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Chemokine production by peripheral blood mononuclear cells in elderly subjects
Affiliation:1. School of Environment, Tsinghua University, Beijing, 100084, China;2. Environmental Simulation and Pollution Control State Key Joint Laboratory, School of Environment, Tsinghua University, Beijing 100084, China;3. College of Engineering, University of Georgia, GA, USA, 30602;1. Civil & Environmental Engineering, Florida A&M University, 2525 Pottsdamer Street, Tallahassee, FL, 32307, United States;2. Department of Civil and Environmental Engineering, FAMU-FSU College of Engineering, 2525 Pottsdamer Street, Tallahassee, FL, 32310, United States;3. Department of Civil and Environmental Engineering, FAMU-FSU College of Engineering, 2525 Pottsdamer Street, Tallahassee, FL, 32310, United States;4. School of the Environment, Florida A&M University, 1515 S. Martin Luther King Jr. Blvd., Tallahassee, FL, 32307, United States;1. Norwegian Institute for Water Research, Gaustadalléen 21, N-0349, Oslo, Norway;2. Forest Research Institute, 15013, Yezin, Myanmar;3. Department of Natural Sciences and Environmental Health, University of South- Eastern Norway, Gullbringvegen 36, N-3800, Bø, Norway;4. Limno Consulting, via Bedollo 303, I-00124, Rome, Italy
Abstract:The function of chemokines in promoting and modulating leukocyte migration is essential for a prompt and efficacious inflammatory response and in host defence against infections. In order to investigate whether this important aspect of immunological response is influenced by ageing, we evaluated the basal levels as well as the ability of peripheral blood mononuclear cells from young and healthy elderly subjects to produce chemokines (IL-8, MCP-1, MIP-Iα, RANTES) in response to stimulation with anti-CD3 monoclonal antibody and lipopolysaccharide (LPS), a gram negative bacterial endotoxin. Our main findings are a spontaneous chemokine production; a 20% decrease of proliferative response to anti-CD3 monoclonal antibody accompanied by an age related increase of MIP-Iα and RANTES production and by a general increase of all chemokine production compared to unstimulated conditions; a proliferative defect of monocytes to LPS challenge associated with an increase of chemokine production compared to basal conditions with a progressive age-related increase of MIP-lα. In conclusion, this study suggests that chemokines could have a compensatory role in balancing the impaired mechanisms involved in ‘specific’ immune response during ageing. The successful activation of this strategy could contribute to the good performance of immune system so maintaining healthy status in elderly.
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