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VESICULAR STOMATITIS VIRUS FOR PRIME BOOST VACCINES

机译:初免疫苗的疱疹性气孔病毒

摘要

The present invention relates to vesicular stomatitis virus (VSV) matrix (M) protein mutants. One mutant M protein includes a glycine changed to a glutamic acid at position (21), a leucine changed to a phenylalanine at position (111) and a methionine changed to an arginine at position (51). Another M protein mutant includes a glycine changed to a glutamic acid at position (22) and a methionine changed to an arginine at positions (48) and (51). Yet another VSV M protein mutant includes a glycine changed to a glutamic acid at position (22), a leucine changed to a phenylalanine at position (110) and a methionine changed to an arginine at positions (48) and (51). The present invention is directed also to recombinant VSVs (rVSV) having these M mutants and to vaccines based on the rVSV having the M mutants of the present invention. These new rVSVs having the mutant M were significantly attenuated and lost virulence, including neurovirulence, and are capable of inducing an immune responses against an antigen of interest. In addition, a rVSV serotype Indiana having the first described M mutant is capable of efficient replication at 31° C., and of poor replication or incapable of replication at about 37° C. or higher.
机译:本发明涉及水泡性口炎病毒(VSV)基质(M)蛋白突变体。一种突变的M蛋白包括在位置(21)变为甘氨酸的甘氨酸,在位置(111)变为丙氨酸的亮氨酸和在位置(51)变为蛋氨酸的蛋氨酸。另一个M蛋白突变体包括在位置(22)处变为谷氨酸的甘氨酸和在位置(48)和(51)处变为精氨酸的甲硫氨酸。另一个VSV M蛋白突变体包括在位置(22)变为甘氨酸的甘氨酸,在位置(110)变为丙氨酸的亮氨酸和在位置(48)和(51)的甲硫氨酸变为精氨酸。本发明还涉及具有这些M突变体的重组VSV(rVSV)和基于具有本发明M突变体的rVSV的疫苗。这些具有突变体M的新的rVSV被显着减毒并丧失了毒力,包括神经毒力,并且能够诱导针对目的抗原的免疫应答。另外,具有首先描述的M突变体的rVSV血清型印第安纳能够在31℃下有效复制,并且在约37℃或更高温度下复制不良或不能复制。

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