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TIM-4 is the ligand for TIM-1, and the TIM-1–TIM-4 interaction regulates T cell proliferation
被引:0
|作者:
Jennifer Hartt Meyers
Sumone Chakravarti
David Schlesinger
Zsolt Illes
Hanspeter Waldner
Sarah E Umetsu
James Kenny
Xin Xiao Zheng
Dale T Umetsu
Rosemarie H DeKruyff
Terry B Strom
Vijay K Kuchroo
机构:
[1] Center for Neurologic Diseases,Department of Neurology
[2] Brigham and Women's Hospital and Harvard Medical School,Division of Immunology
[3] Beth Israel Deaconess Medical Center,Division of Immunology and Allergy, Department of Pediatrics
[4] Harvard Medical School,undefined
[5] Stanford University School of Medicine,undefined
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摘要:
The newly identified TIM family of proteins is associated with regulation of T helper type 1 (TH1) and TH2 immune responses. TIM-1 is genetically linked to asthma and is a receptor for hepatitis A virus, but the endogenous ligand of TIM-1 is not known. Here we show that TIM-4, which is expressed by antigen-presenting cells, is the ligand for TIM-1. In vivo administration of either soluble TIM-1–immunoglobulin (TIM-1–Ig) fusion protein or TIM-4–Ig fusion protein resulted in hyperproliferation of T cells, and TIM-4–Ig costimulated T cell proliferation mediated by CD3 and CD28 in vitro. These data suggest that the TIM-1–TIM-4 interaction is involved in regulating T cell proliferation.
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页码:455 / 464
页数:9
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