• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

低剂量白细胞介素-2 治疗儿童和青年难治性慢性移植物抗宿主病的真实世界经验。

Real-world experience with low-dose IL-2 for children and young adults with refractory chronic graft-versus-host disease.

机构信息

Division of Immunology, Boston Children's Hospital, Boston, MA.

Division of Hematology-Oncology, Boston Children's Hospital, Boston, MA.

出版信息

Blood Adv. 2023 Aug 22;7(16):4647-4657. doi: 10.1182/bloodadvances.2023009729.

DOI:10.1182/bloodadvances.2023009729
PMID:37603347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10448423/
Abstract

The majority of patients with chronic graft-versus-host disease (cGVHD) are steroid refractory (SR), creating a need for safe and effective therapies. Subcutaneous low-dose interleukin-2 (LD IL-2), which preferentially expands CD4+ regulatory T cells (Tregs), has been evaluated in 5 clinical trials at our center with partial responses (PR) in ∼50% of adults and 82% of children by week 8. We now report additional real-world experience with LD IL-2 in 15 children and young adults. We conducted a retrospective chart review of patients with SR-cGVHD at our center who received LD IL-2 from August 2016 to July 2022 not on a research trial. The median age at start of LD IL-2 was 10.4 years (range, 1.2-23.2 years) at a median of 234 days from cGVHD diagnosis (range, 11-542 days). Patients had a median of 2.5 (range, 1-3) active organs at LD IL-2 start and received a median of 3 (range, 1-5) prior therapies. The median duration of LD IL-2 therapy was 462 days (range, 8-1489 days). Most patients received 1 × 106 IU/m2 per day. There were no serious adverse effects. The overall response rate in 13 patients who received >4 weeks of therapy was 85% (complete response, n = 5; PR, n = 6) with responses in diverse organs. Most patients significantly weaned corticosteroids. Tregs preferentially expanded with a median peak fold increase of 2.8 in the ratio of Tregs to CD4+ conventional T cells (range, 2.0-19.8) by 8 weeks on therapy. LD IL-2 is a well-tolerated, steroid-sparing agent with a high response rate in children and young adults with SR-cGVHD.

摘要

大多数慢性移植物抗宿主病(cGVHD)患者对类固醇耐药(SR),这需要安全有效的治疗方法。皮下小剂量白细胞介素 2(LD IL-2)可优先扩增 CD4+调节性 T 细胞(Tregs),在我们中心的 5 项临床试验中进行了评估,在第 8 周时,约 50%的成年人和 82%的儿童有部分反应(PR)。现在,我们报告了在 15 名儿童和年轻成年人中使用 LD IL-2 的额外真实世界经验。我们对我们中心接受 LD IL-2 治疗的 SR-cGVHD 患者进行了回顾性图表审查,这些患者不在研究试验中接受 LD IL-2 治疗。LD IL-2 开始时的中位年龄为 10.4 岁(范围为 1.2-23.2 岁),距 cGVHD 诊断的中位时间为 234 天(范围为 11-542 天)。患者在 LD IL-2 开始时有中位 2.5 个(范围为 1-3 个)活跃器官,接受了中位 3 次(范围为 1-5 次)先前的治疗。LD IL-2 治疗的中位持续时间为 462 天(范围为 8-1489 天)。大多数患者每天接受 1×106 IU/m2。没有严重的不良反应。在接受>4 周治疗的 13 名患者中,总体缓解率为 85%(完全缓解 5 例;部分缓解 6 例),在不同器官中均有缓解。大多数患者显著减少了皮质类固醇的使用。Tregs 优先扩增,在治疗 8 周时,Tregs 与 CD4+常规 T 细胞的比值中位数增加了 2.8 倍(范围为 2.0-19.8)。LD IL-2 是一种耐受性良好的药物,可作为类固醇保存剂,在 SR-cGVHD 的儿童和年轻成年人中具有较高的反应率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/fb9d94ea1477/BLOODA_ADV-2023-009729-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/6bd835934ad6/BLOODA_ADV-2023-009729-fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/9908c96395d6/BLOODA_ADV-2023-009729-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/720de71a914f/BLOODA_ADV-2023-009729-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/12392ffd71a8/BLOODA_ADV-2023-009729-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/fb9d94ea1477/BLOODA_ADV-2023-009729-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/6bd835934ad6/BLOODA_ADV-2023-009729-fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/9908c96395d6/BLOODA_ADV-2023-009729-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/720de71a914f/BLOODA_ADV-2023-009729-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/12392ffd71a8/BLOODA_ADV-2023-009729-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f2/10448423/fb9d94ea1477/BLOODA_ADV-2023-009729-gr4.jpg

相似文献

1
Real-world experience with low-dose IL-2 for children and young adults with refractory chronic graft-versus-host disease.低剂量白细胞介素-2 治疗儿童和青年难治性慢性移植物抗宿主病的真实世界经验。
Blood Adv. 2023 Aug 22;7(16):4647-4657. doi: 10.1182/bloodadvances.2023009729.
2
Durability of clinical and immunologic responses to extended low-dose interleukin-2 therapy in patients with refractory chronic graft-versus-host disease.延长低剂量白细胞介素-2 治疗难治性慢性移植物抗宿主病患者的临床和免疫应答的持久性。
Front Immunol. 2022 Sep 14;13:954966. doi: 10.3389/fimmu.2022.954966. eCollection 2022.
3
A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease.一项关于供者调节性 T 细胞输注联合低剂量白细胞介素-2 治疗激素难治性慢性移植物抗宿主病的 1 期研究。
Blood Adv. 2022 Nov 8;6(21):5786-5796. doi: 10.1182/bloodadvances.2021006625.
4
Dose-escalated interleukin-2 therapy for refractory chronic graft-versus-host disease in adults and children.成人和儿童难治性慢性移植物抗宿主病的递增剂量白细胞介素 2 治疗。
Blood Adv. 2019 Sep 10;3(17):2550-2561. doi: 10.1182/bloodadvances.2019000631.
5
Efficacy, durability, and response predictors of low-dose interleukin-2 therapy for chronic graft-versus-host disease.低剂量白细胞介素-2治疗慢性移植物抗宿主病的疗效、持久性及反应预测指标
Blood. 2016 Jul 7;128(1):130-7. doi: 10.1182/blood-2016-02-702852. Epub 2016 Apr 12.
6
Efficiency and Toxicity of Ruxolitinib as a Salvage Treatment for Steroid-Refractory Chronic Graft-Versus-Host Disease.芦可替尼作为挽救治疗类固醇难治性慢性移植物抗宿主病的疗效和毒性。
Front Immunol. 2021 Jun 30;12:673636. doi: 10.3389/fimmu.2021.673636. eCollection 2021.
7
Organ-specific response after low-dose interleukin-2 therapy for steroid-refractory chronic graft-versus-host disease.低剂量白细胞介素-2 治疗类固醇难治性慢性移植物抗宿主病后的器官特异性反应。
Blood Adv. 2022 Aug 9;6(15):4392-4402. doi: 10.1182/bloodadvances.2022007773.
8
A Prospective Study of Alemtuzumab as a Second-Line Agent for Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric and Young Adult Allogeneic Hematopoietic Stem Cell Transplantation.一项关于阿仑单抗作为儿童和青年成人异基因造血干细胞移植中类固醇难治性急性移植物抗宿主病二线治疗药物的前瞻性研究。
Biol Blood Marrow Transplant. 2016 Dec;22(12):2220-2225. doi: 10.1016/j.bbmt.2016.09.016. Epub 2016 Sep 21.
9
A high-dose pulse steroid regimen for controlling active chronic graft-versus-host disease.一种用于控制活动性慢性移植物抗宿主病的大剂量脉冲类固醇疗法。
Biol Blood Marrow Transplant. 2001;7(9):495-502. doi: 10.1053/bbmt.2001.v7.pm11669216.
10
Extracorporeal photopheresis therapy in the management of steroid-refractory or steroid-dependent cutaneous chronic graft-versus-host disease after allogeneic stem cell transplantation: feasibility and results.体外光化学疗法用于异基因干细胞移植后类固醇难治性或类固醇依赖性皮肤慢性移植物抗宿主病的治疗:可行性及结果
Bone Marrow Transplant. 2003 Mar;31(6):459-65. doi: 10.1038/sj.bmt.1703871.

引用本文的文献

1
Targeted regulatory T cell activation by site-specific PEGylated interleukin-2 mitigates autoimmune inflammation.位点特异性聚乙二醇化白细胞介素-2靶向调节性T细胞激活可减轻自身免疫性炎症。
J Transl Autoimmun. 2025 Aug 8;11:100306. doi: 10.1016/j.jtauto.2025.100306. eCollection 2025 Dec.
2
Low-dose interleukin-2 in patients with mild to moderate Alzheimer's disease: a randomized clinical trial.低剂量白细胞介素-2治疗轻至中度阿尔茨海默病患者:一项随机临床试验。
Alzheimers Res Ther. 2025 Jul 4;17(1):146. doi: 10.1186/s13195-025-01791-x.
3
Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.

本文引用的文献

1
Interleukin-2 immunotherapy reveals human regulatory T cell subsets with distinct functional and tissue-homing characteristics.白细胞介素-2 免疫疗法揭示了具有不同功能和组织归巢特性的人类调节性 T 细胞亚群。
Immunity. 2024 Sep 10;57(9):2232-2250.e10. doi: 10.1016/j.immuni.2024.07.016. Epub 2024 Aug 12.
2
Low-dose interleukin-2 therapy in active systemic lupus erythematosus (LUPIL-2): a multicentre, double-blind, randomised and placebo-controlled phase II trial.低剂量白细胞介素-2 治疗活动期系统性红斑狼疮(LUPIL-2):一项多中心、双盲、随机、安慰剂对照的 II 期临床试验。
Ann Rheum Dis. 2022 Dec;81(12):1685-1694. doi: 10.1136/ard-2022-222501. Epub 2022 Aug 16.
3
移植物抗宿主病小鼠模型:临床转化视角
Methods Mol Biol. 2025;2907:1-56. doi: 10.1007/978-1-0716-4430-0_1.
4
The role of chemokines and interleukins in acute lymphoblastic leukemia: a systematic review.趋化因子和白细胞介素在急性淋巴细胞白血病中的作用:一项系统综述
J Appl Biomed. 2024 Dec;22(4):165-184. doi: 10.32725/jab.2024.024. Epub 2024 Dec 4.
5
Low-dose interleukin 2 therapy halts the progression of post-streptococcal autoimmune complications in a rat model of rheumatic heart disease.低剂量白细胞介素2疗法可阻止风湿性心脏病大鼠模型中链球菌感染后自身免疫并发症的进展。
mBio. 2025 Apr 9;16(4):e0382324. doi: 10.1128/mbio.03823-24. Epub 2025 Feb 25.
6
Oral Chronic Graft-Versus-Host Disease: Pathogenesis, Diagnosis, Current Treatment, and Emerging Therapies.口腔慢性移植物抗宿主病:发病机制、诊断、当前治疗和新兴疗法。
Int J Mol Sci. 2024 Sep 27;25(19):10411. doi: 10.3390/ijms251910411.
7
SARS-CoV-2 infection induces a long-lived pro-inflammatory transcriptional profile.SARS-CoV-2 感染会引起持久的促炎转录特征。
Genome Med. 2023 Sep 12;15(1):69. doi: 10.1186/s13073-023-01227-x.
8
More evidence for low-dose IL-2 for chronic GVHD in children.低剂量白细胞介素-2治疗儿童慢性移植物抗宿主病的更多证据。
Blood Adv. 2023 Aug 22;7(16):4658-4659. doi: 10.1182/bloodadvances.2023010756.
Selective activation and expansion of regulatory T cells using lipid encapsulated mRNA encoding a long-acting IL-2 mutein.
使用包封在脂质中的编码长效 IL-2 突变体的 mRNA 选择性激活和扩增调节性 T 细胞。
Nat Commun. 2022 Jul 5;13(1):3866. doi: 10.1038/s41467-022-31130-9.
4
Organ-specific response after low-dose interleukin-2 therapy for steroid-refractory chronic graft-versus-host disease.低剂量白细胞介素-2 治疗类固醇难治性慢性移植物抗宿主病后的器官特异性反应。
Blood Adv. 2022 Aug 9;6(15):4392-4402. doi: 10.1182/bloodadvances.2022007773.
5
Three US Food and Drug Administration-approved therapies for chronic GVHD.三种美国食品和药物管理局批准的慢性移植物抗宿主病治疗方法。
Blood. 2022 Mar 17;139(11):1642-1645. doi: 10.1182/blood.2021014448.
6
Steroid-refractory chronic graft-versus-host disease: treatment options and patient management.类固醇难治性慢性移植物抗宿主病:治疗选择与患者管理
Bone Marrow Transplant. 2021 Sep;56(9):2079-2087. doi: 10.1038/s41409-021-01389-5. Epub 2021 Jul 3.
7
Selective expansion of regulatory T cells using an orthogonal IL-2/IL-2 receptor system facilitates transplantation tolerance.使用正交白细胞介素-2/白细胞介素-2受体系统选择性扩增调节性T细胞有助于移植耐受。
J Clin Invest. 2021 Apr 15;131(8). doi: 10.1172/JCI139991.
8
Low-dose IL-2 in children with recently diagnosed type 1 diabetes: a Phase I/II randomised, double-blind, placebo-controlled, dose-finding study.低剂量白细胞介素-2用于新诊断的1型糖尿病儿童:一项I/II期随机、双盲、安慰剂对照、剂量探索性研究。
Diabetologia. 2020 Sep;63(9):1808-1821. doi: 10.1007/s00125-020-05200-w. Epub 2020 Jul 1.
9
Immunopathology and biology-based treatment of steroid-refractory graft-versus-host disease.基于免疫病理学和生物学的类固醇难治性移植物抗宿主病的治疗。
Blood. 2020 Jul 23;136(4):429-440. doi: 10.1182/blood.2019000953.
10
IL-2 enhances ex vivo-expanded regulatory T-cell persistence after adoptive transfer.白细胞介素-2可增强过继转移后体外扩增的调节性T细胞的持久性。
Blood Adv. 2020 Apr 28;4(8):1594-1605. doi: 10.1182/bloodadvances.2019001248.