攻击前的高中和抗体和对gp41的持久免疫反应性与恒河猴免受生殖猴免疫缺陷病毒感染或疾病发展的保护有关。

H Petry, U Dittmer, D Jones, G Farrar, H Wachter, D Fuchs, T Nisslein, E Jurkiewicz, G Hunsmann, C Stahl-Hennig, W Lüke
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引用次数: 5

摘要

为了研究多种gp130疫苗制剂的保护效果,我们用gp130低聚物(O-gp130)或两种不同的gp130单体制剂(M1-gp130;M2-gp130)和猴免疫缺陷病毒(SIV)mac32H的50个MID50攻毒。攻毒后,M1-和M2-gp130组和1只O-gp130组的对照动物和所有动物都被有效感染,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和对跨膜蛋白gp41的长期免疫反应有关。虽然O-gp130动物没有出现疾病症状,但3只M1-gp130动物、1只M2-gp130动物和2只对照动物在感染后18个月内死于艾滋病。因此,用病毒衍生的SIVmac32H的gp130寡聚物免疫可以保护SIVmac32H免受生产性感染,并抑制艾滋病样疾病的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prechallenge high neutralizing antibodies and long-lasting immune reactivity to gp41 correlate with protection of rhesus monkeys against productive simian immunodeficiency virus infection or disease development.

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.

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