Moldt Brian, Le Khoa M, Carnathan Diane G, Whitney James B, Schultz Niccole, Lewis Mark G, Borducchi Erica N, Smith Kaitlin M, Mackel Joseph J, Sweat Shelby L, Hodges Andrew P, Godzik Adam, Parren Paul W H I, Silvestri Guido, Barouch Dan H, Burton Dennis R
aDepartment of Immunology and Microbial Science, IAVI Neutralizing Antibody Center and Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery, The Scripps Research Institute, La Jolla, California bEmory Vaccine Center and Yerkes National Primate Research Center, Emory University, Atlanta, Georgia cCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts dBioqual, Inc., Rockville, Maryland eBioinformatics and Systems Biology Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA fGenmab, Utrecht, The Netherlands gRagon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, USA. *Present address: MedImmune, LLC, Gaithersburg, Maryland, USA.
AIDS. 2016 Jun 19;30(10):1543-51. doi: 10.1097/QAD.0000000000001102.
Passive administration of broadly neutralizing antibodies has been shown to protect against both vaginal and rectal challenge in the simian/human immunodeficiency virus (SHIV)/macaque model of HIV transmission. However, the relative efficacy of antibody against the two modes of exposure is unknown and, given differences in the composition and immunology of the two tissue compartments, this is an important gap in knowledge. To investigate the significance of the challenge route for antibody-mediated protection, we performed a comparative protection study in macaques using the highly potent human monoclonal antibody, PGT126.
Animals were administered PGT126 at three different doses before challenged either vaginally or rectally with a single dose of SHIVSF163P3.
Viral loads, PGT126 serum concentrations, and serum neutralizing titers were monitored.
In vaginally challenged animals, sterilizing immunity was achieved in all animals administered 10 mg/kg, in two of five animals administered 2 mg/kg and in one of five animals administered 0.4 mg/kg PGT126. Comparable protection was observed for the corresponding groups challenged rectally as sterilizing immunity was achieved in three of four animals administered 10 mg/kg, in two of four animals administered 2 mg/kg and in none of four animals administered 0.4 mg/kg PGT126. Serological analysis showed similar serum concentrations of PGT126 and serum neutralization titers in animals administered the same antibody dose.
Our data suggest that broadly neutralizing antibody-mediated protection is not strongly dependent on the mucosal route of challenge, which indicates that a vaccine aimed to induce a neutralizing antibody response would have broadly similar efficacy against both primary transmission routes for HIV.
在猿猴/人类免疫缺陷病毒(SHIV)/猕猴艾滋病病毒传播模型中,被动给予广泛中和抗体已被证明可预防阴道和直肠感染。然而,抗体针对这两种暴露方式的相对疗效尚不清楚,鉴于两个组织腔室的组成和免疫学存在差异,这是一个重要的知识空白。为了研究攻击途径对抗体介导的保护作用的重要性,我们使用高效人单克隆抗体PGT126在猕猴中进行了一项比较保护研究。
在动物经阴道或直肠单次给予SHIVSF163P3攻击之前,以三种不同剂量给予PGT126。
监测病毒载量、PGT126血清浓度和血清中和滴度。
在经阴道攻击的动物中,给予10mg/kg的所有动物、给予2mg/kg的五只动物中的两只以及给予0.4mg/kg的五只动物中的一只实现了无菌免疫。在经直肠攻击的相应组中观察到了类似的保护作用,给予10mg/kg的四只动物中的三只、给予2mg/kg的四只动物中的两只以及给予0.4mg/kg的四只动物中无一实现了无菌免疫。血清学分析显示,给予相同抗体剂量的动物中PGT126的血清浓度和血清中和滴度相似。
我们的数据表明,广泛中和抗体介导的保护作用并不强烈依赖于攻击的黏膜途径,这表明旨在诱导中和抗体反应的疫苗对艾滋病病毒的两种主要传播途径将具有大致相似的疗效。