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健康、感染性疾病及特发性CD4+ T淋巴细胞减少症中的T细胞亚群

T-cell subsets in health, infectious disease, and idiopathic CD4+ T lymphocytopenia.

作者信息

Laurence J

机构信息

Department of Medicine, Cornell University Medical College, New York, NY 10021.

出版信息

Ann Intern Med. 1993 Jul 1;119(1):55-62. doi: 10.7326/0003-4819-119-1-199307010-00010.

Abstract

PURPOSE

To update our knowledge about normal absolute values for CD4+ and CD8+ peripheral T-lymphocyte subsets and to show how these values are influenced by infectious disease. These data are discussed in the context of a newly identified syndrome, idiopathic CD4+ T lymphocytopenia and severe unexplained human immunodeficiency virus (HIV)-negative immune suppression (ICL/SUHIS).

DATA IDENTIFICATION

Studies done after 1978, when T-lymphocyte subset analysis using monoclonal antibodies was introduced, identified from a MEDLARS computer search and from personal files.

STUDY SELECTION

All English-language articles that included the number of patients studied; the criteria for patient selection; and the means, ranges, and standard deviations for absolute counts of peripheral T-cell subsets.

RESULTS OF DATA ANALYSIS

The effects of certain bacterial, viral, parasitic, and fungal infections; analytic variance; and biologic factors on T-lymphocyte subsets must be considered in assessing such values in health and disease. Quantitative T-cell abnormalities secondary to advanced HIV infection may be dissociated from physiologic changes, congenital disorders, and most other conditions by documentation of absolute CD4 counts of less than 400/mm3, a progressive depletion of CD4 cells, and a CD4:CD8 ratio of less than 1.0. Designation of ICL/SUHIS as a new syndrome, dependent solely on CD4 cell count, raises the possibility that persons with an extraordinary diversity of conditions, including those with stable, "physiologic" CD4 lymphopenia, will be given the diagnosis.

CONCLUSIONS

Persons with a CD4 count of less than 300 to 400/mm3, a progressive decline in absolute CD4 count, and a CD4:CD8 ratio of less than 1.0 should be aggressively investigated for HIV infection as well as for other causes of immune deficiency, regardless of intercurrent infections. The search for potential novel infectious causes in syndromes such as ICL/SUHIS may be most productive among such a subset of all persons with CD4 counts less than normal levels.

摘要

目的

更新我们关于外周血CD4⁺和CD8⁺T淋巴细胞亚群正常绝对值的知识,并展示这些值如何受到传染病的影响。在一种新发现的综合征——特发性CD4⁺T淋巴细胞减少症和严重不明原因的人类免疫缺陷病毒(HIV)阴性免疫抑制(ICL/SUHIS)的背景下讨论这些数据。

数据识别

1978年引入使用单克隆抗体进行T淋巴细胞亚群分析后进行的研究,通过医学文献分析和检索系统(MEDLARS)计算机检索以及个人档案识别。

研究选择

所有包含研究患者数量、患者选择标准以及外周血T细胞亚群绝对计数的均值、范围和标准差的英文文章。

数据分析结果

在评估健康和疾病状态下的此类数值时,必须考虑某些细菌、病毒、寄生虫和真菌感染、分析方差以及生物学因素对T淋巴细胞亚群的影响。晚期HIV感染继发的定量T细胞异常可通过记录绝对CD4计数低于400/mm³、CD4细胞进行性消耗以及CD4:CD8比值低于1.0,与生理变化、先天性疾病和大多数其他情况相区分。仅根据CD4细胞计数将ICL/SUHIS指定为一种新综合征,增加了包括那些具有稳定的“生理性”CD4淋巴细胞减少症在内的各种情况的人被诊断为此病的可能性。

结论

无论是否并发感染,CD4计数低于300至400/mm³、绝对CD4计数进行性下降且CD4:CD8比值低于1.0的人,都应积极调查是否感染HIV以及其他免疫缺陷原因。在所有CD4计数低于正常水平的人群中,寻找ICL/SUHIS等综合征潜在的新感染病因,在此亚组人群中可能最有成效。

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