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Expansion of CD4(+)CD25(+ )helper T cells without regulatory function in smoking and COPD
BACKGROUND: Regulatory T cells have been implicated in the pathogenesis of COPD by the increased expression of CD25 on helper T cells along with enhanced intracellular expression of FoxP3 and low/absent CD127 expression on the cell surface. METHOD: Regulatory T cells were investigated in BALF from n...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127771/ https://www.ncbi.nlm.nih.gov/pubmed/21651772 http://dx.doi.org/10.1186/1465-9921-12-74 |
Sumario: | BACKGROUND: Regulatory T cells have been implicated in the pathogenesis of COPD by the increased expression of CD25 on helper T cells along with enhanced intracellular expression of FoxP3 and low/absent CD127 expression on the cell surface. METHOD: Regulatory T cells were investigated in BALF from nine COPD subjects and compared to fourteen smokers with normal lung function and nine never-smokers. RESULTS: In smokers with normal lung function, the expression of CD25(+)CD4(+ )was increased, whereas the proportions of FoxP3(+ )and CD127(+ )were unchanged compared to never-smokers. Among CD4(+ )cells expressing high levels of CD25, the proportion of FoxP3(+ )cells was decreased and the percentage of CD127(+ )was increased in smokers with normal lung function. CD4(+)CD25(+ )cells with low/absent CD127 expression were increased in smokers with normal lung function, but not in COPD, when compared to never smokers. CONCLUSION: The reduction of FoxP3 expression in BALF from smokers with normal lung function indicates that the increase in CD25 expression is not associated with the expansion of regulatory T cells. Instead, the high CD127 and low FoxP3 expressions implicate a predominantly non-regulatory CD25(+ )helper T-cell population in smokers and stable COPD. Therefore, we suggest a smoking-induced expansion of predominantly activated airway helper T cells that seem to persist after COPD development. |
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