Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/342766
Type: Artigo
Title: Sickle cell anemia patients display an intricate cellular and serum biomarker network highlighted by tcd4+cd69+lymphocytes, il-17/mip-1 beta, il-12/vegf, and il-10/ip-10 axis
Author: Garcia, Nadja Pinto
Junior, Alexander Leonardo S.
Soares, Geyse Adriana S.
Costa, Thaina Cristina C.
dos Santos, Alicia Patrine C.
Costa, Allyson Guimaraes
Tarrago, Andrea Monteiro
Martins, Rejane Nina
Leao Pontes, Flivia do Carmo
de Almeida, Emerson Garcia
de Paula, Erich Vinicius
Martins-Filho, Olindo Assis
Malheiro, Adriana
Abstract: Sickle cell anemia (SCA) is associated with a chronic proinflammatory state characterized by elevated leukocyte count, mortality from severe recurrent infections, and subsequent vasoocclusive complications with leukocyte adhesion to the endothelium and increased plasma levels of inflammatory cytokines. The immune system has a close connection with morbidity in SCA, but further studies are needed to uncover the involvement of innate and adaptive immunities in modulating the SCA physiopathology. We performed measurements of the frequency of innate and adaptive immunity cells, cytokines, chemokines, and growth factors and immunophenotyping of Toll-like receptor and adhesion molecule expression in the blood of SCA patients and healthy donors to evaluate the different profiles of these biomarkers, the relationship among them, and their correlation to laboratory records and death risk. Immunophenotyping of cells, Toll-like receptors, and adhesion molecules were performed from peripheral blood samples of SCA patients and healthy donors by flow cytometry and cytokine/chemokine/growth factor measurement by the Luminex technique performed from the serum of the same subjects. Cells of adaptive immunity such as IL-12, IL-17, and IL-10 cytokines; IL-8, IP-10, MIP-1 alpha, MIP-1 beta, and RANTES chemokines; and VEGF, FGF-basic, and GM-CSF growth factors were higher in SCA patients than healthy donors regardless of any laboratorial and clinical condition. However, high death risk appears to have relevant biomarkers. In the SCA pathophysiology at steady state, there is a broad immunological biomarker crosstalk highlighted by TCD4+CD69+ lymphocytes, IL-12 and IL-17 inflammatory and IL-10 regulatory cytokines, MIP-1 alpha, MIP-1 beta, and IP-10 chemokines, and VEGF growth factor. High expression of TLR2 in monocytes and VLA-4 in TCD8+ lymphocytes and high levels of MIP-1 beta and RANTES appear to be relevant in high death risk conditions. The high reticulocytosis and high death risk conditions present common correlations, and there seems to be a balance by the Th2 profile
Subject: Anemia falciforme
Country: Reino Unido
Editor: Hindawi
Rights: Aberto
Identifier DOI: 10.1155/2020/4585704
Address: https://www.hindawi.com/journals/jir/2020/4585704/
Date Issue: 2020
Appears in Collections:FCM - Artigos e Outros Documentos

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