Sedegah M, Hedstrom R, Hobart P, Hoffman S L
Malaria Program, Naval Medical Research Institute, Bethesda, MD 20889-5607.
Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9866-70. doi: 10.1073/pnas.91.21.9866.
Immunization with irradiated sporozoites protects animals and humans against malaria, and the circumsporozoite protein is a target of this protective immunity. We now report that adjuvant-free intramuscular injection of mice with plasmid DNA encoding the Plasmodium yoelii circumsporozoite protein induced higher levels of antibodies and cytotoxic T lymphocytes against the P. yoelii circumsporozoite protein than did immunization with irradiated sporozoites. Mice immunized with this vaccine had an 86% reduction in liver-stage parasite burden after challenge with 5 x 10(5) sporozoites (> 10(5) median infectious doses). Eighteen (68%) of 28 mice that received two or three doses of vaccine were protected against challenge with 10(2) sporozoites, and the protection was dependent on CD8+ T cells. These studies demonstrate the utility of plasmid DNA immunization against a nonviral infection. By obviating the requirement for peptide synthesis, expression and purification of recombinant proteins, and adjuvants, this method of immunization provides an important alternative for rapid identification of protective B- and T-cell epitopes and for construction of vaccines to prevent malaria and other infectious diseases.
用辐照子孢子进行免疫可保护动物和人类免受疟疾侵害,而环子孢子蛋白是这种保护性免疫的靶点。我们现在报告,对小鼠进行无佐剂肌肉注射编码约氏疟原虫环子孢子蛋白的质粒DNA,比用辐照子孢子免疫诱导出更高水平的针对约氏疟原虫环子孢子蛋白的抗体和细胞毒性T淋巴细胞。用这种疫苗免疫的小鼠在受到5×10⁵个孢子(>10⁵个半数感染剂量)攻击后,肝期寄生虫负荷降低了86%。28只接受两剂或三剂疫苗的小鼠中有18只(68%)受到保护,免受10²个孢子的攻击,且这种保护依赖于CD8⁺T细胞。这些研究证明了质粒DNA免疫针对非病毒感染的实用性。通过消除对肽合成、重组蛋白表达和纯化以及佐剂的需求,这种免疫方法为快速鉴定保护性B细胞和T细胞表位以及构建预防疟疾和其他传染病的疫苗提供了重要的替代方法。