STRATEGIES TO PREVENT AND/OR TREAT IMMUNE RESPONSES TO SOLUBLE ALLOFACTORS
The present invention relates to the use of immunogenic peptides comprising a T-cell epitope derived from a soluble allofactor and a redox motif such as C-(X)2-[CST] or [CST]-(X)2-C in the prevention and/or suppression of immune responses to said soluble allofactor and in the manufacture of medicaments therefore.
1 - 17 . (canceled)
18 . An isolated peptide of between 12 and 75 amino acids comprising:
a human MHC class II T-cell epitope of a soluble allofactor, wherein the T-cell epitope has a length of 8 to 16 amino acids, and
immediately adjacent to said T-cell epitope or separated from said T-cell epitope by a linker of between 1 and 7 amino acids, a C-(X)2-[CST] (SEQ ID NO: 18) or [CST]-(X)2-C (SEQ ID NO: 19) redox motif, wherein said redox motif does not naturally occur within a region of 11 amino acids N- or C-terminally adjacent to the T-cell epitope in the soluble allofactor from which the peptide is derived.
19 . The peptide according to claim 18 , wherein said redox motif is C-(X)2-C (SEQ ID NO: 21).
20 . The peptide according to claim 18 , wherein said soluble allofactor is a coagulation or fibrinolytic factor.
21 . The peptide according to claim 18 , wherein said soluble allofactor is an antibody used for therapeutic purpose.
22 . The peptide according to claim 18 , wherein said soluble allofactor is a cytokine or a growth factor.
23 . The peptide according to claim 18 , wherein said linker consists of at most 4 amino acids.
24 . The peptide according to claim 18 , wherein said peptide further comprises an endosomal targeting sequence.
25 . The peptide according to claim 18 , wherein at least one X in said redox motif is Gly, Ala, Ser or Thr.
26 . The peptide according to claim 18 , wherein at least one X in said redox motif is His or Pro.
27 . The peptide according to claim 18 , wherein at least one C in said redox motif is methylated.
28 . A method for obtaining a population of soluble allofactor-specific CD4+ T cells with cytotoxic properties, the method comprising the steps of:
providing peripheral blood cells;
contacting said cells in vitro with the isolated peptide of claim 18 ; and
expanding said cells in the presence of IL-2.
29 . A method for obtaining a population of soluble allofactor-specific CD4+ T cells with cytotoxic properties, the method comprising the steps of:
providing the isolated peptide of claim 18 ;
administering said peptide to a subject; and
obtaining said population of soluble allofactor-specific CD4+ T cells from said subject.
30 . A method of eliminating soluble allofactor-specific B cells in a subject expected to receive, receiving or having received the soluble allofactor, said method comprising administering to the subject the isolated peptide of claim 18 .
31 . A method of suppressing immune responses to a soluble allofactor in a subject expected to receive, receiving or having received the soluble allofactor, said method comprising administering to the subject the isolated peptide of claim 18 .