The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT
ABSTRACT Perhaps the best-studied mucosal adjuvants are the bacterially derived ADP-ribosylating enterotoxins. This adjuvant family includes heat-labile enterotoxin of Escherichia coli (LT), cholera toxin (CT), and mutants or subunits of LT and CT. These proteins promote a multifaceted antigen-speci...
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American Society for Microbiology
2018
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oai:doaj.org-article:804b0ebcf2d743a4b4140eb36cdd18d92021-11-15T15:25:51ZThe Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT10.1128/mSphere.00215-182379-5042https://doaj.org/article/804b0ebcf2d743a4b4140eb36cdd18d92018-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00215-18https://doaj.org/toc/2379-5042ABSTRACT Perhaps the best-studied mucosal adjuvants are the bacterially derived ADP-ribosylating enterotoxins. This adjuvant family includes heat-labile enterotoxin of Escherichia coli (LT), cholera toxin (CT), and mutants or subunits of LT and CT. These proteins promote a multifaceted antigen-specific response, including inflammatory Th1, Th2, Th17, cytotoxic T lymphocytes (CTLs), and antibodies. However, more uniquely among adjuvant classes, they induce antigen-specific IgA antibodies and long-lasting memory to coadministered antigens when delivered mucosally or even parenterally. The purpose of this minireview is to describe the general properties, history and creation, preclinical studies, clinical studies, mechanisms of action, and considerations for use of the most promising enterotoxin-based adjuvant to date, LT(R192G/L211A) or dmLT. This review is timely due to completed, ongoing, and planned clinical investigations of dmLT in multiple vaccine formulations by government, nonprofit, and industry groups in the United States and abroad.John D. ClementsElizabeth B. NortonAmerican Society for MicrobiologyarticleadjuvantdmLTmucosal vaccinesMicrobiologyQR1-502ENmSphere, Vol 3, Iss 4 (2018) |
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adjuvant dmLT mucosal vaccines Microbiology QR1-502 |
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adjuvant dmLT mucosal vaccines Microbiology QR1-502 John D. Clements Elizabeth B. Norton The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
description |
ABSTRACT Perhaps the best-studied mucosal adjuvants are the bacterially derived ADP-ribosylating enterotoxins. This adjuvant family includes heat-labile enterotoxin of Escherichia coli (LT), cholera toxin (CT), and mutants or subunits of LT and CT. These proteins promote a multifaceted antigen-specific response, including inflammatory Th1, Th2, Th17, cytotoxic T lymphocytes (CTLs), and antibodies. However, more uniquely among adjuvant classes, they induce antigen-specific IgA antibodies and long-lasting memory to coadministered antigens when delivered mucosally or even parenterally. The purpose of this minireview is to describe the general properties, history and creation, preclinical studies, clinical studies, mechanisms of action, and considerations for use of the most promising enterotoxin-based adjuvant to date, LT(R192G/L211A) or dmLT. This review is timely due to completed, ongoing, and planned clinical investigations of dmLT in multiple vaccine formulations by government, nonprofit, and industry groups in the United States and abroad. |
format |
article |
author |
John D. Clements Elizabeth B. Norton |
author_facet |
John D. Clements Elizabeth B. Norton |
author_sort |
John D. Clements |
title |
The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
title_short |
The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
title_full |
The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
title_fullStr |
The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
title_full_unstemmed |
The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT |
title_sort |
mucosal vaccine adjuvant lt(r192g/l211a) or dmlt |
publisher |
American Society for Microbiology |
publishDate |
2018 |
url |
https://doaj.org/article/804b0ebcf2d743a4b4140eb36cdd18d9 |
work_keys_str_mv |
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