CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:New Frontiers in Monoclonal Antibodies for Relapsed/Refractory Diffuse Large B-Cell Lymphoma.
New Frontiers in Monoclonal Antibodies for Relapsed/Refractory Diffuse Large B-Cell Lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
弥漫大B细胞淋巴瘤(DLBCL)是最常见的侵袭性淋巴瘤。约60%的患者通过R-CHOP作为一线治疗获得治愈,而其余患者则出现原发难治或复发疾病(R/R)。对于既不适合自体干细胞移植也不适合CAR-T 细胞治疗的R/R DLBCL患者,预后较差,代表着重要的未满足需求。单克隆抗体(mAbs)极大地改善了抗癌策略中的治疗选择,为克服这一具有挑战性疾病中的化疗难治性提供了新机遇,即使在原发无应答DLBCL病例中也是如此。目前已有几种具有不同作用机制和靶点的新型mAbs可用于R/R DLBCL。非结合型mAbs诱导针对癌细胞的免疫反应,触发不同机制,包括抗体依赖性细胞介导的细胞毒性(ADCC)、抗体依赖性细胞介导的吞噬作用(ADCP)的激活以及补体依赖性细胞毒性(CDC)。抗体药物偶联物(ADCs)和放射免疫治疗(RIT)分别将细胞毒性载荷或β发射体放射性核素递送至靶细胞及邻近旁观者细胞。双特异性T细胞衔接器(BiTes)和免疫检查点抑制剂(ICIs)重定向并增强针对肿瘤细胞的免疫反应。在此,我们综述基于单克隆抗体的R/R DLBCL治疗策略。
Diffuse large B-cell lymphoma (DLBCL) is the most common aggressive lymphoma. Approximately 60% of patients are cured with R-CHOP as a frontline treatment, while the remaining patients experience primary refractory or relapsed disease (R/R). The prognosis for R/R DLBCL patients who are neither eligible for autologous stem-cell transplantations nor CAR-T-cell treatment is poor, representing an important unmet need. Monoclonal antibodies (mAbs) have dramatically improved therapeutic options in anti-cancer strategies, offering new opportunities to overcome chemo-refractoriness in this challenging disease, even in cases of primary non-responder DLBCL.
Several novel mAbs, characterized by different mechanisms of action and targets, are now available for R/R DLBCL. Unbound mAbs induce an immune response against cancer cells, triggering different mechanisms, including antibody-dependent cellular cytotoxicity (ADCC), activation of antibody-dependent cell-mediated phagocytosis (ADCP) and complement-dependent cytotoxicity (CDC).
Antibody-drug conjugates (ADCs) and radioimmunotherapy (RIT), respectively, deliver a cytotoxic payload or a beta-emitter radionuclide to the targeted cells and nearby bystanders. Bispecific T-cell engagers (BiTes) and immune checkpoint inhibitors (ICIs) redirect and enhance the immune response against tumor cells.
Here, we review therapeutic strategies based on monoclonal antibodies for R/R DLBCL.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。