Article
作者: Cairo, Mitchell S. ; Liao, Yanling ; Mo, Xiaokui ; Overwijk, Willem W. ; Cairo, Mitchell S ; Cripe, Timothy P. ; Luo, Wen ; Gardenswartz, Aliza ; Ayello, Janet ; Rosenblum, Jeremy M ; Marcondes, A. Mario ; Tian, Meijuan ; Marcondes, A Mario ; Overwijk, Willem W ; Cripe, Timothy P ; Chu, Yaya ; Lee, Dean A. ; Rosenblum, Jeremy M. ; Lee, Dean A ; Hoang, Hai
Pediatric patients with recurrent metastatic neuroblastoma (NB) have a dismal 5-year survival. Novel therapeutic approaches are urgently needed. The melanoma cell adhesion molecule (MCAM/CD146/MUC18) is expressed in a variety of pediatric solid tumors, including NB, and constitutes a novel target for immunotherapy. Here, we developed a chimeric antigen receptor (CAR) expressing natural killer (NK) cell-targeting MCAM by non-viral electroporation of CAR mRNA into ex vivo expanded NK cells. Expression of anti-MCAM CAR significantly enhanced NK cell cytotoxic activity compared to mock NK cells against MCAMhigh but not MCAMlow/knockout NB cells in vitro. Anti-MCAM-CAR-NK cell treatment significantly decreased tumor growth and prolonged animal survival in an NB xenograft mouse model. NKTR-255, a polymer-conjugated recombinant human interleukin-15 agonist, significantly stimulated NK cell proliferation and expansion and further enhanced the in vitro cytotoxic activity and in vivo anti-tumor efficacy of anti-MCAM-CAR-NK cells against NB. Our preclinical studies demonstrate that ex vivo expanded and modified anti-MCAM-CAR-NK cells alone and/or in combination with NKTR-255 are promising novel alternative therapeutic approaches to targeting MCAMhigh malignant NB.