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异基因干细胞移植后初始T细胞去除的供体淋巴细胞输注的I期剂量递增研究。

Phase I dose escalation study of naive T-cell depleted donor lymphocyte infusion following allogeneic stem cell transplantation.

作者信息

Maung Ko K, Chen Benny J, Barak Ian, Li Zhiguo, Rizzieri David A, Gasparetto Cristina, Sullivan Keith M, Long Gwynn D, Engemann Ashley M, Waters-Pick Barbara, Nichols Krista Rowe, Lopez Richard, Kang Yubin, Sarantopoulos Stefanie, Sung Anthony D, Chao Nelson J, Horwitz Mitchell E

机构信息

Division of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC, USA.

Cancer Center Biostatistics, Duke Cancer Institute, Duke University Medical Center, Durham, NC, USA.

出版信息

Bone Marrow Transplant. 2021 Jan;56(1):137-143. doi: 10.1038/s41409-020-0991-5. Epub 2020 Jul 5.

Abstract

Prophylactic donor lymphocyte infusions (DLI) are used to augment post-transplant immune recovery to reduce both infectious complications and disease recurrence. Preclinical studies implicate the naive T-cell subset as the primary driver of graft-versus-host disease (GvHD). In this phase I dose escalation study, we assessed the safety of a DLI that was depleted of CD45RA+ naive T cells. Sixteen adult patients received a prophylactic DLI at a median of 113 days (range 76-280 days) following an HLA-identical, non-myeloablative allogeneic hematopoietic stem cell transplantation. Three patients each received the naive T-cell depleted DLI with a CD3+ dose of 1 × 10/kg, 1 × 10/kg, and 5 × 10/kg. The maximum dose of 1 × 10/kg was expanded to 7 patients. No dose-limiting grade III/IV acute GvHD or adverse events attributable to the DLI were observed at any dose level. One patient developed grade 2 acute GvHD of skin and upper intestines, and another developed moderate chronic GvHD of the lungs following the DLI. With a median follow-up of 2.8 years, 2-year progression-free and overall survival is 50.0% and 68.8%, respectively. In conclusion, these data suggest that a DLI that has been depleted of CD45RA+ naive T cells is feasible and carries a low risk of acute or chronic GvHD.

摘要

预防性供体淋巴细胞输注(DLI)用于增强移植后免疫恢复,以减少感染并发症和疾病复发。临床前研究表明,初始T细胞亚群是移植物抗宿主病(GvHD)的主要驱动因素。在这项I期剂量递增研究中,我们评估了去除CD45RA +初始T细胞的DLI的安全性。16例成年患者在接受 HLA 相同的非清髓性异基因造血干细胞移植后的中位113天(范围76 - 280天)接受了预防性DLI。3例患者分别接受了去除初始T细胞的DLI,其CD3 +剂量分别为1×10/kg、1×10/kg和5×10/kg。最大剂量1×10/kg扩大至7例患者。在任何剂量水平均未观察到剂量限制性III/IV级急性GvHD或归因于DLI的不良事件。1例患者在DLI后出现皮肤和上肠道2级急性GvHD,另1例在DLI后出现中度肺部慢性GvHD。中位随访2.8年,2年无进展生存率和总生存率分别为50.0%和68.8%。总之,这些数据表明,去除CD45RA +初始T细胞的DLI是可行的,且急性或慢性GvHD风险较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d74/10805111/2b4cc7e8781e/nihms-1953150-f0001.jpg

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Selective depletion of naïve T cells by targeting CD45RA.通过靶向CD45RA选择性清除初始T细胞。
Front Oncol. 2023 Jan 27;12:1009143. doi: 10.3389/fonc.2022.1009143. eCollection 2022.

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