Latent tuberculosis infection among new recruits to the army in Beijing, China in 2009

被引:12
作者
Wu, Xueqiong [1 ]
Liang, Yan [1 ]
Wang, Lan [1 ]
Wang, Zhiyun [1 ]
Zhang, Chuiying [1 ]
Yang, Yourong [1 ]
Zhang, Junxian [1 ]
机构
[1] 309th Hosp Chinese PLA, Army TB Prevent & Control Key Lab, Inst TB Res, Beijing 100091, Peoples R China
关键词
TB infection; ELISPOT; recombinant CFP-10; ESAT-6 fusion protein; tuberculin skin test; PPD; LINKED IMMUNOSPOT ASSAY; MYCOBACTERIUM-TUBERCULOSIS; SKIN-TEST; DIAGNOSIS; ESAT-6; TESTS; ELISPOT; PROTEIN; RESPONSES; PEPTIDES;
D O I
10.1111/j.1600-0463.2011.02743.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
China is a country with high latent tuberculosis infection (LTI) and has a policy of routine BCG vaccination. To monitor tuberculosis (TB) infection, a total of 907 new recruits to the army were interviewed and routinely examined by chest radiographs. They were intradermally injected with purified protein derivative (PPD) and detected with enzyme-linked immunospot (ELISPOT) assay with recombinant CFP-10/ESAT-6 (rCFP-10/ESAT-6) fusion protein, as a stimulus, from December 2009 to February 2010. The prevalence of LTI among new recruits was estimated as 50.2% and 30.7% by PPD skin test and ELISPOT assay, respectively. Of 452 PPD-negative and 455 PPD-positive volunteers, 132 (29.2%) and 146 (32.1%) were ELISPOT positive, respectively. The overall consistency between these two tests was 51.4% (466/907). Although 65.6% of PPD-positive volunteers and 27.8% of ELISPOT-positive volunteers (spot-forming cells; SFC 12.2 +/- 21.2) could find the vaccination scars on their arms, 21.3% of PPD-positive volunteers and 35.9% of ELISPOT-positive volunteers (SFC 18.3 +/- 34.6) could not. Thus, the TB infection rate in army recruits in China was not as high as previously reported. The results suggest that the ELISPOT technique, we presented, is an accurate method for screening TB infection in China.
引用
收藏
页码:377 / 384
页数:8
相关论文
共 26 条
[1]   The prognosis of latent tuberculosis: can disease be predicted [J].
Andersen, Peter ;
Doherty, T. Mark ;
Pai, Madhukar ;
Weldingh, Karin .
TRENDS IN MOLECULAR MEDICINE, 2007, 13 (05) :175-182
[2]  
Arend SM, 2001, INT J TUBERC LUNG D, V5, P680
[3]   Detection of active tuberculosis infection by T cell responses to early-secreted antigenic target 6-kDa protein and culture filtrate protein 10 [J].
Arend, SM ;
Andersen, P ;
van Meijgaarden, KE ;
Skjot, RLV ;
Subronto, YW ;
van Dissel, JT ;
Ottenhoff, THM .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (05) :1850-1854
[4]   Comparative genomics of BCG vaccines [J].
Behr, MA .
TUBERCULOSIS, 2001, 81 (1-2) :165-168
[5]  
*CTR TUB PROT CONT, REP CHIN TUB MON 200, P86
[6]  
DISTASIO AJ, 1990, MIL MED, V155, P347
[7]  
Doherty TM, 2002, J CLIN MICROBIOL, V40, P704, DOI 10.1128/JCM.40.2.704-706.2002
[8]   Improved diagnostic evaluation of suspected tuberculosis [J].
Dosanjh, Davinder P. S. ;
Hinks, Timothy S. C. ;
Innes, John A. ;
Deeks, Jonathan J. ;
Pasvol, Geoffrey ;
Hackforth, Sarah ;
Varia, Hansa ;
Millington, Kerry A. ;
Gunatheesan, Rubamalar ;
Guyot-Revol, Valerie ;
Lalvani, Ajit .
ANNALS OF INTERNAL MEDICINE, 2008, 148 (05) :325-W72
[9]  
Farhat M, 2006, INT J TUBERC LUNG D, V10, P1192
[10]   Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG [J].
Harboe, M ;
Oettinger, T ;
Wiker, HG ;
Rosenkrands, I ;
Andersen, P .
INFECTION AND IMMUNITY, 1996, 64 (01) :16-22