Lezama-Dávila C M
Centro de Investigaciones en Enfermedades Tropicales, Universidad Autónoma de Campeche, México.
Arch Med Res. 1997 Spring;28(1):47-53.
The objective of this study was to assess the usefulness of parasite-surface molecules reconstituted into liposomes to vaccinate four different strains of mice (C57BL/10, CBA/ca, C57BL/6 and NZB) with different levels of susceptibility to L. m. mexicana infection and to find out possible increases in specific antibody response after vaccination, but before infection with virulent promastigotes. Mice were vaccinated with parasite membrane antigens incorporated into liposomes and antibody levels were recorded. Vaccination was effective to protect CBA/ca and C57BL/6 but not C57BL/10 mice and NZB animals were naturally resistant. Intraperitoneal (ip) was more effective than the subcutaneous (sc) route of inoculation, and the induction of disease-resistance correlated with the production of IgG anti-Leishmania in CBA/ca, C57BL/6 and C57BL/10 mice.
本研究的目的是评估重组成脂质体的寄生虫表面分子对四种不同品系小鼠(C57BL/10、CBA/ca、C57BL/6和NZB)进行疫苗接种的有效性,这些小鼠对墨西哥利什曼原虫感染的易感性程度不同,并找出接种疫苗后、感染强毒前鞭毛体之前特异性抗体反应可能的增加情况。给小鼠接种掺入脂质体的寄生虫膜抗原,并记录抗体水平。疫苗接种有效地保护了CBA/ca和C57BL/6小鼠,但对C57BL/10小鼠无效,而NZB动物天然具有抗性。腹腔内(ip)接种比皮下(sc)接种途径更有效,并且在CBA/ca、C57BL/6和C57BL/10小鼠中,抗病性的诱导与抗利什曼原虫IgG的产生相关。