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Vaccination with live attenuated simian immunodeficiency virus for 21 days protects against superinfection

机译:用减毒的猿猴免疫缺陷病毒活疫苗接种21天可防止重复感染

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摘要

The identification of mechanisms that prevent infection with human immunodeficiency virus (HIV) or simian immunodeficiency virus (SIV) would facilitate the development of an effective AIDS vaccine. In time-course experiments, protection against detectable superinfection with homologous wild-type SIV was achieved within 21 days of inoculation with live attenuated SIV, prior to the development of detectable anti-SIV humoral immunity. Partial protection against superinfection was achieved within 10 days of inoculation with live attenuated SIV, prior to the development of detectable anti-SIV humoral and cellular immunity. Furthermore, co-inoculation of live attenuated SIV with wild-type SIV resulted in a significant reduction in peak virus loads compared to controls that received wild-type SIV alone. These findings imply that innate immunity or non-immune mechanisms are a significant component of early protection against superinfection conferred by inoculation with live attenuated SIV. (C) 2004 Elsevier Inc. All rights reserved.
机译:确定防止感染人类免疫缺陷病毒(HIV)或猿猴免疫缺陷病毒(SIV)的机制将有助于开发有效的艾滋病疫苗。在时程实验中,在开发可检测的抗SIV体液免疫之前,在接种减毒活SIV的21天之内就可以防止同源野生型SIV发生可检测的过度感染。在发展出可检测的抗SIV体液和细胞免疫之前,在接种减毒活SIV的10天内就可以实现对超级感染的部分保护。此外,与单独接受野生型SIV的对照组相比,减毒活的SIV与野生型SIV共同接种导致峰值病毒载量显着降低。这些发现表明,先天免疫或非免疫机制是早期预防早期感染的重要组成部分,该早期预防是通过接种减毒活SIV赋予的。 (C)2004 Elsevier Inc.保留所有权利。

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