Publication:
Increased γδ T cells in acute Plasmodium falciparum malaria

dc.contributor.authorMay Hoen_US
dc.contributor.authorH. Kyle Websteren_US
dc.contributor.authorPongsri Tongtaween_US
dc.contributor.authorKovit Pattanapanyasaten_US
dc.contributor.authorWilliam P. Weidanzen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherDrexel Universityen_US
dc.date.accessioned2018-06-14T09:21:35Z
dc.date.available2018-06-14T09:21:35Z
dc.date.issued1990-01-01en_US
dc.description.abstractThe T cell receptor γδ is normally e xpressed on a small percentage of peripheral lymphocytes. Although the role of γδ T cells in the physiologic immune response is still unknown, there is accumulating evidence that γδ T cells may participate in the immune response to mycobacterial and other infectious organisms. In this study, we have quantitated the number of circulating γδ T cells during acute Plasmodium falciparum malaria. The results indicate that γδ T cells are elevated during the acute infection and remain elevated for at least 4 weeks during convalescence. T cells may participate in the immune response against P. falciparum by functioning as non-MHC restricted cytotoxic cells against intraerythrocytic parasites. Alternatively, lymphokines may be produced on antigen stimulation which may have antiparasitic activity. © 1990.en_US
dc.identifier.citationImmunology Letters. Vol.25, No.1-3 (1990), 139-141en_US
dc.identifier.doi10.1016/0165-2478(90)90105-Yen_US
dc.identifier.issn01652478en_US
dc.identifier.other2-s2.0-0025090884en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/15970
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025090884&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleIncreased γδ T cells in acute Plasmodium falciparum malariaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025090884&origin=inwarden_US

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