Author:
Miyara Makoto,Saichi Melissa,Sterlin Delphine,Anna François,Marot Stéphane,Mathian Alexis,Atif Mo,Quentric Paul,Mohr Audrey,Claër Laetitia,Parizot Christophe,Dorgham Karim,Yssel Hans,Fadlallah Jehane,Chazal Thibaut,Haroche Julien,Luyt Charles-Edouard,Mayaux Julien,Beurton Alexandra,Benameur Neila,Boutolleau David,Burrel Sonia,de Alba Sophia,Mudumba Sasi,Hockett Rick,Gunn Cary,Charneau Pierre,Calvez Vincent,Marcelin Anne-Geneviève,Combes Alain,Demoule Alexandre,Amoura Zahir,Gorochov Guy
Abstract
The capacity of pre-existing immunity to human common coronaviruses (HCoV) to cross-protect against de novo COVID-19is yet unknown. In this work, we studied the sera of 175 COVID-19 patients, 76 healthy donors and 3 intravenous immunoglobulins (IVIG) batches. We found that most COVID-19 patients developed anti-SARS-CoV-2 IgG antibodies before IgM. Moreover, the capacity of their IgGs to react to beta-HCoV, was present in the early sera of most patients before the appearance of anti-SARS-CoV-2 IgG. This implied that a recall-type antibody response was generated. In comparison, the patients that mounted an anti-SARS-COV2 IgM response, prior to IgG responses had lower titres of anti-beta-HCoV IgG antibodies. This indicated that pre-existing immunity to beta-HCoV was conducive to the generation of memory type responses to SARS-COV-2. Finally, we also found that pre-COVID-19-era sera and IVIG cross-reacted with SARS-CoV-2 antigens without neutralising SARS-CoV-2 infectivity in vitro. Put together, these results indicate that whilst pre-existing immunity to HCoV is responsible for recall-type IgG responses to SARS-CoV-2, it does not lead to cross-protection against COVID-19.
Subject
Immunology,Immunology and Allergy