TIM3 comes of age as an inhibitory receptor

Yochai Wolf, Ana C. Anderson, Vijay K. Kuchroo*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review


T cell immunoglobulin and mucin domain-containing protein 3 (TIM3), a member of the TIM family, was originally identified as a receptor expressed on interferon-γ-producing CD4+ and CD8+ T cells. Initial data indicated that TIM3 functioned as a ‘co-inhibitory’ or ‘checkpoint’ receptor, but due to the lack of a definable inhibitory signalling motif, it was also suggested that TIM3 might act as a co-stimulatory receptor. Recent studies have shown that TIM3 is part of a module that contains multiple co-inhibitory receptors (checkpoint receptors), which are co-expressed and co-regulated on dysfunctional or ‘exhausted’ T cells in chronic viral infections and cancer. Furthermore, co-blockade of TIM3 and programmed cell death 1 (PD1) can result in tumour regression in preclinical models and can improve anticancer T cell responses in patients with advanced cancers. Here, we highlight the developments in understanding TIM3 biology, including novel ligand identification and the discovery of loss-of-function mutations associated with human disease. In addition, we summarize emerging data from human clinical trials showing that TIM3 indeed acts as a ‘checkpoint’ receptor and that inhibition of TIM3 enhances the antitumour effect of PD1 blockade.

Original languageEnglish
Pages (from-to)173-185
Number of pages13
JournalNature Reviews Immunology
Issue number3
StatePublished - 1 Mar 2020
Externally publishedYes


Dive into the research topics of 'TIM3 comes of age as an inhibitory receptor'. Together they form a unique fingerprint.

Cite this