High crossreactivity of human T cell responses between Lassa virus lineages

Lassa virus infects hundreds of thousands of people each year across rural West Africa, resulting in a high number of cases of Lassa fever (LF), a febrile disease associated with high morbidity and significant mortality. The lack of approved treatments or interventions underscores the need for an ef...

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Veröffentlicht in:PLoS pathogens 2020-03, Vol.16 (3), p.e1008352-e1008352
Hauptverfasser: Sullivan, Brian M, Sakabe, Saori, Hartnett, Jessica N, Ngo, Nhi, Goba, Augustine, Momoh, Mambu, Demby Sandi, John, Kanneh, Lansana, Cubitt, Beatrice, Garcia, Selma D, Ware, Brian C, Kotliar, Dylan, Robles-Sikisaka, Refugio, Gangavarapu, Karthik, Branco, Luis, Eromon, Philomena, Odia, Ikponmwosa, Ogbaini-Emovon, Ephraim, Folarin, Onikepe, Okogbenin, Sylvanus, Okokhere, Peter O, Happi, Christian, de la Torre, Juan Carlos, Sabeti, Pardis C, Andersen, Kristian G, Garry, Robert F, Grant, Donald S, Schieffelin, John S, Oldstone, Michael B A
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container_issue 3
container_start_page e1008352
container_title PLoS pathogens
container_volume 16
creator Sullivan, Brian M
Sakabe, Saori
Hartnett, Jessica N
Ngo, Nhi
Goba, Augustine
Momoh, Mambu
Demby Sandi, John
Kanneh, Lansana
Cubitt, Beatrice
Garcia, Selma D
Ware, Brian C
Kotliar, Dylan
Robles-Sikisaka, Refugio
Gangavarapu, Karthik
Branco, Luis
Eromon, Philomena
Odia, Ikponmwosa
Ogbaini-Emovon, Ephraim
Folarin, Onikepe
Okogbenin, Sylvanus
Okokhere, Peter O
Happi, Christian
de la Torre, Juan Carlos
Sabeti, Pardis C
Andersen, Kristian G
Garry, Robert F
Grant, Donald S
Schieffelin, John S
Oldstone, Michael B A
description Lassa virus infects hundreds of thousands of people each year across rural West Africa, resulting in a high number of cases of Lassa fever (LF), a febrile disease associated with high morbidity and significant mortality. The lack of approved treatments or interventions underscores the need for an effective vaccine. At least four viral lineages circulate in defined regions throughout West Africa with substantial interlineage nucleotide and amino acid diversity. An effective vaccine should be designed to elicit Lassa virus specific humoral and cell mediated immunity across all lineages. Most current vaccine candidates use only lineage IV antigens encoded by Lassa viruses circulating around Sierra Leone, Liberia, and Guinea but not Nigeria where lineages I-III are found. As previous infection is known to protect against disease from subsequent exposure, we sought to determine whether LF survivors from Nigeria and Sierra Leone harbor memory T cells that respond to lineage IV antigens. Our results indicate a high degree of cross-reactivity of CD8+ T cells from Nigerian LF survivors to lineage IV antigens. In addition, we identified regions within the Lassa virus glycoprotein complex and nucleoprotein that contributed to these responses while T cell epitopes were not widely conserved across our study group. These data are important for current efforts to design effective and efficient vaccine candidates that can elicit protective immunity across all Lassa virus lineages.
doi_str_mv 10.1371/journal.ppat.1008352
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The lack of approved treatments or interventions underscores the need for an effective vaccine. At least four viral lineages circulate in defined regions throughout West Africa with substantial interlineage nucleotide and amino acid diversity. An effective vaccine should be designed to elicit Lassa virus specific humoral and cell mediated immunity across all lineages. Most current vaccine candidates use only lineage IV antigens encoded by Lassa viruses circulating around Sierra Leone, Liberia, and Guinea but not Nigeria where lineages I-III are found. As previous infection is known to protect against disease from subsequent exposure, we sought to determine whether LF survivors from Nigeria and Sierra Leone harbor memory T cells that respond to lineage IV antigens. Our results indicate a high degree of cross-reactivity of CD8+ T cells from Nigerian LF survivors to lineage IV antigens. In addition, we identified regions within the Lassa virus glycoprotein complex and nucleoprotein that contributed to these responses while T cell epitopes were not widely conserved across our study group. 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In addition, we identified regions within the Lassa virus glycoprotein complex and nucleoprotein that contributed to these responses while T cell epitopes were not widely conserved across our study group. 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sullivan, Brian M</au><au>Sakabe, Saori</au><au>Hartnett, Jessica N</au><au>Ngo, Nhi</au><au>Goba, Augustine</au><au>Momoh, Mambu</au><au>Demby Sandi, John</au><au>Kanneh, Lansana</au><au>Cubitt, Beatrice</au><au>Garcia, Selma D</au><au>Ware, Brian C</au><au>Kotliar, Dylan</au><au>Robles-Sikisaka, Refugio</au><au>Gangavarapu, Karthik</au><au>Branco, Luis</au><au>Eromon, Philomena</au><au>Odia, Ikponmwosa</au><au>Ogbaini-Emovon, Ephraim</au><au>Folarin, Onikepe</au><au>Okogbenin, Sylvanus</au><au>Okokhere, Peter O</au><au>Happi, Christian</au><au>de la Torre, Juan Carlos</au><au>Sabeti, Pardis C</au><au>Andersen, Kristian G</au><au>Garry, Robert F</au><au>Grant, Donald S</au><au>Schieffelin, John S</au><au>Oldstone, Michael B A</au><au>Bukreyev, Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High crossreactivity of human T cell responses between Lassa virus lineages</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2020-03-06</date><risdate>2020</risdate><volume>16</volume><issue>3</issue><spage>e1008352</spage><epage>e1008352</epage><pages>e1008352-e1008352</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Lassa virus infects hundreds of thousands of people each year across rural West Africa, resulting in a high number of cases of Lassa fever (LF), a febrile disease associated with high morbidity and significant mortality. The lack of approved treatments or interventions underscores the need for an effective vaccine. At least four viral lineages circulate in defined regions throughout West Africa with substantial interlineage nucleotide and amino acid diversity. An effective vaccine should be designed to elicit Lassa virus specific humoral and cell mediated immunity across all lineages. Most current vaccine candidates use only lineage IV antigens encoded by Lassa viruses circulating around Sierra Leone, Liberia, and Guinea but not Nigeria where lineages I-III are found. As previous infection is known to protect against disease from subsequent exposure, we sought to determine whether LF survivors from Nigeria and Sierra Leone harbor memory T cells that respond to lineage IV antigens. Our results indicate a high degree of cross-reactivity of CD8+ T cells from Nigerian LF survivors to lineage IV antigens. In addition, we identified regions within the Lassa virus glycoprotein complex and nucleoprotein that contributed to these responses while T cell epitopes were not widely conserved across our study group. These data are important for current efforts to design effective and efficient vaccine candidates that can elicit protective immunity across all Lassa virus lineages.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32142546</pmid><doi>10.1371/journal.ppat.1008352</doi><orcidid>https://orcid.org/0000-0003-4277-6037</orcidid><orcidid>https://orcid.org/0000-0002-1619-8678</orcidid><orcidid>https://orcid.org/0000-0002-4329-0795</orcidid><orcidid>https://orcid.org/0000-0002-8048-410X</orcidid><orcidid>https://orcid.org/0000-0001-7283-2920</orcidid><orcidid>https://orcid.org/0000-0002-5683-3250</orcidid><orcidid>https://orcid.org/0000-0001-6642-5739</orcidid><orcidid>https://orcid.org/0000-0002-7474-8156</orcidid><orcidid>https://orcid.org/0000-0002-9873-1121</orcidid><orcidid>https://orcid.org/0000-0002-4203-3252</orcidid><orcidid>https://orcid.org/0000-0001-8161-0182</orcidid><orcidid>https://orcid.org/0000-0002-8171-8115</orcidid><orcidid>https://orcid.org/0000-0001-6024-8612</orcidid><orcidid>https://orcid.org/0000-0002-5027-3440</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1553-7374
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issn 1553-7374
1553-7366
1553-7374
language eng
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source MEDLINE; DOAJ Directory of Open Access Journals; PubMed Central Open Access; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Africa, Western
Amino acids
Antigen-antibody reactions
Antigenic determinants
Antigens
Antigens, Viral - immunology
Authorship
Biology and Life Sciences
CD8 antigen
CD8-Positive T-Lymphocytes - immunology
Cross Reactions
Cross-reactivity
Diseases
Epitopes
Epitopes, T-Lymphocyte - immunology
Female
Fever
Genomics
Glycoproteins
Humans
Humoral immunity
Immunity
Immunoglobulins
Immunological memory
Immunology
Infectious diseases
Laboratories
Lassa fever
Lassa virus - immunology
Lymphocytes
Lymphocytes T
Male
Medical equipment industry
Medicine
Medicine and Health Sciences
Memory cells
Morbidity
Mortality
Nigeria
Nosocomial infections
Nucleotides
R&D
Research & development
Sanitation
Sierra Leone
Species Specificity
T cells
Teaching hospitals
United States
Vaccines
Viruses
title High crossreactivity of human T cell responses between Lassa virus lineages
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