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基因变异的HIV-1/SIV嵌合病毒作为潜在可用于人类的艾滋病减毒活疫苗。

Gene-mutated HIV-1/SIV chimeric viruses as AIDS live attenuated vaccines for potential human use.

作者信息

Hayami M, Igarashi T, Kuwata T, Ui M, Haga T, Ami Y, Shinohara K, Honda M

机构信息

Institute for Virus Research, Kyoto University, Japan.

出版信息

Leukemia. 1999 Apr;13 Suppl 1:S42-7. doi: 10.1038/sj.leu.2401283.

Abstract

To develop an AIDS vaccine for human use as well as a suitable animal model for AIDS research, we constructed a series of HIV-1/SIVmac chimeric viruses (SHIVs). We successfully generated a SHIV (designated as NM-3rN) having the HIV-1 env gene, which enabled the evaluation of the efficacy of HIV-1 Env-targeted vaccines in macaque monkeys instead of chimpanzees. Two NM-3rN derivatives (NM-3 and NM-3n) induced long-term anti-virus immunities without manifesting the disease. The monkeys vaccinated with NM-3 or NM-3n became resistant to a challenge inoculation with NM-3rN. Serum from a monkey vaccinated with NM-3 neutralized not only the parental HIV-1 (NL432), but also an antigenically different HIV-1 (MN). In vivo experiments confirmed the heterologous protection against an SHIV having the HIV-1 (MN) env. In addition to specific immunity including neutralizing antibodies and cytotoxic T lymphocyte activity, nonspecific immunity such as natural killer activity is associated with this protection. These data suggest that the live vaccine has the ability to protect individuals against various types of HIVs. These SHIVs should contribute to the development of future anti-HIV-1 live vaccines in humans.

摘要

为开发供人类使用的艾滋病疫苗以及适合艾滋病研究的动物模型,我们构建了一系列HIV-1/SIVmac嵌合病毒(SHIV)。我们成功构建了一种含有HIV-1 env基因的SHIV(命名为NM-3rN),这使得在猕猴而非黑猩猩中评估针对HIV-1 Env的疫苗的效力成为可能。两种NM-3rN衍生物(NM-3和NM-3n)诱导了长期抗病毒免疫且未出现疾病症状。接种NM-3或NM-3n的猴子对NM-3rN的攻击接种产生了抗性。接种NM-3的猴子的血清不仅中和了亲代HIV-1(NL432),还中和了抗原性不同的HIV-1(MN)。体内实验证实了针对含有HIV-1(MN)env的SHIV的异源保护作用。除了包括中和抗体和细胞毒性T淋巴细胞活性在内的特异性免疫外,非特异性免疫如自然杀伤活性也与这种保护作用相关。这些数据表明,活疫苗有能力保护个体免受各种类型HIV的侵害。这些SHIV应该有助于未来人类抗HIV-1活疫苗的开发。

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