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Antimicrob Agents Chemother. 1991 Dec;35(12):2625-9. doi: 10.1128/AAC.35.12.2625.
2
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Interleukin-6 antagonizes tumor necrosis factor-mediated mycobacteriostatic and mycobactericidal activities in macrophages.白细胞介素-6可拮抗肿瘤坏死因子介导的巨噬细胞对分枝杆菌的抑菌和杀菌活性。
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Effects of the hematoregulatory peptide SK&F 107647 alone and in combination with amphotericin B against disseminated candidiasis in persistently neutropenic rabbits.血液调节肽SK&F 107647单独及与两性霉素B联合应用对持续性中性粒细胞减少兔播散性念珠菌病的影响。
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Effect of granulocyte colony-stimulating factor on the candidacidal activity of polymorphonuclear neutrophils and their collaboration with fluconazole.粒细胞集落刺激因子对多形核中性粒细胞杀念珠菌活性及其与氟康唑协同作用的影响。
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本文引用的文献

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Antibiotic uptake by alveolar macrophages.肺泡巨噬细胞对抗生素的摄取。
J Lab Clin Med. 1980 Mar;95(3):429-39.
2
Treatment of disease due to Mycobacterium intracellulare.胞内分枝杆菌所致疾病的治疗。
Rev Infect Dis. 1981 Sep-Oct;3(5):1052-9. doi: 10.1093/clinids/3.5.1052.
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Pulmonary disease due to Mycobacterium intracellulare.胞内分枝杆菌所致肺部疾病
Am Rev Respir Dis. 1973 Sep;108(3):547-52. doi: 10.1164/arrd.1973.108.3.547.
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Pyrazinamide is not active in vitro against Mycobacterium avium complex.吡嗪酰胺在体外对鸟分枝杆菌复合群无活性。
Am Rev Respir Dis. 1986 Dec;134(6):1287-8. doi: 10.1164/arrd.1986.134.6.1287.
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Mycobacterium avium complex infections in patients with the acquired immunodeficiency syndrome.获得性免疫缺陷综合征患者的鸟分枝杆菌复合群感染
Ann Intern Med. 1986 Aug;105(2):184-8. doi: 10.7326/0003-4819-105-2-184.
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Phagocytosis and intracellular killing of Mycobacterium avium complex by human and murine macrophages.
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Pathology of Mycobacterium avium-intracellulare infection in acquired immunodeficiency syndrome.获得性免疫缺陷综合征中鸟分枝杆菌-胞内分枝杆菌感染的病理学
Hum Pathol. 1987 Jul;18(7):709-14. doi: 10.1016/s0046-8177(87)80242-3.
8
Mycobacterial infections in AIDS patients, with an emphasis on the Mycobacterium avium complex.艾滋病患者的分枝杆菌感染,重点是鸟分枝杆菌复合体。
Rev Infect Dis. 1986 Nov-Dec;8(6):1024-33. doi: 10.1093/clinids/8.6.1024.
9
Mycobacterium avium complex infection in patients with the acquired immunodeficiency syndrome. A clinicopathologic study.获得性免疫缺陷综合征患者的鸟分枝杆菌复合群感染。一项临床病理研究。
Chest. 1988 May;93(5):926-32. doi: 10.1378/chest.93.5.926.
10
Determination of in vitro susceptibility of Mycobacterium avium complex isolates to antimycobacterial agents by various methods.通过多种方法测定鸟分枝杆菌复合群分离株对抗分枝杆菌药物的体外敏感性。
Antimicrob Agents Chemother. 1987 Nov;31(11):1697-702. doi: 10.1128/AAC.31.11.1697.

细胞因子刺激可增强阿奇霉素在人巨噬细胞中的渗透。

Stimulation with cytokines enhances penetration of azithromycin into human macrophages.

作者信息

Bermudez L E, Inderlied C, Young L S

机构信息

Kuzell Institute for Arthritis and Infectious Diseases, California Pacific Medical Center, San Francisco 94115.

出版信息

Antimicrob Agents Chemother. 1991 Dec;35(12):2625-9. doi: 10.1128/AAC.35.12.2625.

DOI:10.1128/AAC.35.12.2625
PMID:1667256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC245442/
Abstract

An effective intracellular concentration of an antimicrobial agent is essential for therapy of infections caused by organisms of the Mycobacterium avium complex. We previously reported on the effect of the combination of azithromycin and tumor necrosis factor (TNF) against M. avium infection in macrophages. We now report that stimulation of macrophages either with recombinant human gamma interferon (IFN-gamma, 10(2) U/ml) or with recombinant human TNF-alpha (10(2) U/ml) resulted in an increase in the intracellular concentration of azithromycin by approximately 200% within 3 h, compared with the concentration in unstimulated macrophages. Infection of macrophages with M. avium complex led to a decrease in the uptake of [14C]azithromycin by infected cells, compared with that by uninfected controls. Stimulation of infected macrophages with recombinant IFN-gamma or TNF-alpha overcame the inhibitory effect associated with infection. These results suggest that the increased bactericidal activity of the TNF-alpha-azithromycin or IFN-gamma-azithromycin combination against M. avium is related to enhanced uptake of the antibiotic by the stimulated phagocyte.

摘要

对于鸟分枝杆菌复合体所致感染的治疗,抗菌药物在细胞内达到有效浓度至关重要。我们之前报道了阿奇霉素与肿瘤坏死因子(TNF)联合用药对巨噬细胞内鸟分枝杆菌感染的影响。我们现在报告,用重组人γ干扰素(IFN-γ,10² U/ml)或重组人TNF-α(10² U/ml)刺激巨噬细胞,与未刺激的巨噬细胞相比,在3小时内阿奇霉素的细胞内浓度增加了约200%。与未感染的对照相比,鸟分枝杆菌复合体感染巨噬细胞导致感染细胞对[¹⁴C]阿奇霉素的摄取减少。用重组IFN-γ或TNF-α刺激感染的巨噬细胞克服了与感染相关的抑制作用。这些结果表明,TNF-α-阿奇霉素或IFN-γ-阿奇霉素联合用药对鸟分枝杆菌杀菌活性的增强与受刺激吞噬细胞对抗生素摄取的增加有关。