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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
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.
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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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