同种异体造血干细胞移植后预防性大剂量粒细胞输注。

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-05-14 DOI:10.1111/vox.70044
Yannis Hadjiyannis, Robert Bubar, Darrell J Triulzi, Joseph Kiss, Christopher C Marino, Randy M Windreich, Paul Szabolcs, Alesia Kaplan
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引用次数: 0

摘要

背景和目的:预防性粒细胞输注(PGTxs)是有争议的。以前的研究面临着许多混杂因素,比如如何获得足够的剂量。在接受造血干细胞移植(HSCT)的患者中,对于持续的、严重的移植前感染,预防性或继发性PGTx很少有报道。在这里,我们回顾了高剂量PGTx在有持续复发感染史的高危HSCT患者中的可行性、安全性和实施情况。材料和方法:我们在三级医疗中心对所有接受高剂量PGTx的HSCT患者进行了回顾性研究(2018-2021),这些患者来自受粒细胞集落刺激因子和地塞米松刺激的供体。PGTx作为预防感染复发/进展的二级预防措施。结果:7例患者在HSCT期间接受了PGTx治疗;95%的输注产品的剂量≥0.6 × 109/kg。输血后绝对中性粒细胞计数(ANC)平均升高5.5±3.7 × 109/L。所有PGTxs耐受性良好,无明显输血反应、不良反应或人白细胞抗原异体免疫。总存活率高(第30天100%),发热率高(85%),无感染。结论:优化后的高剂量PGTx可使ANC显著升高,且耐受性良好。尽管有效性和安全性仍有待确定,但我们强调了为接受HSCT的高风险患者生产和实施优化的高剂量PGTx的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prophylactic high-dose granulocyte transfusions following allogeneic haematopoietic stem cell transplantation.

Background and objectives: Prophylactic granulocyte transfusions (PGTxs) are controversial. Previous studies faced numerous confounders such as achieving an adequate dose. Pre-emptive or secondary PGTx for persistent, severe pre-transplant infections has rarely been reported for patients undergoing haematopoietic stem cell transplantation (HSCT). Here, we reviewed the feasibility, safety and implementation of high-dose PGTx in high-risk patients undergoing HSCT with a history of persistent, recurrent infections.

Materials and methods: We conducted a retrospective review (2018-2021) for all HSCT patients who received high-dose PGTx from donors stimulated with granulocyte colony-stimulating factor and dexamethasone at our tertiary medical centre. PGTx was carried out as secondary prophylaxis to prevent infection recurrence/progression.

Results: Seven patients received PGTx during HSCT; 95% of all transfused products contained a dose ≥0.6 × 109/kg. Post-transfusion absolute neutrophil count (ANC) showed an average increase of 5.5 ± 3.7 × 109/L. All PGTxs were well tolerated, with no evident transfusion reactions, adverse effects or human leukocyte antigen alloimmunization. A high overall survival rate (100% at day 30), afebrile rate (85%) and absence of infections were noted.

Conclusion: Optimized high-dose PGTx resulted in a measurable ANC increase and was well tolerated. Although efficacy and safety remain to be established, we highlight the ability to produce and implement optimized high-dose PGTx for high-risk patients undergoing HSCT.

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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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