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HBcAb 阳性是替诺福韦酯+多替拉韦方案转换后 HIV RNA 无法检出缺失的危险因素。

HBcAb Positivity as a Risk Factor for Missing HIV RNA Undetectability after the 3TC+DTG Switch.

机构信息

Infectious Disease Unit, Policlinico Tor Vergata of Rome, 00133 Rome, Italy.

Department of System Medicine, Tor Vergata University of Rome, 00133 Rome, Italy.

出版信息

Viruses. 2024 Feb 23;16(3):348. doi: 10.3390/v16030348.

DOI:10.3390/v16030348
PMID:38543714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10974397/
Abstract

Hepatitis B Core antibody (HBcAb) positivity is the surrogate marker of hepatitis B occult infection. This condition is not a contraindication for switching to two-drug (2DR) antiretroviral therapy; however, the removal of tenofovir may contribute to poor control of HBV replication. A multicentre retrospective cohort study investigated the impact of HBcAb positivity on HIV control in patients switching to a 2DR with Lamivudine and Dolutegravir (3TC-DTG). In this study, a comparison analysis was conducted between HBcAb-positive and -negative PLWH regarding HIV-RNA suppression, considering: (1): Target Not Detected (TND) < 20 cp/mL; (2) Target Detected (TD) < 20 cp/mL; and (3) Detectable > 20 cp/mL and <50 cp/mL and >50 copies/mL. A total of 267 patients on 2DR with 3TC-DTG were included. In comparison to HBcAb-negative, HBcAb-positive patients were older (45 years [35-54]) and had a lower CD4+ nadir (248 vs. 349 cells/mmc, = 0.007). No difference in the maintenance of virological suppression was present in the two groups of patients before the switch. Although no patient had an HIV-RNA > 20 cp/mL after the switch, significantly fewer HBcAb-positive compared with -negative subjects resulted in TND at 12, 24, and 36 months after the switch: 52 (69.3%) versus 164 (85.4%), = 0.004, 50 [72.5%] versus 143 [89.9%], = 0.001, and 30 [66.7%] versus 90 [92.8%], = 0.001, respectively. HBcAb positivity is associated with an increased risk of suboptimal HIV suppression during the 36 months after 3TC/DTG simplification. This finding reinforces the relevance of the OBI condition in PLWH and raises the issue of careful virological monitoring of such cases.

摘要

乙型肝炎核心抗体(HBcAb)阳性是乙型肝炎隐匿性感染的替代标志物。这种情况不是切换到二药(2DR)抗逆转录病毒治疗的禁忌症;然而,替诺福韦的去除可能导致乙型肝炎病毒复制控制不佳。一项多中心回顾性队列研究调查了 HBcAb 阳性对切换到拉米夫定和度鲁特韦(3TC-DTG)的 2DR 的 HIV 控制的影响。在这项研究中,对 HBcAb 阳性和阴性 PLWH 进行了 HIV-RNA 抑制的比较分析,考虑了:(1)目标未检测到(TND)<20 cp/mL;(2)目标检测到(TD)<20 cp/mL;和(3)检测到>20 cp/mL 和<50 cp/mL 和>50 拷贝/mL。共纳入 267 例接受 2DR 治疗的 3TC-DTG 患者。与 HBcAb 阴性患者相比,HBcAb 阳性患者年龄较大(45 岁[35-54]),CD4+ 最低点较低(248 与 349 个细胞/mmc, = 0.007)。两组患者在切换前的病毒学抑制维持方面没有差异。尽管切换后没有患者的 HIV-RNA > 20 cp/mL,但与 HBcAb 阴性相比,HBcAb 阳性患者在切换后 12、24 和 36 个月时 TND 的比例明显较低:52(69.3%)与 164(85.4%), = 0.004,50 [72.5%]与 143 [89.9%], = 0.001,30 [66.7%]与 90 [92.8%], = 0.001。HBcAb 阳性与切换后 3TC/DTG 简化后 36 个月期间 HIV 抑制不佳的风险增加相关。这一发现强调了隐匿性乙型肝炎感染在 PLWH 中的相关性,并提出了对这种情况进行仔细病毒学监测的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/111de0ea5268/viruses-16-00348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/31f818228378/viruses-16-00348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/edb748974ebd/viruses-16-00348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/111de0ea5268/viruses-16-00348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/31f818228378/viruses-16-00348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/edb748974ebd/viruses-16-00348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/10974397/111de0ea5268/viruses-16-00348-g003.jpg

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