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利用来自鸡蛋黄的特异性免疫球蛋白在小鼠模型中对牛轮状病毒诱导的腹泻进行被动保护。

Passive protection against bovine rotavirus-induced diarrhea in murine model by specific immunoglobulins from chicken egg yolk.

作者信息

Kuroki M, Ikemori Y, Yokoyama H, Peralta R C, Icatlo F C, Kodama Y

机构信息

Immunology Research Institute, Gifu, Japan.

出版信息

Vet Microbiol. 1993 Oct;37(1-2):135-46. doi: 10.1016/0378-1135(93)90188-d.

Abstract

Chicken egg yolk immunoglobulins (yIg) specific against bovine rotavirus (BRV) serotypes 6 (strain Shimane) and 10 (strain KK-3) were used for oral passive immunization of suckling mice against experimental BRV challenge. The protective capacity of the antibody preparation was tested using different concentrations of yIg against a challenge dose of 10(7.5) TCID50 for Shimane and 10(7.0) TCID50 for KK-3 strain. There was a significant homotypic (P < 0.05) and heterotypic (P < 0.01) protection using 160 anti-Shimane or 160 anti-KK-3 neutralizing antibody titer (NAT) compared to control mice given yIg derived from eggs of mock-immunized (control) hens. The titer of infectious BRV recovered from intestinal tissue or luminal chyme decreased with increasing homotypic yIg NAT. A decrease in degree and duration of BRV antigen localization in the villus epithelial lining was observed in mice treated with homotypic yIg at optimum dose for prevention of diarrhea. The NAT in sera of challenged mice increased with decreasing NAT in the yIg given before challenge suggesting that protection was dose-dependent. The present findings indicate that a passive protection could be achieved by the use of yIg against BRV-induced diarrhea in this murine model.

摘要

用针对牛轮状病毒(BRV)血清型6(岛根株)和10(KK - 3株)的鸡卵黄免疫球蛋白(yIg)对乳鼠进行口服被动免疫,以抵抗实验性BRV攻击。针对岛根株10(7.5) TCID50和KK - 3株10(7.0) TCID50的攻击剂量,使用不同浓度的yIg测试抗体制剂的保护能力。与给予来自未免疫(对照)母鸡卵的yIg的对照小鼠相比,使用160抗岛根或160抗KK - 3中和抗体效价(NAT)时有显著的同型(P < 0.05)和异型(P < 0.01)保护作用。从肠道组织或肠腔食糜中回收的感染性BRV滴度随着同型yIg NAT的增加而降低。在用预防腹泻的最佳剂量的同型yIg处理的小鼠中,观察到BRV抗原在绒毛上皮衬里中的定位程度和持续时间降低。攻击小鼠血清中的NAT随着攻击前给予的yIg中NAT的降低而增加,表明保护作用是剂量依赖性的。目前的研究结果表明,在这个小鼠模型中,使用yIg可以实现对BRV诱导腹泻的被动保护。

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