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用半抗原化巨噬细胞诱导对多种过敏原的接触敏感性。

Induction of contact sensitivity to a broad variety of allergens with haptenized macrophages.

作者信息

von Blomberg-van der Flier M, Scheper R J, Boerrigter G H, Polak L

出版信息

J Invest Dermatol. 1984 Aug;83(2):91-5. doi: 10.1111/1523-1747.ep12262604.

Abstract

Using guinea pigs an analysis could be made of various aspects of contact sensitivity (CS) induced by subcutaneous injection of syngeneic haptenized macrophages (oil-induced peritoneal exudate cells, PEC) as compared to epicutaneous sensitization. Very little PEC-bound hapten (dinitrochlorobenzene, or oxazolone) is needed for optimum sensitization. Nevertheless, both sensitization methods induce a state of CS that may last for over 6 months, give rise to hapten-specific antibodies with a similar isotype distribution, and show susceptibility to cyclophosphamide pretreatment. In addition, time courses and microscopic appearance of skin test reactions after either way of sensitization are identical. CS to a broad variety of physicochemically different antigens, including nickel, penicillin, and acrylates, is readily induced by syngeneic PEC, haptenized following a standardized procedure. As Freund's complete adjuvant is known to cause serious side effects like ulceration and long-lasting granuloma formation, immunization with haptenized PEC should now be considered as a clean and effective alternative in experimental CS studies.

摘要

使用豚鼠,可以分析皮下注射同基因半抗原化巨噬细胞(油诱导的腹腔渗出细胞,PEC)诱导的接触敏感性(CS)的各个方面,并与皮内致敏进行比较。最佳致敏所需的PEC结合半抗原(二硝基氯苯或恶唑酮)非常少。然而,两种致敏方法都会诱导一种CS状态,这种状态可能持续超过6个月,产生具有相似同种型分布的半抗原特异性抗体,并显示对环磷酰胺预处理敏感。此外,两种致敏方式后皮肤试验反应的时间进程和微观表现是相同的。通过标准化程序半抗原化的同基因PEC很容易诱导对多种物理化学性质不同的抗原(包括镍、青霉素和丙烯酸酯)产生CS。由于已知弗氏完全佐剂会引起严重的副作用,如溃疡和长期肉芽肿形成,因此在实验性CS研究中,用半抗原化PEC进行免疫现在应被视为一种清洁有效的替代方法。

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