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HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway

BACKGROUND: HIV infection dysregulates the B cell compartment, affecting memory B cell formation and the antibody response to infection and vaccination. Understanding the B cell response to SARS-CoV-2 in people living with HIV (PLWH) may explain the increased morbidity, reduced vaccine efficacy, red...

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Autores principales: Krause, Robert, Snyman, Jumari, Shi-Hsia, Hwa, Muema, Daniel, Karim, Farina, Ganga, Yashica, Ngoepe, Abigail, Zungu, Yenzekile, Gazy, Inbal, Bernstein, Mallory, Khan, Khadija, Mazibuko, Matilda, Mthabela, Ntombifuthi, Ramjit, Dirhona, Limbo, Oliver, Jardine, Joseph, Sok, Devin, Wilson, Ian A, Hanekom, Willem, Sigal, Alex, Kløverpris, Henrik, Ndung'u, Thumbi, Leslie, Alasdair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643005/
https://www.ncbi.nlm.nih.gov/pubmed/36300787
http://dx.doi.org/10.7554/eLife.79924
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author Krause, Robert
Snyman, Jumari
Shi-Hsia, Hwa
Muema, Daniel
Karim, Farina
Ganga, Yashica
Ngoepe, Abigail
Zungu, Yenzekile
Gazy, Inbal
Bernstein, Mallory
Khan, Khadija
Mazibuko, Matilda
Mthabela, Ntombifuthi
Ramjit, Dirhona
Limbo, Oliver
Jardine, Joseph
Sok, Devin
Wilson, Ian A
Hanekom, Willem
Sigal, Alex
Kløverpris, Henrik
Ndung'u, Thumbi
Leslie, Alasdair
author_facet Krause, Robert
Snyman, Jumari
Shi-Hsia, Hwa
Muema, Daniel
Karim, Farina
Ganga, Yashica
Ngoepe, Abigail
Zungu, Yenzekile
Gazy, Inbal
Bernstein, Mallory
Khan, Khadija
Mazibuko, Matilda
Mthabela, Ntombifuthi
Ramjit, Dirhona
Limbo, Oliver
Jardine, Joseph
Sok, Devin
Wilson, Ian A
Hanekom, Willem
Sigal, Alex
Kløverpris, Henrik
Ndung'u, Thumbi
Leslie, Alasdair
author_sort Krause, Robert
collection PubMed
description BACKGROUND: HIV infection dysregulates the B cell compartment, affecting memory B cell formation and the antibody response to infection and vaccination. Understanding the B cell response to SARS-CoV-2 in people living with HIV (PLWH) may explain the increased morbidity, reduced vaccine efficacy, reduced clearance, and intra-host evolution of SARS-CoV-2 observed in some HIV-1 coinfections. METHODS: We compared B cell responses to COVID-19 in PLWH and HIV negative (HIV-ve) patients in a cohort recruited in Durban, South Africa, during the first pandemic wave in July 2020 using detailed flow cytometry phenotyping of longitudinal samples with markers of B cell maturation, homing, and regulatory features. RESULTS: This revealed a coordinated B cell response to COVID-19 that differed significantly between HIV-ve and PLWH. Memory B cells in PLWH displayed evidence of reduced germinal centre (GC) activity, homing capacity, and class-switching responses, with increased PD-L1 expression, and decreased Tfh frequency. This was mirrored by increased extrafollicular (EF) activity, with dynamic changes in activated double negative (DN2) and activated naïve B cells, which correlated with anti-RBD-titres in these individuals. An elevated SARS-CoV-2-specific EF response in PLWH was confirmed using viral spike and RBD bait proteins. CONCLUSIONS: Despite similar disease severity, these trends were highest in participants with uncontrolled HIV, implicating HIV in driving these changes. EF B cell responses are rapid but give rise to lower affinity antibodies, less durable long-term memory, and reduced capacity to adapt to new variants. Further work is needed to determine the long-term effects of HIV on SARS-CoV-2 immunity, particularly as new variants emerge. FUNDING: This work was supported by a grant from the Wellcome Trust to the Africa Health Research Institute (Wellcome Trust Strategic Core Award [grant number 201433/Z/16/Z]). Additional funding was received from the South African Department of Science and Innovation through the National Research Foundation (South African Research Chairs Initiative [grant number 64809]), and the Victor Daitz Foundation.
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spelling pubmed-96430052022-11-15 HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway Krause, Robert Snyman, Jumari Shi-Hsia, Hwa Muema, Daniel Karim, Farina Ganga, Yashica Ngoepe, Abigail Zungu, Yenzekile Gazy, Inbal Bernstein, Mallory Khan, Khadija Mazibuko, Matilda Mthabela, Ntombifuthi Ramjit, Dirhona Limbo, Oliver Jardine, Joseph Sok, Devin Wilson, Ian A Hanekom, Willem Sigal, Alex Kløverpris, Henrik Ndung'u, Thumbi Leslie, Alasdair eLife Epidemiology and Global Health BACKGROUND: HIV infection dysregulates the B cell compartment, affecting memory B cell formation and the antibody response to infection and vaccination. Understanding the B cell response to SARS-CoV-2 in people living with HIV (PLWH) may explain the increased morbidity, reduced vaccine efficacy, reduced clearance, and intra-host evolution of SARS-CoV-2 observed in some HIV-1 coinfections. METHODS: We compared B cell responses to COVID-19 in PLWH and HIV negative (HIV-ve) patients in a cohort recruited in Durban, South Africa, during the first pandemic wave in July 2020 using detailed flow cytometry phenotyping of longitudinal samples with markers of B cell maturation, homing, and regulatory features. RESULTS: This revealed a coordinated B cell response to COVID-19 that differed significantly between HIV-ve and PLWH. Memory B cells in PLWH displayed evidence of reduced germinal centre (GC) activity, homing capacity, and class-switching responses, with increased PD-L1 expression, and decreased Tfh frequency. This was mirrored by increased extrafollicular (EF) activity, with dynamic changes in activated double negative (DN2) and activated naïve B cells, which correlated with anti-RBD-titres in these individuals. An elevated SARS-CoV-2-specific EF response in PLWH was confirmed using viral spike and RBD bait proteins. CONCLUSIONS: Despite similar disease severity, these trends were highest in participants with uncontrolled HIV, implicating HIV in driving these changes. EF B cell responses are rapid but give rise to lower affinity antibodies, less durable long-term memory, and reduced capacity to adapt to new variants. Further work is needed to determine the long-term effects of HIV on SARS-CoV-2 immunity, particularly as new variants emerge. FUNDING: This work was supported by a grant from the Wellcome Trust to the Africa Health Research Institute (Wellcome Trust Strategic Core Award [grant number 201433/Z/16/Z]). Additional funding was received from the South African Department of Science and Innovation through the National Research Foundation (South African Research Chairs Initiative [grant number 64809]), and the Victor Daitz Foundation. eLife Sciences Publications, Ltd 2022-10-27 /pmc/articles/PMC9643005/ /pubmed/36300787 http://dx.doi.org/10.7554/eLife.79924 Text en © 2022, Krause et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Epidemiology and Global Health
Krause, Robert
Snyman, Jumari
Shi-Hsia, Hwa
Muema, Daniel
Karim, Farina
Ganga, Yashica
Ngoepe, Abigail
Zungu, Yenzekile
Gazy, Inbal
Bernstein, Mallory
Khan, Khadija
Mazibuko, Matilda
Mthabela, Ntombifuthi
Ramjit, Dirhona
Limbo, Oliver
Jardine, Joseph
Sok, Devin
Wilson, Ian A
Hanekom, Willem
Sigal, Alex
Kløverpris, Henrik
Ndung'u, Thumbi
Leslie, Alasdair
HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title_full HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title_fullStr HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title_full_unstemmed HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title_short HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway
title_sort hiv skews the sars-cov-2 b cell response towards an extrafollicular maturation pathway
topic Epidemiology and Global Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643005/
https://www.ncbi.nlm.nih.gov/pubmed/36300787
http://dx.doi.org/10.7554/eLife.79924
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