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伴刀豆球蛋白A和植物血凝素P诱导的小鼠对破伤风毒素的抗性。

Resistance induced by concanavalin A and phytohaemagglutinin P against tetanus toxin in mice.

作者信息

Marconi P, Pitzurra M, Vecchiarelli A, Pitzurra L, Bistoni F

出版信息

Ann Immunol (Paris). 1982 Jul-Aug;133D(1):15-27.

PMID:6760792
Abstract

The effect of concanavalin A (ConA), phytohaemagglutinin P (PHA) and Limulus polyphemus haemocyanin (LPH) on the lethal activity of tetanus toxin (TT) is reported. C3H mice treated s.c. with ConA or PHA but not with LPH from 48 h before to 12 h after s.c. TT challenge showed a significant increase in median survival time compared to control mice inoculated with toxin alone. This protective effect was also obtained when PHA or ConA was administered by the i.p. route, TT being injected s.c. In further studies, mice treated with ConA or PHA by different routes (s.c., i.p. or i.v.) were challenged s.c. with graded minimal lethal doses of TT, with or without i.p. administration of horse antitetanus serum (HATS) 24 h after toxin inoculation. The mice treated with ConA or PHA + HATS showed a significantly increased survival rate and a higher percentage of cured mice with respect to control animals treated with lectins alone. In contrast, the mice challenged with TT and treated with HATS alone did not show any increased survival with respect to untreated controls. Sera from ConA- or PHA-treated mice were unable to neutralize the TT. Immune depression in mice by total-body irradiation (400 R) did not abolish the protective activity of the lectins. These results show that in vivo treatment of mice with ConA or PHA but not with LPH can protect against the lethal effects of TT.

摘要

报道了刀豆球蛋白A(ConA)、植物血凝素P(PHA)和鲎血蓝蛋白(LPH)对破伤风毒素(TT)致死活性的影响。从皮下注射TT攻击前48小时至攻击后12小时,皮下注射ConA或PHA而非LPH的C3H小鼠,与仅接种毒素的对照小鼠相比,中位生存时间显著延长。当通过腹腔注射途径给予PHA或ConA,皮下注射TT时,也可获得这种保护作用。在进一步的研究中,通过不同途径(皮下、腹腔或静脉)用ConA或PHA处理的小鼠,皮下注射分级的最小致死剂量的TT,在毒素接种后24小时,腹腔注射或不注射马抗破伤风血清(HATS)。与仅用凝集素处理的对照动物相比,用ConA或PHA + HATS处理的小鼠存活率显著提高,治愈小鼠的百分比更高。相反,用TT攻击并用HATS单独处理的小鼠与未处理的对照相比,存活率没有任何提高。ConA或PHA处理的小鼠血清无法中和TT。全身照射(400 R)导致的小鼠免疫抑制并未消除凝集素的保护活性。这些结果表明,在体内用ConA或PHA而非LPH处理小鼠可预防TT的致死作用。

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