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J‐LEAPS peptide and LEAPS dendritic cell vaccines

The J‐LEAPS vaccines contain a peptide from β‐2‐microglobulin covalently attached to disease‐related peptides of 8–30 amino acids which contain a T cell epitope. The J‐LEAPS vaccines can initiate a protective Th1 immune response or modulate an ongoing Th17 autoimmune response to the peptide. J‐LEAPS...

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Detalles Bibliográficos
Autores principales: Rosenthal, Ken S., Taylor, Patricia, Zimmerman, Daniel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815780/
https://www.ncbi.nlm.nih.gov/pubmed/21895992
http://dx.doi.org/10.1111/j.1751-7915.2011.00278.x
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author Rosenthal, Ken S.
Taylor, Patricia
Zimmerman, Daniel H.
author_facet Rosenthal, Ken S.
Taylor, Patricia
Zimmerman, Daniel H.
author_sort Rosenthal, Ken S.
collection PubMed
description The J‐LEAPS vaccines contain a peptide from β‐2‐microglobulin covalently attached to disease‐related peptides of 8–30 amino acids which contain a T cell epitope. The J‐LEAPS vaccines can initiate a protective Th1 immune response or modulate an ongoing Th17 autoimmune response to the peptide. J‐LEAPS vaccines activate and direct the nature of the subsequent immune response by promoting the maturation of precursor cells into a unique type of dendritic cell that produces interleukin 12, but not IL‐1 or tumour necrosis factor, and presents the antigenic peptide to T cells. Adoptive transfer of JgD‐LEAPS dendritic cells, matured with an anti‐HSV‐1 vaccine, promoted antigen‐specific Th1 protection against lethal challenge with the virus. J‐LEAPS peptide immunogens and J‐LEAPS dendritic cell vaccines have potential applications for antimicrobial prevention and therapy, treatment of autoimmune diseases, and for cancer immunotherapy.
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spelling pubmed-38157802014-02-12 J‐LEAPS peptide and LEAPS dendritic cell vaccines Rosenthal, Ken S. Taylor, Patricia Zimmerman, Daniel H. Microb Biotechnol Minireviews The J‐LEAPS vaccines contain a peptide from β‐2‐microglobulin covalently attached to disease‐related peptides of 8–30 amino acids which contain a T cell epitope. The J‐LEAPS vaccines can initiate a protective Th1 immune response or modulate an ongoing Th17 autoimmune response to the peptide. J‐LEAPS vaccines activate and direct the nature of the subsequent immune response by promoting the maturation of precursor cells into a unique type of dendritic cell that produces interleukin 12, but not IL‐1 or tumour necrosis factor, and presents the antigenic peptide to T cells. Adoptive transfer of JgD‐LEAPS dendritic cells, matured with an anti‐HSV‐1 vaccine, promoted antigen‐specific Th1 protection against lethal challenge with the virus. J‐LEAPS peptide immunogens and J‐LEAPS dendritic cell vaccines have potential applications for antimicrobial prevention and therapy, treatment of autoimmune diseases, and for cancer immunotherapy. Blackwell Publishing Ltd 2012-03 2012-02-20 /pmc/articles/PMC3815780/ /pubmed/21895992 http://dx.doi.org/10.1111/j.1751-7915.2011.00278.x Text en Copyright © 2011 The Authors. Journal compilation © 2011 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Minireviews
Rosenthal, Ken S.
Taylor, Patricia
Zimmerman, Daniel H.
J‐LEAPS peptide and LEAPS dendritic cell vaccines
title J‐LEAPS peptide and LEAPS dendritic cell vaccines
title_full J‐LEAPS peptide and LEAPS dendritic cell vaccines
title_fullStr J‐LEAPS peptide and LEAPS dendritic cell vaccines
title_full_unstemmed J‐LEAPS peptide and LEAPS dendritic cell vaccines
title_short J‐LEAPS peptide and LEAPS dendritic cell vaccines
title_sort j‐leaps peptide and leaps dendritic cell vaccines
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815780/
https://www.ncbi.nlm.nih.gov/pubmed/21895992
http://dx.doi.org/10.1111/j.1751-7915.2011.00278.x
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