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Evaluation of an in vitro assay aimed at measuring protective antibodies against sporozoites.

机译:评估旨在测量针对子孢子的保护性抗体的体外分析。

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摘要

We have evaluated the in vitro biological activities of antibodies directed against sporozoites and compared them with their capacity to protect against challenge with both human and rodent malaria. The anti-Plasmodium falciparum antibodies evaluated with the test included monoclonal antibodies (MAbs) NFS1 and NFS2 as well as polyclonal antibodies contained in human hyperimmune sera directed against sporozoites of P. falciparum. The inhibitory effect of these antibodies was dependent on their concentration. However, total inhibition was not observed except occasionally with highly concentrated MAbs (10-100 micrograms/ml). Strong but also incomplete inhibition was observed with sera from humans living in hyperendemic areas. In the P. yoelii rodent system, we tested sera from mice immunized with subunit vaccines. None of these mice were protected in vivo against challenge with 40-200 sporozoites. In vitro only a sub-total inhibition was achieved (maximum 91% at 1:10 serum dilution). In contrast, we tested sera from mice that received NYS1, an IgG3 MAb, in passive transfer and were protected against challenge with 5000 sporozoites. At 1:10 dilution, 100% inhibition was achieved in vitro while IFA titres from these mice were similar to those of vaccinated mice. These data show a close correlation between in vivo and in vitro findings and thus suggest that the inhibition of liver-stage development assay (ILSDA) appears appropriate to evaluate the potential of antibodies.
机译:我们已经评估了针对子孢子的抗体的体外生物学活性,并将其与其抵抗人类和啮齿类疟疾的能力进行了比较。用该测试评估的抗恶性疟原虫抗体包括单克隆抗体(MAb)NFS1和NFS2,以及针对恶性疟原虫子孢子的人超免疫血清中所含的多克隆抗体。这些抗体的抑制作用取决于它们的浓度。但是,除偶尔使用高浓度的单克隆抗体(10-100微克/毫升)外,未观察到总抑制作用。生活在高流行地区的人类血清中观察到强烈但不完全的抑制作用。在约氏疟原虫啮齿动物系统中,我们测试了用亚单位疫苗免疫的小鼠的血清。这些小鼠均未在体内保护免受40-200子孢子的攻击。在体外,仅实现了部分抑制(在1:10血清稀释度下最大抑制91%)。相比之下,我们测试了接受以被动转移方式接受NYS1(一种IgG3 MAb)的小鼠的血清,并用5000份子孢子保护了小鼠免受血清攻击。在1:10的稀释度下,体外获得了100%的抑制作用,而这些小鼠的IFA滴度与疫苗接种的小鼠相似。这些数据显示了体内和体外发现之间的密切相关性,因此表明抑制肝阶段发育测定(ILSDA)似乎适合评估抗体的潜力。

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