小儿造血干细胞移植后输注高剂量记忆CD45RO+供体淋巴细胞的安全性和有效性

IF 3.2 3区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Cytotherapy Pub Date : 2024-12-01 Epub Date: 2024-07-11 DOI:10.1016/j.jcyt.2024.07.007
Mercedes Gasior Kabat , Ying Li , Victor Galán , Yasmina Mozo , Luisa Sisinni , David Bueno-Sánchez , Dolores Corral , Swati Naik , Carlos Echecopar , Cristina Aguirre-Portolés , Karima Al-Akioui-Sanz , Raquel De Paz , Antonio Marcos , Ana Belén Romero , Aimee Talleur , Víctor Jiménez Yuste , Brandon Triplett , Antonio Pérez-Martínez
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引用次数: 0

摘要

与天真 T 细胞相比,作为供体淋巴细胞输注的记忆 T 细胞(CD45RA-/RO+)产生异体反应和移植物抗宿主疾病(GvHD)的能力较低。本研究旨在评估异基因造血细胞移植(HCT)后大剂量记忆(CD45RA-/RO+)供体淋巴细胞输注(mDLI)的安全性和有效性。mDLI的适应症为 "根据需要 "和 "作为预防方案"。61名被诊断患有恶性疾病(82%)和非恶性疾病(18%)的儿童接受了241次mDLI。患者接受了三次中位 mDLI 输注(1-13 次不等),中位输注剂量为 1.35 × 107/kg CD45RO+,包含 8.96 × 106/kg CD3+CD45RO+ 和 3.81 × 103/kg CD3+CD45RA+。有7名患者在输注4%的mDLI后出现了新的GvHD。在输注 mDLI 前有 GvHD 的患者中,3 名 II-IV 级急性 GvHD 患者在输注 6 次(11%)后病情恶化。65%的 mDLI 输注后巨细胞病毒载量下降。所有患者的两年总生存率(OS)为 64%(95% CI 57%-72%)。对于接受预防性 mDLI 的患者,两年非复发死亡率为 10%(95% CI 9%-11%)。总之,大剂量 mDLI 既可行又安全,即使是活动性 GvHD 患者,发生严重 GvHD 的风险也相对较低。重要的是,mDLI具有积极的作用,包括增强了对CMV病毒血症的控制。
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Safety and Efficacy of High-Dose Memory CD45RO+ Donor Lymphocyte Infusion in Pediatric Recipients after Hematopoietic Stem Cell Transplantation
Memory T selected cells (CD45RA-/RO+) as donor lymphocyte infusion are less capable of producing alloreactivity and graft versus host disease (GvHD) compared with naïve T cells. The objective of this study was to evaluate the safety and efficacy of high-dose memory (CD45RA-/RO+) donor lymphocyte infusion (mDLI) after allogeneic hematopoietic cell transplantation (HCT). Indications for mDLI were “as needed” and “as prophylactic regimen.” Sixty-one children diagnosed with malignant (82%) and non-malignant diseases (18%) received 241 mDLIs. Patients received a median of three infusions (range 1‒13) of mDLI with a median infused dose of 1.35 × 107/kg CD45RO+ containing 8.96 × 106/kg CD3+CD45RO+ and 3.81 × 103/kg CD3+CD45RA+. De novo GvHD developed in 7 patients following 4% of the mDLI infusions. Among patients with GvHD before mDLI, this condition worsened following 6 infusions (11%) in the 3 patients with grade II–IV acute GvHD. A decrease in cytomegalovirus viral load followed 65% of mDLI infusions. Two-year overall survival (OS) for the total cohort was 64% (95% CI 57%‒72%). For patients receiving prophylactic mDLI, the two-year non-relapse mortality was 10% (95% CI 9%‒11%). In summary, high-dose mDLI is feasible and safe, with a relatively low risk of severe GvHD even in patients with active GvHD. Importantly, mDLI was associated with positive effects, including enhanced control of CMV viremia.
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来源期刊
Cytotherapy
Cytotherapy 医学-生物工程与应用微生物
CiteScore
6.30
自引率
4.40%
发文量
683
审稿时长
49 days
期刊介绍: The journal brings readers the latest developments in the fast moving field of cellular therapy in man. This includes cell therapy for cancer, immune disorders, inherited diseases, tissue repair and regenerative medicine. The journal covers the science, translational development and treatment with variety of cell types including hematopoietic stem cells, immune cells (dendritic cells, NK, cells, T cells, antigen presenting cells) mesenchymal stromal cells, adipose cells, nerve, muscle, vascular and endothelial cells, and induced pluripotential stem cells. We also welcome manuscripts on subcellular derivatives such as exosomes. A specific focus is on translational research that brings cell therapy to the clinic. Cytotherapy publishes original papers, reviews, position papers editorials, commentaries and letters to the editor. We welcome "Protocols in Cytotherapy" bringing standard operating procedure for production specific cell types for clinical use within the reach of the readership.
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