Petry H, Dittmer U, Jones D, Farrar G, Wachter H, Fuchs D, Nisslein T, Jurkiewicz E, Hunsmann G, Stahl-Hennig C, Lüke W
Department of Virology and Immunology, German Primate Center, Göttingen.
J Acquir Immune Defic Syndr Hum Retrovirol. 1998 Dec 15;19(5):441-50. doi: 10.1097/00042560-199812150-00002.
To investigate the protective efficacy of various gp130 vaccine preparations, rhesus monkeys were immunized with gp130 oligomers (O-gp130) or two different gp130-monomer preparations (M1-gp130; M2-gp130) and challenged with 50 MID50 of simian immunodeficiency virus (SIV)mac32H. Following challenge the control animals and all animals of the M1- and M2-gp130 group and 1 animal of the O-gp130 group were productively infected, whereas 3 animals of the O-gp130 group resisted the productive virus replication. The protection was correlated with high neutralizing antibodies and a long-lasting immune response to the transmembrane protein gp41. Whereas none of the O-gp130 animals had developed disease symptoms, 3 M1-gp130 animals, 1 M2-gp130 animal, and 2 control animals died as a result of AIDS within 18 months after challenge. Therefore, immunization with virion-derived gp130 oligomers of SIVmac32H can confer protection against the productive infection with SIVmac32H and suppress the development of the AIDS-like disease.
为研究各种gp130疫苗制剂的保护效果,用gp130寡聚体(O-gp130)或两种不同的gp130单体制剂(M1-gp130;M2-gp130)对恒河猴进行免疫,并用50个半数感染剂量(MID50)的猿猴免疫缺陷病毒(SIV)mac32H进行攻击。攻击后,对照动物以及M1-gp130组和M2-gp130组的所有动物以及O-gp130组的1只动物均发生了有效感染,而O-gp130组的3只动物抵抗了病毒的有效复制。这种保护作用与高中和抗体以及对跨膜蛋白gp41的持久免疫反应相关。在O-gp130组动物中,没有一只出现疾病症状,而在攻击后18个月内,3只M1-gp130动物、1只M2-gp130动物和2只对照动物因艾滋病死亡。因此,用SIVmac32H的病毒体衍生gp130寡聚体进行免疫可提供针对SIVmac32H有效感染的保护,并抑制类似艾滋病疾病的发展。