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本文引用的文献

1
Effects of Dextran Sulfate 500 on Cell-Mediated Resistance to Infection with Listeria monocytogenes in Mice.硫酸葡聚糖 500 对小鼠李斯特菌感染的细胞介导抗性的影响。
Infect Immun. 1974 Nov;10(5):1105-9. doi: 10.1128/iai.10.5.1105-1109.1974.
2
The role of cell-mediated immunity in bacterial infections.细胞介导的免疫在细菌感染中的作用。
Rev Infect Dis. 1981 Nov-Dec;3(6):1221-50. doi: 10.1093/clinids/3.6.1221.
3
Modulation of natural killer activity in mice following infection with Listeria monocytogenes.单核细胞增生李斯特菌感染后小鼠自然杀伤活性的调节
Cell Immunol. 1984 Apr 1;84(2):361-71. doi: 10.1016/0008-8749(84)90108-4.
4
Effects of cyclosporin A on experimental infection with Listeria monocytogenes.环孢素A对单核细胞增生李斯特菌实验性感染的影响。
Clin Exp Immunol. 1985 Dec;62(3):491-8.
5
Enhanced accumulation of inflammatory neutrophils and macrophages mediated by transfer of T cells from mice immunized with Listeria monocytogenes.由用单核细胞增生李斯特菌免疫的小鼠的T细胞转移介导的炎性中性粒细胞和巨噬细胞的增强积累。
J Immunol. 1985 May;134(5):3449-54.
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[Risk of infection during treatment with cyclosporin A].[环孢素A治疗期间的感染风险]
Dtsch Med Wochenschr. 1986 Nov 14;111(46):1770-5. doi: 10.1055/s-2008-1068710.
7
T-cell subsets in delayed-type hypersensitivity, protection, and granuloma formation in primary and secondary Listeria infection in mice: superior role of Lyt-2+ cells in acquired immunity.小鼠原发性和继发性李斯特菌感染中迟发型超敏反应、保护性免疫及肉芽肿形成过程中的T细胞亚群:Lyt-2⁺细胞在获得性免疫中的优势作用
Infect Immun. 1988 Aug;56(8):1920-5. doi: 10.1128/iai.56.8.1920-1925.1988.
8
The oral dosage form of FK-506.FK-506的口服剂型。
Transplant Proc. 1987 Oct;19(5 Suppl 6):17-22.
9
Sequential appearance of gamma/delta- and alpha/beta-bearing T cells in the peritoneal cavity during an i.p. infection with Listeria monocytogenes.在腹腔感染单核细胞增生李斯特菌期间,γ/δ和α/β T细胞在腹腔中相继出现。
Eur J Immunol. 1990 Mar;20(3):533-8. doi: 10.1002/eji.1830200311.
10
Chlamydia trachomatis contains a protein similar to the Legionella pneumophila mip gene product.沙眼衣原体含有一种与嗜肺军团菌mip基因产物相似的蛋白质。
Mol Microbiol. 1991 Jan;5(1):109-15. doi: 10.1111/j.1365-2958.1991.tb01831.x.

FK506无法抑制小鼠对单核细胞增生李斯特菌的T细胞介导免疫。

Failure of FK 506 to suppress the T cell-mediated immunity of mice to Listeria monocytogenes.

作者信息

Wagner J A, Kretschmar M, Nichterlein T, Hof H, Quade B

机构信息

Institute of Medical Microbiology, Faculty for Clinical Medicine Mannheim, University of Heidelberg, Germany.

出版信息

Clin Exp Immunol. 1993 Jun;92(3):473-6. doi: 10.1111/j.1365-2249.1993.tb03423.x.

DOI:10.1111/j.1365-2249.1993.tb03423.x
PMID:7685672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1554765/
Abstract

Listeria monocytogenes belongs to the group of intracellular bacteria, which means that they reside and multiply within host cells. The protective immunity against such an infection is mediated by cellular immune mechanisms. Whereas the CD8+ T cell population plays a major role therein, the CD4+ T cells are held to be of minor importance in this defence system. Consequently, one can understand that immune suppression with FK 506 which acts primarily on this latter T cell subset, does not interfere with protective immunity of mice infected with L. monocytogenes. We have demonstrated that the drug blocks neither curing of primary infection, nor formation of granulomas, nor induction of cell populations capable of mediating adoptive transfer of immunity, nor expression of pre-existing immunity.

摘要

单核细胞增生李斯特菌属于细胞内细菌类别,这意味着它们在宿主细胞内生存和繁殖。针对这种感染的保护性免疫是由细胞免疫机制介导的。虽然CD8 + T细胞群体在其中起主要作用,但CD4 + T细胞在这个防御系统中被认为不太重要。因此,可以理解,主要作用于后一种T细胞亚群的FK 506免疫抑制不会干扰感染单核细胞增生李斯特菌的小鼠的保护性免疫。我们已经证明,该药物既不阻断原发性感染的治愈,也不阻断肉芽肿的形成,也不阻断能够介导免疫过继转移的细胞群体的诱导,也不阻断预先存在的免疫的表达。