Biomarkers, methods and kits for the diagnosis of rheumatoid arthritis
The present invention relates to peptides biomarkers that are specifically recognized by autoantibodies present in the sera of patients with Rheumatoid Arthritis (RA). More specifically, the invention provides epitopes of PAD4, of BRAF, and of calpastatin as well as methods and kits for using these sequences for the diagnosis of RA, in particular for the diagnosis of RA in CCP-negative subjects.
1. A kit for detecting the presence of anti-PAD4 autoantibodies or anti-BRAF autoantibodies in a biological sample, said kit comprising:
at least one biomarker,
wherein the at least one biomarker is a PAD4-peptide (i) selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, and SEQ ID NO: 5, or (ii) consisting of a fragment of PAD4 of less than 50 amino acids and comprising a sequence selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, and SEQ ID NO: 5, or
wherein the at least one biomarker is a BRAF-peptide (i) selected from the group consisting of SEQ ID NO: 7, SEQ ID NO: 8, and SEQ ID NO: 9, or (ii) consisting of a fragment of BRAF catalytic domain of less than 50 amino acids and comprising a sequence selected from the group consisting of SEQ ID NO: 7, SEQ ID NO: 8, and SEQ ID NO: 9; and
at least one reagent for detecting a biomarker-antibody complex formed between the biomarker and an autoantibody present in the biological sample, wherein the autoantibody is an anti-PAD4 autoantibody or an anti-BRAF autoantibody that is indicative of rheumatoid arthritis, and wherein the at least one reagent is an anti-human IgG labelled with a detectable moiety.
2. The kit according to claim 1 , wherein the detectable moiety is selected from enzymes, fluorophores, radioisotopes, chemiluminescent moieties and biochemiluminescent moieties.
3. The kit according to claim 2 , wherein:
the at least one biomarker is the PAD4-peptide selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, and SEQ ID NO: 5, or
the at least one biomarker is the BRAF-peptide selected from the group consisting of SEQ ID NO: 7, SEQ ID NO: 8, and SEQ ID NO: 9.
4. The kit according to claim 3 , wherein the detectable moiety is selected from enzymes, fluorophores, radioisotopes, chemiluminescent moieties and biochemiluminescent moieties.
5. The kit according to claim 1 , wherein the fragment of PAD4 of less than 50 amino acids recognizes anti-PAD4 autoantibodies, and wherein the fragment of BRAF catalytic domain of less than 50 amino acids recognizes anti-BRAF autoantibodies.