Khusmith S, Sedegah M, Hoffman S L
Malaria Program, Naval Medical Research Institute, Bethesda, Maryland 20889-5607.
Infect Immun. 1994 Jul;62(7):2979-83. doi: 10.1128/iai.62.7.2979-2983.1994.
BALB/c mice immunized with irradiated Plasmodium yoelii sporozoites produce antibodies and cytotoxic T lymphocytes against the circumsporozoite protein and against a 140-kDa protein, sporozoite surface protein 2 (PySSP2). Approximately 50% of mice immunized with P815 cells transfected with the gene encoding PySSP2 are protected against malaria, and this protection is reversed by in vivo depletion of CD8+ T cells. To determine if CD8+ T cells against PySSP2 are adequate to protect against malaria in the absence of other malaria-specific immune responses, we produced three CD8+ T-cell clones by stimulating spleen cells from mice immunized with irradiated P. yoelii sporozoites with a mitomycin-treated P815 cell clone transfected with the PySSP2 gene. Adoptive transfer of clone TSLB7 protected 100% of mice against P. yoelii. The second clone protected 58% of mice, and the third clone provided no protection. Clone TSLB7 protected even when administered 3 h after sporozoite inoculation at a time when sporozoites had entered hepatocytes, suggesting that it is recognizing and eliminating infected hepatocytes. These studies demonstrate that cytotoxic T lymphocytes against PySSP2 can protect against P. yoelii sporozoite challenge in the absence of other parasite-specific immune responses.
用经辐射的约氏疟原虫子孢子免疫的BALB/c小鼠会产生针对环子孢子蛋白和一种140 kDa蛋白(子孢子表面蛋白2,PySSP2)的抗体和细胞毒性T淋巴细胞。用转染了编码PySSP2基因的P815细胞免疫的小鼠中,约50%受到疟疾保护,且这种保护作用会因体内CD8⁺ T细胞的耗竭而逆转。为了确定在没有其他疟疾特异性免疫反应的情况下,针对PySSP2的CD8⁺ T细胞是否足以预防疟疾,我们通过用经丝裂霉素处理的转染了PySSP2基因的P815细胞克隆刺激用经辐射的约氏疟原虫子孢子免疫的小鼠的脾细胞,产生了三个CD8⁺ T细胞克隆。克隆TSLB7的过继转移使100%的小鼠免受约氏疟原虫感染。第二个克隆保护了58%的小鼠,而第三个克隆没有提供保护。即使在子孢子接种后3小时(此时子孢子已进入肝细胞)给予克隆TSLB7,它仍能提供保护,这表明它正在识别并清除被感染的肝细胞。这些研究表明,在没有其他寄生虫特异性免疫反应的情况下,针对PySSP2的细胞毒性T淋巴细胞可以预防约氏疟原虫子孢子的攻击。