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Tied down by its own receptor

机译:被自己的受体束缚

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摘要

The past 30 years have been marked by a long and discouraging search for an effective HIV vaccine. In 2009, the 'Thai trial' of the candidate vaccine RV144 was the first to demonstrate any success, measuring a 31.2% reduction in the rate of infection, although efficacy decreased over the first year after vaccination. The difficulty in developing a more effective vaccine has forced investigators to explore problems that are posed by other intractable pathogens, including persistence in the host, a high degree of variability of certain regions, masking of common regions, and pathogen-induced inhibition of host immunity. But on page 87 of this issue, Gardner et al. describe research suggesting that protection against HIV infection may be achievable through a gene-therapy approach, rather than by relying on eliciting protective immune responses by vaccination.
机译:在过去的30年中,长期以来一直在寻找有效的HIV疫苗而令人沮丧。 2009年,候选疫苗RV144的“泰国试验”首次证明成功,尽管感染率在接种后的第一年有所降低,但感染率降低了31.2%。开发更有效疫苗的困难迫使研究人员探索其他顽固性病原体带来的问题,包括宿主的持久性,某些区域的高度可变性,共同区域的掩盖以及病原体诱导的宿主免疫抑制。但是在此问题的第87页上,Gardner等人。描述的研究表明,可以通过基因治疗方法来实现针对HIV感染的保护,而不是依靠疫苗接种来引发保护性免疫应答。

著录项

  • 来源
    《Nature》 |2015年第7541期|36-37|共2页
  • 作者

    NANCY L. HAIGWOOD;

  • 作者单位

    Division of Pathobiology & Immunology, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon 97006, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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