Enzyme-linked immunospot assay responses to early secretory antigenic target 6, culture filtrate protein 10, and purified protein derivative among children with tuberculosis: Implications for diagnosis and monitoring of therapy

被引:99
作者
Nicol, MP
Pienaar, D
Wood, K
Eley, B
Wilkinson, RJ
Henderson, H
Smith, L
Samodien, S
Beatty, D
机构
[1] Univ Cape Town, Inst Infect Dis & Mol Med, Div Med Microbiol, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
[2] Univ Cape Town, Sch Child & Adolescent Hlth, ZA-7925 Cape Town, South Africa
[3] Univ London Imperial Coll Sci Technol & Med, Wellcome Trust Ctr Res Clin Trop Med, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1086/429245
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The ability to detect tuberculosis-specific lymphocytes by enzyme-linked immunospot(ELISPOT) assay may have important implications for the diagnosis and monitoring of tuberculosis in children, for which routine methods lack sensitivity. We conducted a study to determine the presence and time course of ELISPOT responses in children with tuberculosis. Methods. Blood samples were obtained from children with a clinical diagnosis of tuberculosis, and interferon-gamma ELISPOT assays were performed using purified protein derivative (PPD), early secretory antigenic target 6 (ESAT-6), and culture filtrate protein 10 (CFP10) as stimulants. A subset of children were retested after 1, 3, and 6 months of therapy. Results. Detectable responses to ESAT-6 or CFP10 were found in 49 of 70 children with clinical tuberculosis but were more frequently found in those with culture-proven disease (P = .05). The number of subjects with responses to PPD increased after 1 month of therapy (P = .0004) and decreased at 3 and 6 months. Conclusion. Tuberculosis-specific ELISPOT testing is a promising tool that should be evaluated as a potential diagnostic test for childhood tuberculosis. We caution against the use of an early decrease in response as a marker of successful antituberculous chemotherapy.
引用
收藏
页码:1301 / 1308
页数:8
相关论文
共 17 条
[11]   Rapid detection of Mycobacterium tuberculosis infection by enumeration of antigen-specific T cells [J].
Lalvani, A ;
Pathan, AA ;
McShane, H ;
Wilkinson, RJ ;
Latif, M ;
Conlon, CP ;
Pasvol, G ;
Hill, AVS .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (04) :824-828
[12]   Enumeration of T cells specific for RD1-encoded antigens suggests a high prevalence of latent Mycobacterium tuberculosis infection in healthy urban Indians [J].
Lalvani, A ;
Nagvenkar, P ;
Udwadia, Z ;
Pathan, AA ;
Wilkinson, KA ;
Shastri, JS ;
Ewer, K ;
Hill, AVS ;
Mehta, A ;
Rodrigues, C .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (03) :469-477
[13]   Enhanced contact tracing and spatial tracking of Mycobacterium tuberculosis infection by enumeration of antigen-specific T cells [J].
Lalvani, A ;
Pathan, AA ;
Durkan, H ;
Wilkinson, KA ;
Whelan, A ;
Deeks, JJ ;
Reece, WHH ;
Latif, M ;
Pasvol, G ;
Hill, AVS .
LANCET, 2001, 357 (9273) :2017-2021
[14]  
Mawa PA, 2004, INT J TUBERC LUNG D, V8, P586
[15]   Transmission of tuberculosis in a high incidence urban community in South Africa [J].
Verver, S ;
Warren, RM ;
Munch, Z ;
Vynnycky, E ;
van Helden, PD ;
Richardson, M ;
van der Spuy, GD ;
Enarson, DA ;
Borgdorff, MW ;
Behr, MA ;
Beyers, N .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2004, 33 (02) :351-357
[16]   Ex vivo characterization of early secretory antigenic target 6-specific T cells at sites of active disease in pleural tuberculosis [J].
Wilkinson, KA ;
Wilkinson, RJ ;
Pathan, A ;
Ewer, K ;
Prakash, M ;
Klenerman, P ;
Maskell, N ;
Davies, R ;
Pasvol, G ;
Lalvani, A .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (01) :184-187
[17]   Tuberculosis in the developing world [J].
Zar, HJ .
PEDIATRIC PULMONOLOGY, 2004, :53-54