Rafati S, Couty-Jouve S, Alimohammadian M H, Louis J A
Department of Immunology, Pasteur Institute of Iran, Tehran.
Clin Exp Immunol. 1997 Nov;110(2):203-11. doi: 10.1111/j.1365-2249.1997.tb08318.x.
Soluble Leishmania antigen (SLA) from both developmental stages of L. major (L. major MRHO/IR/75/ER) were prepared. Three and five subfractions of SLA from amastigote and promastigote were obtained by fast protein liquid chromatography (FPLC), respectively. Biochemical analyses and comparison of amastigote and promastigote SLA were done. The biochemical analyses revealed that the first fraction of L. major amastigote possesses a distinct band on its electrophoretic mobility pattern corresponding to a position of 24 kD, and it has enzymatic activity with characteristics of a cysteine proteinase. The isolated fractions of amastigote were tested for induction of proliferation, interferon-gamma (IFN-gamma) and IL-4 production in cultures of peripheral blood mononuclear cells (PBMC) from individuals who had recovered and also chronic patients of cutaneous leishmaniasis caused by L. major. The cells of recovered individuals compared with chronic cases proliferated profoundly in response to the first fraction of amastigote SLA. In all recovered individuals, the IFN-gamma, but not IL-4, was secreted in response to stimulation with the first fraction of amastigote SLA. In chronic cutaneous leishmaniasis, IFN-gamma was infrequently observed in response to stimulation by all three fractions of amastigote SLA, but secretion of IL-4 was observed. These data indicate that first fraction of amastigote SLA is a strong inducer of primed human immune response to L. major, and may have a protective function.
制备了来自硕大利什曼原虫两个发育阶段(硕大利什曼原虫MRHO/IR/75/ER)的可溶性利什曼原虫抗原(SLA)。分别通过快速蛋白质液相色谱(FPLC)从无鞭毛体和前鞭毛体中获得了3个和5个SLA亚组分。对无鞭毛体和前鞭毛体SLA进行了生化分析和比较。生化分析表明,硕大利什曼原虫无鞭毛体的第一亚组分在其电泳迁移模式上有一条对应于24 kD位置的独特条带,并且它具有半胱氨酸蛋白酶特征的酶活性。对从已康复个体以及由硕大利什曼原虫引起的皮肤利什曼病慢性患者的外周血单个核细胞(PBMC)培养物中分离出的无鞭毛体亚组分进行了增殖诱导、干扰素-γ(IFN-γ)和IL-4产生的检测。与慢性病例相比,已康复个体的细胞对无鞭毛体SLA的第一亚组分有显著增殖反应。在所有已康复个体中,对无鞭毛体SLA的第一亚组分刺激有IFN-γ分泌,但无IL-4分泌。在慢性皮肤利什曼病中,对无鞭毛体SLA的所有三个亚组分刺激很少观察到IFN-γ,但观察到IL-4分泌。这些数据表明,无鞭毛体SLA的第一亚组分是引发人类对硕大利什曼原虫免疫反应的强诱导剂,可能具有保护功能。