Biomarkers for tuberculosis disease activity, cure, and relapse

被引:125
作者
Wallis, Robert S. [2 ]
Doherty, T. Mark [3 ]
Onyebujoh, Phillip [4 ]
Vahedi, Mahnaz [4 ]
Laang, Hannu [5 ]
Olesen, Ole [5 ]
Parida, Shreemanta [6 ]
Zumla, Alimuddin [1 ]
机构
[1] UCL, Sch Med, Windeyer Inst, Ctr Infect Dis & Int Hlth, London W1T 4JF, England
[2] Pfizer, New London, CT USA
[3] Statens Serum Inst, DK-2300 Copenhagen, Denmark
[4] WHO Trop Dis Res, Geneva, Switzerland
[5] European Commiss, Brussels, Belgium
[6] Max Planck Inst Infect Biol, Berlin, Germany
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; ACQUIRED RIFAMYCIN RESISTANCE; POTENTIAL SURROGATE MARKER; INTERFERON-GAMMA RESPONSES; T-CELL RESPONSES; MYCOBACTERIUM-TUBERCULOSIS; PULMONARY TUBERCULOSIS; WHOLE-BLOOD; BACTERICIDAL ACTIVITY; MESSENGER-RNA;
D O I
10.1016/S1473-3099(09)70042-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
New drugs, vaccines, and other therapies will be required to realise the goal of global tuberculosis elimination or control. This Review covers the important role biomarkers can have in accelerating drug development by providing validated surrogate endpoints that can bring enhanced statistical power to small short studies. Candidate biomarkers should differentiate people with active tuberculosis from healthy individuals, normalise with therapy, and reproducibly predict clinical outcomes in diverse patient populations. Although a large number of promising candidate biomarkers have been examined to date, few patients in these studies have reached clinically meaningful outcomes, and few of the studies have been conducted to international research standards. These markers must be further studied in tuberculosis treatment trials to evaluate the kinetics of the responses and their relation to long-term clinical outcomes. These studies will benefit from multidisciplinary collaborations including microbiologists, immunologists, clinicians, tuberculosis control personnel, and the pharmaceutical and biotechnology industry.
引用
收藏
页码:162 / 172
页数:11
相关论文
共 108 条
[21]   Lung diseases at necropsy in African children dying from respiratory illnesses: a descriptive necropsy study [J].
Chintu, C ;
Mudenda, V ;
Lucas, S ;
Nunn, A ;
Lishimpi, K ;
Maswahu, D ;
Kasolo, F ;
Mwaba, P ;
Bhat, G ;
Terunuma, H ;
Zumla, A .
LANCET, 2002, 360 (9338) :985-990
[22]   Detection of Mycobacterium tuberculosis antigens in urinary proteins of tuberculosis patients [J].
Choudhry, V ;
Saxena, RK .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2002, 21 (01) :1-5
[23]   Diagnosis of pulmonary tuberculosis in young children [J].
Coulter, J. B. S. .
ANNALS OF TROPICAL PAEDIATRICS, 2008, 28 (01) :3-12
[24]   Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major [J].
Darrah, Patricia A. ;
Patel, Dipti T. ;
De Luca, Paula M. ;
Lindsay, Ross W. B. ;
Davey, Dylan F. ;
Flynn, Barbara J. ;
Hoff, Soren T. ;
Andersen, Peter ;
Reed, Steven G. ;
Morris, Sheldon L. ;
Roederer, Mario ;
Seder, Robert A. .
NATURE MEDICINE, 2007, 13 (07) :843-850
[25]   Use of nonlinear mixed-effects analysis for improved precision of early pharmacodynamic measures in tuberculosis treatment [J].
Davies, Geraint R. ;
Brindle, Richard ;
Khoo, Saye H. ;
Aarons, Leon J. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (09) :3154-3156
[26]  
Demir T, 2002, INT J TUBERC LUNG D, V6, P155
[27]   Healthy individuals that control a latent infection with Mycobacterium tuberculosis express high evels of Th1 cytokines and the IL-4 antagonist IL-4δ2 [J].
Demissie, A ;
Abebe, M ;
Aseffa, A ;
Rook, G ;
Fletcher, H ;
Zumla, A ;
Weldingh, K ;
Brock, I ;
Andersen, P ;
Doherty, TM .
JOURNAL OF IMMUNOLOGY, 2004, 172 (11) :6938-6943
[28]  
DEMISSIE A, 2006, INFECT IMMUN
[29]   Measurement of sputum Mycobacterium tuberculosis messenger RNA as a surrogate for response to chemotherapy [J].
Desjardin, LE ;
Perkins, MD ;
Wolski, K ;
Haun, S ;
Teixeira, L ;
Chen, Y ;
Johnson, JL ;
Ellner, JJ ;
Dietze, R ;
Bates, J ;
Cave, MD ;
Eisenach, KD .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (01) :203-210
[30]   In vivo and in vitro studies of a novel cytokine, interleukin 4δ2, in pulmonary tuberculosis [J].
Dheda, K ;
Chang, JS ;
Breen, AM ;
Kim, LU ;
Haddock, JA ;
Huggett, JF ;
Johnson, MA ;
Rook, GAW ;
Zumla, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 172 (04) :501-508