Germinal center responses to SARS-CoV-2 mRNA vaccines in healthy and immunocompromised individuals

健康人和免疫功能低下者对SARS-CoV-2 mRNA疫苗的生发中心反应

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作者:Katlyn Lederer ,Emily Bettini ,Kalpana Parvathaneni ,Mark M Painter ,Divyansh Agarwal ,Kendall A Lundgreen ,Madison Weirick ,Kavitha Muralidharan ,Diana Castaño ,Rishi R Goel ,Xiaoming Xu ,Elizabeth M Drapeau ,Sigrid Gouma ,Jordan T Ort ,Moses Awofolaju ,Allison R Greenplate ,Carole Le Coz ,Neil Romberg ,Jennifer Trofe-Clark ,Gregory Malat ,Lisa Jones ,Mark Rosen ,Daniela Weiskopf ,Alessandro Sette ,Behdad Besharatian ,Mary Kaminiski ,Scott E Hensley ,Paul Bates ,E John Wherry ,Ali Naji ,Vijay Bhoj ,Michela Locci

Abstract

Vaccine-mediated immunity often relies on the generation of protective antibodies and memory B cells, which commonly stem from germinal center (GC) reactions. An in-depth comparison of the GC responses elicited by SARS-CoV-2 mRNA vaccines in healthy and immunocompromised individuals has not yet been performed due to the challenge of directly probing human lymph nodes. Herein, through a fine-needle aspiration-based approach, we profiled the immune responses to SARS-CoV-2 mRNA vaccines in lymph nodes of healthy individuals and kidney transplant recipients (KTXs). We found that, unlike healthy subjects, KTXs presented deeply blunted SARS-CoV-2-specific GC B cell responses coupled with severely hindered T follicular helper cell, SARS-CoV-2 receptor binding domain-specific memory B cell, and neutralizing antibody responses. KTXs also displayed reduced SARS-CoV-2-specific CD4 and CD8 T cell frequencies. Broadly, these data indicate impaired GC-derived immunity in immunocompromised individuals and suggest a GC origin for certain humoral and memory B cell responses following mRNA vaccination.

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