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非复制型口服全细胞疫苗可预防产肠毒素大肠杆菌(ETEC)腹泻:刺激抗CFA(CFA/I)和抗肠毒素(抗LT)肠道IgA产生,并预防异源血清型ETEC的攻击。

Non-replicating oral whole cell vaccine protective against enterotoxigenic Escherichia coli (ETEC) diarrhea: stimulation of anti-CFA (CFA/I) and anti-enterotoxin (anti-LT) intestinal IgA and protection against challenge with ETEC belonging to heterologous serotypes.

作者信息

Evans D G, Evans D J, Opekun A R, Graham D Y

机构信息

Mucosal Immunity Laboratory, Veterans Administration Medical Center, Houston, Texas 77211.

出版信息

FEMS Microbiol Immunol. 1988 Dec;1(3):117-25. doi: 10.1111/j.1574-6968.1988.tb02363.x.

DOI:10.1111/j.1574-6968.1988.tb02363.x
PMID:3078739
Abstract

An oral killed (non-replicating) whole-cell anti-ETEC vaccine was prepared by treating enterotoxigenic Escherichia coli strain H-10407 (ST + LT +; 078: H11: CFA/I) with a 100%-lethal amount of colicin E2. Colicin E2 is a potent DNA endonuclease which enters the target bacterial cells without disrupting cellular integrity. Thus the vaccine consists of intact cells lacking chromosomal and plasmid DNA but possessing a normal complement of antigens, including CFA/I and enterotoxin(s), unaltered by chemical- or heat-treatment. Young healthy volunteers were administered two oral doses, one month apart, of approximately 3 x 10(10) vaccine cells. Of 22 vaccinees, 17 (77.3%) showed an intestinal anti-CFA/I IgA response and 19 (86.4%) showed an increase in intestinal anti-LT IgA. Twenty of 22 (90.9%) vaccinees had antibody responses to either CFA/I, LT, or both antigens, demonstrating that colicin E2-treated CFA-positive E. coli cells are an efficient vehicle in terms of delivery of antigens to the gut immune system. We previously demonstrated protection of vaccinees against challenge with the living homologous ETEC (strain H-10407). In this study, two groups of 8 vaccinees were challenged with a diarrheagenic dose of virulent ST + LT + ETEC of heterologous serotype; one group was challenged with a CFA/I-positive 063: H- strain and the other group was challenged with a CFA/II-positive 06: H16 strain. Approximately 75% efficacy was achieved in both challenge groups. None of the 16 vaccinees who had responded to both CFA/I and LT became ill upon challenge while both of the vaccinees who had not responded to either antigen did.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一种口服灭活(非复制性)全细胞抗肠毒素大肠杆菌疫苗,是通过用100%致死剂量的大肠菌素E2处理产肠毒素大肠杆菌菌株H - 10407(ST + LT +;078:H11:CFA/I)制备而成。大肠菌素E2是一种强效DNA内切酶,它能进入靶细菌细胞而不破坏细胞完整性。因此,该疫苗由缺乏染色体和质粒DNA但拥有正常抗原成分(包括CFA/I和肠毒素)的完整细胞组成,这些抗原未因化学或热处理而改变。年轻健康志愿者每隔一个月口服两剂约3×10¹⁰个疫苗细胞。在22名接种疫苗者中,17名(77.3%)出现肠道抗CFA/I IgA反应,19名(86.4%)肠道抗LT IgA增加。22名接种疫苗者中有20名(90.9%)对CFA/I、LT或两种抗原均有抗体反应,这表明经大肠菌素E2处理的CFA阳性大肠杆菌细胞在将抗原递送至肠道免疫系统方面是一种有效的载体。我们之前已证明接种疫苗者可抵御同源活肠毒素大肠杆菌(菌株H - 10407)的攻击。在本研究中,两组各8名接种疫苗者受到致泻剂量的异源血清型强毒ST + LT + 肠毒素大肠杆菌攻击;一组受到CFA/I阳性063:H - 菌株攻击,另一组受到CFA/II阳性06:H16菌株攻击。两个攻击组的疫苗效力均约达75%。对CFA/I和LT均有反应的16名接种疫苗者在受到攻击时均未患病,而对两种抗原均无反应的两名接种疫苗者均患病。(摘要截短于250词)

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