García-Díaz Ana, López-Andújar Pilar, Rodríguez Díaz Jesús, Montava Rebeca, Torres Barceló Clara, Ribes Juan M, Buesa Javier
Departament de Microbiologia, Facultat de Medicina, Hospital Clínic Universitari, Universitat de València, Avda. Blasco Ibáñez 17, 46010 Valencia, Spain.
Vaccine. 2004 Dec 9;23(4):489-98. doi: 10.1016/j.vaccine.2004.06.018.
DNA vaccination using a plasmid encoding the rotavirus inner capsid VP6 has been explored in the mouse model of rotavirus infection. BALB/c mice were immunized with a VP6 DNA vaccine by the intramuscular, nasal and oral routes. VP6 DNA vaccination by the nasal and oral routes induced the production of anti-VP6 IgA antibodies by intestinal lymphoid cells. Intramuscular DNA injection stimulated the production of serum anti-VP6 IgG but not serum anti-VP6 IgA antibodies. Protection against shedding of rotaviruses in stools after oral challenge with the murine EDIM rotavirus strain was investigated in the immunized mice. A significant reduction in the level of rotavirus antigen shedding was demonstrated in those mice immunized at mucosal surfaces, both orally and nasally, with the VP6 DNA vaccine. Intramuscular DNA immunization, which elicited serum anti-VP6 IgG responses but not virus-specific intestinal IgA antibodies, did not provide significant protection against rotavirus challenge.
在轮状病毒感染的小鼠模型中,已经对使用编码轮状病毒内衣壳VP6的质粒进行DNA疫苗接种进行了研究。通过肌肉内、鼻腔和口服途径用VP6 DNA疫苗对BALB/c小鼠进行免疫。鼻腔和口服途径的VP6 DNA疫苗接种诱导肠道淋巴细胞产生抗VP6 IgA抗体。肌肉内注射DNA刺激血清抗VP6 IgG的产生,但不刺激血清抗VP6 IgA抗体的产生。在免疫小鼠中研究了用鼠EDIM轮状病毒株口服攻击后对粪便中轮状病毒排出的保护作用。在用VP6 DNA疫苗经口腔和鼻腔在粘膜表面免疫的那些小鼠中,轮状病毒抗原排出水平显著降低。引起血清抗VP6 IgG反应但不产生病毒特异性肠道IgA抗体的肌肉内DNA免疫,不能提供针对轮状病毒攻击的显著保护。