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使用单抗原细胞系预测HLA限制后第三方病毒特异性T细胞的结果。

Outcomes with third-party virus-specific T cells after the use of single-antigen cell lines to predict HLA restriction.

作者信息

Rubinstein Jeremy D, Pham Giang, Sridharan Anusha, Khoury Ruby, Wang YunZu M, Hudda Zahra, Wilhelm Jamie, Lichtenstein Daniel A, Heyenbruch Daria, Cancelas Jose A, Davies Stella M, Lutzko Carolyn, Grimley Michael S

机构信息

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Division of Oncology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

出版信息

Blood Adv. 2025 Dec 23;9(24):6305-6313. doi: 10.1182/bloodadvances.2025017097.

Abstract

Patients with significant T-cell dysfunction from chemotherapy or hematopoietic stem cell transplant are at significant risk for complications of viral infections. Off-the-shelf third-party virus-specific T cells (TP VSTs) are an effective and well-tolerated treatment for the management of infection with adenovirus, BK polyomavirus, cytomegalovirus, and Epstein-Barr virus. TP VST product selection for any particular patient incorporates maximizing the number of HLA matches between the product and the patient, along with consideration of the antiviral activity of the product. We have previously shown that single-antigen cell lines (SALs), cell lines expressing a single HLA molecule, can be used in a flow cytometric-based assay to determine sites of HLA restriction for TP VST products. We hypothesized that incorporating match at sites of HLA restriction into TP VST product selection would improve response rates. Here we report on 25 patients who received TP VSTs for the treatment of 26 viral infections with at least 1 match at an HLA-restricted site. In this cohort, the overall response rate was 96.2%, with a complete response rate of 69.2%. These data suggest the annotation of VST banks to include SAL-derived HLA restriction could lead to improved product selection and efficacy. This trial was registered at www.clinicaltrials.gov as #NCT02532452.

摘要

因化疗或造血干细胞移植而出现显著T细胞功能障碍的患者,发生病毒感染并发症的风险很高。现成的第三方病毒特异性T细胞(TP VSTs)是治疗腺病毒、BK多瘤病毒、巨细胞病毒和EB病毒感染的一种有效且耐受性良好的治疗方法。为任何特定患者选择TP VST产品时,要使产品与患者之间的HLA匹配数量最大化,同时还要考虑产品的抗病毒活性。我们之前已经表明,单抗原细胞系(SALs),即表达单个HLA分子的细胞系,可用于基于流式细胞术的检测,以确定TP VST产品的HLA限制位点。我们假设,将HLA限制位点的匹配纳入TP VST产品选择中会提高反应率。在此,我们报告了25例接受TP VSTs治疗26次病毒感染的患者,这些患者在HLA限制位点至少有1次匹配。在这个队列中,总体反应率为96.2%,完全缓解率为69.2%。这些数据表明,对VST库进行注释以纳入SAL衍生的HLA限制,可能会改善产品选择并提高疗效。该试验已在www.clinicaltrials.gov上注册,注册号为#NCT02532452。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b5/12744286/c63f6c0352fe/BLOODA_ADV-2025-017097-ga1.jpg

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