在印度西部的一个中心,人类免疫缺陷病毒感染者的免疫病毒学不一致:一项回顾性研究。

Pub Date : 2023-01-01 Epub Date: 2023-06-06 DOI:10.4103/ijstd.ijstd_121_22
Mayank Kacker, Rohit Vashisht, Anil S Menon
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引用次数: 0

摘要

背景和目的:使用血浆HIV病毒载量水平和CD4计数监测人类免疫缺陷病毒(HIV)感染者的治疗。免疫无反应(达到病毒学抑制)或病毒学无反应(实现免疫重建)的患者被称为具有不一致反应。这些患者患获得性免疫缺陷综合征(艾滋病)相关感染/疾病/肿瘤、非艾滋病相关疾病(心血管、神经、肾脏、肝脏疾病)和全因死亡的风险更高。本研究旨在评估在印度抗逆转录病毒疗法(ART)+中心完成至少1年的联合抗逆转录病毒治疗(cART)后,PLHIV中免疫病毒学不一致的患病率,并分析促成因素。方法:本研究是对1月18日至12月21日在印度西部ART+诊所接受cART的PLHIV患者的回顾性研究。根据计算和评估CD4和病毒载量反应的样本量,对496名患者进行了研究。结果:在496名病例中,48名患者(9.7%)存在免疫病毒学不一致。其中,36名患者(75%)有病毒学反应(免疫学无反应),12名患者(25%)有免疫学反应(病毒学无反应)。导致免疫无反应的因素如下——基线CD4水平低(解释和结论:免疫病毒学不一致是影响对cART反应的一个重要因素,与许多并发症有关,如艾滋病和非艾滋病相关事件,甚至死亡。提高依从性以及及时识别和管理机会性感染是有利于降低免疫病毒学差异发生率的措施。)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunovirological discordance among people living with human immunodeficiency virus at a center in Western India: A retrospective study.

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Immunovirological discordance among people living with human immunodeficiency virus at a center in Western India: A retrospective study.

Background and objectives: Treatment of people living with human immunodeficiency virus (HIV) (PLHIV) is monitored using plasma HIV viral load levels and CD4 counts. Patients with either immunological nonresponse (virological suppression achieved) or virological nonresponse (immune reconstitution achieved) are termed as having a discordant response. These patients are at higher risk for acquired immunodeficiency syndrome (AIDS)-related infections/diseases/neoplasms, non-AIDS-related illnesses (cardiovascular, neurological, renal, hepatic diseases), and all-cause death. This study was conducted to assess the prevalence of immunovirological discordance among PLHIV after completion of at least 1 year of combination antiretroviral therapy (cART) at an antiretroviral therapy (ART) plus center in India and analyze contributory factors.

Methods: The study was a retrospective study of PLHIV receiving cART at the ART plus clinic in Western India from January 18 to December 21. Four hundred and ninety-six patients were studied based on sample size calculated and assessed for CD4 and viral load response at 0, 6, and 12 months of ART.

Results: Of the 496 patients, 48 patients (9.7%) had immunovirological discordance. Out of them, 36 patients (75%) had a virological response (immunological nonresponse) and 12 (25%) patients had an immunological response (virological nonresponse). The factors contributing to immunological nonresponse were as follows - low baseline CD4 levels (<100 cells) (36.1%), adherence <95% (33.3%), presence of opportunistic infections (16.6%), and failure on first-line therapy (11.1%). Other factors noted included higher baseline viral load (2.7%), chronic kidney disease (5.5%), and chronic hepatitis B virus co-infection (5.5%). Virological nonresponse was associated with poor adherence to therapy <95% (33%) and failure of first-line regimen (33%). Opportunistic infections were noted among 33% of patients and 8.3% of patients were found to have higher baseline viral load.

Interpretation and conclusion: Immunovirological discordance is an important factor influencing response to cART and is associated with many complications such as AIDS and non-AIDS-related events and even death. Improved adherence and timely identification and management of opportunistic infections are measures that are beneficial in reducing the incidence of immunovirological discordance.

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