抗巨细胞病毒抗体和可溶性CD14水平与长期抗逆转录病毒治疗的HIV感染者免疫衰老的差异关联

IF 5.2 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Ashwini Vinod Shete, Pallavi Shidhaye, Amrita Rao, Nikita Bhawari, Supriya Deshpande, Jyoti Sawant, Rajani Bagul, Ujjwala Ghule, Sunita Kumbhar, Manisha Ghate
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引用次数: 0

摘要

背景:尽管长期抗逆转录病毒治疗(ART)后免疫恢复,但艾滋病毒感染者(PLHIV)表现出加速的衰老和免疫衰老。低水平炎症导致的炎症在介导免疫早衰中起重要作用。正在进行的病毒复制,抗逆转录病毒和亚临床感染的常见病毒,如巨细胞病毒(CMV)是已知的诱导炎症。然而,在印度,由于各种亚临床感染,持续的低水平炎症在普通人群中很常见,因此此类数据很少。因此,我们进行了一项研究,以确定长期抗逆转录病毒治疗的无症状PLHIV患者的免疫衰老程度,并与年龄匹配的对照组进行比较。结果:本研究纳入接受抗逆转录病毒治疗5年以上无症状病毒抑制的PLHIV患者[n = 70, M: F = 36:34]和未感染HIV的对照组[n = 68, M: F = 31:37],年龄在40-55岁之间。采集血样,流式细胞术检测CD4 T细胞免疫衰老标志物水平,ELISA检测抗巨细胞病毒抗体水平,可溶性CD14 (sCD14)水平。比较病例和对照组之间的水平,并与抗巨细胞病毒抗体和sCD14水平相关。通过表达CD4和CD8 T细胞的CD38、CD57、CD28表明,PLHIV患者的naïve T细胞水平明显低于对照组,活化T细胞和免疫衰老T细胞水平明显高于对照组。与对照组相比,PLHIV患者的抗cmv抗体水平较高,但sCD14水平和HLADR + CD8 T细胞水平较低。免疫衰老T细胞与抗巨细胞病毒抗体水平呈正相关,与sCD14水平负相关。以多替韦为基础的治疗持续时间与sCD14水平呈负相关。结论:因此,病例中较高水平的免疫激活和免疫衰老可能表明他们的免疫状态受损,易使PLHIV感染和癌症。该研究表明,即使在无症状的个体中,也需要CMV治疗方案来预防免疫衰老。该研究还表明,dolutegravir诱导sCD14水平的丧失在PLHIV免疫衰老易感中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential associations of anti-cytomegalovirus antibodies and soluble CD14 levels with immunosenescence in people living with HIV on long term antiretroviral therapy.

Background: People living with HIV (PLHIV) demonstrate accelerated aging and immunosenescence in spite of immune-restoration following long-term antiretroviral treatment (ART). Low level inflammation leading to inflammaging plays an important role in mediating premature immunosenescence. Ongoing viral replication, antiretrovirals and subclinical infections with the common viruses like Cytomegalovirus (CMV) are known to induce inflammaging. However such data is scarce in India where persistent low level inflammation is common in general population due to various subclinical infections. Hence we conducted a study to determine the extent of immunosenescence in asymptomatic PLHIV on long term ART in comparison with their age-matched controls.

Results: The study was conducted in asymptomatic virally suppressed PLHIV on ART for more than 5 years [n = 70, M: F = 36:34] and HIV uninfected controls [n = 68, M: F = 31:37] belonging to the age-group of 40-55 years. Blood samples were collected for assessing levels of immunosenescence markers on CD4 T cells by flow cytometry and anti-CMV antibodies as well as soluble CD14 (sCD14) levels by ELISA. The levels were compared between cases and controls and correlated with the levels of anti-CMV antibody and sCD14. PLHIV had significantly lower levels of naïve T cells and higher levels of activated and immunosenescent T cells than controls as indicated by CD38, CD57, CD28 expressing CD4 and CD8 T cells. PLHIV had higher levels of anti-CMV antibodies, but lower levels of sCD14 levels and HLADR + CD8 T cells than those in controls. Immunosenescent T cells correlated positively with anti-CMV antibody levels and negatively with sCD14 levels. Duration of dolutegravir based therapy correlated negatively with sCD14 levels.

Conclusions: Thus, higher levels of immune activation and immunosenescence in the cases possibly indicate their compromised immune status predisposing PLHIV to infections and cancers. The study indicated a need for CMV treatment regimens even in asymptomatic individuals for preventing immunosenescence. The study also indicated a role of dolutegravir induced loss of sCD14 levels in predisposing PLHIV to immunosenescence.

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来源期刊
Immunity & Ageing
Immunity & Ageing GERIATRICS & GERONTOLOGY-IMMUNOLOGY
CiteScore
10.20
自引率
3.80%
发文量
55
期刊介绍: Immunity & Ageing is a specialist open access journal that was first published in 2004. The journal focuses on the impact of ageing on immune systems, the influence of aged immune systems on organismal well-being and longevity, age-associated diseases with immune etiology, and potential immune interventions to increase health span. All articles published in Immunity & Ageing are indexed in the following databases: Biological Abstracts, BIOSIS, CAS, Citebase, DOAJ, Embase, Google Scholar, Journal Citation Reports/Science Edition, OAIster, PubMed, PubMed Central, Science Citation Index Expanded, SCImago, Scopus, SOCOLAR, and Zetoc.
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