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Evaluation of CD4+CD25+FoxP3+ T cell populations,IL-10 production,and their correlation with clinical and biochemical parameters in sickle cell anemia patients with leg ulcers
Affiliation:1. Paediatrics Department, Hospital Sant Joan de Déu (HSJD), Barcelona, Spain;2. Molecular Microbiology Department, HSJD, Barcelona, Spain;3. Paediatric Infectious Diseases Department, HSJD, Barcelona, Spain;4. University of Barcelona, Barcelona, Spain;5. Paediatric Infectious Diseases Research Group, Institut de Recerca Sant Joan de Déu, Barcelona, Spain;6. CIBER of Epidemiology and Public Health (CIBERESP), Madrid, Spain;7. Paediatric Intensive Care Unit, HSJD, Barcelona, Spain;8. Universitat Internacional de Catalunya, Barcelona, Spain
Abstract:Leg ulcers (LUs) are a debilitating complication of sickle cell anemia (SCA), with inflammation known to play a crucial role in their pathogenesis. Many studies have described the roles of T helper type 1 (Th1) and Th2 pathways in SCA; however, defects in anti-inflammatory responses are poorly understood. We evaluated interleukin (IL)-10 levels in serum and peripheral blood mononuclear cells (PBMCs) in SCA patients with leg ulcers (SCALU) and without leg ulcers (SCAWH) in addition to CD4+ CD25+FoxP3+ T cell populations and their its IL-10 expression. In stimulated and unstimulated PBMC cultures, SCALU patients produced higher levels of IL-10 than those in the SCAWH group. Higher levels of IL-10 in SCALU patients correlated with a history of osteonecrosis in stimulated and unstimulated cultures when compared with those in SCAWH. Immunophenotyping revealed that SCALU patients had a higher proportion of CD4+CD25+FoxP3+, Tr1 and CD4+CD25+FoxP3+IL-10+ T cells than other groups. Our findings revealed that IL-10 levels were increased in unstimulated cells from the SCALU group, and that this group also presented with a predominant CD4+ CD25+FoxP3+ cell population despite many of those cells being IL-10 negative.
Keywords:Sickle cell anemia  Leg ulcer  Inflammation  Interleukin 10  T regulatory cells  Immunophenotyping
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