Yang Xinghong, Thornburg Theresa, Holderness Kathryn, Suo Zhiyong, Cao Ling, Lim Timothy, Avci Recep, Pascual David W
Department of Immunology & Infectious Diseases, Montana State University, Bozeman, MT 59717-3610, USA.
J Biomed Biotechnol. 2011;2011:632396. doi: 10.1155/2011/632396. Epub 2011 Oct 9.
To assess whether anticolonization factor antigen I (CFA/I) fimbriae antibodies (Abs) from enterotoxigenic Escherichia coli (ETEC) can protect against various routes of challenge, BALB/c mice were immunized with a live attenuated Salmonella vaccine vector expressing CFA/I fimbriae. Vaccinated mice elicited elevated systemic IgG and mucosal IgA Abs, unlike mice immunized with the empty Salmonella vector. Mice were challenged with wild-type ETEC by the oral, intranasal (i.n.), and intraperitoneal (i.p.) routes. Naïve mice did not succumb to oral challenge, but did to i.n. challenge, as did immunized mice; however, vaccinated mice were protected against i.p. ETEC challenge. Two intramuscular (i.m.) immunizations with CFA/I fimbriae without adjuvant conferred 100% protection against i.p. ETEC challenge, while a single 30 μg dose conferred 88% protection. Bactericidal assays showed that ETEC is highly sensitive to anti-CFA/I sera. These results suggest that parenteral immunization with purified CFA/I fimbriae can induce protective Abs and may represent an alternative method to elicit protective Abs for passive immunity to ETEC.
为评估产肠毒素大肠杆菌(ETEC)的抗定殖因子抗原I(CFA/I)菌毛抗体(Abs)是否能抵御各种途径的攻击,用表达CFA/I菌毛的减毒活沙门氏菌疫苗载体免疫BALB/c小鼠。与用空沙门氏菌载体免疫的小鼠不同,接种疫苗的小鼠诱导产生了升高的全身IgG和黏膜IgA抗体。通过口服、鼻内(i.n.)和腹腔内(i.p.)途径用野生型ETEC攻击小鼠。未免疫的小鼠未死于口服攻击,但死于鼻内攻击,免疫小鼠也是如此;然而,接种疫苗的小鼠对腹腔内ETEC攻击具有抵抗力。两次无佐剂的肌肉内(i.m.)接种CFA/I菌毛可提供100%抵御腹腔内ETEC攻击的保护,而单次30μg剂量可提供88%的保护。杀菌试验表明,ETEC对抗CFA/I血清高度敏感。这些结果表明,用纯化的CFA/I菌毛进行非肠道免疫可诱导产生保护性抗体,可能代表了一种为ETEC被动免疫引发保护性抗体的替代方法。