Campbell J D, Brown D J, Nichani A K, Howie S E, Spooner R L, Glass E J
Division of Molecular Biology, Roslin Institute (Edinburgh), UK.
Clin Exp Immunol. 1997 Jun;108(3):463-70. doi: 10.1046/j.1365-2249.1997.3861290.x.
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-gamma) mRNA. The in vitro response is mirrored during in vivo infection, as greatly elevated amounts of IFN-gamma protein are found in lymph efferent from infected lymph nodes, while expression of IL-4 mRNA within the node stops. IFN-gamma production does not correlate with protection against the parasite, as infected cells flourish during peak IFN-gamma production, and only very small amounts of IFN-gamma are produced during the effective immune response of an immunized animal. Overproduction of IFN-gamma 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.
环形泰勒虫是一种原生动物寄生虫,可感染并转化牛巨噬细胞。被感染的巨噬细胞具有增强的抗原呈递能力,因为它们能够激活来自未接触过该寄生虫动物的大多数T细胞。在体内,引流淋巴结(寄生虫发育的主要部位)中的T细胞被寄生虫“非特异性”激活。此事件之后,免疫反应无法控制感染。针对巨噬细胞内原生动物的保护性免疫反应通常由辅助性T细胞1(Th1)T细胞反应介导。在此,我们研究了环形泰勒虫激活的T细胞产生的细胞因子反应。我们发现,被寄生的巨噬细胞在体外激活T细胞的结果是其细胞因子反应偏向于优先表达干扰素-γ(IFN-γ)mRNA。体外反应在体内感染期间也有体现,因为在来自感染淋巴结的淋巴输出液中发现大量升高的IFN-γ蛋白,而淋巴结内IL-4 mRNA的表达停止。IFN-γ的产生与对寄生虫的保护作用无关,因为被感染细胞在IFN-γ产生高峰期大量繁殖,而在免疫动物的有效免疫反应期间仅产生极少量的IFN-γ。IFN-γ的过量产生和IL-4表达的丧失也可能是B细胞无法到达生发中心亮区的原因,生发中心亮区的发育步骤受到细胞因子的严格调控。