4.6 Review

Immunity and Viral Infections: Modulating Antiviral Response via CRISPR-Cas Systems

期刊

VIRUSES-BASEL
卷 13, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/v13071373

关键词

CRISPR; Cas; interferon effector proteins; interferon induction; pathogen recognition receptor; pathogen-associated molecular pattern; Toll-like receptor; cGAS; STING; DNA sensors; interferon stimulated genes; pooled libraries; epitranscriptomics; HBV; HDV; HCV; HIV; SARS-CoV-2; yellow fever virus; KSHV; HSV; EBOV; ZIKV; influenza A virus; CHIKV

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资金

  1. RFBR-DFG grant [20-515-12010, GL 595/9-1]
  2. RFBR [20-015-00442]
  3. German Ministry of Health via the Robert Koch Institute, Berlin, Germany

向作者/读者索取更多资源

Studying and utilizing virus-host interactions are crucial for developing antiviral agents and mitigating the severity of virus-borne infectious diseases, in which CRISPR systems have played a significant role.
Viral infections cause a variety of acute and chronic human diseases, sometimes resulting in small local outbreaks, or in some cases spreading across the globe and leading to global pandemics. Understanding and exploiting virus-host interactions is instrumental for identifying host factors involved in viral replication, developing effective antiviral agents, and mitigating the severity of virus-borne infectious diseases. The diversity of CRISPR systems and CRISPR-based tools enables the specific modulation of innate immune responses and has contributed impressively to the fields of virology and immunology in a very short time. In this review, we describe the most recent advances in the use of CRISPR systems for basic and translational studies of virus-host interactions.

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