Fang Hao, Aosai Fumie, Mun Hye-Seong, Norose Kazumi, Ahmed Azza Kamal, Furuya Mitsuko, Yano Akihiko
Department of Infection and Host Defense, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8670, Japan.
Int Immunol. 2006 Oct;18(10):1487-97. doi: 10.1093/intimm/dxl081. Epub 2006 Aug 30.
Toxoplasma gondii-derived heat shock protein 70 (T.g.HSP70) is a virulent molecule specific for tachyzoites of T. gondii. The expression of T.g.HSP70 rapidly increases just before death of the host, indicating that T.g.HSP70 functions as a danger signal during lethal acute T. gondii infection. In the present study, T.g.HSP70 was proven to be capable of inducing lethal anaphylactic reaction in T. gondii-infected wild-type (WT) mice. Anaphylactic reaction appeared within the first hour after intraperitoneal injection of T.g.HSP70 and was characterized by a series of consequent symptoms until death. T.g.HSP70-induced anaphylactic reaction was not observed in IFN-gamma knockout (GKO) mice, indicating the involvement of IFN-gamma in the reaction. The anaphylactic reaction was transferable to GKO mice by splenocytes but not serum from infected WT mice. Also, this reaction occurred in B cell-deficient mice, indicating that T.g.HSP70-induced anaphylactic reaction occurred through an Ig-independent pathway. The messenger RNA (mRNA) expression of IFN-gamma increased significantly in splenocytes from T. gondii-infected WT mice after T.g.HSP70 injection. Furthermore, the mRNA expression of platelet-activating factor (PAF) acetylhydrolase in WT, but not GKO mice, distinctly increased during the occurrence of T.g.HSP70-induced anaphylactic reaction, indicating the involvement of PAF in T.g.HSP70-induced anaphylactic reaction. Treatment with PAF receptor antagonist rescued WT mice from the anaphylactic reaction. These data demonstrated the involvement of IFN-gamma-dependent PAF activation in T.g.HSP70-induced anaphylactic reaction.
刚地弓形虫来源的热休克蛋白70(T.g.HSP70)是刚地弓形虫速殖子特有的一种毒力分子。T.g.HSP70的表达在宿主死亡前迅速增加,表明T.g.HSP70在致死性急性刚地弓形虫感染期间作为一种危险信号发挥作用。在本研究中,已证明T.g.HSP70能够在感染刚地弓形虫的野生型(WT)小鼠中诱导致死性过敏反应。过敏反应在腹腔注射T.g.HSP70后的第一小时内出现,其特征是出现一系列随之而来的症状直至死亡。在干扰素-γ基因敲除(GKO)小鼠中未观察到T.g.HSP70诱导的过敏反应,表明干扰素-γ参与了该反应。过敏反应可通过脾细胞转移至GKO小鼠,但不能通过感染的WT小鼠的血清转移。此外,该反应在B细胞缺陷小鼠中也会发生,表明T.g.HSP70诱导的过敏反应是通过一条不依赖免疫球蛋白的途径发生的。注射T.g.HSP70后,感染刚地弓形虫 的WT小鼠脾细胞中干扰素-γ的信使核糖核酸(mRNA)表达显著增加。此外,在T.g.HSP70诱导的过敏反应发生期间,野生型小鼠而非GKO小鼠中血小板活化因子(PAF)乙酰水解酶的mRNA表达明显增加,表明PAF参与了T.g.HSP70诱导的过敏反应。用PAF受体拮抗剂治疗可使WT小鼠免于过敏反应。这些数据证明了干扰素-γ依赖性PAF激活参与了T.g.HSP70诱导的过敏反应。