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Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential
Malaria infection crisis, at which the parasitemia drops precipitously and the parasite loses infectivity to the mosquito vector, occurs in many natural malaria systems, and has not been explained. We demonstrate that in a simian malaria parasite (Plasmodium cynomolgi in its natural host, the toque...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118826/ https://www.ncbi.nlm.nih.gov/pubmed/1900073 |
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collection | PubMed |
description | Malaria infection crisis, at which the parasitemia drops precipitously and the parasite loses infectivity to the mosquito vector, occurs in many natural malaria systems, and has not been explained. We demonstrate that in a simian malaria parasite (Plasmodium cynomolgi in its natural host, the toque monkey), the loss of infectivity during crisis is due to the death of circulating intraerythrocytic gametocytes mediated by crisis serum. These parasite-killing effects in crisis serum are due to the presence in the serum of cytokines tumor necrosis factor and interferon gamma, which are produced by the host as a result of the malaria infection. The killing activity of each cytokine is absolutely dependent upon the presence of additional, as yet unidentified factor(s) in the crisis serum. |
format | Text |
id | pubmed-2118826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21188262008-04-17 Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential J Exp Med Articles Malaria infection crisis, at which the parasitemia drops precipitously and the parasite loses infectivity to the mosquito vector, occurs in many natural malaria systems, and has not been explained. We demonstrate that in a simian malaria parasite (Plasmodium cynomolgi in its natural host, the toque monkey), the loss of infectivity during crisis is due to the death of circulating intraerythrocytic gametocytes mediated by crisis serum. These parasite-killing effects in crisis serum are due to the presence in the serum of cytokines tumor necrosis factor and interferon gamma, which are produced by the host as a result of the malaria infection. The killing activity of each cytokine is absolutely dependent upon the presence of additional, as yet unidentified factor(s) in the crisis serum. The Rockefeller University Press 1991-03-01 /pmc/articles/PMC2118826/ /pubmed/1900073 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 Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title | Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title_full | Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title_fullStr | Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title_full_unstemmed | Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title_short | Cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
title_sort | cytokines kill malaria parasites during infection crisis: extracellular complementary factors are essential |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118826/ https://www.ncbi.nlm.nih.gov/pubmed/1900073 |