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单价铜绿假单胞菌口服疫苗在铜绿假单胞菌实验性感染中的疗效研究。

Investigations on the efficacy of monovalent Pseudomonas aeruginosa vaccine for oral administration in Pseudomonas aeruginosa experimental infection.

作者信息

Meitert E, Sima F, Savulian C, Petrovici M, Chersulick E, Costache G

出版信息

Arch Roum Pathol Exp Microbiol. 1989 Jul-Sep;48(3):237-51.

PMID:2519634
Abstract

Therapeutic efficacy of Pseudomonas aeruginosa vaccine for oral use (10(10) killed germs/ml), prepared from strain 4922, belonging to serotype XV, by Meitert-Meitert scheme, on 4 experimental models in mice (pneumonia, infected burn, septicaemia and urinary tract infection) was studied in comparison with monovalent Ps. aeruginosa vaccine serotype XV (10(9) killed germs/ml) for subcutaneous use and also with associated administration of the two vaccine variants. Mice immunization by using vaccine for oral use was performed by 0.5 ml vaccine per day, for 10 days and vaccine for subcutaneous use was administrated in a volume of 0.5 ml x 2, at 3 days interval. Mice immunization by using the two vaccine types, in association was concomitantly performed and in the same quantity as for separate immunization. In experimental pneumonia, Ps. aeruginosa vaccine for oral use protected mice in 35% of cases, those with infected burns were protected in 33.3% of cases, those with septicemia--in 96.6% of cases and those with urinary tract infection in 50% of cases. As compared to Ps. aeruginosa vaccine for subcutaneous use, the results obtained by vaccine for oral use are less favourable but associated administration of both vaccine variants led to superior results. Thus, in experimental pneumonia, it was obtained a surviving rate of 65% for animals immunized with both vaccine types, in comparison with 50% for animals immunized with vaccine for subcutaneous use only, and in Ps. aeruginosa infected burn, it was obtained a recovering rate of 79.1% for the animals immunized by using both vaccines, in comparison with 70.8% surviving for animals immunized with vaccine for subcutaneous use. In experimental septicaemia and urinary tract infection, combined use of both vaccine variants determined animals surviving and recovering in percents similar to those obtained by separate administration of vaccine for subcutaneous use (in septicemia--100% protection; in urinary tract infection--75% protection).

摘要

采用梅尔特 - 梅尔特方案,由属于血清型XV的4922菌株制备的口服铜绿假单胞菌疫苗(10¹⁰个灭活菌/ml)对小鼠的4种实验模型(肺炎、感染烧伤、败血症和尿路感染)的治疗效果进行了研究,并与皮下使用的单价血清型XV铜绿假单胞菌疫苗(10⁹个灭活菌/ml)以及两种疫苗变体联合给药进行了比较。口服疫苗对小鼠的免疫接种是每天0.5 ml疫苗,共10天,皮下使用的疫苗以0.5 ml×2的剂量,间隔3天给药。同时使用两种疫苗类型对小鼠进行联合免疫接种,剂量与单独免疫接种相同。在实验性肺炎中,口服铜绿假单胞菌疫苗在35%的病例中保护了小鼠,感染烧伤的小鼠在33.3%的病例中得到保护,败血症小鼠在96.6%的病例中得到保护,尿路感染小鼠在50%的病例中得到保护。与皮下使用的铜绿假单胞菌疫苗相比,口服疫苗获得的结果不太理想,但两种疫苗变体联合给药产生了更好的结果。因此,在实验性肺炎中,两种疫苗都接种的动物存活率为65%,而仅接种皮下使用疫苗的动物存活率为50%;在铜绿假单胞菌感染烧伤中,使用两种疫苗免疫的动物恢复率为79.1%,而接种皮下使用疫苗的动物存活率为70.8%。在实验性败血症和尿路感染中,两种疫苗变体联合使用使动物存活和恢复的百分比与单独皮下使用疫苗相似(败血症中——100%保护;尿路感染中——75%保护)。

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