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Article Abstract
The paracaspase Malt1 is a key molecule in mediating Ag receptor-induced NF-κB activation in lymphocytes, but the role of Malt1 in the function of regulatory T (Treg) cells is still unclear. In this article, we reported that specific deletion of Malt1 in Treg cells would lead to -like lethal autoimmune disease, which was caused by Treg cell dysfunction but not number loss. Interestingly, mice, in which Malt1 protease was specifically inactivated in Treg cells, also displayed spontaneous inflammatory disorders, with severe hair loss and skin hyperplasia. Consistently, mice showed enhanced antitumor response because of their decreased function and infiltration of Treg cells, as well as reduced CD8 T cell exhaustion. Gene expression profiling analysis revealed dysregulated expression pattern of Treg effector genes upon Malt1 deletion or its protease inactivation. Together, our data unraveled a critical role of Malt1, especially its protease activity, in maintaining homeostasis and function of Treg cells.
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| http://dx.doi.org/10.4049/jimmunol.1801614 | DOI Listing |
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