Rodrigues M M, Mendonça-Previato L, Charlab R, Barcinski M A
Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Brazil.
Infect Immun. 1987 Dec;55(12):3142-8. doi: 10.1128/iai.55.12.3142-3148.1987.
Immunization of BALB/c mice with gp10/20, a glycoconjugate purified from Leishmania mexicana subsp. amazonensis, induced a delayed-type hypersensitivity response to the antigen, and a significant increase was elicited in the size of the lesion induced by a subcutaneous infection with this parasite. The increase in the lesion size was observed when mice were immunized by the subcutaneous and the intraperitoneal routes. The subcutaneous immunization with gp10/20 was unable to reverse the prophylactic effect of an intravenous injection of irradiated promastigotes. An L3T4+ T-cell line specific for gp10/20 was able to transfer this lesion-enhancing effect and specific delayed-type hypersensitivity reactivity to normal syngeneic recipients. The same T-cell line was a good producer of a hematopoietic growth factor, granulocyte-macrophage colony-stimulating factor.
用从亚马逊利什曼原虫亚种纯化的糖缀合物gp10/20免疫BALB/c小鼠,可诱导对该抗原的迟发型超敏反应,并且在用这种寄生虫进行皮下感染所诱导的损伤大小方面引发了显著增加。当通过皮下和腹腔途径免疫小鼠时,可观察到损伤大小增加。用gp10/20进行皮下免疫无法逆转静脉注射经辐照的前鞭毛体的预防效果。对gp10/20特异的L3T4 + T细胞系能够将这种损伤增强效应和特异的迟发型超敏反应性转移给正常同基因受体。同一个T细胞系是造血生长因子粒细胞-巨噬细胞集落刺激因子的良好产生者。