CXCR6+CD4+ T cells promote mortality during Trypanosoma brucei infection

dc.contributor.authorLiu, Gongguan
dc.contributor.authorAbas, Osama
dc.contributor.authorStrickland, Ashley B.
dc.contributor.authorChen, Yanli
dc.contributor.authorShi, Meiqing
dc.date.accessioned2022-06-13T19:18:00Z
dc.date.available2022-06-13T19:18:00Z
dc.date.issued2021-10-06
dc.description.abstractLiver macrophages internalize circulating bloodborne parasites. It remains poorly understood how this process affects the fate of the macrophages and T cell responses in the liver. Here, we report that infection by Trypanosoma brucei induced depletion of macrophages in the liver, leading to the repopulation of CXCL16-secreting intrahepatic macrophages, associated with substantial accumulation of CXCR6+CD4+ T cells in the liver. Interestingly, disruption of CXCR6 signaling did not affect control of the parasitemia, but significantly enhanced the survival of infected mice, associated with reduced inflammation and liver injury. Infected CXCR6 deficient mice displayed a reduced accumulation of CD4+ T cells in the liver; adoptive transfer experiments suggested that the reduction of CD4+ T cells in the liver was attributed to a cell intrinsic property of CXCR6 deficient CD4+ T cells. Importantly, infected CXCR6 deficient mice receiving wild-type CD4+ T cells survived significantly shorter than those receiving CXCR6 deficient CD4+ T cells, demonstrating that CXCR6+CD4+ T cells promote the mortality. We conclude that infection of T. brucei leads to depletion and repopulation of liver macrophages, associated with a substantial influx of CXCR6+CD4+ T cells that mediates mortality.en_US
dc.description.urihttps://doi.org/10.1371/journal.ppat.1009968
dc.identifierhttps://doi.org/10.13016/hk3z-o1xf
dc.identifier.citationLiu G, Abas O, Strickland AB, Chen Y, Shi M (2021) CXCR6+CD4+ T cells promote mortality during Trypanosoma brucei infection. PLoS Pathog 17(10): e1009968.en_US
dc.identifier.urihttp://hdl.handle.net/1903/28670
dc.language.isoen_USen_US
dc.publisherPLOSen_US
dc.relation.isAvailableAtCollege of Agriculture & Natural Resourcesen_us
dc.relation.isAvailableAtDepartment of Veterinary Medicineen_us
dc.relation.isAvailableAtDigital Repository at the University of Marylanden_us
dc.relation.isAvailableAtUniversity of Maryland (College Park, MD)en_us
dc.titleCXCR6+CD4+ T cells promote mortality during Trypanosoma brucei infectionen_US
dc.typeArticleen_US

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