University of Pennsylvania School of Medicine, Department of Pathology and Laboratory Medicine, Philadelphia, Pennsylvania, USA.
Infect Immun. 2013 Oct;81(10):3709-20. doi: 10.1128/IAI.00180-13. Epub 2013 Jul 29.
A vaccine candidate that elicits humoral and cellular responses to multiple sporozoite and liver-stage antigens may be able to confer protection against Plasmodium falciparum malaria; however, a technology for formulating and delivering such a vaccine has remained elusive. Here, we report the preclinical assessment of an optimized DNA vaccine approach that targets four P. falciparum antigens: circumsporozoite protein (CSP), liver stage antigen 1 (LSA1), thrombospondin-related anonymous protein (TRAP), and cell-traversal protein for ookinetes and sporozoites (CelTOS). Synthetic DNA sequences were designed for each antigen with modifications to improve expression and were delivered using in vivo electroporation (EP). Immunogenicity was evaluated in mice and nonhuman primates (NHPs) and assessed by enzyme-linked immunosorbent assay (ELISA), gamma interferon (IFN-γ) enzyme-linked immunosorbent spot (ELISpot) assay, and flow cytometry. In mice, DNA with EP delivery induced antigen-specific IFN-γ production, as measured by ELISpot assay and IgG seroconversion against all antigens. Sustained production of IFN-γ, interleukin-2, and tumor necrosis factor alpha was elicited in both the CD4(+) and CD8(+) T cell compartments. Furthermore, hepatic CD8(+) lymphocytes produced LSA1-specific IFN-γ. The immune responses conferred to mice by this approach translated to the NHP model, which showed cellular responses by ELISpot assay and intracellular cytokine staining. Notably, antigen-specific CD8(+) granzyme B(+) T cells were observed in NHPs. Collectively, the data demonstrate that delivery of gene sequences by DNA/EP encoding malaria parasite antigens is immunogenic in animal models and can harness both the humoral and cellular arms of the immune system.
一种能够诱导针对多种疟原虫裂殖体和肝期抗原的体液和细胞反应的疫苗候选物,可能能够提供针对恶性疟原虫疟疾的保护;然而,一种用于配制和递送这种疫苗的技术仍然难以捉摸。在这里,我们报告了一种针对恶性疟原虫四个抗原的优化 DNA 疫苗方法的临床前评估:环子孢子蛋白(CSP)、肝期抗原 1(LSA1)、血小板反应蛋白相关的匿名蛋白(TRAP)和细胞穿透蛋白用于配子体和子孢子(CelTOS)。每个抗原的合成 DNA 序列都经过设计,进行了改进以提高表达,并通过体内电穿孔(EP)进行递送。在小鼠和非人灵长类动物(NHP)中评估了免疫原性,并通过酶联免疫吸附试验(ELISA)、γ干扰素(IFN-γ)酶联免疫斑点(ELISpot)试验和流式细胞术进行评估。在小鼠中,DNA 与 EP 递送诱导抗原特异性 IFN-γ产生,通过 ELISpot 试验和针对所有抗原的 IgG 血清转化来衡量。在 CD4(+)和 CD8(+)T 细胞区室中均诱导持续产生 IFN-γ、白细胞介素-2 和肿瘤坏死因子-α。此外,肝脏 CD8(+)淋巴细胞产生 LSA1 特异性 IFN-γ。该方法赋予小鼠的免疫反应转化为 NHP 模型,该模型通过 ELISpot 试验和细胞内细胞因子染色显示细胞反应。值得注意的是,在 NHP 中观察到抗原特异性 CD8(+)颗粒酶 B(+)T 细胞。总的来说,这些数据表明,通过 DNA/EP 传递基因序列编码疟原虫抗原在动物模型中具有免疫原性,并能够利用免疫系统的体液和细胞臂。