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通过在奶牛中进行免疫快速诱导出针对HIV的广泛中和抗体。

Rapid elicitation of broadly neutralizing antibodies to HIV by immunization in cows.

作者信息

Sok Devin, Le Khoa M, Vadnais Melissa, Saye-Francisco Karen L, Jardine Joseph G, Torres Jonathan L, Berndsen Zachary T, Kong Leopold, Stanfield Robyn, Ruiz Jennifer, Ramos Alejandra, Liang Chi-Hui, Chen Patricia L, Criscitiello Michael F, Mwangi Waithaka, Wilson Ian A, Ward Andrew B, Smider Vaughn V, Burton Dennis R

机构信息

Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California 92037, USA.

IAVI Neutralizing Antibody Center, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Nature. 2017 Aug 3;548(7665):108-111. doi: 10.1038/nature23301. Epub 2017 Jul 20.

Abstract

No immunogen to date has reliably elicited broadly neutralizing antibodies to HIV in humans or animal models. Advances in the design of immunogens that antigenically mimic the HIV envelope glycoprotein (Env), such as the soluble cleaved trimer BG505 SOSIP, have improved the elicitation of potent isolate-specific antibody responses in rabbits and macaques, but so far failed to induce broadly neutralizing antibodies. One possible reason for this failure is that the relevant antibody repertoires are poorly suited to target the conserved epitope regions on Env, which are somewhat occluded relative to the exposed variable epitopes. Here, to test this hypothesis, we immunized four cows with BG505 SOSIP. The antibody repertoire of cows contains long third heavy chain complementary determining regions (HCDR3) with an ultralong subset that can reach more than 70 amino acids in length. Remarkably, BG505 SOSIP immunization resulted in rapid elicitation of broad and potent serum antibody responses in all four cows. Longitudinal serum analysis for one cow showed the development of neutralization breadth (20%, n = 117 cross-clade isolates) in 42 days and 96% breadth (n = 117) at 381 days. A monoclonal antibody isolated from this cow harboured an ultralong HCDR3 of 60 amino acids and neutralized 72% of cross-clade isolates (n = 117) with a potent median IC of 0.028 μg ml. Breadth was elicited with a single trimer immunogen and did not require additional envelope diversity. Immunization of cows may provide an avenue to rapidly generate antibody prophylactics and therapeutics to address disease agents that have evolved to avoid human antibody responses.

摘要

迄今为止,尚无免疫原能在人类或动物模型中可靠地引发针对HIV的广泛中和抗体。抗原模拟HIV包膜糖蛋白(Env)的免疫原设计取得了进展,例如可溶性裂解三聚体BG505 SOSIP,已改善了在兔子和猕猴中引发强效的分离株特异性抗体反应,但迄今为止未能诱导出广泛中和抗体。这种失败的一个可能原因是相关抗体库不太适合靶向Env上保守的表位区域,这些区域相对于暴露的可变表位有些隐蔽。在此,为了验证这一假设,我们用BG505 SOSIP免疫了四头奶牛。奶牛的抗体库包含长的第三条重链互补决定区(HCDR3),其中一个超长亚群的长度可达70多个氨基酸。值得注意的是,BG505 SOSIP免疫在所有四头奶牛中迅速引发了广泛而强效的血清抗体反应。对一头奶牛的纵向血清分析显示,在42天时中和广度发展到20%(n = 117个跨分支分离株), 在381天时达到96%(n = 117)。从这头奶牛分离出的一种单克隆抗体含有一个60个氨基酸的超长HCDR3,中和了72%的跨分支分离株(n = 117),中位IC50为0.028μg/ml,效力强劲。仅用一种三聚体免疫原就引发了广度,且不需要额外的包膜多样性。免疫奶牛可能为快速生成抗体预防剂和治疗剂提供一条途径,以应对已进化到能逃避人类抗体反应的病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43a9/5812458/72e253d7e07c/nihms886414f4.jpg

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