Cited by 163HIV Research and Treatmentinterferon and immune responsesHIV/AIDS drug development and treatment

Restriction of HIV-1 and other retroviruses by TRIM5

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Ganser-Pornillos, Barbie K., Pornillos, Owen·2019·Nature Reviews Microbiology

Abstract

Mammalian cells express a variety of innate immune proteins - known as restriction factors - which defend against invading retroviruses such as HIV-1. Two members of the tripartite motif protein family - TRIM5α and TRIMCyp - were identified in 2004 as restriction factors that recognize and inactivate the capsid shell that surrounds and protects the incoming retroviral core. Research on these TRIM5 proteins has uncovered a novel mode of non-self recognition that protects against cross-species transmission of retroviruses. Our developing understanding of the mechanism of TRIM5 restriction underscores the concept that core uncoating and reverse transcription of the viral genome are coordinated processes rather than discrete steps of the post-entry pathway of retrovirus replication. In this Review, we provide an overview of the current state of knowledge of the molecular mechanism of TRIM5-mediated restriction, highlight recent advances and discuss implications for the development of capsid-targeted antiviral therapeutics.

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References 161 · Cited by 163

Authors
Ganser-Pornillos, B. K., & Pornillos, O.
Affiliations
University of Virginia (US)
Corresponding author
Pornillos, Owen
Venue
Nature Reviews Microbiology
Published
2019-07-16
Volume
17
Issue
9
Pages
546-556
ISSN
  • 1740-1526 (ISSN-L)
  • 1740-1534
OpenAlex
W2957306231
Cited by
163
References
161
Citations by year
2026: 18 · 2025: 24 · 2024: 28 · 2023: 19 · 2022: 21 · 2021: 29 · 2020: 20 · 2019: 4
FWCI
2.94
Type
journal article
Language
en
Open access
Locations
  • Nature Reviews Microbiology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute of General Medical Sciences (R01GM112508, P50GM082545)
  • National Institute of Allergy and Infectious Diseases (P50AI150464, R01AI150479)
Topics
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
  • Health Sciences › Medicine › Infectious Diseases › HIV/AIDS drug development and treatment
Keywords
TRIM5, TRIM5α, TRIMCyp, host restriction factors, HIV-1, retroviruses, innate immunity, reverse transcription, interspecies transmission, tripartite motif proteins
MeSH terms
Tripartite Motif Proteins, Antiviral Restriction Factors, Humans, Immunity, Innate, Immunologic Factors, HIV-1, Ubiquitin-Protein Ligases, Reverse Transcription, Host-Pathogen Interactions, Virus Uncoating

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