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CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects
BACKGROUND: Adoptive immune and vaccine therapies have been used to prevent cytomegalovirus (CMV) disease in recipients of hematopoietic progenitor cell transplants, but the nature of T cell responses to CMV have not been completely characterized. METHODS: Peptide pools and individual peptides deriv...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851947/ https://www.ncbi.nlm.nih.gov/pubmed/17391521 http://dx.doi.org/10.1186/1479-5876-5-17 |
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author | Slezak, Stefanie L Bettinotti, Maria Selleri, Silvia Adams, Sharon Marincola, Francesco M Stroncek, David F |
author_facet | Slezak, Stefanie L Bettinotti, Maria Selleri, Silvia Adams, Sharon Marincola, Francesco M Stroncek, David F |
author_sort | Slezak, Stefanie L |
collection | PubMed |
description | BACKGROUND: Adoptive immune and vaccine therapies have been used to prevent cytomegalovirus (CMV) disease in recipients of hematopoietic progenitor cell transplants, but the nature of T cell responses to CMV have not been completely characterized. METHODS: Peptide pools and individual peptides derived from the immune-dominant CMV proteins pp65 and IE-1 and antigen-specific, cytokine flow cytometry were used to characterize the prevalence and frequency of CD4+ and CD8+ memory T cells in 20 healthy CMV-seropositive subjects. RESULTS: CD8+ T cell responses to pp65 were detected in 35% of subjects and to IE-1 in 40% of subjects. CD4+ T cell responses to pp65 were detected in 50% of subjects, but none were detected to IE-1. Several new IE-1 HLA class I epitopes were identified, including 4 restricted to HLA-C antigens. One region of IE-1 spanning amino acids 300 to 327 was rich in class I epitopes. The HLA class I restrictions of IE-1 peptides were more promiscuous than those of pp65 peptides. CONCLUSION: Since naturally occurring CD4+ and CD8+ T cell responses to pp65 were detectable in many subjects, but only CD8+ T cell responses to IE-1 were detected, pp65 may be better than IE-1 for use in vaccine and adoptive immune therapies. |
format | Text |
id | pubmed-1851947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18519472007-04-13 CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects Slezak, Stefanie L Bettinotti, Maria Selleri, Silvia Adams, Sharon Marincola, Francesco M Stroncek, David F J Transl Med Research BACKGROUND: Adoptive immune and vaccine therapies have been used to prevent cytomegalovirus (CMV) disease in recipients of hematopoietic progenitor cell transplants, but the nature of T cell responses to CMV have not been completely characterized. METHODS: Peptide pools and individual peptides derived from the immune-dominant CMV proteins pp65 and IE-1 and antigen-specific, cytokine flow cytometry were used to characterize the prevalence and frequency of CD4+ and CD8+ memory T cells in 20 healthy CMV-seropositive subjects. RESULTS: CD8+ T cell responses to pp65 were detected in 35% of subjects and to IE-1 in 40% of subjects. CD4+ T cell responses to pp65 were detected in 50% of subjects, but none were detected to IE-1. Several new IE-1 HLA class I epitopes were identified, including 4 restricted to HLA-C antigens. One region of IE-1 spanning amino acids 300 to 327 was rich in class I epitopes. The HLA class I restrictions of IE-1 peptides were more promiscuous than those of pp65 peptides. CONCLUSION: Since naturally occurring CD4+ and CD8+ T cell responses to pp65 were detectable in many subjects, but only CD8+ T cell responses to IE-1 were detected, pp65 may be better than IE-1 for use in vaccine and adoptive immune therapies. BioMed Central 2007-03-28 /pmc/articles/PMC1851947/ /pubmed/17391521 http://dx.doi.org/10.1186/1479-5876-5-17 Text en Copyright © 2007 Slezak et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Slezak, Stefanie L Bettinotti, Maria Selleri, Silvia Adams, Sharon Marincola, Francesco M Stroncek, David F CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title | CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title_full | CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title_fullStr | CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title_full_unstemmed | CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title_short | CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects |
title_sort | cmv pp65 and ie-1 t cell epitopes recognized by healthy subjects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851947/ https://www.ncbi.nlm.nih.gov/pubmed/17391521 http://dx.doi.org/10.1186/1479-5876-5-17 |
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