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Lag-3, Tim-3, and TIGIT: Co-inhibitory Receptors with Specialized Functions in Immune Regulation

Journal

IMMUNITY
Volume 44, Issue 5, Pages 989-1004

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2016.05.001

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Funding

  1. NIH [P01 AI073748, P01 NS076410, P01 AI039671, R01 NS045937, R01 CA187975]
  2. Melanoma Research Alliance
  3. Melanoma Research Foundation
  4. American Cancer Society [RSG-11-057-01-LIB]

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Co-inhibitory receptors, such as CTLA-4 and PD-1, have an important role in regulating T cell responses and have proven to be effective targets in the setting of chronic diseases where constitutive co-inhibitory receptor expression on T cells dampens effector T cell responses. Unfortunately, many patients still fail to respond to therapies that target CTLA-4 and PD-1. The next wave of co-inhibitory receptor targets that are being explored in clinical trials include Lag-3, Tim-3, and TIGIT. These receptors, although they belong to the same class of receptors as PD-1 and CTLA-4, exhibit unique functions, especially at tissue sites where they regulate distinct aspects of immunity. Increased understanding of the specialized functions of these receptors will inform the rational application of therapies that target these receptors to the clinic.

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