with the epitope sequence (WO2011147894). WO1998006749 describes fusion proteins of an extracellular binding domain of an MHC II molecule and dimerization domain.

The MHC molecules can be further modified by binding moieties (peptide tags such as His tag, a binding moiety such as biotin, binding proteins such as GST, MBP, antibody tags such as HA tags.)

The MHC molecules can also be modified with detectable labels such as chromophoric groups, radioactive labels, magnetic beads.

In yet another embodiment, the cDNA construct encompassing class II MHC molecules also comprises the sequence of the peptide, so that the engineered molecule constitutively expresses the peptide in fusion with the MHC molecule. It is advantageous in this embodiment to include a linker in between the sequence of class II molecule and the sequence of the peptide, so as to allow proper folding and presentation of the peptide into the cleft of the class II molecule. These linkers are typically a polypeptide sequence of about 15 amino acids with serines and/or glycines to provide enough flexibility for the epitope to tether on the beta chains. The linker can further comprise a protease specific recognition site (e.g. for thrombin) such that after expression and folding, the peptide is presented in its normal configuration.

Soluble forms of MHC class II molecules before or after loading with a peptide, or molecules constitutively expressing the peptide can be used in the form of dimers or polymers, either by reacting several molecules between each other or by insolubilizing such molecules onto a solid phase such as beads or plates. These methods are described in the art.

MHC molecules can occur as multimers, such as tetramers (reviewed in Nepom, cited above) or dextramers (Massilamany (2011) BMC Immunol. 12, 40).

T cell epitopes of the present invention are thought to exert their properties by creating a disulfide bridge between the thioreductase motif and the CD4 molecule. This mechanism of action is substantiated by experimental data (see examples below), but there is no intention to restrict the present invention to this specific mechanism of action.

The methods and tools of the present invention can be used in various applications such as detection, preparation or depletion of antigen-specific CD4+ T cells for diagnosis purposes, phenotypic or functional evaluation, or T cell receptor (TCR) cloning. The CD4+ cell that are obtained our technology could also serve for high sequencing RNA, proteomics and to prepare material for crystallization of T cell receptors.

EXAMPLES

Example 1. Use of Tetramers of MHC Class II Molecules for the Detection of MOG-Specific CD4+ T Lymphocytes in the Naïve Human T Cell Repertoire

Multiple sclerosis is a chronic demyelination disease in which CD4+ T cells towards auto antigens such as the myelin oligodendrocytic glycoprotein (MOG) play a key role. The migration of effector cells through the brain-blood barrier elicits brain tissue destruction.

Such effector CD4+ T cells are generated from peripheral blood naïve T cells after cognate interaction with antigen-presenting cells presenting the MOG epitope within MHC class II complexes. Enumerating (i.e. identifying and quantifying) MOG-specific naïve CD4+ T cells is therefore predictive of disease outcome. However, the frequency of naïve T cell and affinity for MOG epitope are low, which prevents their detection by conventional technology, as for instance soluble tetramers of MHC class II molecules loaded with the MOG epitope.

One of such major MHC class II epitope of MOG is presented by molecules of the class II DR2 haplotype with the common DRB1*1501 allele being expressed by ±75% of patients affected by multiple sclerosis.

Naïve CD4+ T cells are prepared from the peripheral repertoire of DRB1*1501+ subjects susceptible to suffer from multiple sclerosis, using magnetic beads to remove CD4(−) cells and memory cells, as described in the art. Tetramers of DRB1*1501 are made as known in the art (Kasprowicz V et al. (2006) J. Virol. 80, 11209-112017), including a fluorescent label such as Ficoerythrin. A synthetic peptide is produced, which encompasses the corresponding class II-restricted MOG

T cell epitope and a thioreductase motif CGPCSRVVHLYRNGK D [SEQ ID NO: 1], which corresponds to amino acid residues 47-58 of the MOG protein.

Tetramers are loaded with peptide of SEQ ID 1 overnight at room temperature in the appropriate buffer conditions as known in the art. Loaded tetramers are then washed and incubated with naïve CD4+ T cells for 2 h at 37° C. The suspension is then read with a fluorescence-activated cell sorting (facs) system and the proportion of naïve cells specific to the MOG peptide evaluated Control experiments are performed with MHC complex with the same peptide without thioreductase motif. SRVVHLYRNGKD [SEQ ID NO:2].

The experiment shows that only the MHC complex with the peptide containing a thioreductase motif (SEQ ID 1) is able to detect naïve CD4+ T cells specific to the MOG 37-52 sequence.

Example 2. Use of Tetramers of MHC Class II Molecules for the Follow-Up of Specific CD4+ T Cells During Vaccination and for Modulation of the Vaccination Strategy

The effectiveness of vaccination for infectious diseases depends on the number of CD4+ T cells which can be activated by such vaccination. An early and predictive sign of successful vaccination can be found in the increase in the number of vaccine-specific CD4+ T cells, a useful parameter to decide whether the vaccination strategy has to be modified by, for instance, increasing the number of vaccine administrations. Influenza virus vaccination is a significant example in so far as there is only a loose correlation between the concentration of specific antibodies and the robustness of protection.

A major MHC class II-restricted epitope of the virus is located in the hemagglutinin protein. Peptide of sequence CGHCKYVKQNTLKHEMAGG (SEQ ID NO: 3 is therefore produced and loaded onto MHC class II tetramers as described in example 1. A control experiment is performed with tetramers loaded with a peptide with the same epitope but which does not include a thioreductase motif KYVKQNTLK HEMAGG (SEQ ID NO: 4) CD4+ T cells are prepared from peripheral blood in subjects prior to and 3 weeks after influenza vaccine administration. Such cells are incubated with fluorescence-labeled MHC class II tetramers loaded with peptide of SEQ ID 3. The number of cells per million identified by fluorescence labeling is then counted using a facs device.

It is shown that a higher number of CD4+ T cells are detected in peripheral blood when MHC class II tetramers are loaded with peptide of SEQ ID 3 than with peptide of SEQ ID 4. Further, the number of specific CD4+ T cells obtained 3 weeks after the start of the vaccination is determined and the concentration of hemagglutinin-specific antibodies is measured 8 weeks after the start of such vaccination. A close relationship is observed between the number of CD4+ T cells detected using tetramers loaded with peptides of SEQ ID 3 and the concentration of the hemagglutinin-specific antibodies.

Such a correlation between CD4+ cells and hemagglutinin-specific antibodies is not observed when tetramers with the peptide with SEQ ID NO: 3 (i.e. without reducing motif) are to quantify CD4+ cells.

This correlation between CD4+ cells at three weeks and hemagglutinin-specific antibodies at 8 weeks, allows predicting at an early stage after vaccination whether sufficient hemagglutinin-specific antibodies will be formed later on.

Accordingly, subjects with too low a number of CD4+ T cells at 3 weeks are further injected with the vaccine. This method makes it possible to restrict a second vaccination to those individuals which are effectively in need of a re-vaccination.

Example 3. Depletion of Donor-Specific Specific CD4+ T Cells from the Host Repertoire to Improve Bone Marrow Grafting

Bone marrow rejection occurs when CD4+ T lymphocytes from the recipient react towards alloantigens from the donor bone marrow. Both CD4 and CD8 cells are involved in this process, but CD4 cells are required to activate CD8+ T cells. Eliminating recipient's CD4+ T cells would therefore allow successful grafting. Removal of CD4+ T cells specific for alloantigens require a high performance affinity adsorption because of the low frequency of such cells.

The prior art MHC-T cell epitope complexes have not the required affinity to detect and to isolate the relevant CD4+ cells.

In the mouse model, male bone marrow is rejected by syngeneic females due to recognition of H-Y encoded antigens among which the Dby protein plays a major role. A majority of CD4+ T cells recognize an epitope made of residues FNSNRANSS of the murine Dby antigen which is encoded by the H-Y chromosome

A synthetic peptide made of this class II restricted T cell epitope with a thioreductase motif is produced, corresponding to CHGCFNSNRANSS [SEQ ID NO:5] and the corresponding Dby peptide in natural configuration is produced as a control, namely CHGCFNSNRANSS [SEQ ID NO:6].

Lymphocytes from the spleen of female H-2b mice are prepared by magnetic bead sorting. The cells are then incubated with a suspension of beads coated with class II H-2b molecules and loaded with peptide of SEQ ID 5 or of SEQ ID 6. Lymphocytes T cells, containing all CD4+ T cells not retained on beads and CD8+ T cells, are used to reconstitute RAG2 KO mice, which are then engrafted by the bone marrow of a male syngeneic donor. RAG2 KO mice have no functional adaptive immune system and are therefore unable to reject the graft. Rejection is thereby depending only of cells present in the passively transferred population.

It is shown that mice with the depleted Dby specific CD4+ T cells accept the bone marrow, whilst RAG2 KO mice reconstituted with non-depleted Dby-specific CD4+ cells strongly reject it. Depletion of CD4+ T cells with beads coated with control peptide of SEQ ID 6 shows no improvement of graft acceptance.

It is therefore concluded that depletion of CD4+ T cells by beads coated with peptides containing a thioreductase motif is much more efficient in controlling the host response to the allogenic bone marrow.

Example 4. Preparation of Specific CD4+ T Cells for Cell Therapy

Cell therapy consists in isolating cells from a donor, purifying and expanding the relevant cell population in vitro and re-administering his/her own cells to the donor. The success of such approach is highly dependent on the efficacy of the method used to isolate cells.

In insulin-dependent diabetes mellitus (IDDM) the GAD65 antigen plays an important pathogenetic role. Modifying the properties of GAD65-specific CD4+ T cells, as described in WO2008017517, allows to suppress the deleterious response against Langerhans beta cells.

NOD (non-obese diabetic) mice spontaneously develop diabetes by progressive destruction of insulin-producing Langerhans islet cells. NOD mice are considered as a representative pre-clinical model of human IDDM. Effector CD4+ T cells against GAD65 are prepared from the spleen of diseased animals by first depleting non-CD4+ cells. CD4+ cells are then incubated with class II tetramers loaded with a GAD65 class II restricted epitope encompassing a thioreductase motif in flanking residues.

The sequence of the peptide is therefore CRLCKVAPVIKARMM (GAD65 524-543) (SEQ ID NO: 7) A peptide of GAD65 without thioreductase motif is prepared for control experiments KVAPVIKARMM (SEQ ID NO: 8).

Cells are then sorted by facs according to their binding of peptide-loaded tetramers. Positive cells are then maintained in culture and stimulated with APC loaded with peptide of SEQ ID 7 to generate cytolytic CD4+ T cells, as described in the WO2008017517 patent application. It is observed that the yield of GAD65-specific cytolytic CD4+ T cells is significantly increased when peptide of SEQ ID 7 is used instead of peptide of SEQ ID 8.

The yield of GAD65-specific cytolytic CD4+ T cells is also higher than in the method disclosed in WO2008017517, wherein a peptide with SEQ ID NO 7 was added to T cells obtained from the spleen of NOD mice.

Cells expanded in vitro and having acquired cytolytic properties are used for cell transfer in NOD mice and are shown to prevent or suppress the development of IDDM.

Example 5. Preparation of CD4+ T Cells for T Cell Receptor (TCR) Sequencing

One of the risk factors for disease development is linked to the repertoire of T cells available in peripheral blood. Currently, however, an association between TCR family usage and higher risk of developing disease, is identified only when disease is patent, namely when sufficient expansion of specific T cells has already occurred, thereby allowing detection using currently available methods. Detecting such cells before the development of disease would be of much interest and could, in addition, provide the possibility of purging such cells from the repertoire, as described in example 3 above. An example is provided by T cells in germline configuration which recognize an epitope located in the 9-23 region of insulin (Nakayama et al. (2012), Diabetes 61, 857-865, 2012).

Further, during the course of an immune response involving CD4+ T cells, be it in the framework of a spontaneous disease or as a result of vaccination, there is an increase in TCR affinity resulting from selection of T cell clones with higher natural affinity and from mutations introduced in the hypervariable parts of the TCR. It would be advantageous to follow such TCR usage and/or mutations in a number of situations. Thus, maturation of the T cell repertoire during a vaccination with weak antigens is predictive of protection. Further, in autoimmune diseases, change in TCR affinity due to mutations could be predictive of disease worsening.

TCR family usage and detection of TCR mutations requires receptor sequencing, which can only be carried out on highly purified cells obtained in sufficient numbers. The invention allows such methods, as illustrated by the following example.

Expression of human DQ8 MHC class II molecule is associated with reactivity to a major epitope of insulin, located in the beta chain of insulin within the amino acid sequence 9-23. Human peripheral blood naïve T cell repertoire frequently contains cells expressing germline encoded alpha chain sequences, called Trav13-1, associated with various beta chain sequences, but which are sufficient as to confer a low affinity reaction with the B9-23 insulin epitope when presented by DQ8.

Peptides encompassing the sequences of the B9-23 epitope with a thioreductase motif and a one amino acid glycine linker are produced, namely CGHCGSHLVEALYLVCGERG INS9-23 (SEQ ID 9) and control peptides without thioreductase motif and linker SHLVEALYLVCGERG INS9-23 (SEQ ID 10)

Tetramers of DQ8 are produced and loaded with each one of peptides of SEQ ID 9 or SEQ ID 10. Loaded tetramers are incubated with human peripheral blood CD4+ T cells. Cells are washed, analysed by facs and sorted out. Cells are then washed from tetramers and used for TCR alpha chain sequencing using corresponding primers. It is shown that only cells prepared by tetramers loaded with peptide of SEQ ID 9 (containing a thioreductase motif) are obtained in sufficient number as to allow TCR sequencing.

It is therefore concluded that T cell epitopes containing a thioreductase motif are useful to detect and prepare cells carrying a given TCR in numbers sufficient as to allow TCR sequencing.

Sequences Disclosed in the Application:

(MOG 47-58)
[SEQ ID NO: 1]
CGPCSRVVHLYRNGKD
(MOG 47-58)
[SEQ ID NO: 2]
SRVVHLYRNGKD
(influenza hemagglutinin)
[SEQ ID NO: 3]
CGHCKYVKQNTLKHEMAGG
(influenza hemagglutinin)
[SEQ ID NO: 4]
KYVKQNTLKHEMAGG
(Dby)
[SEQ ID NO: 5]
CHGCFNSNRANSS
(Dby)
[SEQ ID NO: 6]
FNSNRANSS
(GAD65 524-543)
[SEQ ID NO: 7]
CRLCKVAPVIKARMM
(GAD65 524-543)
[SEQ ID NO: 8]
KVAPVIKARMM
(INS9-23)
[SEQ ID NO: 9]
CGHC              GSHLVEALYLVCGERG
(INS9-23)
[SEQ ID NO: 10]
SHLVEALYLVCGERG

Claims

1. An isolated complex of: a Major Histocompatibility Complex (MHC) class II molecule anda peptide consisting essentially of (i) an MHC class II restricted CD4+ T cell epitope of an antigenic protein and (ii) a redox motif of [CST]-X-X-C (SEQ ID NO: 11) or C-X-X-[CST] (SEQ ID NO: 12), which are immediately adjacent to each other or separated by a linker of at most 7 amino acids, wherein X is any amino acid, C is cysteine and [CST] is an amino acid selected from cysteine, serine and threonine.

2. The complex according to claim 1, wherein said redox motif is C-X-X-C (SEQ ID NO: 13).

3. The complex according to claim 1, wherein said MHC class II restricted CD4+ T-cell epitope and redox motif are separated by a linker of at most 4 amino acids.

4. The complex according to claim 1, wherein said complex between said peptide and said MHC class II molecule is a covalently bound complex.

5. The complex according to claim 4, wherein said covalently bound complex is a fusion protein of said MHC class II molecule with said peptide.

6. The complex according to claim 1, wherein said complex is attached to a bead or a plate.

7. An in vitro method for detecting class II restricted CD4+ T cells in a sample comprising the steps of: providing a sample comprising cells;contacting the sample with a complex according to claim 1; andmeasuring the binding of said complex with cells in said sample, wherein the binding of said complex to said cells is indicative of CD4+ T cells being present in said sample.

8. The method according to claim 7, wherein said redox motif is C-X-X-C (SEQ ID NO: 13).

9. The method according to claim 7, wherein said MHC class II restricted CD4+ T-cell epitope and redox motif are separated by a linker of at most 4 amino acids.

10. The method according to claim 7, wherein said peptide occurs in a non-covalent complex with the MHC class II molecule and has a length of between 12 and 20 amino acids.

11. The method according to claim 7, wherein said complex is a fusion protein of said MCH class II molecule with said peptide.

12. The method according to claim 7, wherein the sample is a blood sample or a tissue sample.

13. The method according to claim 12, wherein the tissue sample is synovial fluid from a rheumatoid arthritis patient or pleural fluid of a patient with infectious pneumonia.

14. The method according to claim 12, wherein said complex is attached to an insoluble carrier or a substrate.

15. The method according to claim 12, further comprising the step of detecting or isolating subpopulations of detected CD4+ T cells.

16. The method according to claim 7, wherein said CD4+ T cells are one or more selected from the group consisting of Tregs, induced Tregs such as Tr1 or Th3, naïve CD4+ T cells, polarised CD4+ T cells, and cytolytic CD4+ T cells.

17. The method according to claim 7, wherein said sample comprises one or more cells selected from the group consisting of naïve CD4+ T cells, antigen-exposed CD4+ T cells, CD4+ T cells obtained during therapy or during vaccination, and CD4+ T cells in a tissue.

18. The method according to claim 7, wherein said epitope sequence of said peptide is identical to the epitope sequence of said antigenic protein or wherein, the MHC class II anchoring residues of the epitope sequence of said peptide are modified compared to the epitope sequence of said antigenic protein in order to modulate the binding affinity of an epitope to CD4+ cells.

19. The method according to claim 7, wherein said MHC class II molecule in the complex is a multimer.

20. The method according to claim 7, wherein said complex is a soluble complex.

21. The method according to claim 7, further comprising the step of isolating CD4+ T cells which are bound to said complex.