Pomeroy C, Kline S, Jordan M C, Filice G A
Medical Service, Veterans Administration Medical Center, Minneapolis, MN 55417.
J Infect Dis. 1989 Aug;160(2):305-11. doi: 10.1093/infdis/160.2.305.
Reactivation of Toxoplasma gondii infection often occurs concurrently with active cytomegalovirus (CMV) disease in immunocompromised patients, and CMV disease results in immunosuppression. To determine if murine CMV (MCMV) infection decreases resistance to T. gondii, mice with latent T. gondii infection were infected with MCMV. T. gondii infection reactivated, manifested primarily as pneumonia. Lung macrophages supported the growth of T. gondii before, during, and after T. gondii reactivation. Peritoneal macrophages inhibited the growth of T. gondii as pneumonia developed and became permissive as pneumonia resolved. Mice with latent T. gondii infection could survive larger doses of MCMV than could controls. Thus, MCMV infection led to reactivation of latent T. gondii infection in mice. Activation of lung macrophages, assessed by their ability to inhibit replication of T. gondii in vitro, was not associated with control of T. gondii infection.
在免疫功能低下的患者中,弓形虫感染的再激活通常与活动性巨细胞病毒(CMV)疾病同时发生,并且CMV疾病会导致免疫抑制。为了确定鼠巨细胞病毒(MCMV)感染是否会降低对弓形虫的抵抗力,将潜伏有弓形虫感染的小鼠感染MCMV。弓形虫感染再激活,主要表现为肺炎。在弓形虫再激活之前、期间和之后,肺巨噬细胞都支持弓形虫的生长。随着肺炎的发展,腹腔巨噬细胞抑制弓形虫的生长,而随着肺炎的消退,腹腔巨噬细胞变得具有允许性。与对照组相比,潜伏有弓形虫感染的小鼠能够耐受更大剂量的MCMV。因此,MCMV感染导致小鼠潜伏性弓形虫感染的再激活。通过肺巨噬细胞在体外抑制弓形虫复制的能力评估的肺巨噬细胞激活与弓形虫感染的控制无关。