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评估治疗后 HIV 感染患者免疫恢复的遗传药理学。

Evaluation of the pharmacogenetics of immune recovery in treated HIV-infected patients.

机构信息

Hospital Universitari de Tarragona Joan XXIII, IISPV, Universitat Rovira i Virgili , Tarragona , Spain +0034977295833 ; +0034977295833 ;

出版信息

Expert Opin Drug Metab Toxicol. 2014 Jan;10(1):81-101. doi: 10.1517/17425255.2014.854330. Epub 2013 Nov 21.

Abstract

INTRODUCTION

Combination antiretroviral therapy has markedly improved the survival rate and quality of life in patients infected with HIV due to the powerful suppressor effect that current antiretroviral drugs have on the viral load. Consequently, the immune system undergoes a substantial qualitative and quantitative improvement; and this leads to an increase in the absolute CD4(+) T-lymphocyte count and the restoration of lost T-cell responses against certain opportunistic pathogens. Unfortunately, not all patients who successfully suppress plasma viremia experience sufficient CD4(+) T-cell gain and these patients, in turn, are associated with worse outcomes. Pharmacogenetic studies have been used to investigate how a patient's genetic predisposition may affect their response to antiretroviral drugs.

AREAS COVERED

This article reviews the investigations that have been published on the association between host genetic determinants of CD4(+) T-cell gain in treated HIV-infected patients. Studies were identified through a PubMed database search. Longitudinal studies into pharmacogenetic association were specifically selected.

EXPERT OPINION

While the possibility of genetic predisposition to HIV therapeutics has potential, most studies provide inconsistent data. Inconsistency is often due to partial genetic evaluation, different categorization of poor immune recovery or due to small numbers of patients evaluated. Currently, studies still belong to the research laboratory stage and more studies are required to improve our understanding.

摘要

简介

由于目前的抗逆转录病毒药物对病毒载量具有强大的抑制作用,联合抗逆转录病毒疗法显著提高了 HIV 感染者的生存率和生活质量。因此,免疫系统经历了实质性的定性和定量改善;这导致绝对 CD4(+)T 淋巴细胞计数增加,并恢复了对某些机会性病原体失去的 T 细胞反应。不幸的是,并非所有成功抑制血浆病毒血症的患者都能获得足够的 CD4(+)T 细胞,这些患者的预后较差。遗传药理学研究已被用于研究患者的遗传易感性如何影响他们对抗逆转录病毒药物的反应。

涵盖领域

本文综述了已发表的关于治疗后 HIV 感染患者中 CD4(+)T 细胞获得的宿主遗传决定因素的相关性的研究。通过 PubMed 数据库检索确定了研究。专门选择了关于药物遗传学相关性的纵向研究。

专家意见

虽然遗传易感性对 HIV 治疗具有潜在可能性,但大多数研究提供的数据不一致。不一致的原因通常是部分遗传评估、不良免疫恢复的分类不同,或评估的患者数量较少。目前,研究仍处于研究实验室阶段,需要更多的研究来加深我们的理解。

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