Responses of CD27 + CD38 + plasmablasts, and CD24 hi CD27 hi and CD24 hi CD38 hi regulatory B cells during primary dengue virus 2 infection
Humoral immunity is thought to play a central role in mediating the immunopathogenesis of dengue virus (DENV) infection; however, the B-cell responses elicited by primary DENV2 infection are incompletely understood. Follicular helper T cells (Tfh) are important to promote B-cell activation and diffe...
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Veröffentlicht in: | Journal of clinical laboratory analysis 2021-11, Vol.35 (11), p.e24035 |
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container_start_page | e24035 |
container_title | Journal of clinical laboratory analysis |
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creator | Lei, Chenshuang Yu, Qinhua Wang, Hong Liu, JieJing Chen, Sufeng Zhao, Zhao Qiu, Liannv |
description | Humoral immunity is thought to play a central role in mediating the immunopathogenesis of dengue virus (DENV) infection; however, the B-cell responses elicited by primary DENV2 infection are incompletely understood. Follicular helper T cells (Tfh) are important to promote B-cell activation and differentiation.
The present study analyzed the detailed dynamic changes of circulating B-cell subsets and Tfh (cTfh) using flow cytometry to explore their responses to DENV2 infection.
Thirty-six patients with DENV2 and 21 healthy individuals were included. The results showed that CD27
CD38
plasmablasts emerged after DENV2 infection, and correlated with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh, which increased after DENV2 infection, and correlated with DENV2 RNA viral loads. Significantly low levels of CD27
naïve B cells, and CD24
CD27
and CD24
CD38
regulatory B cells (Breg) were observed after DENV2 infection, which correlated negatively with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh cells.
Overall, these results provide insights into the DENV2-elicited B-cell response and revealed previously unidentified CD24
CD27
and CD24
CD38
Breg responses to DENV2 infection. |
doi_str_mv | 10.1002/jcla.24035 |
format | Article |
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The present study analyzed the detailed dynamic changes of circulating B-cell subsets and Tfh (cTfh) using flow cytometry to explore their responses to DENV2 infection.
Thirty-six patients with DENV2 and 21 healthy individuals were included. The results showed that CD27
CD38
plasmablasts emerged after DENV2 infection, and correlated with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh, which increased after DENV2 infection, and correlated with DENV2 RNA viral loads. Significantly low levels of CD27
naïve B cells, and CD24
CD27
and CD24
CD38
regulatory B cells (Breg) were observed after DENV2 infection, which correlated negatively with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh cells.
Overall, these results provide insights into the DENV2-elicited B-cell response and revealed previously unidentified CD24
CD27
and CD24
CD38
Breg responses to DENV2 infection.</description><identifier>ISSN: 0887-8013</identifier><identifier>EISSN: 1098-2825</identifier><identifier>DOI: 10.1002/jcla.24035</identifier><identifier>PMID: 34606646</identifier><language>eng</language><publisher>United States</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antigens, CD - metabolism ; B-Lymphocytes, Regulatory - chemistry ; B-Lymphocytes, Regulatory - immunology ; Dengue - immunology ; Dengue - metabolism ; Dengue Virus - immunology ; Female ; Flow Cytometry ; Humans ; Male ; Middle Aged ; T Follicular Helper Cells - chemistry ; T Follicular Helper Cells - immunology ; Young Adult</subject><ispartof>Journal of clinical laboratory analysis, 2021-11, Vol.35 (11), p.e24035</ispartof><rights>2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c996-dde185aca0847c05e78a31e3602e0276664b20945dddc338b3b15ce64c7a0ec53</citedby><cites>FETCH-LOGICAL-c996-dde185aca0847c05e78a31e3602e0276664b20945dddc338b3b15ce64c7a0ec53</cites><orcidid>0000-0002-2325-7509</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34606646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lei, Chenshuang</creatorcontrib><creatorcontrib>Yu, Qinhua</creatorcontrib><creatorcontrib>Wang, Hong</creatorcontrib><creatorcontrib>Liu, JieJing</creatorcontrib><creatorcontrib>Chen, Sufeng</creatorcontrib><creatorcontrib>Zhao, Zhao</creatorcontrib><creatorcontrib>Qiu, Liannv</creatorcontrib><title>Responses of CD27 + CD38 + plasmablasts, and CD24 hi CD27 hi and CD24 hi CD38 hi regulatory B cells during primary dengue virus 2 infection</title><title>Journal of clinical laboratory analysis</title><addtitle>J Clin Lab Anal</addtitle><description>Humoral immunity is thought to play a central role in mediating the immunopathogenesis of dengue virus (DENV) infection; however, the B-cell responses elicited by primary DENV2 infection are incompletely understood. Follicular helper T cells (Tfh) are important to promote B-cell activation and differentiation.
The present study analyzed the detailed dynamic changes of circulating B-cell subsets and Tfh (cTfh) using flow cytometry to explore their responses to DENV2 infection.
Thirty-six patients with DENV2 and 21 healthy individuals were included. The results showed that CD27
CD38
plasmablasts emerged after DENV2 infection, and correlated with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh, which increased after DENV2 infection, and correlated with DENV2 RNA viral loads. Significantly low levels of CD27
naïve B cells, and CD24
CD27
and CD24
CD38
regulatory B cells (Breg) were observed after DENV2 infection, which correlated negatively with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh cells.
Overall, these results provide insights into the DENV2-elicited B-cell response and revealed previously unidentified CD24
CD27
and CD24
CD38
Breg responses to DENV2 infection.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, CD - metabolism</subject><subject>B-Lymphocytes, Regulatory - chemistry</subject><subject>B-Lymphocytes, Regulatory - immunology</subject><subject>Dengue - immunology</subject><subject>Dengue - metabolism</subject><subject>Dengue Virus - immunology</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>T Follicular Helper Cells - chemistry</subject><subject>T Follicular Helper Cells - immunology</subject><subject>Young Adult</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkN1Kw0AQhRdRbK3e-ACy12rq7G82l1p_oSBI78Nmd1JT0iRkG8Fn8KXd2ip4Mx-cOTPMHELOGUwZAL9ZudpOuQShDsiYQWYSbrg6JGMwJk0MMDEiJyGsAMBkTB-TkZAatJZ6TL7eMHRtEzDQtqSze57SqwhhIrrahrUtYt2Ea2obv-1L-l7tfJH_tTgU2eNyqO2m7T_pHXVY14H6oa-aJe36am2j7LFZDkg_qn4IlNOqKdFtqrY5JUelrQOe7Tkhi8eHxew5mb8-vcxu54nLMp14j8wo6ywYmTpQmBorGAoNHIGnOv5VcMik8t47IUwhCqYcaulSC-iUmJDL3VrXtyH0WOb7w3IG-TbQfBto_hNoNF_szN1QrNH_WX8TFN-VsW2G</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Lei, Chenshuang</creator><creator>Yu, Qinhua</creator><creator>Wang, Hong</creator><creator>Liu, JieJing</creator><creator>Chen, Sufeng</creator><creator>Zhao, Zhao</creator><creator>Qiu, Liannv</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2325-7509</orcidid></search><sort><creationdate>202111</creationdate><title>Responses of CD27 + CD38 + plasmablasts, and CD24 hi CD27 hi and CD24 hi CD38 hi regulatory B cells during primary dengue virus 2 infection</title><author>Lei, Chenshuang ; Yu, Qinhua ; Wang, Hong ; Liu, JieJing ; Chen, Sufeng ; Zhao, Zhao ; Qiu, Liannv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c996-dde185aca0847c05e78a31e3602e0276664b20945dddc338b3b15ce64c7a0ec53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, CD - metabolism</topic><topic>B-Lymphocytes, Regulatory - chemistry</topic><topic>B-Lymphocytes, Regulatory - immunology</topic><topic>Dengue - immunology</topic><topic>Dengue - metabolism</topic><topic>Dengue Virus - immunology</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>T Follicular Helper Cells - chemistry</topic><topic>T Follicular Helper Cells - immunology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lei, Chenshuang</creatorcontrib><creatorcontrib>Yu, Qinhua</creatorcontrib><creatorcontrib>Wang, Hong</creatorcontrib><creatorcontrib>Liu, JieJing</creatorcontrib><creatorcontrib>Chen, Sufeng</creatorcontrib><creatorcontrib>Zhao, Zhao</creatorcontrib><creatorcontrib>Qiu, Liannv</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of clinical laboratory analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lei, Chenshuang</au><au>Yu, Qinhua</au><au>Wang, Hong</au><au>Liu, JieJing</au><au>Chen, Sufeng</au><au>Zhao, Zhao</au><au>Qiu, Liannv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Responses of CD27 + CD38 + plasmablasts, and CD24 hi CD27 hi and CD24 hi CD38 hi regulatory B cells during primary dengue virus 2 infection</atitle><jtitle>Journal of clinical laboratory analysis</jtitle><addtitle>J Clin Lab Anal</addtitle><date>2021-11</date><risdate>2021</risdate><volume>35</volume><issue>11</issue><spage>e24035</spage><pages>e24035-</pages><issn>0887-8013</issn><eissn>1098-2825</eissn><abstract>Humoral immunity is thought to play a central role in mediating the immunopathogenesis of dengue virus (DENV) infection; however, the B-cell responses elicited by primary DENV2 infection are incompletely understood. Follicular helper T cells (Tfh) are important to promote B-cell activation and differentiation.
The present study analyzed the detailed dynamic changes of circulating B-cell subsets and Tfh (cTfh) using flow cytometry to explore their responses to DENV2 infection.
Thirty-six patients with DENV2 and 21 healthy individuals were included. The results showed that CD27
CD38
plasmablasts emerged after DENV2 infection, and correlated with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh, which increased after DENV2 infection, and correlated with DENV2 RNA viral loads. Significantly low levels of CD27
naïve B cells, and CD24
CD27
and CD24
CD38
regulatory B cells (Breg) were observed after DENV2 infection, which correlated negatively with CXCR5
PD-1
or CXCR5
ICOS
PD-1
cTfh cells.
Overall, these results provide insights into the DENV2-elicited B-cell response and revealed previously unidentified CD24
CD27
and CD24
CD38
Breg responses to DENV2 infection.</abstract><cop>United States</cop><pmid>34606646</pmid><doi>10.1002/jcla.24035</doi><orcidid>https://orcid.org/0000-0002-2325-7509</orcidid></addata></record> |
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source | MEDLINE; Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Adolescent Adult Aged Aged, 80 and over Antigens, CD - metabolism B-Lymphocytes, Regulatory - chemistry B-Lymphocytes, Regulatory - immunology Dengue - immunology Dengue - metabolism Dengue Virus - immunology Female Flow Cytometry Humans Male Middle Aged T Follicular Helper Cells - chemistry T Follicular Helper Cells - immunology Young Adult |
title | Responses of CD27 + CD38 + plasmablasts, and CD24 hi CD27 hi and CD24 hi CD38 hi regulatory B cells during primary dengue virus 2 infection |
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