Reduced Mycobacterium tuberculosis association with monocytes from diabetes patients that have poor glucose control

被引:76
作者
Gomez, Diana I. [1 ]
Twahirwa, Marcel [2 ]
Schlesinger, Larry S. [3 ,4 ]
Restrepo, Blanca I. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Sch Publ Hlth Brownsville, Div Epidemiol, Brownsville, TX 78520 USA
[2] Doctors Hosp Renaissance, Joslin Diabet Ctr, Edinburg, TX USA
[3] Ohio State Univ, Ctr Microbial Interface Biol, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Microbial Infect & Immun, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
Tuberculosis; Diabetes; Complement; Monocyte; Mycobacterium; PHAGOCYTOSIS; RECEPTORS; INTERLEUKIN-12; EXPRESSION; ANTIBODIES; INCREASES; METFORMIN; RESPONSES; VIRULENT; STRAINS;
D O I
10.1016/j.tube.2012.10.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The re-emerging importance of type 2 diabetes mellitus (DM) to tuberculosis (TB) control is of growing concern, but the basis for this relationship is poorly understood. Given the importance of mononuclear phagocytes for TB control and the reported alterations in monocytes of DM patients, we evaluated whether the initial interaction between both was affected in diabetics. Mycobacterium tuberculosis-naive individuals with and without DM were group matched by age and gender and the efficiency of M. tuberculosis association (attachment and ingestion) with their monocytes was assessed in the presence of autologous serum. The association of M. tuberculosis with monocytes was significantly lower in diabetics (19.2 +/- 6.1) than non-diabetics (27.5 +/- 7.9; p = 0.02). Multivariate analysis controlling for host socio demographics, DM characteristics and serum lipids indicated that male gender (p = 0.04) and poorly-controlled DM (high HbA(1c) and hyperglycemia; p = 0.01) were significantly associated with the lower interaction of M. tuberculosis with monocytes. Serum heat-inactivation reduced the association of M. tuberculosis to similar levels in both study groups (p = 0.69) suggesting alterations in the complement pathway of DM patients. These findings suggest an altered route of entry of the pathogen in DM patients that may influence the downstream activation of signaling pathways in the monocyte and the survival of mycobacteria. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:192 / 197
页数:6
相关论文
共 39 条
[31]  
Schlesinger LS, 1996, CURR TOP MICROBIOL, V215, P71
[32]  
SCHLESINGER LS, 1993, J IMMUNOL, V150, P2920
[33]  
SCHLESINGER LS, 1990, J IMMUNOL, V144, P2771
[34]   The role of interferon-gamma in the increased tuberculosis risk in type 2 diabetes mellitus [J].
Stalenhoef, J. E. ;
Alisjahbana, B. ;
Nelwan, E. J. ;
van der Ven-Jongekrijg, J. ;
Ottenhoff, T. H. M. ;
van der Meer, J. W. M. ;
Nelwan, R. H. ;
Netea, M. G. ;
van Crevel, R. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2008, 27 (02) :97-103
[35]   Selective suppression of interleukin-12 induction after macrophage receptor ligation [J].
Sutterwala, FS ;
Noel, GJ ;
Clynes, R ;
Mosser, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (11) :1977-1985
[36]   Glutathione deficiency in type 2 diabetes impairs cytokine responses and control of intracellular bacteria [J].
Tan, Kai Soo ;
Lee, Kok Onn ;
Low, Kee Chung ;
Gamage, Akshamal Mihiranga ;
Liu, Yichun ;
Tan, Gek-Yen Gladys ;
Koh, Hui Qi Vanessa ;
Alonso, Sylvie ;
Gan, Yunn-Hwen .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (06) :2289-2300
[37]   Diabetic Mice Display a Delayed Adaptive Immune Response to Mycobacterium tuberculosis [J].
Vallerskog, Therese ;
Martens, Gregory W. ;
Kornfeld, Hardy .
JOURNAL OF IMMUNOLOGY, 2010, 184 (11) :6275-6282
[38]  
World Health Organization, 2011, TUB GLOB FACTS 2011
[39]   Growth of virulent and avirulent Mycobacterium tuberculosis strains in human macrophages [J].
Zhang, M ;
Gong, JH ;
Lin, YG ;
Barnes, PF .
INFECTION AND IMMUNITY, 1998, 66 (02) :794-799