Samykutty Abhilash, Dakshinamoorthy Gajalakshmi, Kalyanasundaram Ramaswamy
Department of Biomedical Sciences, College of Medicine, University of Illinois Rockford, 1601 Parkview Avenue, Rockford, Illinois, USA. 61107.
Procedia Vaccinol. 2010;3:12-18. doi: 10.1016/j.provac.2010.11.003.
Lymphatic filariasis is a mosquito borne parasitic infection that cause severe economic burden in several parts of the world. Currently there is no vaccine available to prevent this infection in human. Multidrug therapy is effective, however, requires annual treatment and there is significant concern of drug resistance. In this manuscript we describe development of a multivalent DNA based vaccine comprising BmALT-2 and BmHSP antigens of lymphatic filariasis. Challenge experiments using third stage infective larvae of Brugia malayi in a mouse model suggested that nearly 90% protection can be achieved using the multivalent formulation in a DNA prime protein boost approach. The vaccination regimen induced significant IgG antibody responses and ELISPOT analysis for secreted cytokines from the spleen cells of vaccinated animals showed that these cells produce significant amount of IL-4. Results from this study thus show that a multivalent vaccine formulation of BmALT-2 and BmHSP is an excellent vaccine for lymphatic filariasis and significant protection can be achieved against a challenge infection with B. malayi in a mouse model.
淋巴丝虫病是一种由蚊子传播的寄生虫感染,在世界上多个地区造成严重的经济负担。目前尚无用于预防人类感染这种疾病的疫苗。多药疗法有效,但需要每年进行治疗,且人们对耐药性问题极为担忧。在本手稿中,我们描述了一种基于多价DNA的疫苗的研发,该疫苗包含淋巴丝虫病的BmALT - 2和BmHSP抗原。在小鼠模型中使用马来布鲁线虫第三期感染性幼虫进行的攻毒实验表明,采用DNA初免 - 蛋白加强方法的多价制剂可实现近90%的保护率。该疫苗接种方案诱导了显著的IgG抗体反应,对接种动物脾细胞分泌的细胞因子进行的ELISPOT分析表明,这些细胞产生大量的IL - 4。因此,本研究结果表明,BmALT - 2和BmHSP的多价疫苗制剂是预防淋巴丝虫病的优良疫苗,在小鼠模型中可对马来布鲁线虫的攻毒感染实现显著保护。