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Human Immunodeficiency Virus Type 1 Elite Neutralizers: Individuals with Broad and Potent Neutralizing Activity Identified by Using a High-Throughput Neutralization Assay together with an Analytical Selection Algorithm▿ †

机译:人类免疫缺陷病毒1型精英中和剂:通过使用高通量中和测定和分析选择算法鉴定具有广泛和有效中和活性的个体

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摘要

The development of a rapid and efficient system to identify human immunodeficiency virus type 1 (HIV-1)-infected individuals with broad and potent HIV-1-specific neutralizing antibody responses is an important step toward the discovery of critical neutralization targets for rational AIDS vaccine design. In this study, samples from HIV-1-infected volunteers from diverse epidemiological regions were screened for neutralization responses using pseudovirus panels composed of clades A, B, C, and D and circulating recombinant forms (CRFs). Initially, 463 serum and plasma samples from Australia, Rwanda, Uganda, the United Kingdom, and Zambia were screened to explore neutralization patterns and selection ranking algorithms. Samples were identified that neutralized representative isolates from at least four clade/CRF groups with titers above prespecified thresholds and ranked based on a weighted average of their log-transformed neutralization titers. Linear regression methods selected a five-pseudovirus subset, representing clades A, B, and C and one CRF01_AE, that could identify top-ranking samples with 50% inhibitory concentration (IC50) neutralization titers of ≥100 to multiple isolates within at least four clade groups. This reduced panel was then used to screen 1,234 new samples from the Ivory Coast, Kenya, South Africa, Thailand, and the United States, and 1% were identified as elite neutralizers. Elite activity is defined as the ability to neutralize, on average, more than one pseudovirus at an IC50 titer of 300 within a clade group and across at least four clade groups. These elite neutralizers provide promising starting material for the isolation of broadly neutralizing monoclonal antibodies to assist in HIV-1 vaccine design.
机译:建立快速有效的系统以鉴定具有广泛且有效的HIV-1特异性中和抗体反应的人类免疫缺陷病毒1型(HIV-1)感染者是朝着发现合理的AIDS疫苗关键中和目标迈出的重要一步设计。在这项研究中,使用由进化枝A,B,C和D组成的假病毒面板和循环重组形式(CRF),筛选了来自不同流行病学区域的HIV-1感染志愿者的样本,以进行中和反应筛选。最初,对来自澳大利亚,卢旺达,乌干达,英国和赞比亚的463个血清和血浆样品进行了筛选,以探索中和模式和选择排名算法。鉴定出的样品中至少有四个滴度/ CRF组的中和代表性分离物的滴度高于预定的阈值,并基于其对数转化的中和滴度的加权平均值进行排名。线性回归方法选择了五个伪病毒子集,分别代表进化枝A,B和C,以及一个CRF01_AE,它们可以鉴定出在至少四个进化枝中具有50%抑制浓度(IC50)中和效价≥100的顶级样本组。然后,使用减少的面板筛选来自科特迪瓦,肯尼亚,南非,泰国和美国的1,234个新样品,其中1%被鉴定为精英中和剂。精英活动定义为在进化枝组内和至少四个进化枝组内平均中和一种以上假病毒的能力,IC50效价为300。这些优秀的中和剂为分离广泛中和的单克隆抗体提供了有希望的起始材料,以帮助设计HIV-1疫苗。

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