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Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages

Lassa virus (LASV) is the causative agent of Lassa fever, an often-fatal hemorrhagic disease that is endemic in West Africa. Seven genetically distinct LASV lineages have been identified. As part of CEPI’s (Coalition for Epidemic Preparedness Innovations) Lassa vaccine development program, we assess...

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Autores principales: Heinrich, Megan L., Boisen, Matthew L., Nelson, Diana K. S., Bush, Duane J., Cross, Robert W., Koval, Anatoliy P., Hoffmann, Andrew R., Beddingfield, Brandon J., Hastie, Kathryn M., Rowland, Megan M., Aimukanova, Irina, Koval, Sophia, Lathigra, Raju, Borisevich, Viktoriya, Momoh, Mambu, Sandi, John Demby, Goba, Augustine, Odia, lkponmwosa, Baimba, Francis, Aiyepada, John O., Ebo, Benevolence, Eromon, Philomena, Ugwu, Chinedu, Folarin, Onikepe, Olumade, Testimony, Onyechi, MacDonald N., Etafo, Johnson, Adeyemi, Rashidat, Ella, Elijah E., Aminu, Maryam, Gomerep, Simji S., Eke, Matthew Afam, Ogunsanya, Olusola, Akpede, George O., Asogun, Danny O., Okogbenin, Sylvanus A., Okokhere, Peter O., Holst, Johan, Shaffer, Jeffrey G., Schieffelin, John S., Geisbert, Thomas W., Saphire, Erica Ollmann, Happi, Christian T., Grant, Donald S., Garry, Robert F., Branco, Luis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525497/
https://www.ncbi.nlm.nih.gov/pubmed/32994446
http://dx.doi.org/10.1038/s41598-020-72539-w
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author Heinrich, Megan L.
Boisen, Matthew L.
Nelson, Diana K. S.
Bush, Duane J.
Cross, Robert W.
Koval, Anatoliy P.
Hoffmann, Andrew R.
Beddingfield, Brandon J.
Hastie, Kathryn M.
Rowland, Megan M.
Aimukanova, Irina
Koval, Sophia
Lathigra, Raju
Borisevich, Viktoriya
Momoh, Mambu
Sandi, John Demby
Goba, Augustine
Odia, lkponmwosa
Baimba, Francis
Aiyepada, John O.
Ebo, Benevolence
Eromon, Philomena
Ugwu, Chinedu
Folarin, Onikepe
Olumade, Testimony
Onyechi, MacDonald N.
Etafo, Johnson
Adeyemi, Rashidat
Ella, Elijah E.
Aminu, Maryam
Gomerep, Simji S.
Eke, Matthew Afam
Ogunsanya, Olusola
Akpede, George O.
Asogun, Danny O.
Okogbenin, Sylvanus A.
Okokhere, Peter O.
Holst, Johan
Shaffer, Jeffrey G.
Schieffelin, John S.
Geisbert, Thomas W.
Saphire, Erica Ollmann
Happi, Christian T.
Grant, Donald S.
Garry, Robert F.
Branco, Luis M.
author_facet Heinrich, Megan L.
Boisen, Matthew L.
Nelson, Diana K. S.
Bush, Duane J.
Cross, Robert W.
Koval, Anatoliy P.
Hoffmann, Andrew R.
Beddingfield, Brandon J.
Hastie, Kathryn M.
Rowland, Megan M.
Aimukanova, Irina
Koval, Sophia
Lathigra, Raju
Borisevich, Viktoriya
Momoh, Mambu
Sandi, John Demby
Goba, Augustine
Odia, lkponmwosa
Baimba, Francis
Aiyepada, John O.
Ebo, Benevolence
Eromon, Philomena
Ugwu, Chinedu
Folarin, Onikepe
Olumade, Testimony
Onyechi, MacDonald N.
Etafo, Johnson
Adeyemi, Rashidat
Ella, Elijah E.
Aminu, Maryam
Gomerep, Simji S.
Eke, Matthew Afam
Ogunsanya, Olusola
Akpede, George O.
Asogun, Danny O.
Okogbenin, Sylvanus A.
Okokhere, Peter O.
Holst, Johan
Shaffer, Jeffrey G.
Schieffelin, John S.
Geisbert, Thomas W.
Saphire, Erica Ollmann
Happi, Christian T.
Grant, Donald S.
Garry, Robert F.
Branco, Luis M.
author_sort Heinrich, Megan L.
collection PubMed
description Lassa virus (LASV) is the causative agent of Lassa fever, an often-fatal hemorrhagic disease that is endemic in West Africa. Seven genetically distinct LASV lineages have been identified. As part of CEPI’s (Coalition for Epidemic Preparedness Innovations) Lassa vaccine development program, we assessed the potential of the human immune system to mount cross-reactive and cross-protective humoral immune responses to antigens from the most prevalent LASV lineages, which are lineages II and III in Nigeria and lineage IV in Sierra Leone. IgG and IgM present in the blood of Lassa fever survivors from Nigeria or Sierra Leone exhibited substantial cross-reactivity for binding to LASV nucleoprotein and two engineered (linked and prefusion) versions of the glycoproteins (GP) of lineages II–IV. There was less cross-reactivity for the Zinc protein. Serum or plasma from Nigerian Lassa fever survivors neutralized LASV pseudoviruses expressing lineage II GP better than they neutralized lineage III or IV GP expressing pseudoviruses. Sierra Leonean survivors did not exhibit a lineage bias. Neutralization titres determined using LASV pseudovirus assays showed significant correlation with titres determined by plaque reduction with infectious LASV. These studies provide guidance for comparison of humoral immunity to LASV of distinct lineages following natural infection or immunization.
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spelling pubmed-75254972020-10-01 Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages Heinrich, Megan L. Boisen, Matthew L. Nelson, Diana K. S. Bush, Duane J. Cross, Robert W. Koval, Anatoliy P. Hoffmann, Andrew R. Beddingfield, Brandon J. Hastie, Kathryn M. Rowland, Megan M. Aimukanova, Irina Koval, Sophia Lathigra, Raju Borisevich, Viktoriya Momoh, Mambu Sandi, John Demby Goba, Augustine Odia, lkponmwosa Baimba, Francis Aiyepada, John O. Ebo, Benevolence Eromon, Philomena Ugwu, Chinedu Folarin, Onikepe Olumade, Testimony Onyechi, MacDonald N. Etafo, Johnson Adeyemi, Rashidat Ella, Elijah E. Aminu, Maryam Gomerep, Simji S. Eke, Matthew Afam Ogunsanya, Olusola Akpede, George O. Asogun, Danny O. Okogbenin, Sylvanus A. Okokhere, Peter O. Holst, Johan Shaffer, Jeffrey G. Schieffelin, John S. Geisbert, Thomas W. Saphire, Erica Ollmann Happi, Christian T. Grant, Donald S. Garry, Robert F. Branco, Luis M. Sci Rep Article Lassa virus (LASV) is the causative agent of Lassa fever, an often-fatal hemorrhagic disease that is endemic in West Africa. Seven genetically distinct LASV lineages have been identified. As part of CEPI’s (Coalition for Epidemic Preparedness Innovations) Lassa vaccine development program, we assessed the potential of the human immune system to mount cross-reactive and cross-protective humoral immune responses to antigens from the most prevalent LASV lineages, which are lineages II and III in Nigeria and lineage IV in Sierra Leone. IgG and IgM present in the blood of Lassa fever survivors from Nigeria or Sierra Leone exhibited substantial cross-reactivity for binding to LASV nucleoprotein and two engineered (linked and prefusion) versions of the glycoproteins (GP) of lineages II–IV. There was less cross-reactivity for the Zinc protein. Serum or plasma from Nigerian Lassa fever survivors neutralized LASV pseudoviruses expressing lineage II GP better than they neutralized lineage III or IV GP expressing pseudoviruses. Sierra Leonean survivors did not exhibit a lineage bias. Neutralization titres determined using LASV pseudovirus assays showed significant correlation with titres determined by plaque reduction with infectious LASV. These studies provide guidance for comparison of humoral immunity to LASV of distinct lineages following natural infection or immunization. Nature Publishing Group UK 2020-09-29 /pmc/articles/PMC7525497/ /pubmed/32994446 http://dx.doi.org/10.1038/s41598-020-72539-w Text en © The Author(s) 2020 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/.
spellingShingle Article
Heinrich, Megan L.
Boisen, Matthew L.
Nelson, Diana K. S.
Bush, Duane J.
Cross, Robert W.
Koval, Anatoliy P.
Hoffmann, Andrew R.
Beddingfield, Brandon J.
Hastie, Kathryn M.
Rowland, Megan M.
Aimukanova, Irina
Koval, Sophia
Lathigra, Raju
Borisevich, Viktoriya
Momoh, Mambu
Sandi, John Demby
Goba, Augustine
Odia, lkponmwosa
Baimba, Francis
Aiyepada, John O.
Ebo, Benevolence
Eromon, Philomena
Ugwu, Chinedu
Folarin, Onikepe
Olumade, Testimony
Onyechi, MacDonald N.
Etafo, Johnson
Adeyemi, Rashidat
Ella, Elijah E.
Aminu, Maryam
Gomerep, Simji S.
Eke, Matthew Afam
Ogunsanya, Olusola
Akpede, George O.
Asogun, Danny O.
Okogbenin, Sylvanus A.
Okokhere, Peter O.
Holst, Johan
Shaffer, Jeffrey G.
Schieffelin, John S.
Geisbert, Thomas W.
Saphire, Erica Ollmann
Happi, Christian T.
Grant, Donald S.
Garry, Robert F.
Branco, Luis M.
Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title_full Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title_fullStr Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title_full_unstemmed Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title_short Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages
title_sort antibodies from sierra leonean and nigerian lassa fever survivors cross-react with recombinant proteins representing lassa viruses of divergent lineages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525497/
https://www.ncbi.nlm.nih.gov/pubmed/32994446
http://dx.doi.org/10.1038/s41598-020-72539-w
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