B cells, not dendritic cells, prime the dominant CD4+ Tfh response to Plasmodium infection

dc.contributor.advisorPepper, Marion
dc.contributor.authorArroyo, Enidza Nicole
dc.date.accessioned2019-10-15T22:58:46Z
dc.date.available2019-10-15T22:58:46Z
dc.date.issued2019-10-15
dc.date.submitted2019
dc.descriptionThesis (Ph.D.)--University of Washington, 2019
dc.description.abstractCD4+ T follicular helper (Tfh) cells dominate the acute response to a blood- stage Plasmodium infection and provide signals to direct B cell differentiation and protective antibody expression. We studied antigen-specific CD4+ Tfh cells responding to Plasmodium infection in order to understand the generation and maintenance of the Tfh response. We discovered that a dominant, phenotypically stable, CXCR5+ Tfh population emerges within the first four days of infection and results in a CXCR5+ CCR7+ Tfh/central memory T cell response that persists well after parasite clearance. We also found that CD4+ T cell priming by B cells was both necessary and sufficient to generate this Tfh-dominant response, whereas priming by conventional dendritic cells was dispensable. This study provides important insights into the development of CD4+ Tfh cells during Plasmodium infection and highlights the heterogeneity of antigen-presenting cells involved in CD4+ T cell priming.
dc.embargo.termsOpen Access
dc.format.mimetypeapplication/pdf
dc.identifier.otherArroyo_washington_0250E_20704.pdf
dc.identifier.urihttp://hdl.handle.net/1773/44832
dc.language.isoen_US
dc.rightsnone
dc.subjectmemory T cells
dc.subjectPlasmodium
dc.subjectT cell priming
dc.subjectT follicular helper cells
dc.subjectImmunology
dc.subject.otherImmunology
dc.titleB cells, not dendritic cells, prime the dominant CD4+ Tfh response to Plasmodium infection
dc.typeThesis

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