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Autoantibodies against chemokines post-SARS-CoV-2 infection correlate with disease course.

Jonathan MuriValentina CecchinatoAndrea CavalliAkanksha A ShanbhagMilos MatkovicMaira BiggiogeroPier Andrea MaidaJacques MoritzChiara ToscanoElaheh GhovehoudRaffaello FurlanFranca BarbicAntonio VozaGuendalina De NadaiCarlo Cervia-HaslerYves ZurbuchenPatrick TaeschlerLilly A MurrayGabriela Danelon-SargentiSimone MoroTao GongPietro PiffarettiFilippo BianchiniVirginia CrivelliLucie PodešvováMattia PedottiDavid JarrossayJacopo SgrignaniSylvia ThelenMario UhrEnos BernasconiAndri RauchAntonio ManzoAdrian CiureaMarco B L RocchiLuca VaraniBernhard MoserBarbara BottazziMarcus ThelenBrian A FallonOnur BoymanAlberto MantovaniChristian GarzoniAlessandra Franzetti-PellandaMariagrazia UguccioniDavide F Robbiani
Published in: Nature immunology (2023)
Infection with severe acute respiratory syndrome coronavirus 2 associates with diverse symptoms, which can persist for months. While antiviral antibodies are protective, those targeting interferons and other immune factors are associated with adverse coronavirus disease 2019 (COVID-19) outcomes. Here we discovered that antibodies against specific chemokines were omnipresent post-COVID-19, were associated with favorable disease outcome and negatively correlated with the development of long COVID at 1 yr post-infection. Chemokine antibodies were also present in HIV-1 infection and autoimmune disorders, but they targeted different chemokines compared with COVID-19. Monoclonal antibodies derived from COVID-19 convalescents that bound to the chemokine N-loop impaired cell migration. Given the role of chemokines in orchestrating immune cell trafficking, naturally arising chemokine antibodies may modulate the inflammatory response and thus bear therapeutic potential.
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