Sagodira S, Iochmann S, Mevelec M N, Dimier-Poisson I, Bout D
Equipe Associée INRA d'Immunologie Parasitaire, UFR des Sciences Pharmaceutiques, 31 Avenue Monge, 37200 Tours, France.
Parasite Immunol. 1999 Oct;21(10):507-16. doi: 10.1046/j.1365-3024.1999.00247.x.
DNA immunization offers a novel approach to inducing humoral and cellular immunity against infectious pathogens. We examined whether such an approach could be used against cryptosporiodiosis, an intestinal disease caused by the protozoan parasite Cryptosporidium parvum. This infection is a major problem for young ruminants and immunosuppressed individuals in whom cryptosporidiosis causes life-threatening symptoms. The life cycle of C. parvum takes place in the enterocytes of the intestinal epithelium. We therefore focused our attention on a route of immunization that might induce a mucosal immunoglobulin (Ig)A response. Eight-week-old BALB/c mice were immunized intranasally with DNA encoding a 15-kDa C. parvum sporozoite antigen (CP15-DNA) cloned onto the plasmid pcDNA3. CP15-DNA-immunized mice developed specific and longlasting production of anti-CP15 Ig A in intestinal secretions and specific IgG in sera 3 months and 1 year after the first DNA inoculation. CP15-DNA-immunized mice also developed an antigen-specific T lymphocyte proliferative response in both spleen and mesenteric lymph nodes. Control mice that received the pcDNA3 plasmid alone did not develop specific humoral and cellular responses. These results indicate that plasmid DNA may provide a powerful means of eliciting intestinal humoral and cellular responses to C. parvum infections in mammals.
DNA免疫提供了一种诱导针对传染性病原体的体液免疫和细胞免疫的新方法。我们研究了这种方法是否可用于对抗隐孢子虫病,这是一种由原生动物寄生虫微小隐孢子虫引起的肠道疾病。这种感染对于幼龄反刍动物和免疫抑制个体来说是一个主要问题,在这些个体中隐孢子虫病会导致危及生命的症状。微小隐孢子虫的生命周期发生在肠上皮细胞的肠细胞中。因此,我们将注意力集中在一种可能诱导黏膜免疫球蛋白(Ig)A反应的免疫途径上。将8周龄的BALB/c小鼠通过鼻腔接种克隆到质粒pcDNA3上的编码15 kDa微小隐孢子虫子孢子抗原(CP15-DNA)的DNA进行免疫。在首次接种DNA后3个月和1年,用CP15-DNA免疫的小鼠在肠道分泌物中产生了特异性且持久的抗CP15 Ig A,在血清中产生了特异性IgG。用CP15-DNA免疫的小鼠在脾脏和肠系膜淋巴结中也产生了抗原特异性T淋巴细胞增殖反应。仅接受pcDNA3质粒的对照小鼠未产生特异性体液和细胞反应。这些结果表明,质粒DNA可能是在哺乳动物中引发针对微小隐孢子虫感染的肠道体液和细胞反应的有力手段。