Stem Cell Transplantation and Cellular Therapies Service, Department of Pediatrics, and.
Department of Pediatrics, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York, USA.
J Clin Invest. 2023 May 15;133(10):e165476. doi: 10.1172/JCI165476.
BackgroundRefractory CMV viremia and disease are associated with significant morbidity and mortality in recipients of hematopoietic stem cell transplant (HCT).MethodsIn phase I/II trials, we treated 67 subjects for CMV viremia or disease arising after HCT with adoptive transfer of banked, third-party, CMVpp65-sensitized T cells (CMVpp65-VSTs). All were evaluable for toxicity and 59 for response. Evaluable subjects had CMV disease or persisting viremia that had failed at least 2 weeks of induction therapy with a median of 3 antiviral drugs; 84.7% had more than 3 of 11 high-risk features. CMVpp65-VSTs were specific for 1 to 3 CMVpp65 epitopes, presented by a limited set of HLA class I or II alleles, and were selected based on high-resolution HLA matching at 2 of 10 HLA alleles and matching for subject and subject's HCT donor for 1 or more alleles through which the CMVpp65-VSTs were restricted.ResultsT cell infusions were well tolerated. Of 59 subjects evaluable for response, 38 (64%) achieved complete or durable partial responses.ConclusionsRecipients responding to CMVpp65VSTs experienced an improved overall survival. Of the risk factors evaluated, transplant type, recipient CD4+ and CD8+ T cell levels prior to adoptive therapy, and the HLA restriction of CMVpp65-VSTs infused each significantly affected responses. In addition, CMVpp65-specific T cells of HCT donor or recipient origin contributed to the durability of both complete and partial responses.Trial RegistrationNCT00674648; NCT01646645; NCT02136797 (NIH).FundingNIH (P01 CA23766, R21 CA162002 and P30 CA008748); Aubrey Fund; Claire Tow Foundation; Major Family Foundation; "Rick" Eisemann Pediatric Research Fund; Banbury Foundation; Edith Robertson Foundation; Larry Smead Foundation.
造血干细胞移植(HCT)后出现难治性 CMV 血症和疾病与受者的发病率和死亡率显著相关。
在 I/II 期试验中,我们用已储存的、第三方的 CMVpp65 致敏 T 细胞(CMVpp65-VSTs)对 67 例 HCT 后发生 CMV 血症或疾病的患者进行了过继性转移治疗。所有患者均进行了毒性评估,59 例进行了反应评估。可评估的患者具有 CMV 疾病或持续病毒血症,在接受中位为 3 种抗病毒药物的至少 2 周诱导治疗后失败;84.7%的患者具有 11 个高危特征中的 3 个以上。CMVpp65-VSTs 针对 1 到 3 个 CMVpp65 表位,由有限的一组 HLA Ⅰ类或Ⅱ类等位基因呈递,并根据 10 个 HLA 等位基因中的 2 个的高分辨率 HLA 匹配以及通过 CMVpp65-VSTs 受限的 1 个或多个等位基因与供体和受者的 HLA 匹配进行选择。
T 细胞输注耐受性良好。在 59 例可评估反应的患者中,38 例(64%)获得完全或持久部分缓解。
对 CMVpp65VSTs 有反应的受者的总生存率得到改善。在所评估的危险因素中,移植类型、过继治疗前受者 CD4+和 CD8+T 细胞水平以及输注的 CMVpp65-VSTs 的 HLA 限制均显著影响反应。此外,HCT 供者或受者来源的 CMVpp65 特异性 T 细胞对完全和部分反应的持久性均有贡献。
NCT00674648;NCT01646645;NCT02136797(NIH)。
NIH(P01 CA23766、R21 CA162002 和 P30 CA008748);Aubrey 基金;Claire Tow 基金会;主要家庭基金会;“Rick”Eisemann 儿科研究基金;Banbury 基金会;Edith Robertson 基金会;Larry Smead 基金会。