Effect of sample handling on analysis of cytokine responses to Mycobacterium tuberculosis in clinical samples using ELISA, ELISPOT and quantitative PCR

被引:50
作者
Doherty, TM
Demissie, A
Menzies, D
Andersen, P
Rook, G
Zumla, A
VACSEL Study Grp
机构
[1] Statens Serum Inst, Dept TB Immunol, DK-2300 Copenhagen, Denmark
[2] Armauer Hansen Res Inst, Addis Ababa, Ethiopia
[3] Resp Axis MUHC Res Inst, Montreal Chest Inst, Montreal, PQ, Canada
[4] UCL Royal Free & Univ Coll Med Sch, Windeyer Inst Med Sci, Ctr Infect Dis & Int Hlth, London, England
关键词
tuberculosis; ELISA; ELISPOT; RT-PCR;
D O I
10.1016/j.jim.2005.01.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Measuring cytokine responses to infection has proven to be invaluable for the understanding of immunity to tuberculosis in the laboratory. However, far less data are available from studies in humans and these have often produced conflicting results. Here we describe a comprehensive multi-center comparison of the most commonly used protocols for cytokine analysis: ELISA, ELISPOT and RT-PCR, in cohorts of TB patients, their household contacts and community controls. In particular, we have studied the effect on these protocols of conditions that commonly prevail in field studies, such as delays between sample collection and analysis, or different source material, such as whole blood or frozen PBMC. The results clearly show that while there is good correlation between the methods under optimal conditions, each method has strengths and weaknesses that render them more or less suitable for particular types of analyses. Researchers should carefully consider these factors when planning human field studies. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 141
页数:13
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