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Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection
Both rectal and vaginal mucosal surfaces serve as transmission routes for pathogenic microorganisms. Vaccination through large intestinal mucosa, previously proven protective for both mucosal sites in animal studies, can be achieved successfully by direct intra-colorectal (i.c.r.) administration, wh...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475749/ https://www.ncbi.nlm.nih.gov/pubmed/22797811 http://dx.doi.org/10.1038/nm.2866 |
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author | Zhu, Qing Talton, James Zhang, Guofeng Cunningham, Tshaka Wang, Zijian Waters, Robert C. Kirk, James Eppler, Bärbel Dennis M, Klinman Sui, Yongjun Gagnon, Susan Belyakov, Igor M. Mumper, Russell J. Berzofsky, Jay A. |
author_facet | Zhu, Qing Talton, James Zhang, Guofeng Cunningham, Tshaka Wang, Zijian Waters, Robert C. Kirk, James Eppler, Bärbel Dennis M, Klinman Sui, Yongjun Gagnon, Susan Belyakov, Igor M. Mumper, Russell J. Berzofsky, Jay A. |
author_sort | Zhu, Qing |
collection | PubMed |
description | Both rectal and vaginal mucosal surfaces serve as transmission routes for pathogenic microorganisms. Vaccination through large intestinal mucosa, previously proven protective for both mucosal sites in animal studies, can be achieved successfully by direct intra-colorectal (i.c.r.) administration, which is, however, clinically impractical. Oral delivery seems preferable, but risks vaccine destruction in the upper gastrointestinal tract. Therefore, we designed a large intestine-targeted oral delivery with pH-dependent microparticles containing vaccine nanoparticles, which induced colorectal immunity in mice comparably to colorectal vaccination and protected against rectal or vaginal viral challenge. Conversely, vaccine targeted to the small intestine induced only small intestinal immunity and provided no rectal or vaginal protection, demonstrating functional compartmentalization within the gut mucosal immune system. Therefore, using this oral vaccine delivery system to target the large intestine, but not the small intestine, may represent a feasible novel strategy for immune protection of rectal and vaginal mucosa. |
format | Online Article Text |
id | pubmed-3475749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34757492013-07-25 Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection Zhu, Qing Talton, James Zhang, Guofeng Cunningham, Tshaka Wang, Zijian Waters, Robert C. Kirk, James Eppler, Bärbel Dennis M, Klinman Sui, Yongjun Gagnon, Susan Belyakov, Igor M. Mumper, Russell J. Berzofsky, Jay A. Nat Med Article Both rectal and vaginal mucosal surfaces serve as transmission routes for pathogenic microorganisms. Vaccination through large intestinal mucosa, previously proven protective for both mucosal sites in animal studies, can be achieved successfully by direct intra-colorectal (i.c.r.) administration, which is, however, clinically impractical. Oral delivery seems preferable, but risks vaccine destruction in the upper gastrointestinal tract. Therefore, we designed a large intestine-targeted oral delivery with pH-dependent microparticles containing vaccine nanoparticles, which induced colorectal immunity in mice comparably to colorectal vaccination and protected against rectal or vaginal viral challenge. Conversely, vaccine targeted to the small intestine induced only small intestinal immunity and provided no rectal or vaginal protection, demonstrating functional compartmentalization within the gut mucosal immune system. Therefore, using this oral vaccine delivery system to target the large intestine, but not the small intestine, may represent a feasible novel strategy for immune protection of rectal and vaginal mucosa. 2012-07-15 2012-08 /pmc/articles/PMC3475749/ /pubmed/22797811 http://dx.doi.org/10.1038/nm.2866 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Zhu, Qing Talton, James Zhang, Guofeng Cunningham, Tshaka Wang, Zijian Waters, Robert C. Kirk, James Eppler, Bärbel Dennis M, Klinman Sui, Yongjun Gagnon, Susan Belyakov, Igor M. Mumper, Russell J. Berzofsky, Jay A. Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title | Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title_full | Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title_fullStr | Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title_full_unstemmed | Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title_short | Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
title_sort | large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475749/ https://www.ncbi.nlm.nih.gov/pubmed/22797811 http://dx.doi.org/10.1038/nm.2866 |
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