4.7 Review

HIV-1 and interferons: who's interfering with whom?

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NATURE REVIEWS MICROBIOLOGY
卷 13, 期 7, 页码 403-413

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NATURE PUBLISHING GROUP
DOI: 10.1038/nrmicro3449

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资金

  1. UK Medical Research Council
  2. European Commission
  3. Wellcome Trust
  4. US National Institutes of Health
  5. Department of Health via a UK National Institute for Health Research comprehensive Biomedical Research Centre award
  6. King's College London
  7. King's College Hospital NHS Foundation Trust
  8. Medical Research Council [G0401570, G1001081, G1000196, MR/M001199/1] Funding Source: researchfish
  9. Wellcome Trust [106223/Z/14/Z] Funding Source: researchfish
  10. MRC [G1001081, G0401570, G1000196, MR/M001199/1] Funding Source: UKRI

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The ability of interferons (IFNs) to inhibit HIV-1 replication in cell culture models has long been recognized, and the therapeutic administration of IFN alpha to HIV-1-infected patients who are not receiving antiretroviral therapy produces a clear but transient decrease in plasma viral load. Conversely, studies of chronic HIV-1 infection in humans and SIV-infected animal models of AIDS show positive correlations between elevated plasma levels of IFNs, increased expression of IFN-stimulated genes (ISGs), biomarkers of inflammation and disease progression. In this Review, we discuss the evidence that IFNs can control HIV-1 replication in vivo and debate the controversial role of IFNs in promoting the pathological sequelae of chronic HIV-1 infection.

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