Sheridan J F, Smith C C, Manak M M, Aurelian L
J Infect Dis. 1984 Mar;149(3):434-8. doi: 10.1093/infdis/149.3.434.
Female CF-1 mice were immunized subcutaneously with a rotavirus vaccine consisting of noninfectious, purified empty capsids from simian rotavirus SA-11 and were given a booster dose at 14-17 days of gestation. The vaccinated animals developed high titers of rotavirus-specific IgG in colostrum and milk. Virus-specific IgA titers were significantly (150-fold) lower, and virus-specific IgM was not detected. These results contrast with those obtained in natural and experimental infections of the gastrointestinal tract with epizootic-diarrhea infant-mouse ( EDIM ) virus; in such cases, intestinal and lacteal virus-specific antibody is primarily of the IgA isotype. Suckling mice born to vaccinated dams were challenged with infectious EDIM virus and monitored for the development of diarrheal disease; these neonates acquired maternal antibody and did not develop diarrhea.
将雌性CF-1小鼠皮下接种由猿猴轮状病毒SA-11的无感染性、纯化空衣壳组成的轮状病毒疫苗,并在妊娠14至17天时给予加强剂量。接种疫苗的动物在初乳和乳汁中产生了高滴度的轮状病毒特异性IgG。病毒特异性IgA滴度显著降低(150倍),且未检测到病毒特异性IgM。这些结果与用流行性腹泻幼鼠(EDIM)病毒对胃肠道进行自然感染和实验感染所获得的结果形成对比;在这种情况下,肠道和乳汁中的病毒特异性抗体主要是IgA同种型。接种疫苗的母鼠所生的乳鼠用感染性EDIM病毒进行攻击,并监测腹泻疾病的发展;这些新生鼠获得了母源抗体,未出现腹泻。