Moser C A, Speaker T J, Offit P A
Section of Infectious Diseases, The Children's Hospital of Philadelphia, Pennsylvania 19104, USA.
J Virol. 1998 May;72(5):3859-62. doi: 10.1128/JVI.72.5.3859-3862.1998.
We determined the capacity of microcapsules formed by the combination of sodium alginate, an aqueous anionic polymer, and spermine hydrochloride, an aqueous cationic amine, to enhance protection against rotavirus challenge in mice. Adult BALB/c mice were orally inoculated with either free or microencapsulated rotavirus (simian rotavirus strain RRV) and challenged 6 or 16 weeks later with murine rotavirus strain EDIM. Virus-specific humoral immune responses were determined at the time of challenge and 4 days after challenge by intestinal fragment culture. We found that spermine-alginate microcapsules enhanced protection against challenge 16 weeks after immunization but not 6 weeks after immunization. Quantities of virus-specific immunoglobulin A produced by small intestinal lamina propria lymphocytes were correlated with the degree of protection against challenge afforded by spermine-alginate microcapsules. Possible mechanisms by which microcapsules enhance protection against rotavirus challenge are discussed.
我们测定了由海藻酸钠(一种水性阴离子聚合物)和盐酸精胺(一种水性阳离子胺)组合形成的微胶囊增强小鼠抗轮状病毒攻击保护能力的情况。成年BALB/c小鼠口服接种游离或微囊化的轮状病毒(猿猴轮状病毒株RRV),并在6周或16周后用鼠轮状病毒株EDIM进行攻击。在攻击时和攻击后4天通过肠段培养测定病毒特异性体液免疫反应。我们发现精胺-海藻酸钠微胶囊在免疫16周后增强了对攻击的保护作用,但在免疫6周后没有。小肠固有层淋巴细胞产生的病毒特异性免疫球蛋白A的量与精胺-海藻酸钠微胶囊提供的抗攻击保护程度相关。讨论了微胶囊增强抗轮状病毒攻击保护作用的可能机制。