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可溶性尿激酶型纤溶酶原激活物受体 (suPAR)、生长分化因子 15 (GDF-15) 和可溶性 C5b-9 (sC5b-9) 水平与 CAR-T 细胞受者的内皮损伤指标显著相关。

Soluble Urokinase-Type Plasminogen Activator Receptor (suPAR), Growth Differentiation Factor-15 (GDF-15), and Soluble C5b-9 (sC5b-9) Levels Are Significantly Associated with Endothelial Injury Indices in CAR-T Cell Recipients.

机构信息

BMT Unit, Hematology Department, George Papanicolaou General Hospital, 57010 Thessaloniki, Greece.

Second Propedeutic Department of Internal Medicine, Hippocration Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.

出版信息

Int J Mol Sci. 2024 Oct 14;25(20):11028. doi: 10.3390/ijms252011028.

DOI:10.3390/ijms252011028
PMID:39456810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11507105/
Abstract

Endothelial injury indices, such as Endothelial Activation and Stress Index (EASIX), modified EASIX (m-EASIX), and simplified EASIX (s-EASIX) scores, have been previously associated with chimeric antigen receptor-T (CAR-T) cell immunotherapy complications. Soluble urokinase-type plasminogen activator receptor (suPAR), growth differentiation factor-15 (GDF-15), and soluble C5b-9 (sC5b-9) have been described as markers of endothelial injury post-hematopoietic stem cell transplantation. In the current study, we examined whether suPAR, GDF-15, and sC5b-9 levels were associated with endothelial injury indices in adult CAR-T cell recipients. The levels of these markers were measured in patients before CAR-T cell infusion and in healthy individuals with immunoenzymatic methods. We studied 45 CAR-T cell recipients and 20 healthy individuals as the control group. SuPAR, GDF-15, and sC5b-9 levels were significantly higher in the patients' group compared to the healthy control group ( < 0.001, in all comparisons). SuPAR levels at baseline were associated with the m-EASIX scores calculated at the same time point ( = 0.020), while suPAR and GDF-15 concentrations were correlated with EASIX scores at day 14 post-infusion ( < 0.001 in both comparisons). Moreover, sC5b-9 levels were correlated with the s-EASIX scores at infusion ( = 0.008) and the EASIX scores at day 14 ( = 0.005). In our study, sC5b9, suPAR, and GDF-15 levels were found to reflect endothelial injury in CAR-T cell recipients.

摘要

内皮损伤指数,如内皮激活和应激指数(EASIX)、改良 EASIX(m-EASIX)和简化 EASIX(s-EASIX)评分,先前与嵌合抗原受体-T(CAR-T)细胞免疫治疗并发症相关。可溶性尿激酶型纤溶酶原激活物受体(suPAR)、生长分化因子 15(GDF-15)和可溶性 C5b-9(sC5b-9)已被描述为造血干细胞移植后内皮损伤的标志物。在本研究中,我们研究了 suPAR、GDF-15 和 sC5b-9 水平是否与成人 CAR-T 细胞接受者的内皮损伤指数相关。使用免疫酶法在 CAR-T 细胞输注前测量这些标志物在患者中的水平,并在健康个体中测量这些标志物的水平。我们研究了 45 名 CAR-T 细胞接受者和 20 名健康个体作为对照组。与健康对照组相比,患者组的 suPAR、GDF-15 和 sC5b-9 水平显著升高(<0.001,所有比较)。基线时的 suPAR 水平与同时计算的 m-EASIX 评分相关(=0.020),而 suPAR 和 GDF-15 浓度与输注后第 14 天的 EASIX 评分相关(在两个比较中均<0.001)。此外,sC5b-9 水平与输注时的 s-EASIX 评分(=0.008)和第 14 天的 EASIX 评分(=0.005)相关。在我们的研究中,发现 sC5b9、suPAR 和 GDF-15 水平反映了 CAR-T 细胞接受者的内皮损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/c008dcffecc6/ijms-25-11028-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/133ba1d7b8a9/ijms-25-11028-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/f727f3dec4ef/ijms-25-11028-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/c008dcffecc6/ijms-25-11028-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/133ba1d7b8a9/ijms-25-11028-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/f727f3dec4ef/ijms-25-11028-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dd/11507105/c008dcffecc6/ijms-25-11028-g003.jpg

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2
Genetic Susceptibility in Endothelial Injury Syndromes after Hematopoietic Cell Transplantation and Other Cellular Therapies: Climbing a Steep Hill.造血细胞移植及其他细胞治疗后内皮损伤综合征中的遗传易感性:艰难前行。
Curr Issues Mol Biol. 2024 May 15;46(5):4787-4802. doi: 10.3390/cimb46050288.
3
What is the role of complement in bystander hemolysis? Old concept, new insights.
CAR-T细胞治疗后免疫效应细胞相关神经毒性综合征及其他精神症状:综述与病例系列
J Clin Med. 2025 Feb 21;14(5):1451. doi: 10.3390/jcm14051451.
4
Invasive Fungal Disease After Chimeric Antigen Receptor-T Immunotherapy in Adult and Pediatric Patients.成人和儿童患者接受嵌合抗原受体T细胞免疫治疗后的侵袭性真菌病
Pathogens. 2025 Feb 8;14(2):170. doi: 10.3390/pathogens14020170.
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Expert Rev Hematol. 2024 Apr-May;17(4-5):107-116. doi: 10.1080/17474086.2024.2348662. Epub 2024 May 6.
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Immune effector cell-associated hematotoxicity: EHA/EBMT consensus grading and best practice recommendations.免疫效应细胞相关血液学毒性:EHA/EBMT 共识分级和最佳实践建议。
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