CD38
NAD+激酶
免疫疗法
多发性骨髓瘤
抗体
医学
癌症研究
酶
化学
免疫学
生物
免疫系统
生物化学
细胞生物学
川地34
干细胞
作者
Barry E. Kennedy,Maryanne Sadek,Manal O. Elnenaei,Tony Reiman,Shashi Gujar
标识
DOI:10.1016/j.trecan.2019.11.005
摘要
Antibodies targeting CD38, a NAD+-degrading enzyme, have emerged as a promising immunotherapy against multiple myeloma (MM). Currently, the mechanisms by which anti-CD38 antibodies establish their therapeutic effects are poorly understood. Here, we advocate for the depletion of NAD+ to enhance the efficacy of anti-CD38-based immunotherapies in MM. Antibodies targeting CD38, a NAD+-degrading enzyme, have emerged as a promising immunotherapy against multiple myeloma (MM). Currently, the mechanisms by which anti-CD38 antibodies establish their therapeutic effects are poorly understood. Here, we advocate for the depletion of NAD+ to enhance the efficacy of anti-CD38-based immunotherapies in MM.
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