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
Hauptverfasser: 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
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container_issue 5
container_start_page e1129
container_title Clinical & translational immunology
container_volume 9
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
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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 &amp; Biomedicine ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Major histocompatibility complex ; neutralising antibodies ; Original ; Peripheral blood ; Science &amp; Technology ; T follicular helper (Tfh) cells ; Vaccination ; Vaccines ; Vaccinology ; viral infection ; Viral infections ; yellow fever ; YF‐17D</subject><ispartof>Clinical &amp; translational immunology, 2020-05, Vol.9 (5), p.e1129-n/a, Article 1129</ispartof><rights>2020 The Authors. published by John Wiley &amp; Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc.</rights><rights>2020 The Authors. Clinical &amp; Translational Immunology published by John Wiley &amp; 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”). 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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 &amp; 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 &amp; 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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 &amp; 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 &amp; 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 &amp; 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Clinical &amp; translational immunology</jtitle></facets><delivery><delcategory>Remote Search 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 &amp; 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>
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2050-0068
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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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