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Immune Evasion Strategies of Trypanosoma cruzi
Microbes have evolved a diverse range of strategies to subvert the host immune system. The protozoan parasite Trypanosoma cruzi, the causative agent of Chagas disease, provides a good example of such adaptations. This parasite targets a broad spectrum of host tissues including both peripheral and ce...
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Published in: | Journal of immunology research 2015-01, Vol.2015 (2015), p.1-7 |
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description | Microbes have evolved a diverse range of strategies to subvert the host immune system. The protozoan parasite Trypanosoma cruzi, the causative agent of Chagas disease, provides a good example of such adaptations. This parasite targets a broad spectrum of host tissues including both peripheral and central lymphoid tissues. Rapid colonization of the host gives rise to a systemic acute response which the parasite must overcome. The parasite in fact undermines both innate and adaptive immunity. It interferes with the antigen presenting function of dendritic cells via an action on host sialic acid-binding Ig-like lectin receptors. These receptors also induce suppression of CD4+ T cells responses, and we presented evidence that the sialylation of parasite-derived mucins is required for the inhibitory effects on CD4 T cells. In this review we highlight the major mechanisms used by Trypanosoma cruzi to overcome host immunity and discuss the role of parasite colonization of the central thymic lymphoid tissue in chronic disease. |
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The protozoan parasite Trypanosoma cruzi, the causative agent of Chagas disease, provides a good example of such adaptations. This parasite targets a broad spectrum of host tissues including both peripheral and central lymphoid tissues. Rapid colonization of the host gives rise to a systemic acute response which the parasite must overcome. The parasite in fact undermines both innate and adaptive immunity. It interferes with the antigen presenting function of dendritic cells via an action on host sialic acid-binding Ig-like lectin receptors. These receptors also induce suppression of CD4+ T cells responses, and we presented evidence that the sialylation of parasite-derived mucins is required for the inhibitory effects on CD4 T cells. In this review we highlight the major mechanisms used by Trypanosoma cruzi to overcome host immunity and discuss the role of parasite colonization of the central thymic lymphoid tissue in chronic disease.</description><identifier>ISSN: 2314-8861</identifier><identifier>EISSN: 2314-7156</identifier><identifier>DOI: 10.1155/2015/178947</identifier><identifier>PMID: 26240832</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Chagas Disease - immunology ; Chagas Disease - parasitology ; Chronic illnesses ; Disease Resistance - immunology ; Host-Parasite Interactions - immunology ; Humans ; Immune Evasion ; Immune Tolerance ; Immunology ; Kinases ; Parasites ; Protozoa ; Review ; T cell receptors ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; Trypanosoma cruzi ; Trypanosoma cruzi - immunology ; Trypanosoma cruzi - pathogenicity ; Virulence Factors</subject><ispartof>Journal of immunology research, 2015-01, Vol.2015 (2015), p.1-7</ispartof><rights>Copyright © 2015 Ana Flávia Nardy et al.</rights><rights>Copyright © 2015 Ana Flavia Nardy et al. 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This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2015 Ana Flávia Nardy et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-9d5b5132dd20c78d13496ff6232622852536217c2e7f85acd24c86a3ebd8c3563</citedby><cites>FETCH-LOGICAL-c594t-9d5b5132dd20c78d13496ff6232622852536217c2e7f85acd24c86a3ebd8c3563</cites><orcidid>0000-0001-9432-9701</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1697156416/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1697156416?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26240832$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kul, Oguz</contributor><creatorcontrib>Flávia Nardy, Ana</creatorcontrib><creatorcontrib>Morrot, Alexandre</creatorcontrib><creatorcontrib>Freire-de-Lima, Célio Geraldo</creatorcontrib><title>Immune Evasion Strategies of Trypanosoma cruzi</title><title>Journal of immunology research</title><addtitle>J Immunol Res</addtitle><description>Microbes have evolved a diverse range of strategies to subvert the host immune system. The protozoan parasite Trypanosoma cruzi, the causative agent of Chagas disease, provides a good example of such adaptations. This parasite targets a broad spectrum of host tissues including both peripheral and central lymphoid tissues. Rapid colonization of the host gives rise to a systemic acute response which the parasite must overcome. The parasite in fact undermines both innate and adaptive immunity. It interferes with the antigen presenting function of dendritic cells via an action on host sialic acid-binding Ig-like lectin receptors. These receptors also induce suppression of CD4+ T cells responses, and we presented evidence that the sialylation of parasite-derived mucins is required for the inhibitory effects on CD4 T cells. 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subjects | Chagas Disease - immunology Chagas Disease - parasitology Chronic illnesses Disease Resistance - immunology Host-Parasite Interactions - immunology Humans Immune Evasion Immune Tolerance Immunology Kinases Parasites Protozoa Review T cell receptors T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism Trypanosoma cruzi Trypanosoma cruzi - immunology Trypanosoma cruzi - pathogenicity Virulence Factors |
title | Immune Evasion Strategies of Trypanosoma cruzi |
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