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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3815780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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