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Beyond T cell exhaustion: TIM-3 regulation of myeloid cells.
Dixon, Karen O; Lahore, Gonzalo Fernandez; Kuchroo, Vijay K.
Affiliation
  • Dixon KO; Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital, and Harvard Medical School, Boston, MA 02115, USA.
  • Lahore GF; Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital, and Harvard Medical School, Boston, MA 02115, USA.
  • Kuchroo VK; Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital, and Harvard Medical School, Boston, MA 02115, USA.
Sci Immunol ; 9(93): eadf2223, 2024 Mar 08.
Article in En | MEDLINE | ID: mdl-38457514
ABSTRACT
T cell immunoglobulin and mucin domain-containing protein 3 (TIM-3) is an important immune checkpoint molecule initially identified as a marker of IFN-γ-producing CD4+ and CD8+ T cells. Since then, our understanding of its role in immune responses has significantly expanded. Here, we review emerging evidence demonstrating unexpected roles for TIM-3 as a key regulator of myeloid cell function, in addition to recent work establishing TIM-3 as a delineator of terminal T cell exhaustion, thereby positioning TIM-3 at the interface between fatigued immune responses and reinvigoration. We share our perspective on the antagonism between TIM-3 and T cell stemness, discussing both cell-intrinsic and cell-extrinsic mechanisms underlying this relationship. Looking forward, we discuss approaches to decipher the underlying mechanisms by which TIM-3 regulates stemness, which has remarkable potential for the treatment of cancer, autoimmunity, and autoinflammation.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis A Virus Cellular Receptor 2 / Neoplasms Limits: Humans Language: En Journal: Sci Immunol Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis A Virus Cellular Receptor 2 / Neoplasms Limits: Humans Language: En Journal: Sci Immunol Year: 2024 Document type: Article Affiliation country: United States