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豚鼠实验性皮肤利什曼病中保护性免疫的机制。III. 对无关抗原的迟发型超敏反应对豚鼠利什曼病损的抑制作用。

Mechanisms of protective immunity in experimental cutaneous leishmaniasis of the guinea-pig. III. Inhibition of leishmanial lesion in the guinea-pig by delayed hypersensitivity reaction to unrelated antigens.

作者信息

Behin R, Mauel J, Rowe D S

出版信息

Clin Exp Immunol. 1977 Aug;29(2):320-5.

Abstract

The purpose of this investigation was to determine whether prior induction of a non-specific delayed reaction at a site of leishmanial infection could modify the course of infection. Groups of animals were made hypersensitive to either DNCB or BCG and a delayed reaction was elicited by corresponding antigen in one or both ears when an infective dose of L. enriettii was inoculated. With various experimental designs the following results were obtained: (a) induction of delayed reaction by DNCB or BCG inhibited the development of leishmanial lesions; (a) the protection was effective only when delayed reaction occurred at the site of infection; (c) to be effective, the reaction had to be continuously present at the site of infection for at least 3--4 weeks; (d) lesions developed normally, in the absence of delayed reaction, in DNCB-tolerant animals treated with DNCB; (E) a protective delayed reaction did not completely eliminate the parasites from the host tissues, since metastatic lesions appeared later at ectopic areas; (f) the suppressed development of a lesion did not confer resistance to reinfection dose of the parasite. It is concluded that cell-mediated immunity plays an important role in healing leishmanial lesions in the guinea-pig and that the final effector mechanism may be sought in the non-specific microbicidal capacity of activated macrophages. The relevance of leishmania-specific delayed reaction in the course of the disease is discussed.

摘要

本研究的目的是确定在利什曼原虫感染部位预先诱导非特异性迟发型反应是否会改变感染进程。将动物分组,使其对二硝基氯苯(DNCB)或卡介苗(BCG)产生超敏反应,当接种感染剂量的恩氏利什曼原虫时,用相应抗原在一只或两只耳朵中引发迟发型反应。通过各种实验设计得到了以下结果:(a)DNCB或BCG诱导的迟发型反应抑制了利什曼原虫病变的发展;(a)只有当迟发型反应发生在感染部位时,这种保护才有效;(c)为了有效,反应必须在感染部位持续存在至少3 - 4周;(d)在用DNCB处理的对DNCB耐受的动物中,在没有迟发型反应的情况下,病变正常发展;(E)保护性迟发型反应并没有完全从宿主组织中清除寄生虫,因为转移性病变后来出现在异位区域;(f)病变发展受到抑制并没有赋予对寄生虫再感染剂量的抗性。得出的结论是,细胞介导的免疫在豚鼠利什曼原虫病变的愈合中起重要作用,并且最终效应机制可能在于活化巨噬细胞的非特异性杀菌能力。文中还讨论了利什曼原虫特异性迟发型反应在疾病过程中的相关性。

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1
[Immunity in Leishmania enriettii infection of the guinea pig].
Z Tropenmed Parasitol. 1965 Oct;16(3):277-83.

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