Tuberculosis: progress and advances in development of new drugs, treatment regimens, and host-directed therapies

被引:257
作者
Tiberi, Simon [1 ]
du Plessis, Nelita [2 ,3 ]
Walzl, Gerhard [2 ,3 ]
Vjecha, Michael J. [4 ]
Rao, Martin [5 ,6 ]
Ntoumi, Francine [7 ,8 ]
Mfinanga, Sayoki [9 ]
Kapata, Nathan [12 ]
Mwaba, Peter [10 ,11 ]
McHugh, Timothy D. [15 ]
Ippolito, Giuseppe [13 ]
Migliori, Giovanni Battista [14 ]
Maeurer, Markus J. [5 ,6 ]
Zumla, Alimuddin [15 ,16 ]
机构
[1] Barts Hlth NHS Trust, Royal London Hosp, Div Infect, London, England
[2] Stellenbosch Univ, South African Dept Sci & Technol, Cape Town, South Africa
[3] Stellenbosch Univ, Natl Res Fdn Ctr Excellence Biomed TB Res, Cape Town, South Africa
[4] Vet Affairs Med Ctr, 50 Irving St NW, Washington, DC 20422 USA
[5] Champalimaud Fdn, Lisbon, Portugal
[6] Krankenhaus NW Frankfurt, Frankfurt, Germany
[7] Fdn Congolaise Rech Med, Brazzaville, Rep Congo
[8] Univ M Ngouabi, Fac Sci & Tech, Brazzaville, Rep Congo
[9] Muhimbili Med Res Ctr, Natl Inst Med Res, Dar Es Salaam, Tanzania
[10] UNZA UCLMS Res & Training Programme, Lusaka, Zambia
[11] Apex Univ, Lusaka, Zambia
[12] Minist Hlth, Inst Publ Hlth, Lusaka, Zambia
[13] Natl Inst Infect Dis, Rome, Italy
[14] IRCCS, Maugeri Care & Res Inst, World Hlth Org Collaborating Ctr TB & Lung Dis, Tradate, Italy
[15] UCL, Ctr Clin Microbiol, Div Infect & Immun, London WC1E 6BT, England
[16] UCL Hosp NHS Fdn Trust, Natl Inst Hlth & Res Biomed Res Ctr, London WC1E 6BT, England
基金
美国国家卫生研究院;
关键词
MULTIDRUG-RESISTANT TUBERCULOSIS; ACTIVATED PROTEIN-KINASE; HIGH-DOSE RIFAMPICIN; MYCOBACTERIUM-TUBERCULOSIS; ANTITUBERCULOSIS DRUGS; PULMONARY TUBERCULOSIS; TREATMENT OUTCOMES; SUPPRESSOR-CELLS; VITAMIN-A; MOXIFLOXACIN;
D O I
10.1016/S1473-3099(18)30110-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Tuberculosis remains the world's leading cause of death from an infectious disease, responsible for an estimated 1 674 000 deaths annually. WHO estimated 600 000 cases of rifampicin-resistant tuberculosis in 2016-of which 490 000 were multidrug resistant (MDR), with less than 50% survival after receiving recommended treatment regimens. Concerted efforts of stakeholders, advocates, and researchers are advancing further development of shorter course, more effective, safer, and better tolerated treatment regimens. We review the developmental pipeline and landscape of new and repurposed tuberculosis drugs, treatment regimens, and host-directed therapies (HDTs) for drug-sensitive and drug-resistant tuberculosis. 14 candidate drugs for drug-susceptible, drug-resistant, and latent tuberculosis are in clinical stages of drug development; nine are novel in phase 1 and 2 trials, and three new drugs are in advanced stages of development for MDR tuberculosis. Specific updates are provided on clinical trials of bedaquiline, delamanid, pretomanid, and other licensed or repurposed drugs that are undergoing investigation, including trials aimed at shortening duration of tuberculosis treatment, improving treatment outcomes and patient adherence, and reducing toxic effects. Ongoing clinical trials for shortening tuberculosis treatment duration, improving treatment outcomes in MDR tuberculosis, and preventing disease in people with latent tuberculosis infection are reviewed. A range of HDTs and immune-based treatments are under investigation as adjunctive therapy for shortening duration of therapy, preventing permanent lung injury, and improving treatment outcomes of MDR tuberculosis. We discuss the HDT development pipeline, ongoing clinical trials, and translational research efforts for adjunct tuberculosis treatment.
引用
收藏
页码:E183 / E198
页数:16
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