An Jianhong, Hu Erqiang, Shi Yang, Fang Yanan, Liu Naijia, Liu Qiang, Wang Qing, Wang Yanhua, He Wu, Wang Angelina, Song Yinghui, Shan Jidong, Zhang Jinghang, Zou Yiyu, Cheng Haiying, Kabarriti Rafi, Cai Wei, Verma Amit, Sica Roberto Alejandro, Deng Wenjun, Yin Shanye
Department of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
Einstein Pathology Single-cell & Bioinformatics laboratory, Bronx, NY, USA.
J Immunother Cancer. 2025 Mar 25;13(3):e011265. doi: 10.1136/jitc-2024-011265.
Adult T-cell leukemia/lymphoma (ATLL), an aggressive T-cell malignancy associated with human T-cell leukemia virus type 1, presents significant therapeutic challenges due to high relapse rates and resistance to therapy. Here, we present the first reported case of ATLL treated with talimogene laherparepvec (T-VEC), an oncolytic viral immunotherapy approved for unresectable melanoma. The patient, who had experienced disease progression despite multiple lines of chemotherapy, radiotherapy, immunotherapy, and targeted therapy, underwent experimental virotherapy with two intratumoral T-VEC injections. The treatment was well-tolerated, with no significant adverse effects, and led to substantial tumor regression and clinical stabilization, suggesting potential remission. Single-cell analysis revealed that T-VEC treatment induced robust local and systemic immune responses, including tumor necrosis, activation of M1 macrophages, and infiltration of CD8+ effector memory T cells. These findings demonstrate T-VEC's safety and efficacy in generating both localized oncolysis and systemic anti-tumor immune response, highlighting its promise as a novel therapeutic approach for refractory ATLL.
成人T细胞白血病/淋巴瘤(ATLL)是一种与1型人类T细胞白血病病毒相关的侵袭性T细胞恶性肿瘤,由于复发率高和对治疗耐药,面临重大治疗挑战。在此,我们报告首例用talimogene laherparepvec(T-VEC)治疗的ATLL病例,T-VEC是一种已获批用于不可切除黑色素瘤的溶瘤病毒免疫疗法。该患者尽管接受了多线化疗、放疗、免疫疗法和靶向治疗,但病情仍进展,接受了两次瘤内注射T-VEC的实验性病毒疗法。治疗耐受性良好,无明显不良反应,并导致肿瘤显著消退和临床稳定,提示可能缓解。单细胞分析显示,T-VEC治疗诱导了强大的局部和全身免疫反应,包括肿瘤坏死、M1巨噬细胞激活和CD8 + 效应记忆T细胞浸润。这些发现证明了T-VEC在产生局部溶瘤和全身抗肿瘤免疫反应方面的安全性和有效性,突出了其作为难治性ATLL新型治疗方法的前景。