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环磷酰胺的作用及抑制细胞在迟发型超敏反应脱敏中的作用。

The effect of cyclophosphamide and role suppressor cells in the desensitization of delayed hypersensitivity.

作者信息

Parker D, Dwyer J M, Turk J L

出版信息

Immunology. 1981 May;43(1):191-6.

PMID:6166543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1555184/
Abstract

Desensitization of guinea-pigs with ovalbumin (OA) or bovine gamma globulin (BGG) induces strong specific desensitization and is associated with a non-specific energy to tuberculin--PPD. Similarly, it was found that animals receiving desensitizing injections of PPD have suppressed delayed hypersensitivity reactions to OA or BGG. PPD also induced strong specific desensitization. Cyclophosphamide (CY) given in one large dose (300 mg/kg) 3 days before immunization failed to affect the specific desensitization induced by all three antigens. However, if CY was given 1 day after immunization, it was not possible to induce specific desensitization. The induction of non-specific desensitization was prevented in all three antigen systems if CY was given either 3 days before or 1 day after immunization. Desensitization with either OA or BGG markedly suppressed the specific 4 hr Arthus reactions.

摘要

用卵清蛋白(OA)或牛γ球蛋白(BGG)对豚鼠进行脱敏可诱导强烈的特异性脱敏,并与对结核菌素——PPD的非特异性反应相关。同样,发现接受PPD脱敏注射的动物对OA或BGG的迟发型超敏反应受到抑制。PPD也诱导了强烈的特异性脱敏。在免疫前3天给予一次大剂量(300mg/kg)的环磷酰胺(CY)未能影响由所有三种抗原诱导的特异性脱敏。然而,如果在免疫后1天给予CY,则无法诱导特异性脱敏。如果在免疫前3天或免疫后1天给予CY,则在所有三种抗原系统中均阻止了非特异性脱敏的诱导。用OA或BGG进行脱敏可显著抑制特异性4小时阿瑟斯反应。

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本文引用的文献

1
Delayed hypersensitivity. III. Specific desensitization of guinea pigs sensitized to protein antigens.迟发型超敏反应。III. 对蛋白质抗原有致敏反应的豚鼠的特异性脱敏
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Suppression of delayed hypersensitivity to tuberculin by antigenic competition. A positive immunoregulatory mechanism sensitive to cyclophosphamide.抗原竞争对结核菌素迟发型超敏反应的抑制。一种对环磷酰胺敏感的阳性免疫调节机制。
Immunology. 1981 Apr;42(4):549-59.
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Suppressor cells in normal immunisation as a basic homeostatic phenomenon.正常免疫中的抑制细胞作为一种基本的稳态现象。
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Further studies on B-lymphocyte suppression in delayed hypersensitivity, indicating a possible mechanism for Jones-Mote hypersensitivity.对迟发型超敏反应中B淋巴细胞抑制作用的进一步研究,揭示了琼斯-莫特超敏反应的一种可能机制。
Immunology. 1973 Apr;24(4):751-8.
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Regulation of delayed hypersensitivity. Failure to transfer delayed hypersensitivity to desensitized guinea pigs.迟发型超敏反应的调节。无法将迟发型超敏反应转移至脱敏豚鼠。
J Exp Med. 1973 Jan 1;137(1):32-41. doi: 10.1084/jem.137.1.32.
6
Functional aspects of the selective depletion of lymphoid tissue by cyclophosphamide.环磷酰胺对淋巴组织选择性耗竭的功能方面
Immunology. 1972 Oct;23(4):493-501.
7
Reversal of immunological tolerance by cyclophosphamide through inhibition of suppressor cell activity.环磷酰胺通过抑制抑制性细胞活性逆转免疫耐受。
Nature. 1974 Jun 14;249(458):654-6. doi: 10.1038/249654a0.
8
In vivo suppression of delayed hypersensitivity: prolongation of desensitization in guinea pigs.体内对迟发型超敏反应的抑制:豚鼠脱敏作用的延长
J Exp Med. 1975 Sep 1;142(3):588-99. doi: 10.1084/jem.142.3.588.
9
Reversal by cyclophosphamide of tolerance in contact sensitization. Tolerance induced by prior feeding with DNCB.环磷酰胺对接触致敏中耐受性的逆转作用。先前喂食二硝基氯苯诱导的耐受性。
Immunology. 1975 May;28(5):939-42.
10
Epicutaneous induction of hyporeactivity in contact sensitization. Demonstration of suppressor cells induced by contact with 2,4-dinitrothiocyanatebenzene.接触致敏中表皮诱导低反应性。接触2,4-二硝基硫氰酸苯诱导的抑制细胞的证明。
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