Ehigiator Humphrey N, Romagnoli Pablo, Priest Jeffrey W, Secor W Evan, Mead Jan R
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30033, USA.
Parasitol Res. 2007 Sep;101(4):943-50. doi: 10.1007/s00436-007-0565-0. Epub 2007 May 9.
Cp23 has been identified as one of the immunodominant antigens involved in the immune response to Cryptosporidium parvum infection. Thus, in this study, Cp23 antigen was investigated as a vaccine candidate using the DNA vaccine model in adult interleukin-12 (IL-12) knockout (KO) mice, which are susceptible to C. parvum infection. Our data show that subcutaneous immunization in the ear with DNA encoding Cp23 (Cp23-DNA) cloned into the pUMVCb4 vector induced a significant anti-Cp23 immunoglobulin G1 (IgG1) and IgG2a antibody response and specific in vitro spleen cell proliferation to recombinant Cp23 as compared to control mice. Long-term memory responses were also detected after administration of the Cp23-DNA vaccine. Furthermore, Cp23-DNA vaccination induced a 50-60% reduction in oocysts shedding, indicating a partial protection against C. parvum infection in IL-12 KO mice. However, it is possible that this protective response was nonspecific because mice immunized with vector only also exhibited lower oocyst shedding than the naive controls. These results suggest that DNA encoding for immunodominant C. parvum antigens may provide an effective means of eliciting humoral and cellular responses and possibly in generating protective immunity against C. parvum infections in mammals.
Cp23已被确定为参与对微小隐孢子虫感染免疫反应的免疫显性抗原之一。因此,在本研究中,使用DNA疫苗模型在易受微小隐孢子虫感染的成年白细胞介素-12(IL-12)基因敲除(KO)小鼠中研究了Cp23抗原作为候选疫苗。我们的数据表明,与对照小鼠相比,将克隆到pUMVCb4载体中的编码Cp23的DNA(Cp23-DNA)经耳部皮下免疫可诱导显著的抗Cp23免疫球蛋白G1(IgG1)和IgG2a抗体反应以及对重组Cp23的特异性体外脾细胞增殖。在给予Cp23-DNA疫苗后还检测到了长期记忆反应。此外,Cp23-DNA疫苗接种使卵囊排出减少了50-60%,表明对IL-12基因敲除小鼠的微小隐孢子虫感染有部分保护作用。然而,这种保护反应可能是非特异性的,因为仅用载体免疫的小鼠与未免疫的对照相比也表现出较低的卵囊排出。这些结果表明,编码微小隐孢子虫免疫显性抗原的DNA可能提供一种有效的手段来引发体液和细胞反应,并可能产生针对哺乳动物微小隐孢子虫感染的保护性免疫。