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T细胞受体切除环和HIV-1 2-LTR游离型DNA用于预测未接受有效治疗患者的艾滋病发病情况。

T cell receptor excision circles and HIV-1 2-LTR episomal DNA to predict AIDS in patients not receiving effective therapy.

作者信息

Goedert J J, O'Brien T R, Hatzakis A, Kostrikis L G

机构信息

Viral Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.

出版信息

AIDS. 2001 Nov 23;15(17):2245-50. doi: 10.1097/00002030-200111230-00005.

Abstract

OBJECTIVE

To determine whether improved prediction of AIDS-free survival following HIV-1 seroconversion is achieved by measuring HIV-1 2-LTR episomal DNA (2-LTR) circles and T cell receptor rearrangement excision circles (TREC), reflecting HIV replication and lymphocyte emigration from the thymus, respectively.

DESIGN

Subanalysis of a cohort of 154 patients with hemophilia who became HIV positive between 1978 and 1985 and were followed prospectively.

METHODS

Relative hazards (RH) of AIDS, in the absence of highly effective anti-HIV therapy, were estimated for age, HIV-1 viral load, CD4 lymphocyte count and levels of HIV-1 2-LTR circles and TREC [per 106 peripheral blood mononuclear cells (PBMC)].

RESULTS

TREC correlated significantly with CD4 cell counts (r = 0.30) and age (r = -0.60). 2-LTR circles correlated significantly with HIV-1 viral load (r = 0.35). If viral load, CD4 lymphocytes and age were included in a proportional hazards model, the risk of AIDS during a median of 11.6 years of follow-up was increased significantly with fewer TREC (adjusted RH, 2.0 per log10 copies/106 PBMC) and more 2-LTR circles (RH, 1.7 per log10 copies/106 PBMC). AIDS prediction with TREC and 2-LTR circles held for most subgroups defined by median viral load, CD4 lymphocytes and age.

CONCLUSIONS

PBMC that have high levels of HIV-1 replication and low levels of recent thymic emigrants are associated with a substantially increased risk of AIDS. It is not known if measurement of either TREC or 2-LTR circles will complement HIV-1 viral load as an estimation of the risk of AIDS for patients who are receiving highly effective anti-HIV therapy.

摘要

目的

通过检测分别反映HIV复制及胸腺淋巴细胞迁出的HIV-1 2-LTR游离型DNA(2-LTR)环和T细胞受体重排切除环(TREC),确定HIV-1血清转化后无艾滋病生存的预测是否得到改善。

设计

对1978年至1985年间HIV呈阳性且接受前瞻性随访的154例血友病患者队列进行亚分析。

方法

在未进行高效抗HIV治疗的情况下,针对年龄、HIV-1病毒载量、CD4淋巴细胞计数以及HIV-1 2-LTR环和TREC水平[每106个外周血单个核细胞(PBMC)]估算艾滋病的相对风险(RH)。

结果

TREC与CD4细胞计数(r = 0.30)和年龄(r = -0.60)显著相关。2-LTR环与HIV-1病毒载量(r = 0.35)显著相关。如果将病毒载量、CD4淋巴细胞和年龄纳入比例风险模型,在中位随访11.6年期间,TREC越少(校正RH,每log10拷贝/106 PBMC为2.0)和2-LTR环越多(RH,每log10拷贝/106 PBMC为1.7),艾滋病风险显著增加。根据中位病毒载量、CD4淋巴细胞和年龄定义的大多数亚组中,TREC和2-LTR环对艾滋病预测均有效。

结论

HIV-1复制水平高且近期胸腺迁出细胞水平低的PBMC与艾滋病风险大幅增加相关。对于接受高效抗HIV治疗的患者,尚不清楚检测TREC或2-LTR环是否能作为HIV-1病毒载量的补充来评估艾滋病风险。

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