Regulatory role of promoter and 3′ UTR variants of vitamin D receptor gene on cytokine response in pulmonary tuberculosis

被引:45
作者
Selvaraj, P. [1 ]
Vidyarani, M. [1 ]
Alagarasu, K. [1 ]
Anand, S. Prabhu [1 ]
Narayanan, P. R. [1 ]
机构
[1] Indian Council Med Res, Dept Immunol, TB Res Ctr, Madras 600031, Tamil Nadu, India
关键词
vitamin D receptor; cytokines; gene polymorphism; tuberculosis;
D O I
10.1007/s10875-007-9152-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vitamin D receptor (VDR) gene variants are shown to regulate immune response in tuberculosis. We studied the influence of VDR promoter (Cdx-2 and A1012G), 3' untranslated region (Apa I, Bsm I, and Taq I) and start codon (Fok I) polymorphisms on 1,25(OH)(2)D-3-modulated IL-12p40, IFN-gamma, IL-10, and IL-5 response to live Mycobacterium tuberculosis and its culture filtrate antigen (CFA) in 60 normal healthy subjects and 51 pulmonary tuberculosis patients. In peripheral blood mononuclear cell cultures with CFA and 1,25(OH)(2)D-3, IL-12p40, and IFN-gamma levels were significantly decreased (p<0.05) and IL-10 levels were significantly increased (p<0.05) in patients with GG genotype. The extended genotype bbaaTT (baT haplotype) was associated with decreased IL-12p40 and IFN-gamma levels and significantly increased IL-10 levels (p<0.05). The Cdx-2 GG genotype and baT haplotype are associated with a suppressed Th1 and increased IL-10 response, which suggests that 1,25(OH)(2)D-3 probably through the VDR polymorphic variants augments the anti-inflammatory response at the site of M. tuberculosis infection.
引用
收藏
页码:306 / 313
页数:8
相关论文
共 22 条
[1]   The polymorphism in the caudal-related homeodomain protein Cdx-2 binding element in the human vitamin D receptor gene [J].
Arai, H ;
Miyamoto, KI ;
Yoshida, M ;
Yamamoto, H ;
Taketani, Y ;
Morita, K ;
Kubota, M ;
Yoshida, S ;
Ikeda, M ;
Watabe, F ;
Kanemasa, Y ;
Takeda, E .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (07) :1256-1264
[2]   1,25(OH)2D3 PRODUCTION BY LYMPHOCYTE-T AND ALVEOLAR MACROPHAGES RECOVERED BY LAVAGE FROM NORMOCALCEMIC PATIENTS WITH TUBERCULOSIS [J].
CADRANEL, J ;
GARABEDIAN, M ;
MILLERON, B ;
GUILLOZO, H ;
AKOUN, G ;
HANCE, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (05) :1588-1593
[3]   Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors [J].
Carling, T ;
Rastad, J ;
Åkerström, G ;
Westin, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (07) :2255-2259
[4]   Effect of vitamin D3 on phagocytic potential of macrophages with live Mycobacterium tuberculosis and lymphoproliferative response in pulmonary tuberculosis [J].
Chandra, G ;
Selvaraj, P ;
Jawahar, MS ;
Banurekha, VV ;
Narayanan, PR .
JOURNAL OF CLINICAL IMMUNOLOGY, 2004, 24 (03) :249-257
[5]  
CHARPY J, 1950, Bull Med, V64, P555
[6]   The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels [J].
Correa, P ;
Rastad, J ;
Schwarz, P ;
Westin, G ;
Kindmark, A ;
Lundgren, E ;
Åkerström, G ;
Carling, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (05) :1690-1694
[7]   Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly [J].
Fang, Y ;
Van Meurs, JBJ ;
Bergink, AP ;
Hofman, A ;
Van Duijn, CM ;
Van Leeuwen, JP ;
Ap Pols, H ;
Uitterlinden, AG .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (09) :1632-1641
[8]   A novel polymorphism in the 1A promoter region of the vitamin D receptor is associated with altered susceptibilty and prognosis in malignant melanoma [J].
Halsall, JA ;
Osborne, JE ;
Potter, L ;
Pringle, JH ;
Hutchinson, PE .
BRITISH JOURNAL OF CANCER, 2004, 91 (04) :765-770
[9]   The genomics and genetics of human infectious disease susceptibility [J].
Hill, AVS .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2001, 2 :373-400
[10]   Immunomodulating effect of vitamin D3 derivatives on type-1 cellular immunity [J].
Imazeki, Ikuo ;
Matsuzaki, Junko ;
Tsuji, Keiko ;
Nishimura, Takashi .
BIOMEDICAL RESEARCH-TOKYO, 2006, 27 (01) :1-9