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Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes
Irradiated malaria sporozoites can induce CD8+ T cells that are required for protection against infection. However, the parasite antigens targeted by this immune response are unknown. We have discovered a 16-amino acid epitope from the Plasmodium yoelii circumsporozoite (CS) protein that is recogniz...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1990
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187765/ https://www.ncbi.nlm.nih.gov/pubmed/1689762 |
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collection | PubMed |
description | Irradiated malaria sporozoites can induce CD8+ T cells that are required for protection against infection. However, the parasite antigens targeted by this immune response are unknown. We have discovered a 16-amino acid epitope from the Plasmodium yoelii circumsporozoite (CS) protein that is recognized by cytotoxic T cells from immune mice. Lymphocytes stimulated with this peptide can kill P. yoelii liver stage parasites in vitro in an MHC-restricted, antigen- specific manner. Thus, epitopes from the CS protein are presented on the surface of infected hepatocytes and can be targets for T cells, even though intact CS protein has not been detected on the surface of the infected hepatocyte. A vaccine that induced CTL to parasite antigens might protect humans against malaria by eliminating liver stage parasites. |
format | Text |
id | pubmed-2187765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21877652008-04-17 Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes J Exp Med Articles Irradiated malaria sporozoites can induce CD8+ T cells that are required for protection against infection. However, the parasite antigens targeted by this immune response are unknown. We have discovered a 16-amino acid epitope from the Plasmodium yoelii circumsporozoite (CS) protein that is recognized by cytotoxic T cells from immune mice. Lymphocytes stimulated with this peptide can kill P. yoelii liver stage parasites in vitro in an MHC-restricted, antigen- specific manner. Thus, epitopes from the CS protein are presented on the surface of infected hepatocytes and can be targets for T cells, even though intact CS protein has not been detected on the surface of the infected hepatocyte. A vaccine that induced CTL to parasite antigens might protect humans against malaria by eliminating liver stage parasites. The Rockefeller University Press 1990-03-01 /pmc/articles/PMC2187765/ /pubmed/1689762 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title | Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title_full | Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title_fullStr | Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title_full_unstemmed | Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title_short | Cytotoxic T cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
title_sort | cytotoxic t cells recognize a peptide from the circumsporozoite protein on malaria-infected hepatocytes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187765/ https://www.ncbi.nlm.nih.gov/pubmed/1689762 |