Vanam Uma, Pandey Vivek, Prabhu Prince R, Dakshinamurthy Gajalakshmi, Reddy Maryada Venkata Rami, Kaliraj Perumal
Centre for Biotechnology, Anna University, Chennai, India.
Am J Trop Med Hyg. 2009 Feb;80(2):319-24.
An attempt was made to study the immunoprophylactic efficacy of recombinant Brugia malayi transglutaminase (BmTGA) as protein vaccine along with two other recombinant proteins, Brugia malayi abundant larval transcript-2 (BmALT-2) and Brugia malayi thioredoxin peroxidase (BmTPX), in single and multiple antigen form for human lymphatic filariasis. Parasite challenge studies in jirds exhibited protection of 30%, 69%, and 43% against BmTGA, BmALT-2, and BmTPX, respectively, in single antigen vaccination mode. The protective efficacy of BmTGA was enhanced significantly (74%) by immunizing the jirds in multiple antigen vaccination mode along with BmTPX, whereas immunizing with the combination of BmTGA and BmALT2 conferred only 47% protection. The same protection profiles were obtained by in vitro antibody-dependent cellular cytotoxicity, using live microfilariae and L3 stage larvae. The immune response was Th2 biased, irrespective of single or multiple vaccinations. The combination of BmTGA and BmTPX seems to be a promising vaccine candidate against lymphatic filariasis.
人们尝试研究重组马来布鲁线虫转谷氨酰胺酶(BmTGA)作为蛋白质疫苗与另外两种重组蛋白——马来布鲁线虫丰富幼虫转录本-2(BmALT-2)和马来布鲁线虫硫氧还蛋白过氧化物酶(BmTPX),以单一抗原和多抗原形式用于人类淋巴丝虫病的免疫预防效果。在沙鼠身上进行的寄生虫攻击试验显示,在单一抗原疫苗接种模式下,针对BmTGA、BmALT-2和BmTPX的保护率分别为30%、69%和43%。通过与BmTPX一起以多抗原疫苗接种模式免疫沙鼠,BmTGA的保护效果显著提高(74%),而用BmTGA和BmALT2组合免疫仅提供47%的保护。使用活微丝蚴和L3期幼虫进行体外抗体依赖性细胞毒性试验也获得了相同的保护情况。无论单次还是多次接种,免疫反应均偏向Th2型。BmTGA和BmTPX的组合似乎是一种有前景的抗淋巴丝虫病疫苗候选物。