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刺激或免疫激活的巨噬细胞对单核细胞增生李斯特菌免疫应答诱导的影响。

Effects of stimulated or immunologically activated macrophages on the induction of immune responses to Listeria monocytogenes.

作者信息

Yoshikai Y, Ohga S, Takeda Y, Nomoto K

机构信息

Department of Immunology, Kyushu University, Fukuoka, Japan.

出版信息

Immunobiology. 1990 Feb;180(2-3):124-37. doi: 10.1016/S0171-2985(11)80323-2.

DOI:10.1016/S0171-2985(11)80323-2
PMID:2345013
Abstract

The influences of peritoneal macrophages induced by proteose peptone, Corynebacterium parvum (C. parvum) or Bacillus Calmette Guérin (BCG) on the initiation and development of immune responses and protection against Listeria monocytogenes infection were studied in mice. Mice treated intraperitoneally (i.p.) with proteose peptone 4 days previously showed much the same level of protection against an intraperitoneal infection with Listeria as untreated mice. Mice treated i.p. with C. parvum 4 days previously, of which peritoneal macrophages had increased abilities for intracellular killing of Listeria and O2- generation as compared with peptone-elicited macrophages, exhibited an enhanced resistance against the listerial infection. The degree of immune responses, as assessed by delayed footpad reaction (DFR), was rather depressed in these mice because C. parvum-activated macrophages acting as scavenger cells reduced the amount of effective antigenic stimulation. BCG-activated peritoneal macrophages from mice treated i.p. with BCG 14 days previously showed a strong ability for antigen presentation in correlation with increases in the number of Ia-bearing macrophages and in the level of interleukin 1 (IL 1) production. These mice showed an early appearance of DFR response and a markedly enhanced resistance against the listerial infection. These results suggested that the differences in macrophage activities as scavenger cells, cytokine-secreting cells and antigen presenting cells may account for the differences in the responsiveness against listerial infection in peptone-, C. parvum- and BCG-treated mice.

摘要

研究了经蛋白胨、短小棒状杆菌(C. parvum)或卡介苗(BCG)诱导的小鼠腹腔巨噬细胞对免疫反应的启动和发展以及抵抗单核细胞增生李斯特菌感染的保护作用。4天前经腹腔注射(i.p.)蛋白胨处理的小鼠,对腹腔感染李斯特菌的保护水平与未处理的小鼠大致相同。4天前经腹腔注射C. parvum处理的小鼠,其腹腔巨噬细胞对李斯特菌的细胞内杀伤能力和O2-生成能力比蛋白胨诱导的巨噬细胞有所增强,对李斯特菌感染表现出更强的抵抗力。通过足垫迟发型反应(DFR)评估,这些小鼠的免疫反应程度相当低,因为作为清除细胞的C. parvum激活的巨噬细胞减少了有效抗原刺激的量。14天前经腹腔注射BCG处理的小鼠的BCG激活的腹腔巨噬细胞,与含Ia巨噬细胞数量增加和白细胞介素1(IL 1)产生水平增加相关,表现出很强的抗原呈递能力。这些小鼠早期出现DFR反应,对李斯特菌感染的抵抗力明显增强。这些结果表明,作为清除细胞、细胞因子分泌细胞和抗原呈递细胞的巨噬细胞活性差异,可能解释了蛋白胨、C. parvum和BCG处理的小鼠对李斯特菌感染反应性的差异。

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Effects of stimulated or immunologically activated macrophages on the induction of immune responses to Listeria monocytogenes.刺激或免疫激活的巨噬细胞对单核细胞增生李斯特菌免疫应答诱导的影响。
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引用本文的文献

1
Increased susceptibility to primary infection with Listeria monocytogenes in germfree mice may be due to lack of accumulation of L-selectin+ CD44+ T cells in sites of inflammation.无菌小鼠对单核细胞增生李斯特菌原发性感染的易感性增加,可能是由于炎症部位缺乏L-选择素+CD44+T细胞的积累。
Infect Immun. 1996 Aug;64(8):3280-7. doi: 10.1128/iai.64.8.3280-3287.1996.
2
Difference in the functional maturation of T cells against Listeria monocytogenes in lymph nodes and spleen.淋巴结和脾脏中针对单核细胞增生李斯特菌的T细胞功能成熟的差异。
Immunology. 1992 Feb;75(2):238-44.
3
Effect of recombinant human granulocyte colony-stimulating factor (rh G-CSF) on murine resistance against Listeria monocytogenes.
重组人粒细胞集落刺激因子(rh G-CSF)对小鼠抗单核细胞增生李斯特菌抵抗力的影响。
Immunology. 1992 Mar;75(3):475-80.