Impaired phenotype and function of monocyte derived dendritic cells in pulmonary tuberculosis

被引:18
作者
Rajashree, R. [1 ]
Krishnan, Gokula [2 ]
Das, Sulochana D. [1 ]
机构
[1] ICMR, Dept Immunol, Chennai 600031, Tamil Nadu, India
[2] Inst Thorac Med, Dept Pulmonol, Chennai 600031, Tamil Nadu, India
关键词
Pulmonary tuberculosis; Mycobacterium tuberculosis; Dendritic cells; Lipopolysaccharide; Differentiation; Maturation; MYCOBACTERIUM-TUBERCULOSIS; IN-VITRO; INTERFERON-GAMMA; IL-10; PRODUCTION; T-CELLS; EXPRESSION; MATURATION; INFECTION; DIFFERENTIATION; MACROPHAGES;
D O I
10.1016/j.tube.2008.07.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pulmonary tuberculosis (PTB) is often associated with impaired immunological functions. Blood monocytes, which can differentiate into dendritic Cells upon cytokine stimulation, play a central role in adequate immune reactivity. Here, we investigated the morphologic, phenotypic and functional characteristics of in vitro-generated monocyte derived dendritic cells (MoDC) from PTB patients in comparison with healthy Subjects. Phenotypic analysis revealed a defective differentiation of MoDC in PTB patients as assessed by a strong down regulation of CD1a, MHC II, CD80 and CD83 expression and impaired allosimulatory function under the influence of IL-4 and GM-CSF. In contrast, the expression of CD86 was not affected and remained same as in healthy subjects. Furthermore, the maturation Status Of lipopolysaccharide (LPS) stimulated MoDC was not optimal in PTB. However, the MoDC of PTB patients produced significantly higher levels of TNF-alpha and IL-6 but lower levels of IL-12 compared to healthy Subjects. These findings suggest that there is a fundamental defect in the differentiation and maturation of dendritic cells during PTB that may compromise the antigen presentation and Subsequent immune functions. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 83
页数:7
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