首页> 美国卫生研究院文献>Journal of Virology >Orally administered microencapsulated reovirus can bypass suckled neutralizing maternal antibody that inhibits active immunization of neonates.
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Orally administered microencapsulated reovirus can bypass suckled neutralizing maternal antibody that inhibits active immunization of neonates.

机译:口服微囊化呼肠孤病毒可以绕过乳汁中和母体抗体从而抑制新生儿的主动免疫。

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摘要

Purified reovirus serotype 1, encapsulated in biodegradable aqueous microcapsules, was found to bypass maternal antibody passively transferred by suckling to neonates. Genetically identical, immunocompetent F1 scid/+ mice were generated by the reciprocal crosses of C.B17 scid/scid and normal congenic +/+ adult mice. The immunocompetent +/+ dams were either orally infected with reovirus prior to mating or not. Thus, these immunocompetent F1 pups developed either in the absence or in presence of passively transferred maternal immunity. The F1 mice were orally immunized on day 10 with either live virus, microencapsulated reovirus, or empty microcapsules plus live virus. The immune responses were assessed in the neonatal gut-associated lymphoid tissues (GALT). Examination of reovirus specific immunoglobulin A in the serum and GALT, taken on days 7, 14, and 21 postimmunization, clearly demonstrated that microencapsulated reovirus could bypass the normal effect of maternal antibodies, passively acquired by suckling, to inhibit active priming of neonates by oral route. These observations seem relevant to the development of efficacious oral vaccines that also allow passive, protective immunity via suckled maternal antibodies while permitting active oral immunization of neonates.
机译:发现纯化的呼肠孤病毒血清型1封装在可生物降解的水微囊中,可以绕过母乳喂养而被动转移给新生儿的抗体。通过C.B17 scid / scid与正常同基因+ / +成年小鼠的反向杂交,产生了具有遗传学上相同的,具有免疫能力的F1 scid / +小鼠。具有免疫能力的+ / +坝在交配前口服呼肠孤病毒感染或没有。因此,这些有免疫能力的F1幼仔在没有或没有被动转移母体免疫的情况下发展。在第10天用活病毒,微囊化呼肠孤病毒或空的微胶囊加活病毒对F1小鼠进行口服免疫。在新生儿肠相关淋巴组织(GALT)中评估免疫应答。免疫后第7、14和21天对血清和GALT中呼肠孤病毒特异性免疫球蛋白A的检查清楚地表明,微囊化的呼肠孤病毒可以绕过母乳喂养的被动获得的母体抗体的正常作用,从而抑制口服后新生儿的主动引发路线。这些观察结果似乎与有效的口服疫苗的开发有关,该疫苗还允许通过哺乳的母体抗体进行被动的保护性免疫,同时允许新生儿的主动口服免疫。

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