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一种针对埃尔托型霍乱的口服减毒活疫苗的研发。

Development of a live, oral, attenuated vaccine against El Tor cholera.

作者信息

Taylor D N, Killeen K P, Hack D C, Kenner J R, Coster T S, Beattie D T, Ezzell J, Hyman T, Trofa A, Sjogren M H

机构信息

Division of Communicable Diseases and Immunology, Walter Reed Army Institute of Research, Washington, DC.

出版信息

J Infect Dis. 1994 Dec;170(6):1518-23. doi: 10.1093/infdis/170.6.1518.

Abstract

Vibrio cholerae El Tor strains from Peru, Bangladesh, and Bahrain were attenuated by deletion of a genetic element that encodes virulence factors and RS1. The B subunit of ctx (ctxB) was reintroduced into the recA gene of the deletion mutants, rendering them unable to recombine with exogenous genetic elements and generating Peru-3, Bang-3, and Bah-3. Fifteen volunteers received one dose of various vaccine strains at 4 x 10(6) to 1 x 10(8) cfu. All strains colonized the gut. A > or = 4-fold rise in vibriocidal titer was observed in 14 volunteers, with titers of > or = 1600 in 13. Peru-3 was the least reactogenic, but 2 of 6 volunteers had loose stools. Peru-14, a filamentous motility-deficient mutant of Peru-3, was well tolerated and colonized 18 of 21 volunteers at doses of 2 x 10(6) to 1 x 10(9) cfu. Also, when 8 Peru-3 or Peru-5 vaccinees, 5 Peru-14 vaccinees, and 8 controls were challenged with 2 x 10(6) cfu V. cholerae El Tor Inaba (N16961), 11 vaccinees were protected compared with no controls. Peru-14 shows promise as a safe, effective, single-dose oral vaccine against El Tor cholera.

摘要

来自秘鲁、孟加拉国和巴林的霍乱弧菌埃尔托生物型菌株通过缺失编码毒力因子和RS1的遗传元件而减毒。将ctx的B亚基(ctxB)重新导入缺失突变体的recA基因中,使其无法与外源性遗传元件重组,从而产生了秘鲁-3、孟加拉-3和巴林-3。15名志愿者接受了一剂4×10⁶至1×10⁸cfu的各种疫苗菌株。所有菌株都在肠道定殖。14名志愿者的杀弧菌滴度升高了≥4倍,13人的滴度≥1600。秘鲁-3的反应原性最低,但6名志愿者中有2人出现腹泻。秘鲁-14是秘鲁-3的丝状运动缺陷型突变体,耐受性良好,在2×10⁶至1×10⁹cfu剂量下,21名志愿者中有18人定殖。此外,当8名秘鲁-3或秘鲁-5疫苗接种者、5名秘鲁-14疫苗接种者和8名对照者用2×10⁶cfu霍乱弧菌埃尔托生物型稻叶(N16961)进行攻击时,与无对照者相比,11名疫苗接种者受到了保护。秘鲁-14作为一种安全、有效的单剂量口服抗埃尔托霍乱疫苗显示出前景。

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