Suppr超能文献

HIV-1 感染者接受 Vacc-4x 和罗米地辛治疗后 HIV-1 储存库的遗传特征。

Genetic characterization of the HIV-1 reservoir after Vacc-4x and romidepsin therapy in HIV-1-infected individuals.

机构信息

Centre for Virus Research, The Westmead Institute for Medical Research, The University of Sydney, Sydney, New South Wales, Australia.

The Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.

出版信息

AIDS. 2018 Aug 24;32(13):1793-1802. doi: 10.1097/QAD.0000000000001861.

Abstract

OBJECTIVE

Therapeutic HIV-1 immunization followed by latency reversal has been suggested as a strategy to eradicate HIV-1. Here we investigate the phylogenetic composition of the HIV-1 regions targeted by the therapeutic HIV-1 peptide vaccine Vacc-4x in participants in a clinical trial.

DESIGN

Seventeen participants on suppressive antiretroviral therapy were vaccinated with six doses of Vacc-4x followed by three doses of romidepsin. Seven study participants were selected for sequencing analysis. All participants underwent an analytical treatment interruption.

METHODS

Single-genome/proviral sequencing of the p24-RT region was performed to genetically characterize proviral DNA, cell-associated RNA and outgrowth viruses during therapy as well as plasma HIV-1 RNA during an analytical treatment interruption.

RESULTS

There were no changes in cell-associated HIV-1 RNA (P = 0.83) and DNA (P = 0.09) diversity over the course of the study and no difference between cell-associated HIV-1 RNA and DNA diversity (P = 0.32). Only one participant showed signs of potential vaccine-related selection in the rebounding plasma virus. In five of seven participants, we identified human leukocyte antigen-specific cytotoxic T lymphocytes (CTL) epitopes containing nonsilent mutations in 100% of the sequences.

CONCLUSION

We detected no evidence of selective immune pressure reflected in proviral diversity or by occurrence of specific mutation in the vaccine-targeted epitopes. Preexisting CTL epitope mutations may affect the potency of this therapeutic vaccine. This highlights the challenges of developing effective HIV-1 therapeutic vaccines.

摘要

目的

治疗性 HIV-1 免疫接种后再加上潜伏期逆转已被提出作为消除 HIV-1 的一种策略。在此,我们研究了在临床试验中的参与者中,治疗性 HIV-1 肽疫苗 Vacc-4x 靶向的 HIV-1 区域的系统发育组成。

设计

17 名接受抑制性抗逆转录病毒治疗的参与者接受了六剂 Vacc-4x 疫苗接种,然后接受了三剂罗米地辛治疗。有 7 名研究参与者被选中进行测序分析。所有参与者都经历了分析性治疗中断。

方法

对 p24-RT 区域的单基因/前病毒序列进行了分析,以对治疗过程中前病毒 DNA、细胞相关 RNA 和外生病毒以及分析性治疗中断期间的血浆 HIV-1 RNA 进行遗传特征分析。

结果

在研究过程中,细胞相关 HIV-1 RNA(P=0.83)和 DNA(P=0.09)多样性没有变化,细胞相关 HIV-1 RNA 和 DNA 多样性之间也没有差异(P=0.32)。只有一名参与者在反弹的血浆病毒中显示出潜在的与疫苗相关的选择迹象。在 7 名参与者中的 5 名中,我们在 100%的序列中发现了人类白细胞抗原特异性细胞毒性 T 淋巴细胞(CTL)表位,其中包含非沉默突变。

结论

我们没有发现选择免疫压力在前病毒多样性中反映的证据,也没有在疫苗靶向表位中出现特定突变的证据。预先存在的 CTL 表位突变可能会影响这种治疗性疫苗的效力。这突显了开发有效 HIV-1 治疗性疫苗的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ea/6072375/2a9c86023da7/aids-32-1793-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验