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Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization
Llamas (Lama glama) naturally produce heavy chain–only antibodies (Abs) in addition to conventional Abs. The variable regions (VHH) in these heavy chain–only Abs demonstrate comparable affinity and specificity for antigens to conventional immunoglobulins despite their much smaller size. To date, imm...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371729/ https://www.ncbi.nlm.nih.gov/pubmed/22641382 http://dx.doi.org/10.1084/jem.20112655 |
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author | McCoy, Laura E. Quigley, Anna Forsman Strokappe, Nika M. Bulmer-Thomas, Bianca Seaman, Michael S. Mortier, Daniella Rutten, Lucy Chander, Nikita Edwards, Carolyn J. Ketteler, Robin Davis, David Verrips, Theo Weiss, Robin A. |
author_facet | McCoy, Laura E. Quigley, Anna Forsman Strokappe, Nika M. Bulmer-Thomas, Bianca Seaman, Michael S. Mortier, Daniella Rutten, Lucy Chander, Nikita Edwards, Carolyn J. Ketteler, Robin Davis, David Verrips, Theo Weiss, Robin A. |
author_sort | McCoy, Laura E. |
collection | PubMed |
description | Llamas (Lama glama) naturally produce heavy chain–only antibodies (Abs) in addition to conventional Abs. The variable regions (VHH) in these heavy chain–only Abs demonstrate comparable affinity and specificity for antigens to conventional immunoglobulins despite their much smaller size. To date, immunizations in humans and animal models have yielded only Abs with limited ability to neutralize HIV-1. In this study, a VHH phagemid library generated from a llama that was multiply immunized with recombinant trimeric HIV-1 envelope proteins (Envs) was screened directly for HIV-1 neutralization. One VHH, L8CJ3 (J3), neutralized 96 of 100 tested HIV-1 strains, encompassing subtypes A, B, C, D, BC, AE, AG, AC, ACD, CD, and G. J3 also potently neutralized chimeric simian-HIV strains with HIV subtypes B and C Env. The sequence of J3 is highly divergent from previous anti–HIV-1 VHH and its own germline sequence. J3 achieves broad and potent neutralization of HIV-1 via interaction with the CD4-binding site of HIV-1 Env. This study may represent a new benchmark for immunogens to be included in B cell–based vaccines and supports the development of VHH as anti–HIV-1 microbicides. |
format | Online Article Text |
id | pubmed-3371729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33717292012-12-04 Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization McCoy, Laura E. Quigley, Anna Forsman Strokappe, Nika M. Bulmer-Thomas, Bianca Seaman, Michael S. Mortier, Daniella Rutten, Lucy Chander, Nikita Edwards, Carolyn J. Ketteler, Robin Davis, David Verrips, Theo Weiss, Robin A. J Exp Med Article Llamas (Lama glama) naturally produce heavy chain–only antibodies (Abs) in addition to conventional Abs. The variable regions (VHH) in these heavy chain–only Abs demonstrate comparable affinity and specificity for antigens to conventional immunoglobulins despite their much smaller size. To date, immunizations in humans and animal models have yielded only Abs with limited ability to neutralize HIV-1. In this study, a VHH phagemid library generated from a llama that was multiply immunized with recombinant trimeric HIV-1 envelope proteins (Envs) was screened directly for HIV-1 neutralization. One VHH, L8CJ3 (J3), neutralized 96 of 100 tested HIV-1 strains, encompassing subtypes A, B, C, D, BC, AE, AG, AC, ACD, CD, and G. J3 also potently neutralized chimeric simian-HIV strains with HIV subtypes B and C Env. The sequence of J3 is highly divergent from previous anti–HIV-1 VHH and its own germline sequence. J3 achieves broad and potent neutralization of HIV-1 via interaction with the CD4-binding site of HIV-1 Env. This study may represent a new benchmark for immunogens to be included in B cell–based vaccines and supports the development of VHH as anti–HIV-1 microbicides. The Rockefeller University Press 2012-06-04 /pmc/articles/PMC3371729/ /pubmed/22641382 http://dx.doi.org/10.1084/jem.20112655 Text en © 2012 McCoy et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article McCoy, Laura E. Quigley, Anna Forsman Strokappe, Nika M. Bulmer-Thomas, Bianca Seaman, Michael S. Mortier, Daniella Rutten, Lucy Chander, Nikita Edwards, Carolyn J. Ketteler, Robin Davis, David Verrips, Theo Weiss, Robin A. Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title | Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title_full | Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title_fullStr | Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title_full_unstemmed | Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title_short | Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization |
title_sort | potent and broad neutralization of hiv-1 by a llama antibody elicited by immunization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371729/ https://www.ncbi.nlm.nih.gov/pubmed/22641382 http://dx.doi.org/10.1084/jem.20112655 |
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