Objectives Over 50% of rheumatoid arthritis (RA) patients harbor a variety of Anti-Modified Protein Antibodies (AMPA) against different post-translationally modified (PTM) proteins, including anti... Show moreObjectives Over 50% of rheumatoid arthritis (RA) patients harbor a variety of Anti-Modified Protein Antibodies (AMPA) against different post-translationally modified (PTM) proteins, including anti-carbamylated protein (anti-CarP) antibodies. At present it is unknown how AMPA are generated and how autoreactive B cell responses against PTM proteins are induced. Here we studied whether PTM foreign antigens can breach B cell tolerance towards PTM self-proteins. Methods Serum reactivity towards five carbamylated proteins was determined for 160 RA-patients and 40 healthy individuals. Antibody cross-reactivity was studied by inhibition experiments. Mass spectrometry was performed to identify carbamylated self-proteins in human rheumatic joint tissue. Mice were immunized with carbamylated- or non-modified (auto)antigens and analyzed for autoantibody responses. Results We show that anti-CarP antibodies in RA are highly cross-reactive towards multiple carbamylated proteins, including modified self- as well as modified non-self proteins. Studies in mice show that anti-CarP antibody responses recognizing carbamylated self-proteins are not only induced by immunization with carbamylated self-proteins but also by immunization with carbamylated proteins of non-self origin. Similar to the data observed with sera from RA patients, the murine anti-CarP antibody response was, both at the monoclonal- and polyclonal level, highly cross-reactive towards multiple carbamylated proteins, including carbamylated self-proteins. Conclusions Self-reactive AMPA-responses can be induced by exposure to foreign proteins containing PTM. These data show how autoreactive B cell responses against PTM self-proteins can be induced by exposure to PTM foreign proteins and provide new insights on the breach of autoreactive B cell tolerance. Show less
