Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/40181
Título : Germinal center responses to SARS-CoV-2 mRNA vaccines in healthy and immunocompromised individuals
Autor : Castaño Monsalve, Diana María
Lederer, Katlyn
Bettini, Emily
Parvathaneni, Kalpana
Painter, Mark M.
Agarwal, Divyansh
Lundgreen, Kendall A.
Weirick, Madison
Muralidharan, Kavitha
Goel, Rishi R.
Xu, Xiaoming
Drapeau, Elizabeth M.
Gouma, Sigrid
Ort, Jordan T.
Awofolaju, Moses
Greenplate, Allison R.
Coz, Carole Le
Romberg, Neil
Trofe Clark, Jennifer
Malat, Gregory
Locci, Michela
metadata.dc.subject.*: SARS-CoV-2
Células T Auxiliares Foliculares
T Follicular Helper Cells
Biopsia con Aguja Fina
Biopsy, Fine-Needle
Huésped Inmunocomprometido
Immunocompromised Host
Centro Germinal
Germinal Center
Células B de Memoria
Memory B Cells
Anticuerpos Neutralizantes
Antibodies, Neutralizing
Vacunas de ARNm
mRNA Vaccines
https://id.nlm.nih.gov/mesh/D000086402
https://id.nlm.nih.gov/mesh/D000084522
https://id.nlm.nih.gov/mesh/D044963
https://id.nlm.nih.gov/mesh/D016867
https://id.nlm.nih.gov/mesh/D018858
https://id.nlm.nih.gov/mesh/D000091245
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D000087503
Fecha de publicación : 2022
Editorial : MDPI
Citación : Lederer K, Bettini E, Parvathaneni K, Painter MM, Agarwal D, Lundgreen KA, Weirick M, Muralidharan K, Castaño D, Goel RR, Xu X, Drapeau EM, Gouma S, Ort JT, Awofolaju M, Greenplate AR, Le Coz C, Romberg N, Trofe-Clark J, Malat G, Jones L, Rosen M, Weiskopf D, Sette A, Besharatian B, Kaminiski M, Hensley SE, Bates P, Wherry EJ, Naji A, Bhoj V, Locci M. Germinal center responses to SARS-CoV-2 mRNA vaccines in healthy and immunocompromised individuals. Cell. 2022 Mar 17;185(6):1008-1024.e15. doi: 10.1016/j.cell.2022.01.027. Epub 2022 Feb 2.
Resumen : 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.
metadata.dc.identifier.eissn: 2073-4410
metadata.dc.identifier.doi: 10.1016/j.cell.2022.01.027
Aparece en las colecciones: Artículos de Revista en Ciencias Médicas

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