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CD28: Direct and Critical Receptor for Superantigen Toxins

Every adaptive immune response requires costimulation through the B7/CD28 axis, with CD28 on T-cells functioning as principal costimulatory receptor. Staphylococcal and streptococcal superantigen toxins hyperstimulate the T-cell-mediated immune response by orders of magnitude, inducing a lethal cyto...

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Detalles Bibliográficos
Autores principales: Kaempfer, Raymond, Arad, Gila, Levy, Revital, Hillman, Dalia, Nasie, Iris, Rotfogel, Ziv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798871/
https://www.ncbi.nlm.nih.gov/pubmed/24022021
http://dx.doi.org/10.3390/toxins5091531
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author Kaempfer, Raymond
Arad, Gila
Levy, Revital
Hillman, Dalia
Nasie, Iris
Rotfogel, Ziv
author_facet Kaempfer, Raymond
Arad, Gila
Levy, Revital
Hillman, Dalia
Nasie, Iris
Rotfogel, Ziv
author_sort Kaempfer, Raymond
collection PubMed
description Every adaptive immune response requires costimulation through the B7/CD28 axis, with CD28 on T-cells functioning as principal costimulatory receptor. Staphylococcal and streptococcal superantigen toxins hyperstimulate the T-cell-mediated immune response by orders of magnitude, inducing a lethal cytokine storm. We show that to elicit an inflammatory cytokine storm and lethality, superantigens must bind directly to CD28. Blocking access of the superantigen to its CD28 receptor with peptides mimicking the contact domains in either toxin or CD28 suffices to protect mice effectively from lethal shock. Our finding that CD28 is a direct receptor of superantigen toxins broadens the scope of microbial pathogen recognition mechanisms.
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spelling pubmed-37988712013-10-21 CD28: Direct and Critical Receptor for Superantigen Toxins Kaempfer, Raymond Arad, Gila Levy, Revital Hillman, Dalia Nasie, Iris Rotfogel, Ziv Toxins (Basel) Review Every adaptive immune response requires costimulation through the B7/CD28 axis, with CD28 on T-cells functioning as principal costimulatory receptor. Staphylococcal and streptococcal superantigen toxins hyperstimulate the T-cell-mediated immune response by orders of magnitude, inducing a lethal cytokine storm. We show that to elicit an inflammatory cytokine storm and lethality, superantigens must bind directly to CD28. Blocking access of the superantigen to its CD28 receptor with peptides mimicking the contact domains in either toxin or CD28 suffices to protect mice effectively from lethal shock. Our finding that CD28 is a direct receptor of superantigen toxins broadens the scope of microbial pathogen recognition mechanisms. MDPI 2013-09-09 /pmc/articles/PMC3798871/ /pubmed/24022021 http://dx.doi.org/10.3390/toxins5091531 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Kaempfer, Raymond
Arad, Gila
Levy, Revital
Hillman, Dalia
Nasie, Iris
Rotfogel, Ziv
CD28: Direct and Critical Receptor for Superantigen Toxins
title CD28: Direct and Critical Receptor for Superantigen Toxins
title_full CD28: Direct and Critical Receptor for Superantigen Toxins
title_fullStr CD28: Direct and Critical Receptor for Superantigen Toxins
title_full_unstemmed CD28: Direct and Critical Receptor for Superantigen Toxins
title_short CD28: Direct and Critical Receptor for Superantigen Toxins
title_sort cd28: direct and critical receptor for superantigen toxins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798871/
https://www.ncbi.nlm.nih.gov/pubmed/24022021
http://dx.doi.org/10.3390/toxins5091531
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