Further kinetic experiments revealed that soon after exposure to tumor-derived monocytes, NK cells underwent a rapid, transient activation, but then they became exhausted, Selleckchem Ponatinib and eventually died. The monocytes from HCC tissues, but not from nontumoral liver, strongly express CD48 proteins; and such monocyte-induced NK cell dysfunction

was markedly attenuated by blocking CD48 receptor 2B4 on NK cells, but not by blockade of NKG2D and NKp30. Conclusion: These data reveal that human NK cells are regulated by a fine-tuned collaborative action between different types of immune cells, which may reflect a novel immune-escape mechanism by which tumors dynamically regulate their functions at distinct tumor microenvironments. (HEPATOLOGY 2013) Natural killer Hormones antagonist (NK) cells constitute a major component of host defense against tumors by secretion of granules containing lytic enzymes or by triggering apoptosis.1, 2 Clinical and experimental studies have demonstrated that dysfunction of NK cells often leads to advanced disease progression in several types of human solid tumors.3, 4 Compared to other organs, NK cells constitute a predominant lymphocyte population in the liver,5 and studies in mice indicate that liver-infiltrating NK cells play a critical role in clearing viral infection.6, 7 However, very little is known about the nature, regulation, and functions of NK cells in human hepatocellular

carcinoma (HCC). NK cell activity is regulated by both activating and inhibitory receptors. Activation of NK cells is mediated through the interaction of NK cell surface activation receptors with their ligands on target cells. Alternatively, interaction of an inhibitory receptor with its ligand negatively regulates NK cell activity.8, 9 In addition to being expressed on target cells, the

regulatory ligands for NK cell activation are also found on activated antigen-presenting cells (APCs).8 However, there is substantial evidence that the inflammatory response associated with activated APCs can be rerouted selleck products in a tumor-promoting direction.10, 11 Macrophages (Mψ) markedly outnumber other APCs in solid tumors,12-14 and we recently found that tumor environments can alter the normal development of Mψ that is intended to trigger transient early activation of monocytes in peritumoral stroma, which in turn induces formation of suppressive Mψ in the intratumoral region.15 Thus, functional data on NK cells in the presence of monocytes/Mψ in different niches of a tumor are essential for understanding their roles and potential mechanisms in tumor immunopathogenesis. The CD48 molecule is a costimulatory ligand of the CD2 family receptors, and it has been found on various hematopoietic cells, particularly on APCs.16 CD48 binds CD2 and other molecules, although its high-affinity receptor in both mouse and human systems is 2B4. The interactions between 2B4 and CD48 are closely associated with inflammatory disorders.