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孕期的免疫保护机制。I. 妊娠小鼠针对单核细胞增生李斯特菌的细胞介导免疫。

Immune protective mechanisms during pregnancy. I. Cell-mediated immunity against Listeria monocytogenes in pregnant mice.

作者信息

Shinomiya N, Tsuru S, Taniguchi M, Fujisawa H, Ikeda M, Zinnaka Y, Nomoto K

出版信息

Immunology. 1986 Nov;59(3):373-8.

Abstract

Characteristics of protective mechanisms during pregnancy were investigated using neonatally thymectomized (NTx) and/or pregnant mice infected with sublethal doses of Listeria monocytogenes, of which the explosive growth at an early phase of 2 or 3 days after infection is prevented by non-immune macrophages, and complete elimination at a late phase from 4 to 10 days after infection is attributed to the augmented functions of macrophages in co-operation with lymphokine-producing sensitized T lymphocytes. Although in virgin control mice there was a gradual decline of bacteria from the day after infection, viable bacteria in pregnant mice showed an increase in number until Day 3. In such pregnant mice, carbon clearance was suppressed. Thus, the enhanced bacterial growth in pregnant mice within 3 days may be attributable to the suppressed functions of non-immune macrophages. Complete elimination of Listeria from Day 4 was observed in pregnant sham-operated mice as well as in non-pregnant and pregnant NTx mice. Twenty-four hour reaction of delayed-type in normal mice induced by sheep red blood cells (SRBC) in incomplete Freund's adjuvant (IFA) was not affected by pregnancy, while 48 hr reaction in mice immunized with SRBC in complete Freund's adjuvant (CFA) was suppressed by pregnancy. We have reported previously that macrophage migration inhibitory factor (MIF) was produced in the latter but not in the former, and that the tuberculin type of delayed hypersensitivity accompanied by MIF production scarcely participated in acquired resistance to Listeria. Effective elimination of Listeria in pregnant and/or NTx mice at a late phase may be attributable to the activity of cellular immunity comparable to 24 hr reaction. These results suggest that T cells showing a low degree of thymus dependency in the ontogenic development may be the major component required for acquired protective immunity against Listeria and may account for the protection in pregnant mice.

摘要

利用新生期胸腺切除(NTx)和/或感染亚致死剂量单核细胞增生李斯特菌的怀孕小鼠,研究了孕期保护机制的特征。在感染后2或3天的早期阶段,非免疫巨噬细胞可阻止该菌的爆发性生长,而在感染后4至10天的后期阶段,其被彻底清除则归因于巨噬细胞与产生淋巴因子的致敏T淋巴细胞协同作用后功能增强。尽管在未孕对照小鼠中,感染后一天起细菌数量逐渐减少,但怀孕小鼠体内的活菌数量在第3天前呈增加趋势。在这类怀孕小鼠中,碳清除功能受到抑制。因此,怀孕小鼠在3天内细菌生长增强可能归因于非免疫巨噬细胞功能受到抑制。在假手术的怀孕小鼠以及未孕和怀孕的NTx小鼠中,均观察到从第4天起李斯特菌被彻底清除。正常小鼠用不完全弗氏佐剂(IFA)中的绵羊红细胞(SRBC)诱导的24小时迟发型反应不受怀孕影响,而用完全弗氏佐剂(CFA)中的SRBC免疫的小鼠的48小时反应则受到怀孕抑制。我们之前曾报道,后者会产生巨噬细胞迁移抑制因子(MIF),而前者不会,并且伴有MIF产生的结核菌素型迟发型超敏反应几乎不参与对李斯特菌的获得性抗性。怀孕和/或NTx小鼠在后期有效清除李斯特菌可能归因于与24小时反应相当的细胞免疫活性。这些结果表明,在个体发育过程中胸腺依赖性程度较低的T细胞可能是获得性抗李斯特菌保护性免疫所需的主要成分,并且可以解释怀孕小鼠中的保护作用。

相似文献

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Impairment of T cell-mediated immunity to Listeria monocytogenes in pregnant mice.
Microbiol Immunol. 1986;30(2):165-76. doi: 10.1111/j.1348-0421.1986.tb00931.x.

本文引用的文献

2
THYMECTOMY IN NEWBORN AND ADULT MICE.新生小鼠和成年小鼠的胸腺切除术
Transplantation. 1963 Oct;1:521-5. doi: 10.1097/00007890-196301040-00011.

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