Rosenberg Y J, Janossy G
The Immune Research Corporation Inc, 6701 Democracy Blvd. 201, Suit 20189, Bethesda, MD 20817, USA.
Semin Immunol. 1999 Apr;11(2):139-54. doi: 10.1006/smim.1999.0169.
In humans, blood is commonly monitored to provide surrogates of disease progression and assess immune status. However, the varied, rapid and atypical alterations in lymphocyte subsets which may occur in blood in response to pathogens, are not predictive of changes in the bulk of the immune system. A hallmark of human and simian immunodeficiency virus (SIV) infections is the profound loss of blood CD4(+) lymphocytes, a feature widely accepted as being a consequence of direct or indirect viral killing of CD4(+) cells throughout the body. However, in recording declining CD4 counts and CD4/8 ratios in the blood, little attention has been paid to migratory behaviour or the composition and tissue distribution of various lymphocyte subsets. This article compares the lymphocyte subsets in blood and various tissues in normal and virus-infected individuals prior to and following drug treatment and indicates an absence of selective CD4(+) cell decreases or increases, highlighting the importance of lymphocyte trafficking and compartmentalization in regulating blood T cell levels and suggesting a reevaluation of the currently favoured paradigm.
在人类中,血液通常被监测以提供疾病进展的替代指标并评估免疫状态。然而,血液中淋巴细胞亚群因病原体而可能发生的多样、快速且非典型的变化,并不能预测整个免疫系统的变化。人类免疫缺陷病毒(HIV)和猴免疫缺陷病毒(SIV)感染的一个标志是血液中CD4(+)淋巴细胞的大量减少,这一特征被广泛认为是全身CD4(+)细胞直接或间接被病毒杀伤的结果。然而,在记录血液中CD4计数和CD4/8比值下降时,很少有人关注各种淋巴细胞亚群的迁移行为或组成及组织分布。本文比较了正常个体和病毒感染个体在药物治疗前后血液和各种组织中的淋巴细胞亚群,结果表明不存在选择性的CD4(+)细胞减少或增加,突出了淋巴细胞迁移和分隔在调节血液T细胞水平中的重要性,并建议重新评估当前流行的范式。