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Distinct dynamics of antigen-specific induction and differentiation of different CD11c+Tbet+ B-cell subsets
CD11c+Tbet+ B cells are enriched in autoimmunity and chronic infections and also expand on immune challenge in healthy individuals. CD11c+Tbet+ B cells remain an enigmatic B-cell population because of their intrinsic heterogeneity. We investigated severe acute respiratory syndrome coronavirus 2 (SAR...
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Published in: | Journal of allergy and clinical immunology 2023-09, Vol.152 (3), p.689-699.e6 |
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container_title | Journal of allergy and clinical immunology |
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creator | Steuten, Juulke Bos, Amélie V. Kuijper, Lisan H. Claireaux, Mathieu Olijhoek, Wouter Elias, George Duurland, Mariel C. Jorritsma, Tineke Marsman, Casper Paul, Alberta G.A. Garcia Vallejo, Juan J. van Gils, Marit J. Wieske, Luuk Kuijpers, Taco W. Eftimov, Filip van Ham, S. Marieke ten Brinke, Anja |
description | CD11c+Tbet+ B cells are enriched in autoimmunity and chronic infections and also expand on immune challenge in healthy individuals. CD11c+Tbet+ B cells remain an enigmatic B-cell population because of their intrinsic heterogeneity.
We investigated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen-specific development and differentiation properties of 3 separate CD11c+ B-cell subsets—age-associated B cells (ABCs), double-negative 2 (DN2) B cells, and activated naive B cells—and compared them to their canonical CD11c− counterparts.
Dynamics of the response of the 3 CD11c+ B-cell subsets were assessed at SARS-CoV-2 vaccination in healthy donors by spectral flow cytometry. Distinct CD11c+ B-cell subsets were functionally characterized by optimized in vitro cultures.
In contrast to a durable expansion of antigen-specific CD11c− memory B cells over time, both ABCs and DN2 cells were strongly expanded shortly after second vaccination and subsequently contracted. Functional characterization of antibody-secreting cell differentiation dynamics revealed that CD11c+Tbet+ B cells were primed for antibody-secreting cell differentiation compared to relevant canonical CD11c− counterparts.
Overall, CD11c+Tbet+ B cells encompass heterogeneous subpopulations, of which primarily ABCs as well as DN2 B cells respond early to immune challenge and display a pre–antibody-secreting cell phenotype. |
doi_str_mv | 10.1016/j.jaci.2023.02.020 |
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We investigated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen-specific development and differentiation properties of 3 separate CD11c+ B-cell subsets—age-associated B cells (ABCs), double-negative 2 (DN2) B cells, and activated naive B cells—and compared them to their canonical CD11c− counterparts.
Dynamics of the response of the 3 CD11c+ B-cell subsets were assessed at SARS-CoV-2 vaccination in healthy donors by spectral flow cytometry. Distinct CD11c+ B-cell subsets were functionally characterized by optimized in vitro cultures.
In contrast to a durable expansion of antigen-specific CD11c− memory B cells over time, both ABCs and DN2 cells were strongly expanded shortly after second vaccination and subsequently contracted. Functional characterization of antibody-secreting cell differentiation dynamics revealed that CD11c+Tbet+ B cells were primed for antibody-secreting cell differentiation compared to relevant canonical CD11c− counterparts.
Overall, CD11c+Tbet+ B cells encompass heterogeneous subpopulations, of which primarily ABCs as well as DN2 B cells respond early to immune challenge and display a pre–antibody-secreting cell phenotype.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2023.02.020</identifier><identifier>PMID: 36858158</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>activated naive ; age-associated B cell ; antibody-secreting cell differentiation ; B-Lymphocyte Subsets ; CD11c+Tbet+ atypical B cell ; Cell Differentiation ; COVID-19 ; COVID-19 Vaccines ; double negative 2 ; Humans ; SARS-CoV-2 ; SARS-CoV-2 vaccination</subject><ispartof>Journal of allergy and clinical immunology, 2023-09, Vol.152 (3), p.689-699.e6</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2450-423af4f84fc772d8cc1603abfd610ef84cd8a50cbdd2ccbaf62c171679552c283</citedby><cites>FETCH-LOGICAL-c2450-423af4f84fc772d8cc1603abfd610ef84cd8a50cbdd2ccbaf62c171679552c283</cites><orcidid>0000-0002-6647-2233</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36858158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steuten, Juulke</creatorcontrib><creatorcontrib>Bos, Amélie V.</creatorcontrib><creatorcontrib>Kuijper, Lisan H.</creatorcontrib><creatorcontrib>Claireaux, Mathieu</creatorcontrib><creatorcontrib>Olijhoek, Wouter</creatorcontrib><creatorcontrib>Elias, George</creatorcontrib><creatorcontrib>Duurland, Mariel C.</creatorcontrib><creatorcontrib>Jorritsma, Tineke</creatorcontrib><creatorcontrib>Marsman, Casper</creatorcontrib><creatorcontrib>Paul, Alberta G.A.</creatorcontrib><creatorcontrib>Garcia Vallejo, Juan J.</creatorcontrib><creatorcontrib>van Gils, Marit J.</creatorcontrib><creatorcontrib>Wieske, Luuk</creatorcontrib><creatorcontrib>Kuijpers, Taco W.</creatorcontrib><creatorcontrib>Eftimov, Filip</creatorcontrib><creatorcontrib>van Ham, S. Marieke</creatorcontrib><creatorcontrib>ten Brinke, Anja</creatorcontrib><creatorcontrib>T2B Consortium</creatorcontrib><title>Distinct dynamics of antigen-specific induction and differentiation of different CD11c+Tbet+ B-cell subsets</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>CD11c+Tbet+ B cells are enriched in autoimmunity and chronic infections and also expand on immune challenge in healthy individuals. CD11c+Tbet+ B cells remain an enigmatic B-cell population because of their intrinsic heterogeneity.
We investigated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen-specific development and differentiation properties of 3 separate CD11c+ B-cell subsets—age-associated B cells (ABCs), double-negative 2 (DN2) B cells, and activated naive B cells—and compared them to their canonical CD11c− counterparts.
Dynamics of the response of the 3 CD11c+ B-cell subsets were assessed at SARS-CoV-2 vaccination in healthy donors by spectral flow cytometry. Distinct CD11c+ B-cell subsets were functionally characterized by optimized in vitro cultures.
In contrast to a durable expansion of antigen-specific CD11c− memory B cells over time, both ABCs and DN2 cells were strongly expanded shortly after second vaccination and subsequently contracted. Functional characterization of antibody-secreting cell differentiation dynamics revealed that CD11c+Tbet+ B cells were primed for antibody-secreting cell differentiation compared to relevant canonical CD11c− counterparts.
Overall, CD11c+Tbet+ B cells encompass heterogeneous subpopulations, of which primarily ABCs as well as DN2 B cells respond early to immune challenge and display a pre–antibody-secreting cell phenotype.</description><subject>activated naive</subject><subject>age-associated B cell</subject><subject>antibody-secreting cell differentiation</subject><subject>B-Lymphocyte Subsets</subject><subject>CD11c+Tbet+ atypical B cell</subject><subject>Cell Differentiation</subject><subject>COVID-19</subject><subject>COVID-19 Vaccines</subject><subject>double negative 2</subject><subject>Humans</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 vaccination</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kF9LwzAUxYMobk6_gA_SR2F0JmmbpuCLbv6DgS_zOaQ3N5K6tbNphX17Uzd9FC6EnPzO4eYQcsnojFEmbqpZpcHNOOXJjPIw9IiMGS3yWEieHZMxpQWLRZ4WI3LmfUXDPZHFKRklQmaSZXJMPhbOd66GLjK7Wm8c-Kixka4794517LcIzjqIXG166FxThycTGWctthgg_aMFx58UzReMwXRVYjeN7mPA9Tryfemx8-fkxOq1x4vDOSFvjw-r-XO8fH16md8tY-BpRuOUJ9qmVqYW8pwbCcAETXRpjWAUgw5G6oxCaQwHKLUVHFjORF5kGQcukwm53udu2-azR9-pjfPDIrrGpveK55IJVvB0QPkehbbxvkWrtq3b6HanGFVDyapSQ8lqKFlRHoYG09Uhvy83aP4sv60G4HYPYPjll8NWeXBYAxrXInTKNO6__G8FGY5V</recordid><startdate>202309</startdate><enddate>202309</enddate><creator>Steuten, Juulke</creator><creator>Bos, Amélie V.</creator><creator>Kuijper, Lisan H.</creator><creator>Claireaux, Mathieu</creator><creator>Olijhoek, Wouter</creator><creator>Elias, George</creator><creator>Duurland, Mariel C.</creator><creator>Jorritsma, Tineke</creator><creator>Marsman, Casper</creator><creator>Paul, Alberta G.A.</creator><creator>Garcia Vallejo, Juan J.</creator><creator>van Gils, Marit J.</creator><creator>Wieske, Luuk</creator><creator>Kuijpers, Taco W.</creator><creator>Eftimov, Filip</creator><creator>van Ham, S. Marieke</creator><creator>ten Brinke, Anja</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6647-2233</orcidid></search><sort><creationdate>202309</creationdate><title>Distinct dynamics of antigen-specific induction and differentiation of different CD11c+Tbet+ B-cell subsets</title><author>Steuten, Juulke ; Bos, Amélie V. ; Kuijper, Lisan H. ; Claireaux, Mathieu ; Olijhoek, Wouter ; Elias, George ; Duurland, Mariel C. ; Jorritsma, Tineke ; Marsman, Casper ; Paul, Alberta G.A. ; Garcia Vallejo, Juan J. ; van Gils, Marit J. ; Wieske, Luuk ; Kuijpers, Taco W. ; Eftimov, Filip ; van Ham, S. 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Marieke</au><au>ten Brinke, Anja</au><aucorp>T2B Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct dynamics of antigen-specific induction and differentiation of different CD11c+Tbet+ B-cell subsets</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2023-09</date><risdate>2023</risdate><volume>152</volume><issue>3</issue><spage>689</spage><epage>699.e6</epage><pages>689-699.e6</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><abstract>CD11c+Tbet+ B cells are enriched in autoimmunity and chronic infections and also expand on immune challenge in healthy individuals. CD11c+Tbet+ B cells remain an enigmatic B-cell population because of their intrinsic heterogeneity.
We investigated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen-specific development and differentiation properties of 3 separate CD11c+ B-cell subsets—age-associated B cells (ABCs), double-negative 2 (DN2) B cells, and activated naive B cells—and compared them to their canonical CD11c− counterparts.
Dynamics of the response of the 3 CD11c+ B-cell subsets were assessed at SARS-CoV-2 vaccination in healthy donors by spectral flow cytometry. Distinct CD11c+ B-cell subsets were functionally characterized by optimized in vitro cultures.
In contrast to a durable expansion of antigen-specific CD11c− memory B cells over time, both ABCs and DN2 cells were strongly expanded shortly after second vaccination and subsequently contracted. Functional characterization of antibody-secreting cell differentiation dynamics revealed that CD11c+Tbet+ B cells were primed for antibody-secreting cell differentiation compared to relevant canonical CD11c− counterparts.
Overall, CD11c+Tbet+ B cells encompass heterogeneous subpopulations, of which primarily ABCs as well as DN2 B cells respond early to immune challenge and display a pre–antibody-secreting cell phenotype.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36858158</pmid><doi>10.1016/j.jaci.2023.02.020</doi><orcidid>https://orcid.org/0000-0002-6647-2233</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | activated naive age-associated B cell antibody-secreting cell differentiation B-Lymphocyte Subsets CD11c+Tbet+ atypical B cell Cell Differentiation COVID-19 COVID-19 Vaccines double negative 2 Humans SARS-CoV-2 SARS-CoV-2 vaccination |
title | Distinct dynamics of antigen-specific induction and differentiation of different CD11c+Tbet+ B-cell subsets |
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