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Neutralizing antibody titers conferring protection to macaques from a simian/human immunodeficiency virus challenge using the TZM-bl assay.

机译:使用TZM-bl分析,中和抗体滴度可保护猿猴免受猿猴/人类免疫缺陷病毒攻击。

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We previously reported that passive transfer of polyclonal neutralizing antibodies (NAbs) sufficient to generate a titer of 1:38 in the plasma would confer sterilizing protection to 99% of macaques challenged intravenously with 75 TCID(50) of SHIV(DH12). Neutralizing activity in that study was measured in an MT4 cell assay in which infection was completely blocked (EC(100)). In the current study, the TZM-bl system was used to measure EC(50) neutralizing titers in several of the same macaque plasma samples and the relationship between these titers and in vivo protection was determined. The antiviral EC(50) NAb titers measured in individual plasma samples were higher than those previously obtained in the MT4 system. Furthermore, the geometric mean EC(50) NAb titers against pseudotyped SHIV(DH12) were 33-fold greater than the EC(100) titers measured in the MT4 cell assay against the replication-competent SHIV(DH12) inoculated into animals. An augmented probit regression model was used to generate curves relating TZM-bl EC(50) NAb titers and protection from a virus challenge; estimated titers conferring various levels of protection were then determined. In TZM-bl assays using pseudotyped SHIV(DH12), representative percent in vivo protection/estimated EC(50) titers were 99%/1:4467, 90%/1:1175, 80%/1:676, 50%/1:234, and 33%/1:141. Because it is likely that contributions from other arms of the immune system will contribute to vaccine-induced control, the range of EC(50) NAb titers we have derived may be more informative for evaluating the protective value of NAb activity from TZM-bl assays.
机译:我们先前曾报道过,多克隆中和抗体(NAbs)的被动转移足以在血浆中产生效价为1:38,将对99%的猕猴静脉注射75 TCID(50)的SHIV(DH12)进行灭菌保护。该研究的中和活性是通过MT4细胞测定法测定的,其中感染被完全阻止(EC(100))。在当前的研究中,TZM-bl系统用于测量某些相同猕猴血浆样品中的EC(50)中和效价,并确定了这些效价与体内保护之间的关系。在单个血浆样品中测得的抗病毒EC(50)NAb滴度高于以前在MT4系统中获得的滴度。此外,针对假型SHIV(DH12)的几何平均EC(50)NAb滴度比在MT4细胞分析中针对接种到动物中的具有复制能力的SHIV(DH12)的EC(100)滴度高33倍。使用增强的概率回归模型生成与TZM-bl EC(50)NAb效价和病毒攻击防护相关的曲线;然后确定赋予各种保护水平的估计效价。在使用假型SHIV(DH12)的TZM-b1分析中,体内保护/估计EC(50)滴度的代表性百分比为99%/ 1:4467、90%/ 1:1175、80%/ 1:676、50%/ 1 :234,和33%/ 1:141。由于免疫系统其他方面的贡献可能会有助于疫苗诱导的控制,因此我们得出的EC(50)NAb效价范围对于评估TZM-bl分析中NAb活性的保护价值可能更具参考价值。 。

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