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环磷酰胺对迟发型超敏反应表达及诱导的影响。

Effects of cyclophosphamide on the expression and induction of delayed hypersensitivity.

作者信息

Himeno K, Nomoto K, Takeya K

出版信息

Microbiol Immunol. 1978;22(11):719-30. doi: 10.1111/j.1348-0421.1978.tb00425.x.

Abstract

Erythematous delayed reactions without induration, presumably assigned to Jones-Mote type, were characterized by the resistance to treatment with cyclophosphamide (CY) before elicitation or immunization in guinea pigs immunized with BGG in IFA or CFA. CY-treatment before elicitation converted delayed erythematous reactions from negative to positive at late intervals after immunization with BGG in IFA. Such a treatment augmented erythematous delayed reactions in animals immunized with BGG in CFA, but abolished induration at the reaction sites. CY-treatment before elicitation or immunization reduced the numbers of basophils at the reaction sites, although erythematous delayed reactions were augmented. Effector T cells responsible for delayed erythematous reaction without induration appear to persist for a long period of time after immunization in the presence of antibody production or tuberculin hypersensitivity and the expression of their function may be inhibited by suppressive mechanisms.

摘要

无硬结的红斑性迟发型反应,推测属于琼斯-莫特型,其特征是在用不完全弗氏佐剂(IFA)或完全弗氏佐剂(CFA)中卡介苗(BGG)免疫的豚鼠中,在激发或免疫前用环磷酰胺(CY)治疗时具有抗性。在用IFA中的BGG免疫后,激发前的CY治疗在免疫后期将迟发型红斑反应从阴性转变为阳性。这种治疗增强了用CFA中的BGG免疫的动物的红斑性迟发型反应,但消除了反应部位的硬结。激发或免疫前的CY治疗减少了反应部位的嗜碱性粒细胞数量,尽管红斑性迟发型反应增强了。负责无硬结的红斑性迟发型反应的效应T细胞在免疫后似乎在抗体产生或结核菌素超敏反应存在的情况下长期持续存在,其功能的表达可能受到抑制机制的抑制。

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