Plasma immune mediators as laboratorial biomarkers for Sickle Cell Disease patients according to the hydroxyurea therapy and disease severity

被引:1
|
作者
de Oliveira Toledo, Silvia Leticia [1 ]
Ladeira, Valeria Sutana [2 ]
Nogueira, Leilismara Sousa [3 ]
Resende Ferreira, Leticia Goncalves [1 ]
Oliveira, Marina Mendes [2 ]
Reno, Cristiane de Oliveira [1 ]
dos Santos, Herica Lima [1 ]
Alves Coelho-dos-Reis, Jordana Grazziela [4 ]
Campi-Azevedo, Ana Carolina [5 ,6 ]
Teixeira-Carvalho, Andrea [5 ,6 ]
Martins-Filho, Olindo Assis [5 ,6 ]
Alves Rios, Danyelle Romana [1 ]
Barros-Pinheiro, Melina [1 ]
机构
[1] Univ Fed Sao Joao Rei, Campus Ctr Oeste Dona Lindu, BR-35501296 Divinopolis, MG, Brazil
[2] Fundacao Ctr Hematol & Hemoterapia Estado Minas, HEMOMINAS, Hemonucleo Reg Divinopolis, Divinopolis, MG, Brazil
[3] Univ Fed Alfenas, Dept Anal Clin & Toxicol, Alfenas, MG, Brazil
[4] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Microbiol, Belo Horizonte, MG, Brazil
[5] Fundacao Oswaldo Cruz, FIOCRUZ Minas, Inst Rene Rachou, Belo Horizonte, MG, Brazil
[6] Fundacao Oswaldo Cruz, FIOCRUZ Minas, Inst Rene Rachou, Grp Integrad Pesquisas Biomarcadores, Ave Augusto de Lima 1715, BR-30190002 Belo Horizonte, MG, Brazil
关键词
Sickle Cell Disease; Biomarkers; Cytokine; Inflammation; Hydroxyurea; ENDOTHELIAL GROWTH-FACTOR; INFLAMMATORY CYTOKINES; NETWORK MODEL; NITRIC-OXIDE; CHILDREN; ANEMIA; STATE; RECEPTORS; HISTORY; MARKER;
D O I
10.1016/j.bcmd.2022.102703
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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页数:12
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