Memory B cell development elicited by mRNA booster vaccinations in the elderly

Author:

Wang Zijun1ORCID,Muecksch Frauke23ORCID,Raspe Raphael1ORCID,Johannsen Frederik1ORCID,Turroja Martina1ORCID,Canis Marie2ORCID,ElTanbouly Mohamed A.1ORCID,Santos Gabriela S. Silva1ORCID,Johnson Brianna1ORCID,Baharani Viren A.12ORCID,Patejak Rachel2ORCID,Yao Kai-Hui1ORCID,Chirco Bennett J.1ORCID,Millard Katrina G.1ORCID,Shimeliovich Irina1ORCID,Gazumyan Anna1ORCID,Oliveira Thiago Y.1ORCID,Bieniasz Paul D.24ORCID,Hatziioannou Theodora2ORCID,Caskey Marina1ORCID,Nussenzweig Michel C.14ORCID

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University 1 , New York, NY, USA

2. Laboratory of Retrovirology, The Rockefeller University 2 , New York, NY, USA

3. University of Heidelberg 3 Department of Infectious Diseases, Virology, , Heidelberg, Germany

4. Howard Hughes Medical Institute 4 , Maryland, MD, USA

Abstract

Despite mRNA vaccination, elderly individuals remain especially vulnerable to severe consequences of SARS-CoV-2 infection. Here, we compare the memory B cell responses in a cohort of elderly and younger individuals who received mRNA booster vaccinations. Plasma neutralizing potency and breadth were similar between the two groups. By contrast, the absolute number of SARS-CoV-2–specific memory B cells was lower in the elderly. Antibody sequencing revealed that the SARS-CoV-2–specific elderly memory compartments were more clonal and less diverse. Notably, memory antibodies from the elderly preferentially targeted the ACE2-binding site on the RBD, while those from younger individuals targeted less accessible but more conserved epitopes. Nevertheless, individual memory antibodies elicited by booster vaccines in the elderly and younger individuals showed similar levels of neutralizing activity and breadth against SARS-CoV-2 variants. Thus, the relatively diminished protective effects of vaccination against serious disease in the elderly are associated with a smaller number of antigen-specific memory B cells that express altered antibody repertoires.

Funder

National Center for Advancing Translational Sciences

National Institutes of Health

Clinical and Translational Science Award

Advancement of Translational Research

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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