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循环中迁移抑制因子和干扰素与小鼠迟发型超敏反应。

Migration inhibitory factor and interferon in the circulation of mice with delayed hypersensitivity.

机构信息

Department of Microbiology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15213.

出版信息

Infect Immun. 1973 Jan;7(1):68-75. doi: 10.1128/iai.7.1.68-75.1973.

Abstract

When mice infected with Mycobacterium tuberculosis strain BCG were inoculated intravenously with old tuberculin (OT) or living BCG cells, both migration inhibitory factor (MIF) and interferon appeared in the circulation within a few hours. In such animals, which showed delayed hypersensitivity by footpad tests, as little as 1.5 mg of OT or as few as 1.7 x 10(6) bacteria per mouse were capable of eliciting circulating MIF and interferon. Uninfected animals inoculated with large doses of OT or living BCG cells did not produce MIF or interferon. When nonspecific stimuli such as bacterial lipopolysaccharide (LPS; from Salmonella typhimurium strain LT-2), heat-killed Brucella abortus, Newcastle disease virus (NDV), and polyinosinic acid:polycytidilic acid (poly I:C) were inoculated intravenously into BCG-infected mice, MIF was produced in the circulation of animals challenged with LPS or Brucella but not in those challenged with NDV or poly I:C, although all the stimuli were capable of eliciting an interferon response. The interferon elicited in BCG-infected mice by specific antigen differed in at least one important property from the viral inhibitor produced by the nonspecific stimuli. The interferon which appeared after injection of OT or living BCG cells was destroyed by treatment at pH 2 for 24 hr at 4C, whereas the interferons produced after injection of the nonspecific stimuli were stable under the same conditions. The MIF activity in plasma from sensitized mice inoculated with specific antigen was also destroyed by treatment at pH 2. When mouse plasma containing both MIF and interferon activity was filtered through Sephadex G-100, both mediators were excluded in the same peak fractions. Sensitization of mice with complete Freund adjuvant instead of infection with BCG cells produces a different pattern of response. Although hypersensitive to specific antigen by footpad swelling tests, mice sensitized with complete Freund adjuvant failed to produce MIF or interferon when they were inoculated intravenously with OT or living BCG cells.

摘要

当感染结核分枝杆菌 BCG 株的小鼠经静脉内接种旧结核菌素(OT)或活卡介苗细胞时,移行抑制因子(MIF)和干扰素在数小时内出现在循环中。在这些通过足垫试验显示迟发型超敏反应的动物中,只需 1.5mg OT 或每只小鼠 1.7x10(6)个细菌就能够引发循环中的 MIF 和干扰素。未感染的动物用大剂量 OT 或活卡介苗细胞接种不会产生 MIF 或干扰素。当非特异性刺激物,如细菌脂多糖(LPS;来自鼠伤寒沙门氏菌 LT-2 株)、热灭活布鲁氏菌流产株、新城疫病毒(NDV)和聚肌苷酸:聚胞苷酸(poly I:C)经静脉内接种到感染 BCG 的小鼠中时,在 LPS 或布鲁氏菌挑战的动物循环中产生 MIF,但在 NDV 或 poly I:C 挑战的动物中则不产生,尽管所有刺激物均能够引发干扰素反应。与非特异性刺激物产生的病毒抑制剂相比,特异性抗原在感染 BCG 的小鼠中引发的干扰素在至少一个重要特性上有所不同。注射 OT 或活卡介苗细胞后出现的干扰素在 pH2 下于 4°C 孵育 24 小时会被破坏,而注射非特异性刺激物后产生的干扰素在相同条件下则稳定。用特异性抗原接种致敏小鼠的血浆中的 MIF 活性也会在 pH2 下被破坏。当含有 MIF 和干扰素活性的小鼠血浆通过 Sephadex G-100 过滤时,两种介质都在相同的峰级分中被排除。用完全弗氏佐剂而不是感染卡介苗细胞致敏小鼠会产生不同的反应模式。尽管通过足垫肿胀试验对特异性抗原敏感,但用完全弗氏佐剂致敏的小鼠在静脉内接种 OT 或活卡介苗细胞时不会产生 MIF 或干扰素。

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