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环磷酰胺介导的肺部迟发型超敏反应增强。

Cyclophosphamide-mediated enhancement of delayed hypersensitivity reactions in the lung.

作者信息

Enander I, Ahlstedt S, Nygren H

出版信息

Int Arch Allergy Appl Immunol. 1986;79(3):291-5. doi: 10.1159/000233989.

DOI:10.1159/000233989
PMID:3949410
Abstract

The appearance of mononuclear cells, mast cells and mucous cells in the airways was studied in Balb/c mice in relation to cell-mediated immunity reflected as delayed hypersensitivity (DH). The animals were pretreated with cyclophosphamide (Cy) to increase cell-mediated immunity and to decrease the influence of antibodies. Mice pretreated with Cy and epicutaneously sensitized with picrylchloride (PiCl) had stronger DH reactions as compared with sensitized mice not pretreated with Cy. The Cy treatment decreased the IgG antibody formation after sensitization. The Cy-pretreated, sensitized and challenged mice had increased numbers of mucus-producing cells and to some extent also mononuclear cells in their lungs compared with sensitized and challenged non-Cy-treated animals. However, the mucous cell numbers were also increased in Cy-treated, but nonsensitized mice in which most of the airway epithelium had differentiated into mucus-containing cells. The present results indicate that local cell-mediated immunity involves the appearance of mononuclear cells and mucus-producing cells in the lung. This inflammatory reaction is enhanced by Cy treatment, although mucous cell differentiation seems to be induced by exposure to Cy alone.

摘要

在Balb/c小鼠中,研究了气道中单核细胞、肥大细胞和黏液细胞的出现情况,并将其与作为迟发型超敏反应(DH)反映的细胞介导免疫相关联。用环磷酰胺(Cy)对动物进行预处理,以增强细胞介导免疫并减少抗体的影响。与未用Cy预处理的致敏小鼠相比,用Cy预处理并经皮用苦味酸氯(PiCl)致敏的小鼠具有更强的DH反应。Cy处理降低了致敏后IgG抗体的形成。与未用Cy处理的致敏和激发小鼠相比,经Cy预处理、致敏和激发的小鼠肺部产生黏液的细胞数量增加,单核细胞数量在一定程度上也增加。然而,在仅用Cy处理但未致敏的小鼠中,黏液细胞数量也增加,其中大部分气道上皮已分化为含黏液的细胞。目前的结果表明,局部细胞介导免疫涉及肺中单核细胞和产生黏液细胞的出现。这种炎症反应通过Cy处理而增强,尽管黏液细胞分化似乎仅由暴露于Cy诱导。

相似文献

1
Cyclophosphamide-mediated enhancement of delayed hypersensitivity reactions in the lung.环磷酰胺介导的肺部迟发型超敏反应增强。
Int Arch Allergy Appl Immunol. 1986;79(3):291-5. doi: 10.1159/000233989.
2
Regulation by T cells of delayed hypersensitivity reaction in mouse lung as reflected by mononuclear cells, mast cells and mucus-producing cells.通过单核细胞、肥大细胞和黏液产生细胞反映出的小鼠肺中迟发型超敏反应的T细胞调节。
Int Arch Allergy Appl Immunol. 1988;85(3):374-80. doi: 10.1159/000234535.
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Immunological suppression of delayed hypersensitivity responses in mouse lungs as reflected by numbers of mononuclear cells, mast cells and mucus-producing cells.通过单核细胞、肥大细胞和黏液分泌细胞数量反映的小鼠肺部迟发型超敏反应的免疫抑制。
Int Arch Allergy Appl Immunol. 1988;85(1):99-103. doi: 10.1159/000234481.
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Regulation of the delayed hypersensitivity reaction in the lung reflected as mononuclear, mast cell and mucus cell appearance after T helper cell depletion and adoptive transfer.肺中迟发型超敏反应的调节表现为辅助性T细胞耗竭及过继转移后单核细胞、肥大细胞和黏液细胞的出现。
Int Arch Allergy Appl Immunol. 1987;82(3-4):361-3. doi: 10.1159/000234227.
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Mononuclear cells, mast cells and mucous cells as part of the delayed hypersensitivity response to aerosolized antigen in mice.单核细胞、肥大细胞和黏液细胞作为小鼠对雾化抗原迟发型超敏反应的一部分。
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Enhancement of sheep erythrocyte (SRBC)-induced pleurisy in non-sensitized mice by cyclophosphamide: demonstration of natural cell-mediated immune reactivity to SRBC.环磷酰胺增强未致敏小鼠中绵羊红细胞(SRBC)诱导的胸膜炎:对SRBC天然细胞介导免疫反应性的证明
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Regulation of delayed-type hypersensitivity. III. Effect of cyclophosphamide on the suppressor cells for delayed-type hypersensitivity to sheep erythrocytes in mice.迟发型超敏反应的调节。III. 环磷酰胺对小鼠绵羊红细胞迟发型超敏反应抑制细胞的影响。
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Comparative analysis of the effects of cyclophosphamide and dexamethasone on intestinal immunity and microbiota in delayed hypersensitivity mice.环磷酰胺和地塞米松对迟发性超敏反应小鼠肠道免疫及微生物区系影响的比较分析。
PLoS One. 2024 Oct 17;19(10):e0312147. doi: 10.1371/journal.pone.0312147. eCollection 2024.

引用本文的文献

1
Effect of cyclophosphamide on the candidacidal activity of rabbit peritoneal macrophages.环磷酰胺对兔腹腔巨噬细胞杀念珠菌活性的影响。
Folia Microbiol (Praha). 1988;33(5):401-6. doi: 10.1007/BF02925851.
2
Regulation of delayed-type hypersensitivity-like responses in the mouse lung, determined with histological procedures: serotonin, T-cell suppressor-inducer factor and high antigen dose tolerance regulate the magnitude of T-cell dependent inflammatory reactions.用组织学方法测定小鼠肺中迟发型超敏样反应的调节:血清素、T细胞抑制诱导因子和高抗原剂量耐受性调节T细胞依赖性炎症反应的程度。
Immunology. 1989 Sep;68(1):51-8.