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Invariant NKT cell response to dengue virus infection in human
Dengue viral infection is a global health threat without vaccine or specific treatment. The clinical outcome varies from asymptomatic, mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF). While adaptive immune responses were found to be detrimental in the dengue pathogenesis, the roles o...
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Published in: | PLoS neglected tropical diseases 2014-06, Vol.8 (6), p.e2955-e2955 |
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creator | Matangkasombut, Ponpan Chan-In, Wilawan Opasawaschai, Anunya Pongchaikul, Pisut Tangthawornchaikul, Nattaya Vasanawathana, Sirijitt Limpitikul, Wannee Malasit, Prida Duangchinda, Thaneeya Screaton, Gavin Mongkolsapaya, Juthathip |
description | Dengue viral infection is a global health threat without vaccine or specific treatment. The clinical outcome varies from asymptomatic, mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF). While adaptive immune responses were found to be detrimental in the dengue pathogenesis, the roles of earlier innate events remain largely uninvestigated. Invariant natural killer T (iNKT) cells represent innate-like T cells that could dictate subsequent adaptive response but their role in human dengue virus infection is not known. We hypothesized that iNKT cells play a role in human dengue infection.
Blood samples from a well-characterized cohort of children with DF, DHF, in comparison to non-dengue febrile illness (OFI) and healthy controls at various time points were studied. iNKT cells activation were analyzed by the expression of CD69 by flow cytometry. Their cytokine production was then analyzed after α-GalCer stimulation. Further, the CD1d expression on monocytes, and CD69 expression on conventional T cells were measured.
iNKT cells were activated during acute dengue infection. The level of iNKT cell activation associates with the disease severity. Furthermore, these iNKT cells had altered functional response to subsequent ex vivo stimulation with α-GalCer. Moreover, during acute dengue infection, monocytic CD1d expression was also upregulated and conventional T cells also became activated.
iNKT cells might play an early and critical role in the pathogenesis of severe dengue viral infection in human. Targeting iNKT cells and CD1d serve as a potential therapeutic strategy for severe dengue infection in the future. |
doi_str_mv | 10.1371/journal.pntd.0002955 |
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Blood samples from a well-characterized cohort of children with DF, DHF, in comparison to non-dengue febrile illness (OFI) and healthy controls at various time points were studied. iNKT cells activation were analyzed by the expression of CD69 by flow cytometry. Their cytokine production was then analyzed after α-GalCer stimulation. Further, the CD1d expression on monocytes, and CD69 expression on conventional T cells were measured.
iNKT cells were activated during acute dengue infection. The level of iNKT cell activation associates with the disease severity. Furthermore, these iNKT cells had altered functional response to subsequent ex vivo stimulation with α-GalCer. Moreover, during acute dengue infection, monocytic CD1d expression was also upregulated and conventional T cells also became activated.
iNKT cells might play an early and critical role in the pathogenesis of severe dengue viral infection in human. Targeting iNKT cells and CD1d serve as a potential therapeutic strategy for severe dengue infection in the future.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0002955</identifier><identifier>PMID: 24945350</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Antigens, CD - metabolism ; Antigens, CD1d - metabolism ; Antigens, Differentiation, T-Lymphocyte - metabolism ; Biology and Life Sciences ; Case-Control Studies ; Child ; Child, Preschool ; Cytokines - immunology ; Dengue ; Dengue - immunology ; Dengue fever ; Dengue Virus ; Female ; Flow Cytometry ; Galactosylceramides - pharmacology ; Humans ; Immune response ; Immune system ; Immunity, Innate ; Immunophenotyping ; Infant ; Killer cells ; Lectins, C-Type - metabolism ; Lymphocyte Activation ; Male ; Medical research ; Medicine and Health Sciences ; Monocytes - immunology ; Monocytes - virology ; Natural Killer T-Cells - immunology ; Natural Killer T-Cells - virology ; Observations ; Physiological aspects ; Severe Dengue - immunology ; T-Lymphocytes - immunology ; T-Lymphocytes - virology ; Viral infections</subject><ispartof>PLoS neglected tropical diseases, 2014-06, Vol.8 (6), p.e2955-e2955</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Matangkasombut et al 2014 Matangkasombut et al</rights><rights>2014 Matangkasombut et al. 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 credited: Matangkasombut P, Chan-in W, Opasawaschai A, Pongchaikul P, Tangthawornchaikul N, et al. (2014) Invariant NKT Cell Response to Dengue Virus Infection in Human. PLoS Negl Trop Dis 8(6): e2955. doi:10.1371/journal.pntd.0002955</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c596t-cdc7355f578cc82e71c2384e961ef69b8654305661c4bd9445a8b7525e24b64c3</citedby><cites>FETCH-LOGICAL-c596t-cdc7355f578cc82e71c2384e961ef69b8654305661c4bd9445a8b7525e24b64c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063705/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063705/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,37011,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24945350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Marques, Ernesto T. A.</contributor><creatorcontrib>Matangkasombut, Ponpan</creatorcontrib><creatorcontrib>Chan-In, Wilawan</creatorcontrib><creatorcontrib>Opasawaschai, Anunya</creatorcontrib><creatorcontrib>Pongchaikul, Pisut</creatorcontrib><creatorcontrib>Tangthawornchaikul, Nattaya</creatorcontrib><creatorcontrib>Vasanawathana, Sirijitt</creatorcontrib><creatorcontrib>Limpitikul, Wannee</creatorcontrib><creatorcontrib>Malasit, Prida</creatorcontrib><creatorcontrib>Duangchinda, Thaneeya</creatorcontrib><creatorcontrib>Screaton, Gavin</creatorcontrib><creatorcontrib>Mongkolsapaya, Juthathip</creatorcontrib><title>Invariant NKT cell response to dengue virus infection in human</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Dengue viral infection is a global health threat without vaccine or specific treatment. The clinical outcome varies from asymptomatic, mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF). While adaptive immune responses were found to be detrimental in the dengue pathogenesis, the roles of earlier innate events remain largely uninvestigated. Invariant natural killer T (iNKT) cells represent innate-like T cells that could dictate subsequent adaptive response but their role in human dengue virus infection is not known. We hypothesized that iNKT cells play a role in human dengue infection.
Blood samples from a well-characterized cohort of children with DF, DHF, in comparison to non-dengue febrile illness (OFI) and healthy controls at various time points were studied. iNKT cells activation were analyzed by the expression of CD69 by flow cytometry. Their cytokine production was then analyzed after α-GalCer stimulation. Further, the CD1d expression on monocytes, and CD69 expression on conventional T cells were measured.
iNKT cells were activated during acute dengue infection. The level of iNKT cell activation associates with the disease severity. Furthermore, these iNKT cells had altered functional response to subsequent ex vivo stimulation with α-GalCer. Moreover, during acute dengue infection, monocytic CD1d expression was also upregulated and conventional T cells also became activated.
iNKT cells might play an early and critical role in the pathogenesis of severe dengue viral infection in human. Targeting iNKT cells and CD1d serve as a potential therapeutic strategy for severe dengue infection in the future.</description><subject>Adolescent</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, CD1d - metabolism</subject><subject>Antigens, Differentiation, T-Lymphocyte - metabolism</subject><subject>Biology and Life Sciences</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytokines - immunology</subject><subject>Dengue</subject><subject>Dengue - immunology</subject><subject>Dengue fever</subject><subject>Dengue Virus</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Galactosylceramides - pharmacology</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunity, Innate</subject><subject>Immunophenotyping</subject><subject>Infant</subject><subject>Killer cells</subject><subject>Lectins, C-Type - metabolism</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Monocytes - immunology</subject><subject>Monocytes - virology</subject><subject>Natural Killer T-Cells - immunology</subject><subject>Natural Killer T-Cells - virology</subject><subject>Observations</subject><subject>Physiological aspects</subject><subject>Severe Dengue - immunology</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - virology</subject><subject>Viral infections</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptUl1r2zAUNWNj7br9g7EZCmMvySRLV7JeCqXsI6xsL92zkOXrRMGRMskO7N9PXtySwNCDxNU5R-denaJ4S8mSMkk_bcMYvemXez-0S0JIpQCeFZdUMVhUksHzk_NF8SqlLSGgoKYvi4uKKw4MyGVxs_IHE53xQ_nj-0Npse_LiGkffMJyCGWLfj1ieXBxTKXzHdrBBZ9P5WbcGf-6eNGZPuGbeb8qfn35_HD3bXH_8-vq7vZ-YUGJYWFbm11AB7K2tq5QUluxmqMSFDuhmloAZwSEoJY3reIcTN1IqAAr3ghu2VXx_qi770PSc-tJU-ASRK0kyYjVEdEGs9X76HYm_tHBOP2vEOJamzg426PGmhpZM9FWrOGKoeJtI1F1wCQnnFVZ62Z-bWx22Fr0QzT9mej5jXcbvQ4HzYlgkkAW-DgLxPB7xDTonUvTbI3HME6-meKyYkpm6PURujbZWp5wyIp2gutbVjMqhYDJ0fI_qLxa3DkbPHYu188IH04IGzT9sEmhH6ffS-dAfgTaGFKK2D21SYmegvY4bT0FTc9By7R3pyN6Ij0mi_0FV-nNxQ</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Matangkasombut, Ponpan</creator><creator>Chan-In, Wilawan</creator><creator>Opasawaschai, Anunya</creator><creator>Pongchaikul, Pisut</creator><creator>Tangthawornchaikul, Nattaya</creator><creator>Vasanawathana, Sirijitt</creator><creator>Limpitikul, Wannee</creator><creator>Malasit, Prida</creator><creator>Duangchinda, Thaneeya</creator><creator>Screaton, Gavin</creator><creator>Mongkolsapaya, Juthathip</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140601</creationdate><title>Invariant NKT cell response to dengue virus infection in human</title><author>Matangkasombut, Ponpan ; Chan-In, Wilawan ; Opasawaschai, Anunya ; Pongchaikul, Pisut ; Tangthawornchaikul, Nattaya ; Vasanawathana, Sirijitt ; Limpitikul, Wannee ; Malasit, Prida ; Duangchinda, Thaneeya ; Screaton, Gavin ; Mongkolsapaya, Juthathip</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c596t-cdc7355f578cc82e71c2384e961ef69b8654305661c4bd9445a8b7525e24b64c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, CD1d - metabolism</topic><topic>Antigens, Differentiation, T-Lymphocyte - metabolism</topic><topic>Biology and Life Sciences</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cytokines - immunology</topic><topic>Dengue</topic><topic>Dengue - immunology</topic><topic>Dengue fever</topic><topic>Dengue Virus</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Galactosylceramides - pharmacology</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunity, Innate</topic><topic>Immunophenotyping</topic><topic>Infant</topic><topic>Killer cells</topic><topic>Lectins, C-Type - metabolism</topic><topic>Lymphocyte Activation</topic><topic>Male</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Monocytes - immunology</topic><topic>Monocytes - virology</topic><topic>Natural Killer T-Cells - immunology</topic><topic>Natural Killer T-Cells - virology</topic><topic>Observations</topic><topic>Physiological aspects</topic><topic>Severe Dengue - immunology</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - virology</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matangkasombut, Ponpan</creatorcontrib><creatorcontrib>Chan-In, Wilawan</creatorcontrib><creatorcontrib>Opasawaschai, Anunya</creatorcontrib><creatorcontrib>Pongchaikul, Pisut</creatorcontrib><creatorcontrib>Tangthawornchaikul, Nattaya</creatorcontrib><creatorcontrib>Vasanawathana, Sirijitt</creatorcontrib><creatorcontrib>Limpitikul, Wannee</creatorcontrib><creatorcontrib>Malasit, Prida</creatorcontrib><creatorcontrib>Duangchinda, Thaneeya</creatorcontrib><creatorcontrib>Screaton, Gavin</creatorcontrib><creatorcontrib>Mongkolsapaya, Juthathip</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matangkasombut, Ponpan</au><au>Chan-In, Wilawan</au><au>Opasawaschai, Anunya</au><au>Pongchaikul, Pisut</au><au>Tangthawornchaikul, Nattaya</au><au>Vasanawathana, Sirijitt</au><au>Limpitikul, Wannee</au><au>Malasit, Prida</au><au>Duangchinda, Thaneeya</au><au>Screaton, Gavin</au><au>Mongkolsapaya, Juthathip</au><au>Marques, Ernesto T. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Invariant NKT cell response to dengue virus infection in human</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>8</volume><issue>6</issue><spage>e2955</spage><epage>e2955</epage><pages>e2955-e2955</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Dengue viral infection is a global health threat without vaccine or specific treatment. The clinical outcome varies from asymptomatic, mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF). While adaptive immune responses were found to be detrimental in the dengue pathogenesis, the roles of earlier innate events remain largely uninvestigated. Invariant natural killer T (iNKT) cells represent innate-like T cells that could dictate subsequent adaptive response but their role in human dengue virus infection is not known. We hypothesized that iNKT cells play a role in human dengue infection.
Blood samples from a well-characterized cohort of children with DF, DHF, in comparison to non-dengue febrile illness (OFI) and healthy controls at various time points were studied. iNKT cells activation were analyzed by the expression of CD69 by flow cytometry. Their cytokine production was then analyzed after α-GalCer stimulation. Further, the CD1d expression on monocytes, and CD69 expression on conventional T cells were measured.
iNKT cells were activated during acute dengue infection. The level of iNKT cell activation associates with the disease severity. Furthermore, these iNKT cells had altered functional response to subsequent ex vivo stimulation with α-GalCer. Moreover, during acute dengue infection, monocytic CD1d expression was also upregulated and conventional T cells also became activated.
iNKT cells might play an early and critical role in the pathogenesis of severe dengue viral infection in human. Targeting iNKT cells and CD1d serve as a potential therapeutic strategy for severe dengue infection in the future.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24945350</pmid><doi>10.1371/journal.pntd.0002955</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Antigens, CD - metabolism Antigens, CD1d - metabolism Antigens, Differentiation, T-Lymphocyte - metabolism Biology and Life Sciences Case-Control Studies Child Child, Preschool Cytokines - immunology Dengue Dengue - immunology Dengue fever Dengue Virus Female Flow Cytometry Galactosylceramides - pharmacology Humans Immune response Immune system Immunity, Innate Immunophenotyping Infant Killer cells Lectins, C-Type - metabolism Lymphocyte Activation Male Medical research Medicine and Health Sciences Monocytes - immunology Monocytes - virology Natural Killer T-Cells - immunology Natural Killer T-Cells - virology Observations Physiological aspects Severe Dengue - immunology T-Lymphocytes - immunology T-Lymphocytes - virology Viral infections |
title | Invariant NKT cell response to dengue virus infection in human |
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