Back to Search Start Over

Anti-chemokine antibodies after SARS-CoV-2 infection correlate with favorable disease course

Authors :
Jonathan Muri
Valentina Cecchinato
Andrea Cavalli
Akanksha A. Shanbhag
Milos Matkovic
Maira Biggiogero
Pier Andrea Maida
Jacques Moritz
Chiara Toscano
Elaheh Ghovehoud
Raffaello Furlan
Franca Barbic
Antonio Voza
Guendalina De Nadai
Carlo Cervia
Yves Zurbuchen
Patrick Taeschler
Lilly A. Murray
Gabriela Danelon-Sargenti
Simone Moro
Tao Gong
Pietro Piffaretti
Filippo Bianchini
Virginia Crivelli
Lucie Podešvová
Mattia Pedotti
David Jarrossay
Jacopo Sgrignani
Sylvia Thelen
Mario Uhr
Enos Bernasconi
Andri Rauch
Antonio Manzo
Adrian Ciurea
Marco B.L. Rocchi
Luca Varani
Bernhard Moser
Barbara Bottazzi
Marcus Thelen
Brian A. Fallon
Onur Boyman
Alberto Mantovani
Christian Garzoni
Alessandra Franzetti-Pellanda
Mariagrazia Uguccioni
Davide F. Robbiani
Source :
bioRxiv
Publication Year :
2022

Abstract

Infection by SARS-CoV-2 leads to diverse symptoms, which can persist for months. While antiviral antibodies are protective, those targeting interferons and other immune factors are associated with adverse COVID-19 outcomes. Instead, we discovered that antibodies against specific chemokines are omnipresent after COVID-19, associated with favorable disease, and predictive of lack of long COVID symptoms at one year post infection. Anti-chemokine antibodies are present also in HIV-1 infection and autoimmune disorders, but they target different chemokines than those in COVID-19. Monoclonal antibodies derived from COVID- 19 convalescents that bind to the chemokine N-loop impair cell migration. Given the role of chemokines in orchestrating immune cell trafficking, naturally arising anti-chemokine antibodies associated with favorable COVID-19 may be beneficial by modulating the inflammatory response and thus bear therapeutic potential.One-Sentence Summary:Naturally arising anti-chemokine antibodies associate with favorable COVID-19 and predict lack of long COVID.

Subjects

Subjects :
Article

Details

Database :
OpenAIRE
Journal :
bioRxiv : the preprint server for biology
Accession number :
edsair.doi.dedup.....ca04d395480f1e2dd56c6ba09c24dc0b