Biedermann K, Flepp M, Fierz W, Joller-Jemelka H, Kleihues P
Department of Gynecology and Obstetrics, University Hospital of Zurich, Switzerland.
J Perinat Med. 1995;23(3):191-203. doi: 10.1515/jpme.1995.23.3.191.
Toxoplasmosis is a chronic, latent infection which can be reactivated in the presence of immunosuppression. The critical question in obstetrics is whether toxoplasmosis may be reactivated in the presence of the physiological "immunosuppression" of pregnancy. Standard in vitro tests, done in 24 healthy pregnant women and compared with the literature, show no significant changes in humoral and cellular immunity during pregnancy. However, the fact that some infections occur more frequently and more severely than in non-pregnant women (e.g. those due to cytomegalovirus (CMV) and human papilloma virus (HPV) points to a degree of pregnancy-associated immunosuppression. Non-rejection of the semiallogenic fetus is achieved in presence of maternal immunocompetence and is explained mainly by local changes in immune function, mediated by inhibitors of decidual, placental and fetal origin, and by the absence of class II histocompatibility antigens at the fetomaternal interface. Immune status allowing reactivation of toxoplasmosis was studied in a selected group of (predominantly male) AIDS patients from the Swiss HIV Cohort study. Shortly before (cerebral) reactivation of toxoplasmosis, 92% of these patients had very low CD4 lymphocyte counts (mean 50 cells/microliters, i.e. lower than ever recorded in a normal uncomplicated pregnancy). In a larger population of 48 women receiving immunosuppressive therapy after organ transplantation, not a single case of cerebral toxoplasmosis was observed during pregnancy, while in the 105 HIV-positive women in the Swiss HIV and Pregnancy study, there was only one case of cerebral toxoplasmosis during pregnancy and the puerperium (20 CD4/microliters), even though some 17% of those sampled (18/105) had CD4 levels below 200 cells/microliters on at least one occasion during pregnancy. These findings explain why latent toxoplasmosis is not reactivated in normal pregnancy, and why it is only likely in an immunosuppressed mother when her CD4 lymphocyte count is very low (< 200 cells/microliters). In such cases, a prophylactic treatment to prevent maternal reactivation and vertical transmission of toxoplasmosis may be useful.
弓形虫病是一种慢性潜伏感染,在免疫抑制情况下可能会被激活。产科的关键问题是,在妊娠生理性“免疫抑制”情况下,弓形虫病是否会被激活。对24名健康孕妇进行的标准体外试验,并与文献对比,结果显示孕期体液免疫和细胞免疫无显著变化。然而,某些感染(如由巨细胞病毒(CMV)和人乳头瘤病毒(HPV)引起的感染)在孕妇中比非孕妇更频繁、更严重地发生,这一事实表明存在一定程度的妊娠相关免疫抑制。在母体免疫功能正常的情况下,半同种异体胎儿不被排斥,这主要是由蜕膜、胎盘和胎儿来源的抑制剂介导的免疫功能局部变化以及母胎界面处II类组织相容性抗原的缺失所解释。在瑞士HIV队列研究中,对一组(主要为男性)艾滋病患者进行了研究,观察了允许弓形虫病激活的免疫状态。在弓形虫病(脑部)激活前不久,这些患者中有92%的CD4淋巴细胞计数极低(平均50个细胞/微升,即低于正常无并发症妊娠所记录的最低值)。在48名器官移植后接受免疫抑制治疗的女性的更大群体中,孕期未观察到一例脑部弓形虫病病例,而在瑞士HIV与妊娠研究中的105名HIV阳性女性中,孕期和产褥期仅有一例脑部弓形虫病病例(CD4为20/微升),尽管约17%的采样者(18/105)在孕期至少有一次CD4水平低于200个细胞/微升。这些发现解释了为什么正常妊娠时潜伏的弓形虫病不会被激活,以及为什么只有当免疫抑制母亲的CD4淋巴细胞计数非常低(<200个细胞/微升)时才可能激活。在这种情况下,预防性治疗以防止母亲弓形虫病激活和垂直传播可能是有用的。