Author:
Wang Chong,Li Yan-Yuan,Li Xiang,Wei Li-Liang,Yang Xiu-Yun,Xu Dan-Dan,Jiang Ting-Ting,Li Zhong-Jie,Chen Zhong-Liang,Zhang Xing,Liu Ji-Yan,Ping Ze-Peng,Li Ji-Cheng
Abstract
Abstract
Background
Mycobacterium tuberculosis infection can activate the immune system, leading to characteristic pathological changes such as inflammatory granuloma, caseous necrosis, and cavity formation.
Methods
Clinical data of 187 cases of pulmonary tuberculosis (PTB) were analyzed using statistical methods, while serum levels of complement C4b (C4b), fibronectin (FN), and prolidase (PEPD) were detected using the ELISA method among the control, minimal PTB, moderate PTB, and advanced PTB groups.
Results
We found significantly higher levels of serum C4b and PEPD (P = 0.018, P = 0.003), and significantly lower levels of serum FN (P < 0.001) in PTB patients. Furthermore, the serum levels of 3 proteins were significantly different among 3 PTB groups. FN level was significantly higher in the moderate PTB group, compared with patients in the minimal and advanced PTB groups (P < 0.05, P < 0.01). PEPD level was significantly higher in the moderate PTB group, compared with the minimal PTB group (P < 0.05). Analysis of clinical data showed that serum albumin, C-reactive protein (CRP), prealbumin, and C4 were significantly higher (P < 0.05), while serum globulin was significantly lower in patients with PTB (P < 0.001). A significant negative correlation was found between C4b and albumin, prealbumin. On the other hand, a significant positive correlation was found between C4b and globulin, CRP, PEPD, as well as between PEPD and CRP (P < 0.05).
Conclusions
Our study showed that C4b, FN, and PEPD are associated with tissue damage, granuloma formation, and cavity formation, respectively, in patients with PTB. The present study provides a new experimental basis to understand the pathogenesis and pathological changes of PTB.
Publisher
Springer Science and Business Media LLC
Reference27 articles.
1. World Health Organization: Global tuberculosis report 2012. http://www.who.int/tb/publications/global_report/gtbr12_main.pdf,
2. Technical Guidance Group of the Fifth National TB Epidemiological Survey, The Office of the Fifth National TB Epidemiological Survey: The fifth national tuberculosis epidemiological survey in 2010. Chin J Antituber. 2012, 34 (8): 485-508.
3. Dunkelberger JR, Song WC: Complement and its role in innate and adaptive immune responses. Cell Res. 2010, 20 (1): 34-50. 10.1038/cr.2009.139.
4. Kleinnijenhuis J, Oosting M, Joosten LA, Netea MG, Van Crevel R: Innate immune recognition of Mycobacterium tuberculosis. Clin Dev Immunol. 2011, 2011: 405310-
5. Vankayalapati R, Barnes PF: Innate and adaptive immune responses to human Mycobacterium tuberculosis infection. Tuberculosis (Edinb). 2009, 89 (Suppl 1): S77-S80.