ESAT-6 and CFP-10 can be combined to reduce the cost of testing for Mycobacterium tuberculosis infection, but CFP-10 responses associate with active disease

被引:14
作者
Fox, Annette [1 ]
Jeffries, David J. [1 ]
Hill, Philip C. [1 ]
Hammond, Abdulrahman S. [1 ]
Lugos, Moses D. [1 ]
Jackson-Sillah, Dolly [1 ]
Donkor, Simon A. [1 ]
Owiafe, Patrick K. [1 ]
McAdam, Keith P. W. J. [1 ]
Brookes, Roger H. [1 ]
机构
[1] MRC Labs, TB Div, Bacterial Dis Programme, Banjul, Gambia
基金
英国医学研究理事会;
关键词
tuberculosis; infection; disease; ESAT-6; CFP-10; ELISPOT;
D O I
10.1016/j.trstmh.2007.03.001
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Commercial tests measuring IFN-gamma responses to ESAT-6 and CFP-10 are available for diagnosing Mycobacterium tuberculosis infection. Measures that minimize cost and complexity will facilitate their application in less-developed countries. We investigated whether overlapping peptides representing both ESAT-6 and CFP-10 are required to detect M. tuberculosis infection in a high TB-burden country, and whether they can be combined in a single pool. ESAT-6 and CFP-10 peptides were compared in IFN-gamma enzyme-linked immunospot (ELISPOT) in 183 HIV-negative smear-positive TB cases and 1673 HIV-negative household contacts. Separate peptide pools for each antigen were compared with a combined pool in 498 contacts. Forty per cent of responsive contacts recognized both antigens, 51% only ESAT-6 and 10% only CFP-10, whereas 56% of responsive cases recognized both antigens, 30% only ESAT-6 and 13% only CFP-10. Accordingly, CFP-10 response rates were higher for TB cases (odds ratio 2.409, P < 0.001). Low purified protein derivative response rates indicated that responses to CFP-10 only were nonspecific in contacts. Agreement between peptides in separate versus combined pools was good (kappa = 0.758, r = 0.840). Therefore a combined ESAT-6/CFP-10 peptide pool provided maximum sensitivity and efficiency, but CFP-10 was mainly required to detect active disease. (C) 2007 Royal Society of Tropical Medicine and Hygiene. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:691 / 698
页数:8
相关论文
共 33 条
[1]   Tuberculin skin testing compared with T-cell responses to Mycobacterium tuberculosis-specific and nonspecific antigens for detection of latent infection in persons with recent tuberculosis contact [J].
Arend, SM ;
Engelhard, ACF ;
Groot, G ;
de Boer, K ;
Andersen, P ;
Ottenhoff, THW ;
van Dissel, JT .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (06) :1089-1096
[2]   Antigenic equivalence of human T-cell responses to Mycobacterium tuberculosis-specific RD1-encoded protein antigens ESAT-6 and culture filtrate protein 10 and to mixtures of synthetic peptides [J].
Arend, SM ;
Geluk, A ;
van Meijgaarden, KE ;
van Dissel, JT ;
Theisen, M ;
Andersen, P ;
Ottenhoff, THM .
INFECTION AND IMMUNITY, 2000, 68 (06) :3314-3321
[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 by whole-genome DNA microarray [J].
Behr, MA ;
Wilson, MA ;
Gill, WP ;
Salamon, H ;
Schoolnik, GK ;
Rane, S ;
Small, PM .
SCIENCE, 1999, 284 (5419) :1520-1523
[5]   A Mycobacterium tuberculosis operon encoding ESAT-6 and a novel low-molecular-mass culture filtrate protein (CFP-10) [J].
Berthet, FX ;
Rasmussen, PB ;
Rosenkrands, I ;
Andersen, P ;
Gicquel, B .
MICROBIOLOGY-UK, 1998, 144 :3195-3203
[6]   BCG-induced increase in interferon-gamma response to mycobacterial antigens and efficacy of BCG vaccination in Malawi and the UK: two randomised controlled studies [J].
Black, GF ;
Weir, RE ;
Floyd, S ;
Bliss, L ;
Warndorff, DK ;
Crampin, AC ;
Ngwira, B ;
Sichali, L ;
Nazareth, B ;
Blackwell, JM ;
Branson, K ;
Chaguluka, SD ;
Donovan, L ;
Jarman, E ;
King, E ;
Fine, PEM ;
Dockrell, HM .
LANCET, 2002, 359 (9315) :1393-1401
[7]   Rapid detection of active and latent tuberculosis infection in HIV-positive individuals by enumeration of Mycobacterium tuberculosis-specific T cells [J].
Chapman, ALN ;
Munkanta, M ;
Wilkinson, KA ;
Pathan, AA ;
Ewer, K ;
Ayles, H ;
Reece, WH ;
Mwinga, A ;
Godfrey-Faussett, P ;
Lalvani, A .
AIDS, 2002, 16 (17) :2285-2293
[8]   MTSA-10, the product of the Rv3874 gene of Mycobacterium tuberculosis, elicits tuberculosis-specific, delayed-type hypersensitivity in guinea pigs [J].
Colangeli, R ;
Spencer, JS ;
Bifani, P ;
Williams, A ;
Lyashchenko, K ;
Keen, MA ;
Hill, PJ ;
Belisle, J ;
Gennaro, ML .
INFECTION AND IMMUNITY, 2000, 68 (02) :990-993
[9]   Mycobacterium africanum elicits an attenuated T cell response to early secreted antigenic target, 6 kDa, in patients with tuberculosis and their household contacts [J].
de Jong, BC ;
Hill, PC ;
Brookes, RH ;
Gagneux, S ;
Jeffries, DJ ;
Otu, JK ;
Donkor, SA ;
Fox, A ;
McAdam, KPWJ ;
Small, PM ;
Adegbola, RA .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (09) :1279-1286
[10]   Cost-optimisation of screening for latent tuberculosis in close contacts [J].
Diel, R. ;
Nienhaus, A. ;
Lange, C. ;
Schaberg, T. .
EUROPEAN RESPIRATORY JOURNAL, 2006, 28 (01) :35-44