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

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...

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Veröffentlicht in:Cell Jg. 185; H. 6; S. 1008
Hauptverfasser: Lederer, Katlyn, Bettini, Emily, Parvathaneni, Kalpana, Painter, Mark M, Agarwal, Divyansh, Lundgreen, Kendall A, Weirick, Madison, Muralidharan, Kavitha, Castaño, Diana, Goel, Rishi R, Xu, Xiaoming, Drapeau, Elizabeth M, Gouma, Sigrid, Ort, Jordan T, Awofolaju, Moses, Greenplate, Allison R, Le Coz, Carole, Romberg, Neil, Trofe-Clark, Jennifer, Malat, Gregory, Jones, Lisa, Rosen, Mark, Weiskopf, Daniela, Sette, Alessandro, Besharatian, Behdad, Kaminiski, Mary, Hensley, Scott E, Bates, Paul, Wherry, E John, Naji, Ali, Bhoj, Vijay, Locci, Michela
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 17.03.2022
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ISSN:1097-4172, 1097-4172
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Zusammenfassung: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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ISSN:1097-4172
1097-4172
DOI:10.1016/j.cell.2022.01.027