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雾化递送合成 mRNA 至阴道黏膜可导致对 HIV 的广泛中和抗体的持久表达。

Aerosol Delivery of Synthetic mRNA to Vaginal Mucosa Leads to Durable Expression of Broadly Neutralizing Antibodies against HIV.

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30332, USA.

Department of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.

出版信息

Mol Ther. 2020 Mar 4;28(3):805-819. doi: 10.1016/j.ymthe.2020.01.002. Epub 2020 Jan 10.

Abstract

There is a clear need for low-cost, self-applied, long-lasting approaches to prevent human immunodeficiency virus (HIV) infection in both men and women, even with the advent of pre-exposure prophylaxis (PrEP). Broadly neutralizing antibodies represent an option to improve HIV prophylaxis, but intravenous delivery, cold-chain stability requirements, low cervicovaginal concentrations, and cost may preclude their use. Here, we present an approach to express the anti-GP120 broadly neutralizing antibody PGT121 in the primary site of inoculation, the female reproductive tract, using synthetic mRNA. Expression is achieved through aerosol delivery of unformulated mRNA in water. We demonstrated high levels of antibody expression for over 28 days with a single mRNA administration in the reproductive tract of sheep. In rhesus macaques, neutralizing antibody titers in secretions developed within 4 h and simian-HIV (SHIV) infection of ex vivo explants was prevented. Persistence of PGT121 in vaginal secretions and epithelium was achieved through the incorporation of a glycosylphosphatidylinositol (GPI) anchor into the heavy chain of the antibody. Overall, we present a new paradigm to deliver neutralizing antibodies to the female reproductive tract for the prevention of HIV infections.

摘要

目前,人们迫切需要低成本、可自行使用、长效的方法来预防男性和女性的人类免疫缺陷病毒(HIV)感染,即使已经出现了暴露前预防(PrEP)措施。广泛中和抗体是改善 HIV 预防的一种选择,但静脉内给药、冷链稳定性要求、宫颈阴道内浓度低和成本可能会限制其使用。在这里,我们提出了一种使用合成 mRNA 在接种的主要部位(女性生殖道)表达抗-GP120 广泛中和抗体 PGT121 的方法。通过将未配方的 mRNA 以气雾剂形式递送至水中来实现表达。我们证明了在绵羊生殖道中单次给予 mRNA 即可在超过 28 天内实现高水平的抗体表达。在恒河猴中,在 4 小时内即可在分泌物中产生中和抗体滴度,并可防止猴免疫缺陷病毒(SHIV)对离体组织的感染。通过将糖基磷脂酰肌醇(GPI)锚定在抗体的重链中,实现了 PGT121 在阴道分泌物和上皮中的持续存在。总的来说,我们提出了一种将中和抗体递送至女性生殖道以预防 HIV 感染的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed0/7054722/00bf5ae4a2a8/fx1.jpg

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