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CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes
CD8(+) T cells are crucial for control of a number of medically important protozoan parasites, including Trypanosoma cruzi, the agent of human Chagas disease. Yet, in contrast to the wealth of information from viral and bacterial infections, little is known about the antigen specificity or the gener...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526708/ https://www.ncbi.nlm.nih.gov/pubmed/16879036 http://dx.doi.org/10.1371/journal.ppat.0020077 |
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author | Martin, Diana L Weatherly, D. Brent Laucella, Susana A Cabinian, Melissa A Crim, Matthew T Sullivan, Susan Heiges, Mark Craven, Sarah H Rosenberg, Charles S Collins, Matthew H Sette, Alessandro Postan, Miriam Tarleton, Rick L |
author_facet | Martin, Diana L Weatherly, D. Brent Laucella, Susana A Cabinian, Melissa A Crim, Matthew T Sullivan, Susan Heiges, Mark Craven, Sarah H Rosenberg, Charles S Collins, Matthew H Sette, Alessandro Postan, Miriam Tarleton, Rick L |
author_sort | Martin, Diana L |
collection | PubMed |
description | CD8(+) T cells are crucial for control of a number of medically important protozoan parasites, including Trypanosoma cruzi, the agent of human Chagas disease. Yet, in contrast to the wealth of information from viral and bacterial infections, little is known about the antigen specificity or the general development of effector and memory T-cell responses in hosts infected with protozoans. In this study we report on a wide-scale screen for the dominant parasite peptides recognized by CD8(+) T cells in T. cruzi–infected mice and humans. This analysis demonstrates that in both hosts the CD8(+) T-cell response is highly focused on epitopes encoded by members of the large trans-sialidase family of genes. Responses to a restricted set of immunodominant peptides were especially pronounced in T. cruzi–infected mice, with more than 30% of the CD8(+) T-cell response at the peak of infection specific for two major groups of trans-sialidase peptides. Experimental models also demonstrated that the dominance patterns vary depending on the infective strain of T. cruzi, suggesting that immune evasion may be occurring at a population rather than single-parasite level. |
format | Text |
id | pubmed-1526708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-15267082006-09-07 CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes Martin, Diana L Weatherly, D. Brent Laucella, Susana A Cabinian, Melissa A Crim, Matthew T Sullivan, Susan Heiges, Mark Craven, Sarah H Rosenberg, Charles S Collins, Matthew H Sette, Alessandro Postan, Miriam Tarleton, Rick L PLoS Pathog Research Article CD8(+) T cells are crucial for control of a number of medically important protozoan parasites, including Trypanosoma cruzi, the agent of human Chagas disease. Yet, in contrast to the wealth of information from viral and bacterial infections, little is known about the antigen specificity or the general development of effector and memory T-cell responses in hosts infected with protozoans. In this study we report on a wide-scale screen for the dominant parasite peptides recognized by CD8(+) T cells in T. cruzi–infected mice and humans. This analysis demonstrates that in both hosts the CD8(+) T-cell response is highly focused on epitopes encoded by members of the large trans-sialidase family of genes. Responses to a restricted set of immunodominant peptides were especially pronounced in T. cruzi–infected mice, with more than 30% of the CD8(+) T-cell response at the peak of infection specific for two major groups of trans-sialidase peptides. Experimental models also demonstrated that the dominance patterns vary depending on the infective strain of T. cruzi, suggesting that immune evasion may be occurring at a population rather than single-parasite level. Public Library of Science 2006-08 2006-08-04 /pmc/articles/PMC1526708/ /pubmed/16879036 http://dx.doi.org/10.1371/journal.ppat.0020077 Text en © 2006 Martin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Martin, Diana L Weatherly, D. Brent Laucella, Susana A Cabinian, Melissa A Crim, Matthew T Sullivan, Susan Heiges, Mark Craven, Sarah H Rosenberg, Charles S Collins, Matthew H Sette, Alessandro Postan, Miriam Tarleton, Rick L CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title | CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title_full | CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title_fullStr | CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title_full_unstemmed | CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title_short | CD8(+) T-Cell Responses to Trypanosoma cruzi Are Highly Focused on Strain-Variant trans-Sialidase Epitopes |
title_sort | cd8(+) t-cell responses to trypanosoma cruzi are highly focused on strain-variant trans-sialidase epitopes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526708/ https://www.ncbi.nlm.nih.gov/pubmed/16879036 http://dx.doi.org/10.1371/journal.ppat.0020077 |
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