Dynamic changes in circulating T follicular helper cell composition predict neutralising antibody responses after yellow fever vaccination
Objectives T follicular helper (Tfh) cells are the principal T helper cell subset that provides help to B cells for potent antibody responses against various pathogens. In this study, we took advantage of the live‐attenuated yellow fever virus (YFV) vaccine strain, YF‐17D, as a model system for stud...
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Veröffentlicht in: | Clinical & translational immunology 2020-05, Vol.9 (5), p.e1129-n/a, Article 1129 |
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creator | Huber, Johanna E Ahlfeld, Julia Scheck, Magdalena K Zaucha, Magdalena Witter, Klaus Lehmann, Lisa Karimzadeh, Hadi Pritsch, Michael Hoelscher, Michael Sonnenburg, Frank Dick, Andrea Barba‐Spaeth, Giovanna Krug, Anne B Rothenfußer, Simon Baumjohann, Dirk |
description | Objectives
T follicular helper (Tfh) cells are the principal T helper cell subset that provides help to B cells for potent antibody responses against various pathogens. In this study, we took advantage of the live‐attenuated yellow fever virus (YFV) vaccine strain, YF‐17D, as a model system for studying human antiviral immune responses in vivo following exposure to an acute primary virus challenge under safe and highly controlled conditions, to comprehensively analyse the dynamics of circulating Tfh (cTfh) cells.
Methods
We tracked and analysed the response of cTfh and other T and B cell subsets in peripheral blood of healthy volunteers by flow cytometry over the course of 4 weeks after YF‐17D vaccination.
Results
Using surface staining of cell activation markers to track YFV‐specific T cells, we found increasing cTfh cell frequencies starting at day 3 and peaking around 2 weeks after YF‐17D vaccination. This kinetic was confirmed in a subgroup of donors using MHC multimer staining for four known MHC class II epitopes of YF‐17D. The subset composition of cTfh cells changed dynamically during the course of the immune response and was dominated by the cTfh1‐polarised subpopulation. Importantly, frequencies of cTfh1 cells correlated with the strength of the neutralising antibody response, whereas frequencies of cTfh17 cells were inversely correlated.
Conclusion
In summary, we describe detailed cTfh kinetics during YF‐17D vaccination. Our results suggest that cTfh expansion and polarisation can serve as a prognostic marker for vaccine success. These insights may be leveraged in the future to improve current vaccine design and strategies.
We tracked circulating T follicular helper (cTfh) cells in the blood of healthy individuals who received the yellow fever (YF) vaccine YF‐17D. We found that cTfh1‐polarised cells dominated the cTfh response and that their frequency on day 14 predicted YF virus‐neutralising antibody levels detected on day 28 after vaccination, thus highlighting the prognostic value of cTfh cells for monitoring of vaccine outcomes. |
doi_str_mv | 10.1002/cti2.1129 |
format | Article |
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T follicular helper (Tfh) cells are the principal T helper cell subset that provides help to B cells for potent antibody responses against various pathogens. In this study, we took advantage of the live‐attenuated yellow fever virus (YFV) vaccine strain, YF‐17D, as a model system for studying human antiviral immune responses in vivo following exposure to an acute primary virus challenge under safe and highly controlled conditions, to comprehensively analyse the dynamics of circulating Tfh (cTfh) cells.
Methods
We tracked and analysed the response of cTfh and other T and B cell subsets in peripheral blood of healthy volunteers by flow cytometry over the course of 4 weeks after YF‐17D vaccination.
Results
Using surface staining of cell activation markers to track YFV‐specific T cells, we found increasing cTfh cell frequencies starting at day 3 and peaking around 2 weeks after YF‐17D vaccination. This kinetic was confirmed in a subgroup of donors using MHC multimer staining for four known MHC class II epitopes of YF‐17D. The subset composition of cTfh cells changed dynamically during the course of the immune response and was dominated by the cTfh1‐polarised subpopulation. Importantly, frequencies of cTfh1 cells correlated with the strength of the neutralising antibody response, whereas frequencies of cTfh17 cells were inversely correlated.
Conclusion
In summary, we describe detailed cTfh kinetics during YF‐17D vaccination. Our results suggest that cTfh expansion and polarisation can serve as a prognostic marker for vaccine success. These insights may be leveraged in the future to improve current vaccine design and strategies.
We tracked circulating T follicular helper (cTfh) cells in the blood of healthy individuals who received the yellow fever (YF) vaccine YF‐17D. We found that cTfh1‐polarised cells dominated the cTfh response and that their frequency on day 14 predicted YF virus‐neutralising antibody levels detected on day 28 after vaccination, thus highlighting the prognostic value of cTfh cells for monitoring of vaccine outcomes.</description><identifier>ISSN: 2050-0068</identifier><identifier>EISSN: 2050-0068</identifier><identifier>DOI: 10.1002/cti2.1129</identifier><identifier>PMID: 32419947</identifier><language>eng</language><publisher>HOBOKEN: Wiley</publisher><subject>Antibodies ; Antibody response ; Cell activation ; Chemokines ; Controlled conditions ; Cytokines ; Epitopes ; Experiments ; Flow cytometry ; Helper cells ; Immunology ; Infections ; Life Sciences ; Life Sciences & Biomedicine ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Major histocompatibility complex ; neutralising antibodies ; Original ; Peripheral blood ; Science & Technology ; T follicular helper (Tfh) cells ; Vaccination ; Vaccines ; Vaccinology ; viral infection ; Viral infections ; yellow fever ; YF‐17D</subject><ispartof>Clinical & translational immunology, 2020-05, Vol.9 (5), p.e1129-n/a, Article 1129</ispartof><rights>2020 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc.</rights><rights>2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Attribution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>31</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000537716300005</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c6039-5926fb5a3c07954dfa1325c2259b85a189eb4e1ce03a2b8b9145e4bfc8f422d73</citedby><cites>FETCH-LOGICAL-c6039-5926fb5a3c07954dfa1325c2259b85a189eb4e1ce03a2b8b9145e4bfc8f422d73</cites><orcidid>0000-0002-7667-4285 ; 0000-0003-3589-7535 ; 0000-0001-5111-6845 ; 0000-0002-9556-7207 ; 0000-0003-2069-9501 ; 0000-0003-1151-7614 ; 0000-0001-8385-8288 ; 0000-0002-4879-4159 ; 0000-0003-2264-4395 ; 0000-0001-7383-8750 ; 0000-0002-5153-3371 ; 0000-0002-3590-1525</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221214/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221214/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,1419,2106,2118,11571,27933,27934,28257,45583,45584,46061,46485,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32419947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://pasteur.hal.science/pasteur-02876541$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Huber, Johanna E</creatorcontrib><creatorcontrib>Ahlfeld, Julia</creatorcontrib><creatorcontrib>Scheck, Magdalena K</creatorcontrib><creatorcontrib>Zaucha, Magdalena</creatorcontrib><creatorcontrib>Witter, Klaus</creatorcontrib><creatorcontrib>Lehmann, Lisa</creatorcontrib><creatorcontrib>Karimzadeh, Hadi</creatorcontrib><creatorcontrib>Pritsch, Michael</creatorcontrib><creatorcontrib>Hoelscher, Michael</creatorcontrib><creatorcontrib>Sonnenburg, Frank</creatorcontrib><creatorcontrib>Dick, Andrea</creatorcontrib><creatorcontrib>Barba‐Spaeth, Giovanna</creatorcontrib><creatorcontrib>Krug, Anne B</creatorcontrib><creatorcontrib>Rothenfußer, Simon</creatorcontrib><creatorcontrib>Baumjohann, Dirk</creatorcontrib><title>Dynamic changes in circulating T follicular helper cell composition predict neutralising antibody responses after yellow fever vaccination</title><title>Clinical & translational immunology</title><addtitle>CLIN TRANSL IMMUNOL</addtitle><addtitle>Clin Transl Immunology</addtitle><description>Objectives
T follicular helper (Tfh) cells are the principal T helper cell subset that provides help to B cells for potent antibody responses against various pathogens. In this study, we took advantage of the live‐attenuated yellow fever virus (YFV) vaccine strain, YF‐17D, as a model system for studying human antiviral immune responses in vivo following exposure to an acute primary virus challenge under safe and highly controlled conditions, to comprehensively analyse the dynamics of circulating Tfh (cTfh) cells.
Methods
We tracked and analysed the response of cTfh and other T and B cell subsets in peripheral blood of healthy volunteers by flow cytometry over the course of 4 weeks after YF‐17D vaccination.
Results
Using surface staining of cell activation markers to track YFV‐specific T cells, we found increasing cTfh cell frequencies starting at day 3 and peaking around 2 weeks after YF‐17D vaccination. This kinetic was confirmed in a subgroup of donors using MHC multimer staining for four known MHC class II epitopes of YF‐17D. The subset composition of cTfh cells changed dynamically during the course of the immune response and was dominated by the cTfh1‐polarised subpopulation. Importantly, frequencies of cTfh1 cells correlated with the strength of the neutralising antibody response, whereas frequencies of cTfh17 cells were inversely correlated.
Conclusion
In summary, we describe detailed cTfh kinetics during YF‐17D vaccination. Our results suggest that cTfh expansion and polarisation can serve as a prognostic marker for vaccine success. These insights may be leveraged in the future to improve current vaccine design and strategies.
We tracked circulating T follicular helper (cTfh) cells in the blood of healthy individuals who received the yellow fever (YF) vaccine YF‐17D. We found that cTfh1‐polarised cells dominated the cTfh response and that their frequency on day 14 predicted YF virus‐neutralising antibody levels detected on day 28 after vaccination, thus highlighting the prognostic value of cTfh cells for monitoring of vaccine outcomes.</description><subject>Antibodies</subject><subject>Antibody response</subject><subject>Cell activation</subject><subject>Chemokines</subject><subject>Controlled conditions</subject><subject>Cytokines</subject><subject>Epitopes</subject><subject>Experiments</subject><subject>Flow cytometry</subject><subject>Helper cells</subject><subject>Immunology</subject><subject>Infections</subject><subject>Life Sciences</subject><subject>Life Sciences & Biomedicine</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Major histocompatibility complex</subject><subject>neutralising antibodies</subject><subject>Original</subject><subject>Peripheral blood</subject><subject>Science & Technology</subject><subject>T follicular helper (Tfh) cells</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Vaccinology</subject><subject>viral infection</subject><subject>Viral infections</subject><subject>yellow 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Johanna E</creator><creator>Ahlfeld, Julia</creator><creator>Scheck, Magdalena K</creator><creator>Zaucha, Magdalena</creator><creator>Witter, Klaus</creator><creator>Lehmann, Lisa</creator><creator>Karimzadeh, Hadi</creator><creator>Pritsch, Michael</creator><creator>Hoelscher, Michael</creator><creator>Sonnenburg, Frank</creator><creator>Dick, Andrea</creator><creator>Barba‐Spaeth, Giovanna</creator><creator>Krug, Anne B</creator><creator>Rothenfußer, Simon</creator><creator>Baumjohann, Dirk</creator><general>Wiley</general><general>John Wiley & Sons, Inc</general><general>Nature Publishing Group</general><general>John Wiley and Sons 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changes in circulating T follicular helper cell composition predict neutralising antibody responses after yellow fever vaccination</title><author>Huber, Johanna E ; Ahlfeld, Julia ; Scheck, Magdalena K ; Zaucha, Magdalena ; Witter, Klaus ; Lehmann, Lisa ; Karimzadeh, Hadi ; Pritsch, Michael ; Hoelscher, Michael ; Sonnenburg, Frank ; Dick, Andrea ; Barba‐Spaeth, Giovanna ; Krug, Anne B ; Rothenfußer, Simon ; Baumjohann, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6039-5926fb5a3c07954dfa1325c2259b85a189eb4e1ce03a2b8b9145e4bfc8f422d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antibodies</topic><topic>Antibody response</topic><topic>Cell activation</topic><topic>Chemokines</topic><topic>Controlled conditions</topic><topic>Cytokines</topic><topic>Epitopes</topic><topic>Experiments</topic><topic>Flow cytometry</topic><topic>Helper cells</topic><topic>Immunology</topic><topic>Infections</topic><topic>Life Sciences</topic><topic>Life Sciences & Biomedicine</topic><topic>Lymphocytes</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Major histocompatibility complex</topic><topic>neutralising antibodies</topic><topic>Original</topic><topic>Peripheral blood</topic><topic>Science & Technology</topic><topic>T follicular helper (Tfh) cells</topic><topic>Vaccination</topic><topic>Vaccines</topic><topic>Vaccinology</topic><topic>viral infection</topic><topic>Viral infections</topic><topic>yellow fever</topic><topic>YF‐17D</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huber, Johanna E</creatorcontrib><creatorcontrib>Ahlfeld, Julia</creatorcontrib><creatorcontrib>Scheck, Magdalena K</creatorcontrib><creatorcontrib>Zaucha, Magdalena</creatorcontrib><creatorcontrib>Witter, Klaus</creatorcontrib><creatorcontrib>Lehmann, Lisa</creatorcontrib><creatorcontrib>Karimzadeh, Hadi</creatorcontrib><creatorcontrib>Pritsch, Michael</creatorcontrib><creatorcontrib>Hoelscher, Michael</creatorcontrib><creatorcontrib>Sonnenburg, Frank</creatorcontrib><creatorcontrib>Dick, Andrea</creatorcontrib><creatorcontrib>Barba‐Spaeth, Giovanna</creatorcontrib><creatorcontrib>Krug, Anne B</creatorcontrib><creatorcontrib>Rothenfußer, Simon</creatorcontrib><creatorcontrib>Baumjohann, Dirk</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huber, Johanna E</au><au>Ahlfeld, Julia</au><au>Scheck, Magdalena K</au><au>Zaucha, Magdalena</au><au>Witter, Klaus</au><au>Lehmann, Lisa</au><au>Karimzadeh, Hadi</au><au>Pritsch, Michael</au><au>Hoelscher, Michael</au><au>Sonnenburg, Frank</au><au>Dick, Andrea</au><au>Barba‐Spaeth, Giovanna</au><au>Krug, Anne B</au><au>Rothenfußer, Simon</au><au>Baumjohann, Dirk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic changes in circulating T follicular helper cell composition predict neutralising antibody responses after yellow fever vaccination</atitle><jtitle>Clinical & translational immunology</jtitle><stitle>CLIN TRANSL IMMUNOL</stitle><addtitle>Clin Transl Immunology</addtitle><date>2020-05</date><risdate>2020</risdate><volume>9</volume><issue>5</issue><spage>e1129</spage><epage>n/a</epage><pages>e1129-n/a</pages><artnum>1129</artnum><issn>2050-0068</issn><eissn>2050-0068</eissn><abstract>Objectives
T follicular helper (Tfh) cells are the principal T helper cell subset that provides help to B cells for potent antibody responses against various pathogens. In this study, we took advantage of the live‐attenuated yellow fever virus (YFV) vaccine strain, YF‐17D, as a model system for studying human antiviral immune responses in vivo following exposure to an acute primary virus challenge under safe and highly controlled conditions, to comprehensively analyse the dynamics of circulating Tfh (cTfh) cells.
Methods
We tracked and analysed the response of cTfh and other T and B cell subsets in peripheral blood of healthy volunteers by flow cytometry over the course of 4 weeks after YF‐17D vaccination.
Results
Using surface staining of cell activation markers to track YFV‐specific T cells, we found increasing cTfh cell frequencies starting at day 3 and peaking around 2 weeks after YF‐17D vaccination. This kinetic was confirmed in a subgroup of donors using MHC multimer staining for four known MHC class II epitopes of YF‐17D. The subset composition of cTfh cells changed dynamically during the course of the immune response and was dominated by the cTfh1‐polarised subpopulation. Importantly, frequencies of cTfh1 cells correlated with the strength of the neutralising antibody response, whereas frequencies of cTfh17 cells were inversely correlated.
Conclusion
In summary, we describe detailed cTfh kinetics during YF‐17D vaccination. Our results suggest that cTfh expansion and polarisation can serve as a prognostic marker for vaccine success. These insights may be leveraged in the future to improve current vaccine design and strategies.
We tracked circulating T follicular helper (cTfh) cells in the blood of healthy individuals who received the yellow fever (YF) vaccine YF‐17D. We found that cTfh1‐polarised cells dominated the cTfh response and that their frequency on day 14 predicted YF virus‐neutralising antibody levels detected on day 28 after vaccination, thus highlighting the prognostic value of cTfh cells for monitoring of vaccine outcomes.</abstract><cop>HOBOKEN</cop><pub>Wiley</pub><pmid>32419947</pmid><doi>10.1002/cti2.1129</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-7667-4285</orcidid><orcidid>https://orcid.org/0000-0003-3589-7535</orcidid><orcidid>https://orcid.org/0000-0001-5111-6845</orcidid><orcidid>https://orcid.org/0000-0002-9556-7207</orcidid><orcidid>https://orcid.org/0000-0003-2069-9501</orcidid><orcidid>https://orcid.org/0000-0003-1151-7614</orcidid><orcidid>https://orcid.org/0000-0001-8385-8288</orcidid><orcidid>https://orcid.org/0000-0002-4879-4159</orcidid><orcidid>https://orcid.org/0000-0003-2264-4395</orcidid><orcidid>https://orcid.org/0000-0001-7383-8750</orcidid><orcidid>https://orcid.org/0000-0002-5153-3371</orcidid><orcidid>https://orcid.org/0000-0002-3590-1525</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2050-0068 |
ispartof | Clinical & translational immunology, 2020-05, Vol.9 (5), p.e1129-n/a, Article 1129 |
issn | 2050-0068 2050-0068 |
language | eng |
recordid | cdi_pubmed_primary_32419947 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Wiley Online Library (Open Access Collection); PubMed Central |
subjects | Antibodies Antibody response Cell activation Chemokines Controlled conditions Cytokines Epitopes Experiments Flow cytometry Helper cells Immunology Infections Life Sciences Life Sciences & Biomedicine Lymphocytes Lymphocytes B Lymphocytes T Major histocompatibility complex neutralising antibodies Original Peripheral blood Science & Technology T follicular helper (Tfh) cells Vaccination Vaccines Vaccinology viral infection Viral infections yellow fever YF‐17D |
title | Dynamic changes in circulating T follicular helper cell composition predict neutralising antibody responses after yellow fever vaccination |
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