Cargando…
Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics
Eliciting broadly neutralizing antibodies (bNAbs) against the four dengue virus serotypes (DENV1-4) that are spreading into new territories is an important goal of vaccine design. To define bNAb targets, we characterized 28 antibodies belonging to expanded and hypermutated clonal families identified...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927745/ https://www.ncbi.nlm.nih.gov/pubmed/31820734 http://dx.doi.org/10.7554/eLife.52384 |
_version_ | 1783482347656577024 |
---|---|
author | Durham, Natasha D Agrawal, Aditi Waltari, Eric Croote, Derek Zanini, Fabio Fouch, Mallorie Davidson, Edgar Smith, Olivia Carabajal, Esteban Pak, John E Doranz, Benjamin J Robinson, Makeda Sanz, Ana M Albornoz, Ludwig L Rosso, Fernando Einav, Shirit Quake, Stephen R McCutcheon, Krista M Goo, Leslie |
author_facet | Durham, Natasha D Agrawal, Aditi Waltari, Eric Croote, Derek Zanini, Fabio Fouch, Mallorie Davidson, Edgar Smith, Olivia Carabajal, Esteban Pak, John E Doranz, Benjamin J Robinson, Makeda Sanz, Ana M Albornoz, Ludwig L Rosso, Fernando Einav, Shirit Quake, Stephen R McCutcheon, Krista M Goo, Leslie |
author_sort | Durham, Natasha D |
collection | PubMed |
description | Eliciting broadly neutralizing antibodies (bNAbs) against the four dengue virus serotypes (DENV1-4) that are spreading into new territories is an important goal of vaccine design. To define bNAb targets, we characterized 28 antibodies belonging to expanded and hypermutated clonal families identified by transcriptomic analysis of single plasmablasts from DENV-infected individuals. Among these, we identified J9 and J8, two somatically related bNAbs that potently neutralized DENV1-4. Mutagenesis studies showed that the major recognition determinants of these bNAbs are in E protein domain I, distinct from the only known class of human bNAbs against DENV with a well-defined epitope. B cell repertoire analysis from acute-phase peripheral blood suggested that J9 and J8 followed divergent somatic hypermutation pathways, and that a limited number of mutations was sufficient for neutralizing activity. Our study suggests multiple B cell evolutionary pathways leading to DENV bNAbs targeting a new epitope that can be exploited for vaccine design. |
format | Online Article Text |
id | pubmed-6927745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69277452019-12-26 Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics Durham, Natasha D Agrawal, Aditi Waltari, Eric Croote, Derek Zanini, Fabio Fouch, Mallorie Davidson, Edgar Smith, Olivia Carabajal, Esteban Pak, John E Doranz, Benjamin J Robinson, Makeda Sanz, Ana M Albornoz, Ludwig L Rosso, Fernando Einav, Shirit Quake, Stephen R McCutcheon, Krista M Goo, Leslie eLife Immunology and Inflammation Eliciting broadly neutralizing antibodies (bNAbs) against the four dengue virus serotypes (DENV1-4) that are spreading into new territories is an important goal of vaccine design. To define bNAb targets, we characterized 28 antibodies belonging to expanded and hypermutated clonal families identified by transcriptomic analysis of single plasmablasts from DENV-infected individuals. Among these, we identified J9 and J8, two somatically related bNAbs that potently neutralized DENV1-4. Mutagenesis studies showed that the major recognition determinants of these bNAbs are in E protein domain I, distinct from the only known class of human bNAbs against DENV with a well-defined epitope. B cell repertoire analysis from acute-phase peripheral blood suggested that J9 and J8 followed divergent somatic hypermutation pathways, and that a limited number of mutations was sufficient for neutralizing activity. Our study suggests multiple B cell evolutionary pathways leading to DENV bNAbs targeting a new epitope that can be exploited for vaccine design. eLife Sciences Publications, Ltd 2019-12-10 /pmc/articles/PMC6927745/ /pubmed/31820734 http://dx.doi.org/10.7554/eLife.52384 Text en © 2019, Durham et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology and Inflammation Durham, Natasha D Agrawal, Aditi Waltari, Eric Croote, Derek Zanini, Fabio Fouch, Mallorie Davidson, Edgar Smith, Olivia Carabajal, Esteban Pak, John E Doranz, Benjamin J Robinson, Makeda Sanz, Ana M Albornoz, Ludwig L Rosso, Fernando Einav, Shirit Quake, Stephen R McCutcheon, Krista M Goo, Leslie Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title | Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title_full | Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title_fullStr | Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title_full_unstemmed | Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title_short | Broadly neutralizing human antibodies against dengue virus identified by single B cell transcriptomics |
title_sort | broadly neutralizing human antibodies against dengue virus identified by single b cell transcriptomics |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927745/ https://www.ncbi.nlm.nih.gov/pubmed/31820734 http://dx.doi.org/10.7554/eLife.52384 |
work_keys_str_mv | AT durhamnatashad broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT agrawaladiti broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT waltarieric broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT crootederek broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT zaninifabio broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT fouchmallorie broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT davidsonedgar broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT smitholivia broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT carabajalesteban broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT pakjohne broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT doranzbenjaminj broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT robinsonmakeda broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT sanzanam broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT albornozludwigl broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT rossofernando broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT einavshirit broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT quakestephenr broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT mccutcheonkristam broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics AT gooleslie broadlyneutralizinghumanantibodiesagainstdenguevirusidentifiedbysinglebcelltranscriptomics |