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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1997 Jun;108(3):463–470. doi: 10.1046/j.1365-2249.1997.3861290.x

A non-protective T helper 1 response against the intra-macrophage protozoan Theileria annulata

J D M CAMPBELL *, D J BROWN *, A K NICHANI , S E M HOWIE , R L SPOONER §, E J GLASS *
PMCID: PMC1904671  PMID: 9182893

Abstract

Theileria annulata is a protozoan parasite which infects and transforms bovine macrophages. Infected macrophages possess augmented antigen presentation capabilities, as they are able to activate the majority of T cells from unexposed animals. In vivo, T cells in the draining lymph node (principal site of parasite development) are activated ‘non-specifically’ by the parasite. This event is followed by failure of the immune response to control the infection. Protective immune responses against intra-macrophage protozoa are usually mediated by T helper 1 (Th1) T cell responses. Here we examine the cytokine responses made by T. annulata-activated T cells. We show that the outcome of in vitro activation of T cells by parasitized macrophages is a skewing of their cytokine responses towards preferential expression of interferon-gamma (IFN-γ) mRNA. The in vitro response is mirrored during in vivo infection, as greatly elevated amounts of IFN-γ protein are found in lymph efferent from infected lymph nodes, while expression of IL-4 mRNA within the node stops. IFN-γ production does not correlate with protection against the parasite, as infected cells flourish during peak IFN-γ production, and only very small amounts of IFN-γ are produced during the effective immune response of an immunized animal. Overproduction of IFN-γ and loss of IL-4 expression are also likely to account for the failure of B cells to reach the light zone of germinal centres, a developmental step which is tightly regulated by cytokines.

Keywords: Theileria annulata, cytokines, T cells, interferon-gamma

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