血浆免疫介质作为镰状细胞病患者根据羟基脲治疗和疾病严重程度的实验室生物标志物

IF 2.1 4区 医学 Q3 HEMATOLOGY
Sílvia Letícia de Oliveira Toledo , Valéria Sutana Ladeira , Leilismara Sousa Nogueira , Letícia Gonçalves Resende Ferreira , Marina Mendes Oliveira , Cristiane de Oliveira Renó , Hérica Lima dos Santos , Jordana Grazziela Alves Coelho-dos-Reis , Ana Carolina Campi-Azevedo , Andréa Teixeira-Carvalho , Olindo Assis Martins-Filho , Danyelle Romana Alves Rios , Melina Barros-Pinheiro
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引用次数: 1

摘要

在本工作中,评估了镰状细胞病(SCD)严重程度以及羟基脲治疗对患者全身免疫特征的影响。基于高通量趋化因子、细胞因子和生长因子多重分析,与健康对照组(n=40)相比,有可能获得接受或不接受羟基脲治疗的SCD患者的全身免疫谱。总体而言,患有严重疾病的SCD患者几乎所有分析的生物标志物水平都有所提高。我们的数据表明CXCL8、CCL3和CXCL10是SCD的通用生物标志物。结果还表明,有HU治疗指征的HU未治疗患者的血浆免疫介质表现出更显著的增加,其方式与严重SCD疾病患者相似。总之,这些发现提供了全面的证据,可能对进一步的治疗策略和SCD临床管理有启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma immune mediators as laboratorial biomarkers for Sickle Cell Disease patients according to the hydroxyurea therapy and disease severity

In the present work, the impact of Sickle Cell Disease (SCD) degrees of severity, as well hydroxyurea treatment on the systemic immunological signatures of patients was evaluated. Based on a high-throughput chemokine, cytokine and growth factor multiplex analysis, it was possible to obtain the systemic immunological profile of patients with SCD (n = 40), treated or not with hydroxyurea, as compared to healthy controls (n = 40). Overall, SCD patients with severe disease displayed increased levels of almost all biomarkers analyzed. Our data demonstrated that CXCL8, CCL3 and CXCL10 were pointed out as universal biomarkers of SCD. The results also indicated that HU-untreated patients with indication of HU-therapy display a more prominent increase on plasma immune mediators in a similar way as those with severe SCD disease. Together, these findings provided a comprehensive landscape of evidence that may have implications for further therapeutic strategies and SCD clinical management.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
42
审稿时长
14 days
期刊介绍: Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.
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