Darcy F, Torpier G, Cesbron-Delauw M F, Decoster A, Ridel P R, Duquesne V, Charif H, Godard I, Pierce R J, Auriault C
Centre d'Immunologie et de Biologie Parasitaires, Unité Mixte INSERM U 167, CNRS 624, Institut Pasteur, Lille.
Ann Biol Clin (Paris). 1989;47(7):451-7.
Toxoplasma gondii is an ubiquitous protozoan parasite which induces severe pathology in in utero infected children and in immunosuppressed patients (particularly in the case of AIDS). Previous work that focused on toxoplasma somatic antigens failed to demonstrate an efficient protection against highly virulent T. gondii strains. The authors therefore first studied the role of parasite excreted-secreted (ES) antigens in the immune response. They describe here the preparation of excreted-secreted antigens in cell-free medium from tachyzoites, the intracellular proliferative stage present during acute infection. Major ES antigens have Mr of 108 K, 97 K, 86 K, 57 K, 42 K, 39 K, 28.5 K, 27 K and 21 K. The protective role of ES antigens has been demonstrated using congenitally athymic (Nu/Nu) rats that are highly sensitive to T. gondii infection (+/+ Fischer rats are resistant). The humoral and cellular components of this protection have been studied by the passive transfer either of sera or of T lymphocytes from ES-immunized +/+ Fischer rats into Nu/Nu rats. Adoptive transfers were carried out 24 hours before infection with the highly virulent T. gondii RH strain. Based on the concept of concomitant immunity, the authors have characterized antigens from tachyzoites and bradyzoites (the encysted stage persisting during chronic infection) which share common epitopes. Four tachyzoite antigens, P63, GP43, P39 and GP 28.5 have been shown by immunoprecipitation to cross-react with bradyzoite antigens. Two monoclonal antibodies raised against ES antigens permitted to demonstrate the localization of the 28.5 K and 27 K antigens inside the dense granules of tachyzoites and bradyzoites.(ABSTRACT TRUNCATED AT 250 WORDS)
刚地弓形虫是一种普遍存在的原生动物寄生虫,可在子宫内感染的儿童和免疫抑制患者(尤其是艾滋病患者)中引发严重病变。以往针对弓形虫体细胞抗原的研究未能证明对高毒力弓形虫菌株有有效保护作用。因此,作者首先研究了寄生虫排泄分泌(ES)抗原在免疫反应中的作用。他们在此描述了从速殖子(急性感染期间存在的细胞内增殖阶段)在无细胞培养基中制备排泄分泌抗原的方法。主要的ES抗原分子量分别为108K、97K、86K、57K、42K、39K、28.5K、27K和21K。使用对弓形虫感染高度敏感的先天性无胸腺(Nu/Nu)大鼠(+/+费希尔大鼠具有抗性)证明了ES抗原的保护作用。通过将ES免疫的+/+费希尔大鼠的血清或T淋巴细胞被动转移到Nu/Nu大鼠中,研究了这种保护的体液和细胞成分。在感染高毒力弓形虫RH株前24小时进行过继转移。基于伴随免疫的概念,作者鉴定了速殖子和缓殖子(慢性感染期间持续存在的包囊阶段)中具有共同表位的抗原。通过免疫沉淀已证明四种速殖子抗原P63、GP43、P39和GP 28.5与缓殖子抗原发生交叉反应。两种针对ES抗原产生的单克隆抗体能够证明28.5K和27K抗原在速殖子和缓殖子致密颗粒内的定位。(摘要截短于250字)