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The Impact of Sustained Immunization Regimens on the Antibody Response to Oligomannose Glycans
[Image: see text] The high mannose patch (HMP) of the HIV envelope protein (Env) is the structure most frequently targeted by broadly neutralizing antibodies; therefore, many researchers have attempted to use mimics of this region as a vaccine immunogen. In our previous efforts, vaccinating rabbits...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091532/ https://www.ncbi.nlm.nih.gov/pubmed/32109354 http://dx.doi.org/10.1021/acschembio.0c00053 |
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author | Nguyen, Dung N. Redman, Richard L. Horiya, Satoru Bailey, Jennifer K. Xu, Bokai Stanfield, Robyn L. Temme, J. Sebastian LaBranche, Celia C. Wang, Shiyu Rodal, Avital A. Montefiori, David C. Wilson, Ian A. Krauss, Isaac J. |
author_facet | Nguyen, Dung N. Redman, Richard L. Horiya, Satoru Bailey, Jennifer K. Xu, Bokai Stanfield, Robyn L. Temme, J. Sebastian LaBranche, Celia C. Wang, Shiyu Rodal, Avital A. Montefiori, David C. Wilson, Ian A. Krauss, Isaac J. |
author_sort | Nguyen, Dung N. |
collection | PubMed |
description | [Image: see text] The high mannose patch (HMP) of the HIV envelope protein (Env) is the structure most frequently targeted by broadly neutralizing antibodies; therefore, many researchers have attempted to use mimics of this region as a vaccine immunogen. In our previous efforts, vaccinating rabbits with evolved HMP mimic glycopeptides containing Man(9) resulted in an overall antibody response targeting the glycan core and linker rather than the full glycan or Manα1→2Man tips of Man(9) glycans. A possible reason could be processing of our immunogen by host serum mannosidases. We sought to test whether more prolonged dosing could increase the antibody response to intact glycans, possibly by increasing the availability of intact Man(9) to germinal centers. Here, we describe a study investigating the impact of immunization regimen on antibody response by testing immunogen delivery through bolus, an exponential series of mini doses, or a continuously infusing mini-osmotic pump. Our results indicate that, with our glycopeptide immunogens, standard bolus immunization elicited the strongest HIV Env-binding antibody response, even though higher overall titers to the glycopeptide were elicited by the exponential and pump regimens. Antibody selectivity for intact glycan was, if anything, slightly better in the bolus-immunized animals. |
format | Online Article Text |
id | pubmed-7091532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70915322020-03-25 The Impact of Sustained Immunization Regimens on the Antibody Response to Oligomannose Glycans Nguyen, Dung N. Redman, Richard L. Horiya, Satoru Bailey, Jennifer K. Xu, Bokai Stanfield, Robyn L. Temme, J. Sebastian LaBranche, Celia C. Wang, Shiyu Rodal, Avital A. Montefiori, David C. Wilson, Ian A. Krauss, Isaac J. ACS Chem Biol [Image: see text] The high mannose patch (HMP) of the HIV envelope protein (Env) is the structure most frequently targeted by broadly neutralizing antibodies; therefore, many researchers have attempted to use mimics of this region as a vaccine immunogen. In our previous efforts, vaccinating rabbits with evolved HMP mimic glycopeptides containing Man(9) resulted in an overall antibody response targeting the glycan core and linker rather than the full glycan or Manα1→2Man tips of Man(9) glycans. A possible reason could be processing of our immunogen by host serum mannosidases. We sought to test whether more prolonged dosing could increase the antibody response to intact glycans, possibly by increasing the availability of intact Man(9) to germinal centers. Here, we describe a study investigating the impact of immunization regimen on antibody response by testing immunogen delivery through bolus, an exponential series of mini doses, or a continuously infusing mini-osmotic pump. Our results indicate that, with our glycopeptide immunogens, standard bolus immunization elicited the strongest HIV Env-binding antibody response, even though higher overall titers to the glycopeptide were elicited by the exponential and pump regimens. Antibody selectivity for intact glycan was, if anything, slightly better in the bolus-immunized animals. American Chemical Society 2020-02-28 2020-03-20 /pmc/articles/PMC7091532/ /pubmed/32109354 http://dx.doi.org/10.1021/acschembio.0c00053 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Nguyen, Dung N. Redman, Richard L. Horiya, Satoru Bailey, Jennifer K. Xu, Bokai Stanfield, Robyn L. Temme, J. Sebastian LaBranche, Celia C. Wang, Shiyu Rodal, Avital A. Montefiori, David C. Wilson, Ian A. Krauss, Isaac J. The Impact of Sustained Immunization Regimens on the Antibody Response to Oligomannose Glycans |
title | The Impact of Sustained Immunization Regimens on the
Antibody Response to Oligomannose Glycans |
title_full | The Impact of Sustained Immunization Regimens on the
Antibody Response to Oligomannose Glycans |
title_fullStr | The Impact of Sustained Immunization Regimens on the
Antibody Response to Oligomannose Glycans |
title_full_unstemmed | The Impact of Sustained Immunization Regimens on the
Antibody Response to Oligomannose Glycans |
title_short | The Impact of Sustained Immunization Regimens on the
Antibody Response to Oligomannose Glycans |
title_sort | impact of sustained immunization regimens on the
antibody response to oligomannose glycans |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091532/ https://www.ncbi.nlm.nih.gov/pubmed/32109354 http://dx.doi.org/10.1021/acschembio.0c00053 |
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