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1
Effects of BCG infection on the susceptibility of mouse macrophages to endotoxin.卡介苗感染对小鼠巨噬细胞对内毒素敏感性的影响。
Infect Immun. 1979 Apr;24(1):59-64. doi: 10.1128/iai.24.1.59-64.1979.
2
BCG-induced enhancement of endotoxin sensitivity in C3H/HeJ mice. I. In vivo studies.卡介苗诱导C3H/HeJ小鼠内毒素敏感性增强。I. 体内研究。
J Immunol. 1980 Apr;124(4):2004-9.
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Interaction of BCG-activated macrophages with neoplastic and nonneoplastic cell lines in vitro : quantitation of the cytotoxic reaction by release of tritiated thymidine from prelabeled target cells.卡介苗激活的巨噬细胞与肿瘤和非肿瘤细胞系在体外的相互作用:通过预标记靶细胞释放氚标记胸腺嘧啶核苷对细胞毒性反应进行定量分析。
J Natl Cancer Inst. 1975 May;54(5):1177-84. doi: 10.1093/jnci/54.5.1177.
4
Aspects of beneficial endotoxin-mediated effects.有益内毒素介导效应的各个方面。
Klin Wochenschr. 1982 Jul 15;60(14):746-8. doi: 10.1007/BF01716569.
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Strain-dependent cytotoxic effects of endotoxin for mouse peritoneal macrophages.内毒素对小鼠腹腔巨噬细胞的菌株依赖性细胞毒性作用。
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Macrophage stimulation by bacterial lipopolysaccharides. III. Selective unresponsiveness of C3H/HeJ macrophages to the lipid A differentiation signal.细菌脂多糖对巨噬细胞的刺激作用。III. C3H/HeJ巨噬细胞对脂质A分化信号的选择性无反应性。
J Immunol. 1979 Nov;123(5):2304-10.
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Endotoxin-induced interferon-gamma production in culture cells derived from BCG-infected C3H/HeJ mice.内毒素诱导卡介苗感染的C3H/HeJ小鼠来源培养细胞产生γ干扰素
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Killing in vitro of Trypanosoma cruzi by macrophages from mice immunized with T. cruzi or BCG, and absence of cross-immunity on challege in vivo.用克氏锥虫或卡介苗免疫的小鼠巨噬细胞对克氏锥虫的体外杀伤作用,以及体内攻击时无交叉免疫现象。
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Infect Immun. 1982 Jun;36(3):1096-101. doi: 10.1128/iai.36.3.1096-1101.1982.

引用本文的文献

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Increased toxicity of endotoxin for tumor-bearing mice and mice responding to bacterial pathogens: macrophage activation as a common denominator.内毒素对荷瘤小鼠和对细菌病原体有反应的小鼠的毒性增加:巨噬细胞激活作为一个共同因素。
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Effect of route of Mycobacterium bovis BCG administration on induction of suppression of sporozoite immunity in rodent malaria.牛分枝杆菌卡介苗接种途径对啮齿类动物疟疾子孢子免疫抑制诱导的影响。
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Enhancement of resistance to infections by endotoxin-induced serum factor from Mycobacterium bovis BCG-infected mice.卡介苗感染小鼠的内毒素诱导血清因子增强对感染的抵抗力
Infect Immun. 1980 Jun;28(3):654-9. doi: 10.1128/iai.28.3.654-659.1980.
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Production of lymphocyte activating factor in vivo.体内淋巴细胞激活因子的产生。
Immunology. 1983 Dec;50(4):637-44.
8
Increased sensitivity of Corynebacterium parvum-treated mice to toxic effects of indomethacin and lipopolysaccharide.短小棒状杆菌处理的小鼠对吲哚美辛和脂多糖毒性作用的敏感性增加。
Infect Immun. 1985 Feb;47(2):408-14. doi: 10.1128/iai.47.2.408-414.1985.
9
Evidence for lipid peroxidation in endotoxin-poisoned mice.内毒素中毒小鼠脂质过氧化的证据。
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10
Alteration of non-specific resistance to infection with Listeria monocytogenes.对单核细胞增生李斯特菌感染的非特异性抵抗力的改变。
Infection. 1988;16 Suppl 2:S112-7. doi: 10.1007/BF01639732.

本文引用的文献

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LYSOSOMAL ACID HYDROLASES IN MICE INFECTED WITH BCG.感染卡介苗小鼠的溶酶体酸性水解酶
J Exp Med. 1965 May 1;121(5):727-38. doi: 10.1084/jem.121.5.727.
2
HYDROLASES OF MONONUCLEAR EXUDATE CELLS AND TUBERCULOSIS. I. EXUDATE CHARACTERISTICS, ESTERASES, PROTEINASES, AND LIPASE.单核渗出细胞水解酶与结核病。I. 渗出液特征、酯酶、蛋白酶和脂肪酶
Arch Pathol. 1963 Nov;76:581-91.
3
Hyperreactivity to endotoxin in mice infected with mycobacteria. Induction and elicitation of the reactions.感染分枝杆菌的小鼠对内毒素的高反应性。反应的诱导与激发。
Immunology. 1961 Oct;4(4):354-65.
4
Effects of bacterial endotoxin on metabolism. I. Carbohydrate depletion and the protective role of cortisone.细菌内毒素对代谢的影响。I. 碳水化合物消耗及可的松的保护作用。
J Exp Med. 1959 Sep 1;110(3):389-405. doi: 10.1084/jem.110.3.389.
5
The effect of Mycobacterium tuberculosis (BCG) infection on the resistance of mice to bacterial endotoxin and Salmonella enteritidis infection.结核分枝杆菌(卡介苗)感染对小鼠抵抗细菌内毒素和肠炎沙门氏菌感染能力的影响。
Br J Exp Pathol. 1959 Jun;40(3):281-90.
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Sensitivity of mice to endotoxin after vaccination with BCG (Bacillus Calmette-Guérin).卡介苗(Bacillus Calmette-Guérin)接种后小鼠对内毒素的敏感性。
Proc Soc Exp Biol Med. 1958 Oct;99(1):167-9. doi: 10.3181/00379727-99-24282.
7
Increased susceptibility of mice with brucellosis to bacterial endotoxins.患布鲁氏菌病的小鼠对细菌内毒素的易感性增加。
J Immunol. 1958 Oct;81(4):271-5.
8
Detection of endotoxin in human blood and demonstration of an inhibitor.人体血液中内毒素的检测及一种抑制剂的证明
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9
The in vitro induction and release of a cell toxin by immune C57B1-6 mouse peritoneal macrophages.免疫C57B1-6小鼠腹腔巨噬细胞对细胞毒素的体外诱导与释放
Cell Immunol. 1972 Jan;3(1):88-100. doi: 10.1016/0008-8749(72)90229-8.
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Acid phosphatase isoenzyme in human leukocytes in normal and pathologic conditions.正常及病理状态下人类白细胞中的酸性磷酸酶同工酶
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卡介苗感染对小鼠巨噬细胞对内毒素敏感性的影响。

Effects of BCG infection on the susceptibility of mouse macrophages to endotoxin.

作者信息

Peavy D L, Baughn R E, Musher D M, Musher D M

出版信息

Infect Immun. 1979 Apr;24(1):59-64. doi: 10.1128/iai.24.1.59-64.1979.

DOI:10.1128/iai.24.1.59-64.1979
PMID:378847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC414261/
Abstract

Mice infected intravenously with Mycobacterium bovis (BCG) are 100 to 1,000 times more sensitive to the lethal effects of bacterial lipopolysaccharides (LPS). Since BCG infection results in macrophage activation and LPS may cause pathophysiological effects through interaction with this cell type, it was of interest to determine whether macrophages from BCG-infected animals were more susceptible to the toxic effects of LPS in vitro. When LPS-susceptible, C57BL/6 mice were infected with BCG, a significant reduction in the 50% lethal dose of LPS was first observed after 7 days and persisted for several weeks. Macrophages from these animals had greatly increased susceptibility to LPS in vitro, which correlated with the development of acquired cellular resistance as determined by their ability to inhibit the growth of Listeria monocytogenes. In contrast, BCG infection of C3H/HeJ mice, a strain resistant to LPS, did not alter the 50% lethal dose of LPS for these animals or increase the sensitivity of their peritoneal macrophages to LPS in vitro. These results indicate that susceptibility of BCG-infected mice to the lethal effects of LPS parallels the susceptibility of their macrophages in vitro; release of vasoactive substances from LPS-susceptible activated macrophages in vivo may be, in part, responsible for lethality.

摘要

静脉注射牛分枝杆菌(卡介苗)的小鼠对细菌脂多糖(LPS)的致死作用敏感程度要高出100至1000倍。由于卡介苗感染会导致巨噬细胞活化,且LPS可能通过与这种细胞类型相互作用而产生病理生理效应,因此确定卡介苗感染动物的巨噬细胞在体外是否对LPS的毒性作用更敏感就很有意义。当LPS敏感的C57BL/6小鼠感染卡介苗后,首次观察到LPS的50%致死剂量在7天后显著降低,并持续数周。这些动物的巨噬细胞在体外对LPS的敏感性大大增加,这与通过抑制单核细胞增生李斯特菌生长能力所确定的获得性细胞抗性的发展相关。相比之下,对LPS有抗性的C3H/HeJ小鼠感染卡介苗后,这些动物的LPS 50%致死剂量并未改变,其腹腔巨噬细胞在体外对LPS的敏感性也未增加。这些结果表明,卡介苗感染小鼠对LPS致死作用的敏感性与其巨噬细胞在体外的敏感性相似;体内LPS敏感的活化巨噬细胞释放血管活性物质可能部分导致了致死性。