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Additionally, myeloma has long been associated with quantitative and functional deficient T cells, particularly in the progressive, refractory disease. Acquisition of T cells from healthy donors is an attractive solution to the problem of insufficient and inferior CAR T cells. There are a few known allogenic compounds in MM that have gained IND clearance from the FDA, namely, UCARTCS1 (SLAMF7), CTX120 (BCMA), ALLO-715 (BCMA), CYAD-211 (BCMA), and PBCAR269A (BCMA)97,98. These products were conceived using different technologies including the non-gene editing method to eliminate TCR (CYAD-211) and single-step platform to concurrently knock-out TCR while knocking-in CAR (PBCAR269A)99. Another BCMA allogeneic compound (ALLO-605) that is being evaluated pre-clinically incorporates additional chimeric features to enhance cytokine signaling100. Besides addressing the T-cell quality, off-the-shelf accessibility of these products also means that we can by-pass the long and complex autologous manufacturing process, thus, allowing for more rapid frontline therapies. The sustained availability of these allogenic CAR T cells will be useful for eradication of residual malignant cells, without the need for multiple rounds of painstaking autologous T-cell harvesting from the patients. In short, a cell bank with universal CAR T cells for allogeneic cell transfer would provide more flexibility in the application, faster delivery to the patients with less cost-intensive manufacturing. d2c66b5586