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
{"title":"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","authors":"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","doi":"10.1016/j.bcmd.2022.102703","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>In the present work, the impact of Sickle Cell Disease (SCD) degrees of severity, as well </span>hydroxyurea<span> treatment<span> 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 (</span></span></span><em>n</em><span><span> = 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 </span>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.</span></p></div>","PeriodicalId":8972,"journal":{"name":"Blood Cells Molecules and Diseases","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Plasma immune mediators as laboratorial biomarkers for Sickle Cell Disease patients according to the hydroxyurea therapy and disease severity\",\"authors\":\"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\",\"doi\":\"10.1016/j.bcmd.2022.102703\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>In the present work, the impact of Sickle Cell Disease (SCD) degrees of severity, as well </span>hydroxyurea<span> treatment<span> 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 (</span></span></span><em>n</em><span><span> = 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 </span>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.</span></p></div>\",\"PeriodicalId\":8972,\"journal\":{\"name\":\"Blood Cells Molecules and Diseases\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Blood Cells Molecules and Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1079979622000602\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Blood Cells Molecules and Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1079979622000602","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
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.
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.