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Cancer immunotherapy based on blocking immune suppression mediated by an immune modulator LAIR-1
Published in OncoImmunology, 2020
Lijun Xu, Shanlong Wang, Jufeng Li, Jie Li, Bingyu Li
Inhibitory receptors containing ITIMs (immunoreceptor tyrosine-based inhibitory motifs) play an important role in the regulation of the immune system.1 These receptors contain ITIM motifs in their intracellular domains and are classified as inhibitory receptors because these motifs can recruit phosphatases such as SHP-1, SHP-2, and SHIP to negatively regulate cell activation.2 The leukocyte-associated immunoglobulin-like receptor 1 (LAIR-1) is a collagen-binding ITIM-bearing inhibitory receptor important for the regulation of immune responses and is expressed on the majority of immune cell subsets, including T cells, NK cells, monocytes, macrophages, and dendritic cells.3–7 LAIR-1 can inhibit the cytotoxic activity of effector T cells upon CD3 cross-linking2,8–10 or antigen stimulation.11 Furthermore, the inhibitory capacity of LAIR-1 in T cell clones correlates to surface expression density.12