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人类免疫缺陷病毒缓慢进展者:来自印度北部一例病例的20年随访

Slow progressor of human immunodeficiency virus: 20 years follow-up of a case from North India.

作者信息

Sehgal S, Minz R W, Saikia B, Pasricha N

机构信息

Department of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Indian J Med Microbiol. 2014 Jan-Mar;32(1):75-6. doi: 10.4103/0255-0857.124325.

Abstract

A case of human immunodeficiency virus (HIV) infection from North India is described with a 20-year follow-up. Patient first reported in 1993 when he was detected HIV positive, remained healthy without treatment, married in 1999 and did not transmit the disease to his children or his wife and was lost to follow-up. He was thought to be an elite controller. After 15 years of the initial visit, his CD4 cells, however, were found to be low, with a viral load of 10,000/copies/ml. He was negative for human leukocyte antigen B57 and B27 alleles with a normal expression of CCR5 and CXCR4 on CD4 cells. Lymphocytes showed a significant production of tumour necrosis factor alpha and interferon γ, but not of interleukin (IL)-2, IL4 or IL10. It is possible that gut infection, common in India, could have triggered T cell activation in the ensuing years, resulting in activation of HIV. The case illustrates the significance of long-term follow-up of these patients for timely institution of anti-retroviral therapy.

摘要

本文描述了一例来自印度北部的人类免疫缺陷病毒(HIV)感染病例,并进行了20年的随访。患者于1993年首次报告,当时检测出HIV阳性,未经治疗保持健康,1999年结婚,未将疾病传染给子女或妻子,随后失访。他被认为是一名精英控制者。然而,在初次就诊15年后,发现他的CD4细胞数量较低,病毒载量为10,000拷贝/毫升。他的人类白细胞抗原B57和B27等位基因呈阴性,CD4细胞上CCR5和CXCR4表达正常。淋巴细胞显示肿瘤坏死因子α和干扰素γ产生显著,但白细胞介素(IL)-2、IL4或IL10未产生。印度常见的肠道感染可能在随后几年引发了T细胞活化,导致HIV激活。该病例说明了对这些患者进行长期随访以便及时开始抗逆转录病毒治疗的重要性。

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