决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Carbonic anhydrase IX: An atypical target for innovative therapies in cancer.
碳酸酐酶(CAs)是参与多种需要组织 pH 调节的病理生理过程的金属酶。
碳酸酐酶(CA)是一类金属酶,参与多种需要组织 pH 调节的病理生理过程。CA IX 是一种肿瘤相关 CA 亚型,可由缺氧诱导,并参与肿瘤细胞对酸中毒环境的适应。多种驱动肿瘤的通路均可诱导 CA IX 表达,而 CA IX 又与癌细胞侵袭和转移特征、干细胞样特征诱导、药物耐药及复发相关。在对其功能和结构完成表征后,研究人员开发了靶向 CA IX 的策略,以抑制其在肿瘤组织中的活性;迄今该领域的治疗选择和生物学研究指标均取得快速发展。小分子抑制剂、杂合/双靶向药物、靶向抗体和过继细胞疗法(基于 CAR-T)已进入临床前开发阶段;一种磺酰胺类 CA IX 抑制剂和一种抗体已进入 Ib/II 期临床试验,用于不同实体瘤的治疗和成像。本文将讨论 CA IX 在癌症中的生物学和药理学最新进展,以及其治疗性靶向策略。
Carbonic anhydrases (CAs), are metallo-enzymes implicated in several pathophysiological processes where tissue pH regulation is required. CA IX is a tumor-associated CA isoform induced by hypoxia and involved in the adaptation of tumor cells to acidosis. Indeed, several tumor-driving pathways can induce CA IX expression, and this in turn has been associated to cancer cells invasion and metastatic features as well as to induction of stem-like features, drug resistance and recurrence. After its functional and structural characterization CA IX targeting approaches have been developed to inhibit its activity in neoplastic tissues, and to date this field has seen an incredible acceleration in terms of therapeutic options and biological readouts. Small molecules inhibitors, hybrid/dual targeting drugs, targeting antibodies and adoptive (CAR-T based) cell therapy have been developed at preclinical level, whereas a sulfonamide CA IX inhibitor and an antibody entered Phase Ib/II clinical trials for the treatment and imaging of different solid tumors. Here recent advances on CA IX biology and pharmacology in cancer, and its therapeutic targeting will be discussed.
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