Key result
Elevated HERV-K Env autoantibodies in RA and JIA correlate with seropositivity and citrullinated Env reactivity.
Why the study?
Autoantibodies against HERV-K proteins have been reported in rheumatoid arthritis, but their clinical relevance remained unresolved, and reactivity with citrullinated epitopes on HERV-K Env was untested.
Do patients with rheumatoid arthritis or juvenile idiopathic arthritis have elevated autoantibodies against unmodified and citrullinated HERV-K Env protein compared to healthy controls?
Case-Control
Do patients with rheumatoid arthritis or juvenile idiopathic arthritis have elevated autoantibodies against unmodified and citrullinated HERV-K Env protein compared to healthy controls?
Anti-HERV-K immunity is elevated in RA and JIA and may be connected to pathogenic protein citrullination in RA.
Anti-citrullinated HERV-K Env reactivity should not yet alter RA management; extends prior observations but remains hypothesis-generating for citrullination links.
OBJECTIVE: Autoantibodies against proteins encoded by human endogenous retrovirus K (HERV-K) have been reported in patients with rheumatoid arthritis (RA), but their relevance, if any, has remained unresolved. We revisited this question and tested if such autoantibodies may react with citrullinated epitopes on the envelope (Env) protein of HERV-K. METHODS: Immunoblotting and ELISAs were conducted with unmodified Env protein and with Env citrullinated by protein arginine deiminase 4 (PAD4). Sera from 100 patients with RA, plasma from 32 patients with juvenile idiopathic arthritis (JIA), and healthy adult and pediatric controls were included. Antibody reactivity was evaluated for correlations with clinical and laboratory variables of the patients. RESULTS: We replicated and expanded upon published data suggesting that patients with RA or JIA have autoantibodies against HERV-K Env, some with high titers. Anti-HERV-K antibodies correlated with cigarette smoking and with circulating myeloperoxidase-DNA complexes indicative of nonapoptotic neutrophil cell death. Further, most of the patients with RA, but not those with JIA, had autoantibodies that reacted more strongly with Env that was citrullinated by PAD4. These anticitrullinated Env autoantibodies correlated with seropositivity and tended to be higher in patients with erosive disease. CONCLUSION: Our data suggest that anti-HERV-K immunity is elevated in RA and JIA and may have a connection with pathogenic protein citrullination in RA.
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Wang et al. (2021) conducted a case-control in Rheumatoid arthritis and juvenile idiopathic arthritis. Rheumatoid arthritis and juvenile idiopathic arthritis vs. Healthy adult and pediatric controls was evaluated on Reactivity of autoantibodies against unmodified and citrullinated HERV-K Env protein. Autoantibodies against HERV-K Env were elevated in RA and JIA patients, and in RA patients, these antibodies reacted more strongly with citrullinated Env and correlated with seropositivity.
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