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Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies
Induction of broadly neutralizing antibodies (bnAbs) is a primary goal of HIV vaccine development. VRC01-class bnAbs are important vaccine leads because their precursor B cells targeted by an engineered priming immunogen are relatively common among humans. This priming immunogen has demonstrated the...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018249/ https://www.ncbi.nlm.nih.gov/pubmed/27610570 http://dx.doi.org/10.1016/j.cell.2016.08.005 |
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author | Briney, Bryan Sok, Devin Jardine, Joseph G. Kulp, Daniel W. Skog, Patrick Menis, Sergey Jacak, Ronald Kalyuzhniy, Oleksandr de Val, Natalia Sesterhenn, Fabian Le, Khoa M. Ramos, Alejandra Jones, Meaghan Saye-Francisco, Karen L. Blane, Tanya R. Spencer, Skye Georgeson, Erik Hu, Xiaozhen Ozorowski, Gabriel Adachi, Yumiko Kubitz, Michael Sarkar, Anita Wilson, Ian A. Ward, Andrew B. Nemazee, David Burton, Dennis R. Schief, William R. |
author_facet | Briney, Bryan Sok, Devin Jardine, Joseph G. Kulp, Daniel W. Skog, Patrick Menis, Sergey Jacak, Ronald Kalyuzhniy, Oleksandr de Val, Natalia Sesterhenn, Fabian Le, Khoa M. Ramos, Alejandra Jones, Meaghan Saye-Francisco, Karen L. Blane, Tanya R. Spencer, Skye Georgeson, Erik Hu, Xiaozhen Ozorowski, Gabriel Adachi, Yumiko Kubitz, Michael Sarkar, Anita Wilson, Ian A. Ward, Andrew B. Nemazee, David Burton, Dennis R. Schief, William R. |
author_sort | Briney, Bryan |
collection | PubMed |
description | Induction of broadly neutralizing antibodies (bnAbs) is a primary goal of HIV vaccine development. VRC01-class bnAbs are important vaccine leads because their precursor B cells targeted by an engineered priming immunogen are relatively common among humans. This priming immunogen has demonstrated the ability to initiate a bnAb response in animal models, but recall and maturation toward bnAb development has not been shown. Here, we report the development of boosting immunogens designed to guide the genetic and functional maturation of previously primed VRC01-class precursors. Boosting a transgenic mouse model expressing germline VRC01 heavy chains produced broad neutralization of near-native isolates (N276A) and weak neutralization of fully native HIV. Functional and genetic characteristics indicate that the boosted mAbs are consistent with partially mature VRC01-class antibodies and place them on a maturation trajectory that leads toward mature VRC01-class bnAbs. The results show how reductionist sequential immunization can guide maturation of HIV bnAb responses. |
format | Online Article Text |
id | pubmed-5018249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50182492016-09-19 Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies Briney, Bryan Sok, Devin Jardine, Joseph G. Kulp, Daniel W. Skog, Patrick Menis, Sergey Jacak, Ronald Kalyuzhniy, Oleksandr de Val, Natalia Sesterhenn, Fabian Le, Khoa M. Ramos, Alejandra Jones, Meaghan Saye-Francisco, Karen L. Blane, Tanya R. Spencer, Skye Georgeson, Erik Hu, Xiaozhen Ozorowski, Gabriel Adachi, Yumiko Kubitz, Michael Sarkar, Anita Wilson, Ian A. Ward, Andrew B. Nemazee, David Burton, Dennis R. Schief, William R. Cell Article Induction of broadly neutralizing antibodies (bnAbs) is a primary goal of HIV vaccine development. VRC01-class bnAbs are important vaccine leads because their precursor B cells targeted by an engineered priming immunogen are relatively common among humans. This priming immunogen has demonstrated the ability to initiate a bnAb response in animal models, but recall and maturation toward bnAb development has not been shown. Here, we report the development of boosting immunogens designed to guide the genetic and functional maturation of previously primed VRC01-class precursors. Boosting a transgenic mouse model expressing germline VRC01 heavy chains produced broad neutralization of near-native isolates (N276A) and weak neutralization of fully native HIV. Functional and genetic characteristics indicate that the boosted mAbs are consistent with partially mature VRC01-class antibodies and place them on a maturation trajectory that leads toward mature VRC01-class bnAbs. The results show how reductionist sequential immunization can guide maturation of HIV bnAb responses. Cell Press 2016-09-08 /pmc/articles/PMC5018249/ /pubmed/27610570 http://dx.doi.org/10.1016/j.cell.2016.08.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Briney, Bryan Sok, Devin Jardine, Joseph G. Kulp, Daniel W. Skog, Patrick Menis, Sergey Jacak, Ronald Kalyuzhniy, Oleksandr de Val, Natalia Sesterhenn, Fabian Le, Khoa M. Ramos, Alejandra Jones, Meaghan Saye-Francisco, Karen L. Blane, Tanya R. Spencer, Skye Georgeson, Erik Hu, Xiaozhen Ozorowski, Gabriel Adachi, Yumiko Kubitz, Michael Sarkar, Anita Wilson, Ian A. Ward, Andrew B. Nemazee, David Burton, Dennis R. Schief, William R. Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title | Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title_full | Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title_fullStr | Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title_full_unstemmed | Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title_short | Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies |
title_sort | tailored immunogens direct affinity maturation toward hiv neutralizing antibodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018249/ https://www.ncbi.nlm.nih.gov/pubmed/27610570 http://dx.doi.org/10.1016/j.cell.2016.08.005 |
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