1. Antibody and T cell memory immune response after two doses of the BNT162b2 mRNA vaccine in older adults with and without prior SARS-CoV-2 infection
- Author
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K. Faure, Annie Sobaszek, F. Vuotto, Enagnon Kazali Alidjinou, B. Corroyer-Simovic, J. Podvin, Dominique Huvent-Grelle, Alain Duhamel, Anne Goffard, Julien Labreuche, Dominique Deplanque, Arnaud Dendooven, Miczek S, François Puisieux, Guillaume Lefèvre, Julie Demaret, Myriam Labalette, Laurence Bocket, Jacques Trauet, and Daniel Dreuil
- Subjects
biology ,business.industry ,T cell ,Antibody titer ,Titer ,medicine.anatomical_structure ,Immune system ,Immunology ,biology.protein ,Medicine ,Young adult ,Antibody ,business ,Neutralizing antibody ,CD8 - Abstract
We quantified S1-specific IgG, neutralizing antibody titers, specific IFNγ secreting T cells and functionality of specific CD4+ and CD8+ T cells in 130 young adults (median age 44.0 years) and 106 older residents living in a long-term care facility (86.5 years) after 2 doses of BNT162b2. Three months after the first injection, humoral and cellular memory responses were dramatically impaired in the 54 COVID-19-naive older compared to the 121 COVID-19-naive younger adults. Notably, older participants’ neutralizing antibodies, detected in 76.5% (versus 100% in young adults,P< 0.0001), were ten times lower than the younger’s antibody titers (P< 0.0001). Antibody and T cell responses were greater among the 52 COVID-19-recovered than among the 54 COVID-19-naive older adults (P< 0.0001). Our study shows that 2 doses of BNT162b2 does not guarantee long-term protection against SARS-CoV-2 in the older. An additional dose should be considered to boost their specific memory response.
- Published
- 2021
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