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Reply to Levis and Rendini.对莱维斯和伦迪尼的回复。
J Infect Dis. 2017 May 1;215(9):1488-1489. doi: 10.1093/infdis/jix084.
2
Clofazimine Mechanisms of Action in Mycobacteria, HIV, and Cancer.氯法齐明在分枝杆菌、HIV和癌症中的作用机制
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Effects of clofazimine on planktonic and biofilm growth of Mycobacterium tuberculosis and Mycobacterium smegmatis.氯法齐明对结核分枝杆菌和耻垢分枝杆菌浮游菌及生物膜生长的影响。
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In vitro activity of aminoglycosides, clofazimine, d-cycloserine and dapsone against 83 Mycobacterium avium complex clinical isolates.氨基糖苷类、氯法齐明、环丝氨酸和氨苯砜对 83 株鸟分枝杆菌复合体临床分离株的体外活性。
J Microbiol Immunol Infect. 2018 Oct;51(5):636-643. doi: 10.1016/j.jmii.2017.05.001. Epub 2017 Jun 28.
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High efficacy of clofazimine and its synergistic effect with amikacin against rapidly growing mycobacteria.氯法齐明的高效性及其与阿米卡星的协同作用对快速生长分枝杆菌。
Int J Antimicrob Agents. 2010 Apr;35(4):400-4. doi: 10.1016/j.ijantimicag.2009.12.008.
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Clofazimine Prevents the Regrowth of Mycobacterium abscessus and Mycobacterium avium Type Strains Exposed to Amikacin and Clarithromycin.氯法齐明可预防暴露于阿米卡星和克拉霉素的脓肿分枝杆菌和鸟分枝杆菌标准菌株的再生长。
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Chest. 2016 May;149(5):1285-93. doi: 10.1378/chest.15-0543. Epub 2016 Jan 12.
8
[Bacteriostatic and bactericidal study of rifabutine and clofazimine in combination against Mycobacterium avium-intracellulare and Mycobacterium xenopi].
Pathol Biol (Paris). 1989 Jun;37(5 Pt 2):585-90.
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Clofazimine drug susceptibility testing for Mycobacterium tuberculosis: the case of using the right diluent.氯法齐明药物敏感性检测结核分枝杆菌:使用正确稀释剂的案例。
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Safety and Effectiveness of Clofazimine for Primary and Refractory Nontuberculous Mycobacterial Infection.氯法齐明治疗原发性和复发性非结核分枝杆菌感染的安全性和有效性。
Chest. 2017 Oct;152(4):800-809. doi: 10.1016/j.chest.2017.04.175. Epub 2017 May 5.

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Luteolin as a potential host-directed immunotherapy adjunct to isoniazid treatment of tuberculosis.木犀草素作为异烟肼治疗结核病的潜在宿主导向免疫治疗佐剂。
PLoS Pathog. 2021 Aug 20;17(8):e1009805. doi: 10.1371/journal.ppat.1009805. eCollection 2021 Aug.
2
Luteolin-mediated Kv1.3 K+ channel inhibition augments BCG vaccine efficacy against tuberculosis by promoting central memory T cell responses in mice.木犀草素介导的 Kv1.3 K+ 通道抑制通过促进小鼠中央记忆 T 细胞反应增强卡介苗疫苗对结核病的疗效。
PLoS Pathog. 2020 Sep 21;16(9):e1008887. doi: 10.1371/journal.ppat.1008887. eCollection 2020 Sep.

本文引用的文献

1
Immunology: Channelling potassium to fight cancer.免疫学:通过引导钾元素来对抗癌症。
Nature. 2016 Sep 22;537(7621):497-499. doi: 10.1038/nature19467. Epub 2016 Sep 14.
2
Blockade of the Kv1.3 K+ Channel Enhances BCG Vaccine Efficacy by Expanding Central Memory T Lymphocytes.阻断Kv1.3钾离子通道通过扩增中枢记忆性T淋巴细胞增强卡介苗疫苗效力。
J Infect Dis. 2016 Nov 1;214(9):1456-1464. doi: 10.1093/infdis/jiw395. Epub 2016 Aug 28.
3
Immune reconstitution inflammatory syndrome in HIV-infected patients.HIV感染患者的免疫重建炎症综合征
HIV AIDS (Auckl). 2015 Feb 12;7:49-64. doi: 10.2147/HIV.S42328. eCollection 2015.
4
Clofazimine shortens the duration of the first-line treatment regimen for experimental chemotherapy of tuberculosis.氯法齐明可缩短结核病实验性化疗一线治疗方案的疗程。
Proc Natl Acad Sci U S A. 2015 Jan 20;112(3):869-74. doi: 10.1073/pnas.1416951112. Epub 2015 Jan 5.
5
Involvement of Kv1.3 and p38 MAPK signaling in HIV-1 glycoprotein 120-induced microglia neurotoxicity.Kv1.3 通道和 p38MAPK 信号通路参与 HIV-1 糖蛋白 120 诱导的小胶质细胞神经毒性。
Cell Death Dis. 2012 Jan 19;3(1):e254. doi: 10.1038/cddis.2011.140.
6
Early secreted antigen ESAT-6 of Mycobacterium tuberculosis promotes protective T helper 17 cell responses in a toll-like receptor-2-dependent manner.结核分枝杆菌早期分泌抗原 ESAT-6 通过 Toll 样受体 2 依赖性途径促进保护性辅助性 T 细胞 17 反应。
PLoS Pathog. 2011 Nov;7(11):e1002378. doi: 10.1371/journal.ppat.1002378. Epub 2011 Nov 10.
7
Regulatory T cells in cancer.肿瘤微环境中的调节性 T 细胞。
Adv Cancer Res. 2010;107:57-117. doi: 10.1016/S0065-230X(10)07003-X.
8
Adjunctive corticosteroid therapy for tuberculosis: a critical reappraisal of the literature.结核病的辅助性皮质类固醇治疗:对文献的批判性重新评估
Clin Infect Dis. 1997 Oct;25(4):872-87. doi: 10.1086/515543.
9
Interleukin-6 production by bladder tumors is upregulated by BCG immunotherapy.卡介苗免疫疗法可上调膀胱肿瘤产生白细胞介素-6的水平。
J Urol. 1995 Aug;154(2 Pt 1):572-5. doi: 10.1097/00005392-199508000-00072.
10
Clofazimine (lamprene or B663) in lepra reactions.
Lepr Rev. 1981 Jun;52(2):135-40. doi: 10.5935/0305-7518.19810015.

Reply to Levis and Rendini.

作者信息

Singh Dhiraj Kumar, Dwivedi Ved Prakash, Ranganathan Anand, Bishai William R, Van Kaer Luc, Das Gobardhan

机构信息

Special Centre for Molecular Medicine, Jawaharlal Nehru University, and.

International Centre for Genetic Engineering and Biotechnology, New Delhi, India.

出版信息

J Infect Dis. 2017 May 1;215(9):1488-1489. doi: 10.1093/infdis/jix084.

DOI:10.1093/infdis/jix084
PMID:28199694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5451602/
Abstract
摘要