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Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria

Elucidating the adaptive immune characteristics of natural protection to Lassa fever (LF) is vital in designing and selecting optimal vaccine candidates. With rejuvenated interest in LF and a call for accelerated research on the Lassa virus (LASV) vaccine, there is a need to define the correlates of...

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Autores principales: Ugwu, Chinedu, Olumade, Testimony, Nwakpakpa, Ebenezer, Onyia, Venatius, Odeh, Elizabeth, Duruiheoma, Rosemary Ogonna, Ojide, Chiedozie K., Eke, Matthew Afam, Nwafor, Ifeanyi Emmanuel, Chika-Igwenyi, Nneka, Abu, Augustine M., Azuogu, Benedict, Ajayi, Nnennaya, Ogah, Emeka, Ayodeji, Oluwafemi, Abejegah, Chukwuyem, Adedosu, Nelson, Oyejide, Nicholas, Abah, Sylvester, Omidele, Abiola, Ingbian, Winifred, Osoba, Emmanuel, Eromon, Philomena, Oluniyi, Paul, Ogunsanya, Olusola, Happi, Anise, Otuh, Patricia, Nadesalingam, Angalee, Carnell, George, Krause, Nina, Aguinam, Ernest, Kinsley, Rebecca, Storisteanu, Daniel Matthew L., Tonks, Paul, Nelson, Diana, McAlister, Carley, Boisen, Matthew, Garry, Robert, Wright, Edward, Temperton, Nigel, Frost, Simon, Heeney, Jonathan Luke, Happi, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790078/
https://www.ncbi.nlm.nih.gov/pubmed/36567369
http://dx.doi.org/10.1038/s41598-022-26045-w
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author Ugwu, Chinedu
Olumade, Testimony
Nwakpakpa, Ebenezer
Onyia, Venatius
Odeh, Elizabeth
Duruiheoma, Rosemary Ogonna
Ojide, Chiedozie K.
Eke, Matthew Afam
Nwafor, Ifeanyi Emmanuel
Chika-Igwenyi, Nneka
Abu, Augustine M.
Azuogu, Benedict
Ajayi, Nnennaya
Ogah, Emeka
Ayodeji, Oluwafemi
Abejegah, Chukwuyem
Adedosu, Nelson
Oyejide, Nicholas
Abah, Sylvester
Omidele, Abiola
Ingbian, Winifred
Osoba, Emmanuel
Eromon, Philomena
Oluniyi, Paul
Ogunsanya, Olusola
Happi, Anise
Otuh, Patricia
Nadesalingam, Angalee
Carnell, George
Krause, Nina
Aguinam, Ernest
Kinsley, Rebecca
Storisteanu, Daniel Matthew L.
Tonks, Paul
Nelson, Diana
McAlister, Carley
Boisen, Matthew
Garry, Robert
Wright, Edward
Temperton, Nigel
Frost, Simon
Heeney, Jonathan Luke
Happi, Christian
author_facet Ugwu, Chinedu
Olumade, Testimony
Nwakpakpa, Ebenezer
Onyia, Venatius
Odeh, Elizabeth
Duruiheoma, Rosemary Ogonna
Ojide, Chiedozie K.
Eke, Matthew Afam
Nwafor, Ifeanyi Emmanuel
Chika-Igwenyi, Nneka
Abu, Augustine M.
Azuogu, Benedict
Ajayi, Nnennaya
Ogah, Emeka
Ayodeji, Oluwafemi
Abejegah, Chukwuyem
Adedosu, Nelson
Oyejide, Nicholas
Abah, Sylvester
Omidele, Abiola
Ingbian, Winifred
Osoba, Emmanuel
Eromon, Philomena
Oluniyi, Paul
Ogunsanya, Olusola
Happi, Anise
Otuh, Patricia
Nadesalingam, Angalee
Carnell, George
Krause, Nina
Aguinam, Ernest
Kinsley, Rebecca
Storisteanu, Daniel Matthew L.
Tonks, Paul
Nelson, Diana
McAlister, Carley
Boisen, Matthew
Garry, Robert
Wright, Edward
Temperton, Nigel
Frost, Simon
Heeney, Jonathan Luke
Happi, Christian
author_sort Ugwu, Chinedu
collection PubMed
description Elucidating the adaptive immune characteristics of natural protection to Lassa fever (LF) is vital in designing and selecting optimal vaccine candidates. With rejuvenated interest in LF and a call for accelerated research on the Lassa virus (LASV) vaccine, there is a need to define the correlates of natural protective immune responses to LF. Here, we describe cellular and antibody immune responses present in survivors of LF (N = 370) and their exposed contacts (N = 170) in a LASV endemic region in Nigeria. Interestingly, our data showed comparable T cell and binding antibody responses from both survivors and their contacts, while neutralizing antibody responses were primarily seen in the LF survivors and not their contacts. Neutralizing antibody responses were found to be cross-reactive against all five lineages of LASV with a strong bias to Lineage II, the prevalent strain in southern Nigeria. We demonstrated that both T cell and antibody responses were not detectable in peripheral blood after a decade in LF survivors. Notably LF survivors maintained high levels of detectable binding antibody response for six months while their contacts did not. Lastly, as potential vaccine targets, we identified the regions of the LASV Glycoprotein (GP) and Nucleoprotein (NP) that induced the broadest peptide-specific T cell responses. Taken together this data informs immunological readouts and potential benchmarks for clinical trials evaluating LASV vaccine candidates.
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spelling pubmed-97900782022-12-27 Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria Ugwu, Chinedu Olumade, Testimony Nwakpakpa, Ebenezer Onyia, Venatius Odeh, Elizabeth Duruiheoma, Rosemary Ogonna Ojide, Chiedozie K. Eke, Matthew Afam Nwafor, Ifeanyi Emmanuel Chika-Igwenyi, Nneka Abu, Augustine M. Azuogu, Benedict Ajayi, Nnennaya Ogah, Emeka Ayodeji, Oluwafemi Abejegah, Chukwuyem Adedosu, Nelson Oyejide, Nicholas Abah, Sylvester Omidele, Abiola Ingbian, Winifred Osoba, Emmanuel Eromon, Philomena Oluniyi, Paul Ogunsanya, Olusola Happi, Anise Otuh, Patricia Nadesalingam, Angalee Carnell, George Krause, Nina Aguinam, Ernest Kinsley, Rebecca Storisteanu, Daniel Matthew L. Tonks, Paul Nelson, Diana McAlister, Carley Boisen, Matthew Garry, Robert Wright, Edward Temperton, Nigel Frost, Simon Heeney, Jonathan Luke Happi, Christian Sci Rep Article Elucidating the adaptive immune characteristics of natural protection to Lassa fever (LF) is vital in designing and selecting optimal vaccine candidates. With rejuvenated interest in LF and a call for accelerated research on the Lassa virus (LASV) vaccine, there is a need to define the correlates of natural protective immune responses to LF. Here, we describe cellular and antibody immune responses present in survivors of LF (N = 370) and their exposed contacts (N = 170) in a LASV endemic region in Nigeria. Interestingly, our data showed comparable T cell and binding antibody responses from both survivors and their contacts, while neutralizing antibody responses were primarily seen in the LF survivors and not their contacts. Neutralizing antibody responses were found to be cross-reactive against all five lineages of LASV with a strong bias to Lineage II, the prevalent strain in southern Nigeria. We demonstrated that both T cell and antibody responses were not detectable in peripheral blood after a decade in LF survivors. Notably LF survivors maintained high levels of detectable binding antibody response for six months while their contacts did not. Lastly, as potential vaccine targets, we identified the regions of the LASV Glycoprotein (GP) and Nucleoprotein (NP) that induced the broadest peptide-specific T cell responses. Taken together this data informs immunological readouts and potential benchmarks for clinical trials evaluating LASV vaccine candidates. Nature Publishing Group UK 2022-12-25 /pmc/articles/PMC9790078/ /pubmed/36567369 http://dx.doi.org/10.1038/s41598-022-26045-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ugwu, Chinedu
Olumade, Testimony
Nwakpakpa, Ebenezer
Onyia, Venatius
Odeh, Elizabeth
Duruiheoma, Rosemary Ogonna
Ojide, Chiedozie K.
Eke, Matthew Afam
Nwafor, Ifeanyi Emmanuel
Chika-Igwenyi, Nneka
Abu, Augustine M.
Azuogu, Benedict
Ajayi, Nnennaya
Ogah, Emeka
Ayodeji, Oluwafemi
Abejegah, Chukwuyem
Adedosu, Nelson
Oyejide, Nicholas
Abah, Sylvester
Omidele, Abiola
Ingbian, Winifred
Osoba, Emmanuel
Eromon, Philomena
Oluniyi, Paul
Ogunsanya, Olusola
Happi, Anise
Otuh, Patricia
Nadesalingam, Angalee
Carnell, George
Krause, Nina
Aguinam, Ernest
Kinsley, Rebecca
Storisteanu, Daniel Matthew L.
Tonks, Paul
Nelson, Diana
McAlister, Carley
Boisen, Matthew
Garry, Robert
Wright, Edward
Temperton, Nigel
Frost, Simon
Heeney, Jonathan Luke
Happi, Christian
Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title_full Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title_fullStr Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title_full_unstemmed Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title_short Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
title_sort humoral and cellular immune responses to lassa fever virus in lassa fever survivors and their exposed contacts in southern nigeria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790078/
https://www.ncbi.nlm.nih.gov/pubmed/36567369
http://dx.doi.org/10.1038/s41598-022-26045-w
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