Cargando…
Superantigen antagonist peptides
The production of superantigenic exotoxins by Gram positive bacteria underlies the pathology of toxic shock syndrome. Future treatment strategies for superantigen-mediated diseases are likely to be directed at blocking the three-way interaction between superantigen, T cell receptor and major histoco...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2001
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC137266/ https://www.ncbi.nlm.nih.gov/pubmed/11299061 http://dx.doi.org/10.1186/cc986 |
_version_ | 1782120418273918976 |
---|---|
author | Llewelyn, Martin Cohen, Jonathan |
author_facet | Llewelyn, Martin Cohen, Jonathan |
author_sort | Llewelyn, Martin |
collection | PubMed |
description | The production of superantigenic exotoxins by Gram positive bacteria underlies the pathology of toxic shock syndrome. Future treatment strategies for superantigen-mediated diseases are likely to be directed at blocking the three-way interaction between superantigen, T cell receptor and major histocompatibility class II molecule, which inititates an excessive and disordered inflammatory response. In this article, we review the first published data to address one such strategy in the context of other recognised and experimental treatments. |
format | Text |
id | pubmed-137266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1372662003-02-27 Superantigen antagonist peptides Llewelyn, Martin Cohen, Jonathan Crit Care Commentary The production of superantigenic exotoxins by Gram positive bacteria underlies the pathology of toxic shock syndrome. Future treatment strategies for superantigen-mediated diseases are likely to be directed at blocking the three-way interaction between superantigen, T cell receptor and major histocompatibility class II molecule, which inititates an excessive and disordered inflammatory response. In this article, we review the first published data to address one such strategy in the context of other recognised and experimental treatments. BioMed Central 2001 2001-02-26 /pmc/articles/PMC137266/ /pubmed/11299061 http://dx.doi.org/10.1186/cc986 Text en Copyright © 2001 BioMed Central Ltd |
spellingShingle | Commentary Llewelyn, Martin Cohen, Jonathan Superantigen antagonist peptides |
title | Superantigen antagonist peptides |
title_full | Superantigen antagonist peptides |
title_fullStr | Superantigen antagonist peptides |
title_full_unstemmed | Superantigen antagonist peptides |
title_short | Superantigen antagonist peptides |
title_sort | superantigen antagonist peptides |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC137266/ https://www.ncbi.nlm.nih.gov/pubmed/11299061 http://dx.doi.org/10.1186/cc986 |
work_keys_str_mv | AT llewelynmartin superantigenantagonistpeptides AT cohenjonathan superantigenantagonistpeptides |