AbstractWe have recently reported that LAG-3 (CD223) mediates the alternative, IFNα-deficient activation of pDCs at tumor sites. Our findings define a novel tumor-driven strategy that promotes immunosuppression by pDCs, and we have provided more detailed information regarding the immunomodulatory role of LAG-3. The translational relevance of our results for the treatment of tumors and autoimmune diseases is discussed herein.
Via Krishan Maggon
CD223