Litcius/Paper detail

TRIM proteins: A ‘swiss army knife’ of antiviral immunity

Elise Chabot, David Durantel, Julie Lucifora

2025PLoS Pathogens18 citationsDOIOpen Access PDF

Abstract

With their modular structure and E3 ubiquitin ligase activity, Tripartite motif (TRIM) proteins interact with a wide range of cellular and viral substrates. This review summarizes how they have emerged as key players in the antiviral response. Shortly, TRIM proteins were shown (i) to enhance pro-inflammatory cytokines production by interacting with pattern recognition receptors and downstream components of immune signaling pathways, (ii) to interfere with viral trafficking by interacting with the cytoskeleton, and (iii) to exhibit direct antiviral effects by targeting viral proteins for proteasomal degradation or inducing autophagy. This combination of actions underscores TRIMs as a potent innate defense system, but also makes them vulnerable to viral evasion strategies.

Topics & Concepts

Ubiquitin ligaseCell biologyInnate immune systemUbiquitinSignal transducing adaptor proteinBiologyAutophagyTrimPattern recognition receptorImmune systemComputational biologySignal transductionImmunologyGeneticsGeneApoptosisOperating systemComputer scienceinterferon and immune responsesCytomegalovirus and herpesvirus researchViral Infections and Vectors