Báo cáo sinh học: Serum cytokine profiles in healthy young and elderly population assessed using multiplexed bead-based immunoassays
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Serum cytokine profiles in healthy young and elderly population assessed using multiplexed bead-based immunoassays
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Báo cáo sinh học: "Serum cytokine profiles in healthy young and elderly population assessed using multiplexed bead-based immunoassays"Kim et al. Journal of Translational Medicine 2011, 9:113http://www.translational-medicine.com/content/9/1/113 RESEARCH Open AccessSerum cytokine profiles in healthy young andelderly population assessed using multiplexedbead-based immunoassaysHyun Ok Kim1†, Han-Soo Kim1†, Jong-Chan Youn2, Eui-Cheol Shin3 and Sungha Park2* Abstract Background: Lipid metabolites and cytokines, including chemokines and growth factors, are the key regulators of immune cell function and differentiation, and thus, dysregulation of these regulators is associated with various human diseases. However, previous studies demonstrating a positive correlation of cytokine levels with aging may have been influenced by various environmental factors and underlying diseases. Also, data regarding cytokine profiling in the elderly are limited to a small subset of cytokines. Methods: We compared the profiles of 22 cytokines, including chemokines and growth factors, in a case- controlled study group of a gender-matched, healthy cohort of 55 patients over the age of 65 and 55 patients under the age of 45. Assessment of serum cytokine concentrations was performed using commercially-available multiplex bead-based sandwich immunoassays. Results: Soluble CD40 ligand (sCD40L) and transforming growth factor alpha (TGF-a) levels were significantly higher in the elderly patients, whereas granulocyte colony-stimulating factor (G-CSF), granulocyte-monocyte colony-stimulating factor (GM-CSF), and monocyte chemoattractant protein-1 (MCP-1) levels were significantly lower in the elderly patients. The partial correlation analysis demonstrating the correlation between cytokine levels when controlled for gender, systolic blood pressure, total cholesterol, HDL cholesterol, triglyceride, and serum creatinine levels further demonstrated that G-CSF, GM-CSF, and MCP-1 had significant negative correlations with age, whereas sCD40L and TGF-a had significant positive correlations. Conclusions: Future studies will focus on examining the significance of these age-related changes in circulating cytokines and other biological markers and their potential contribution to the development of different age- associated diseases.Background accumulation of regulatory T cells contributes to impairedAging is accompanied by a decline in immune functions, CD8 and natural killer cell activities [3,4]. Also, a decreasereferred to as immune aging or immune senescence. Para- in naïve T cells may result in impaired acquired immunedoxically, life-long exposure to environmental factors and responses, whereas clonal expansion of CD25 null T cellscountless interactions with infectious agents leads to a may result in increased secretion of tumor necrosis factor- alpha (TNF- a ) and interleukin-6 (IL-6), resulting in achronic inflammatory state in older individuals, termedinflammaging, characterized by an increase in proinflam- heightened degree of inflammation [5].matory mediators present in serum [1,2]. Changes in T- Lipid metabolites and cytokines, including chemokinescell homeostasis with aging are associated with a decline and growth factors, are the key regulators of immune cellin immunity and increased inflammation. Increased function and differentiation. Thus, dysregulation of these regulators is associated with various human diseases. Age-associated elevation of inflammatory factors includ-* Correspondence: shpark0530@yuhs.ac ing TNF- a , IL-6, prostaglandin E 2 (PGE 2 ), and IL-1 b† Contributed equally2 Division of Cardiology, Yonsei Cardiovascular Center, Yonsei University have been described previously [6-8]. This elevation mayCollege of Medicine, Seoul 120-752, Republic of Korea be attributable to both the derangement of inflammationFull list of author information is available at the end of the article ...
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Báo cáo sinh học: "Serum cytokine profiles in healthy young and elderly population assessed using multiplexed bead-based immunoassays"Kim et al. Journal of Translational Medicine 2011, 9:113http://www.translational-medicine.com/content/9/1/113 RESEARCH Open AccessSerum cytokine profiles in healthy young andelderly population assessed using multiplexedbead-based immunoassaysHyun Ok Kim1†, Han-Soo Kim1†, Jong-Chan Youn2, Eui-Cheol Shin3 and Sungha Park2* Abstract Background: Lipid metabolites and cytokines, including chemokines and growth factors, are the key regulators of immune cell function and differentiation, and thus, dysregulation of these regulators is associated with various human diseases. However, previous studies demonstrating a positive correlation of cytokine levels with aging may have been influenced by various environmental factors and underlying diseases. Also, data regarding cytokine profiling in the elderly are limited to a small subset of cytokines. Methods: We compared the profiles of 22 cytokines, including chemokines and growth factors, in a case- controlled study group of a gender-matched, healthy cohort of 55 patients over the age of 65 and 55 patients under the age of 45. Assessment of serum cytokine concentrations was performed using commercially-available multiplex bead-based sandwich immunoassays. Results: Soluble CD40 ligand (sCD40L) and transforming growth factor alpha (TGF-a) levels were significantly higher in the elderly patients, whereas granulocyte colony-stimulating factor (G-CSF), granulocyte-monocyte colony-stimulating factor (GM-CSF), and monocyte chemoattractant protein-1 (MCP-1) levels were significantly lower in the elderly patients. The partial correlation analysis demonstrating the correlation between cytokine levels when controlled for gender, systolic blood pressure, total cholesterol, HDL cholesterol, triglyceride, and serum creatinine levels further demonstrated that G-CSF, GM-CSF, and MCP-1 had significant negative correlations with age, whereas sCD40L and TGF-a had significant positive correlations. Conclusions: Future studies will focus on examining the significance of these age-related changes in circulating cytokines and other biological markers and their potential contribution to the development of different age- associated diseases.Background accumulation of regulatory T cells contributes to impairedAging is accompanied by a decline in immune functions, CD8 and natural killer cell activities [3,4]. Also, a decreasereferred to as immune aging or immune senescence. Para- in naïve T cells may result in impaired acquired immunedoxically, life-long exposure to environmental factors and responses, whereas clonal expansion of CD25 null T cellscountless interactions with infectious agents leads to a may result in increased secretion of tumor necrosis factor- alpha (TNF- a ) and interleukin-6 (IL-6), resulting in achronic inflammatory state in older individuals, termedinflammaging, characterized by an increase in proinflam- heightened degree of inflammation [5].matory mediators present in serum [1,2]. Changes in T- Lipid metabolites and cytokines, including chemokinescell homeostasis with aging are associated with a decline and growth factors, are the key regulators of immune cellin immunity and increased inflammation. Increased function and differentiation. Thus, dysregulation of these regulators is associated with various human diseases. Age-associated elevation of inflammatory factors includ-* Correspondence: shpark0530@yuhs.ac ing TNF- a , IL-6, prostaglandin E 2 (PGE 2 ), and IL-1 b† Contributed equally2 Division of Cardiology, Yonsei Cardiovascular Center, Yonsei University have been described previously [6-8]. This elevation mayCollege of Medicine, Seoul 120-752, Republic of Korea be attributable to both the derangement of inflammationFull list of author information is available at the end of the article ...
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