CARD8 is an inflammasome sensor for HIV-1 protease activity

Science. 2021 Mar 19;371(6535):eabe1707. doi: 10.1126/science.abe1707. Epub 2021 Feb 4.

Abstract

HIV-1 has high mutation rates and exists as mutant swarms within the host. Rapid evolution of HIV-1 allows the virus to outpace the host immune system, leading to viral persistence. Approaches to targeting immutable components are needed to clear HIV-1 infection. Here, we report that the caspase recruitment domain-containing protein 8 (CARD8) inflammasome senses HIV-1 protease activity. HIV-1 can evade CARD8 sensing because its protease remains inactive in infected cells before viral budding. Premature intracellular activation of the viral protease triggered CARD8 inflammasome-mediated pyroptosis of HIV-1-infected cells. This strategy led to the clearance of latent HIV-1 in patient CD4+ T cells after viral reactivation. Thus, our study identifies CARD8 as an inflammasome sensor of HIV-1, which holds promise as a strategy for the clearance of persistent HIV-1 infection.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkynes / pharmacology
  • Anti-HIV Agents / pharmacology
  • Benzoxazines / pharmacology
  • CARD Signaling Adaptor Proteins / chemistry
  • CARD Signaling Adaptor Proteins / metabolism*
  • CD4-Positive T-Lymphocytes / physiology
  • CD4-Positive T-Lymphocytes / virology
  • Caspase 1 / metabolism
  • Cyclopropanes / pharmacology
  • Enzyme Activation
  • HIV Infections / drug therapy
  • HIV Infections / virology*
  • HIV Protease / metabolism*
  • HIV-1 / drug effects
  • HIV-1 / physiology*
  • Humans
  • Inflammasomes / metabolism*
  • Macrophages / physiology
  • Macrophages / virology
  • Neoplasm Proteins / chemistry
  • Neoplasm Proteins / metabolism*
  • Pyroptosis*
  • Reverse Transcriptase Inhibitors / pharmacology
  • Rilpivirine / pharmacology
  • THP-1 Cells
  • Virus Latency

Substances

  • Alkynes
  • Anti-HIV Agents
  • Benzoxazines
  • CARD Signaling Adaptor Proteins
  • CARD8 protein, human
  • Cyclopropanes
  • Inflammasomes
  • Neoplasm Proteins
  • Reverse Transcriptase Inhibitors
  • Caspase 1
  • HIV Protease
  • p16 protease, Human immunodeficiency virus 1
  • Rilpivirine
  • efavirenz