Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1997-5-5
pubmed:abstractText
In this study, the changes in some of the cellular components of the immune system and the activity of the cytokine interleukin 2, important for immune activation and lymphocyte proliferation, were measured in a large cross-sectional study of all age groups including octogenarian and nonagenarian subjects. In 206 apparently well community-living subjects, the absolute lymphocyte count and T and B cell numbers fell a little in old and very old subjects. Within the T cell compartment, helper/inducer CD4+ T cells, together with their subsets identified as 'naive' (CD4+/CD45RA+) and 'memory' (CD4+/CD45RO+) cells, also showed a decline with increased age. The suppressor/cytotoxic CD8+ subset showed no age-related change. The levels of the cytokine interleukin 2 were very low in octogenarian and nonagenarian subjects, while the soluble interleukin 2 receptor levels increased with increasing age. The interleukin 2 levels were associated with number and percentage of the 'memory' (CD4+/CD45RO+) subset of T cells which mediates the host response to previously met antigens. Since the interleukin 2 values were very low in the oldest groups and were associated with a reduced 'memory' (CD4+/CD45RO+) compartment, this suggests a possible mechanism of why the very elderly subject is more susceptible to morbidity and mortality from infectious or other agents.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0304-324X
pubmed:author
pubmed:issnType
Print
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
69-78
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:9138976-Adult, pubmed-meshheading:9138976-Aged, pubmed-meshheading:9138976-Aged, 80 and over, pubmed-meshheading:9138976-Aging, pubmed-meshheading:9138976-Antibodies, Monoclonal, pubmed-meshheading:9138976-Antigens, CD19, pubmed-meshheading:9138976-Antigens, CD4, pubmed-meshheading:9138976-Antigens, CD45, pubmed-meshheading:9138976-Antigens, CD8, pubmed-meshheading:9138976-B-Lymphocytes, pubmed-meshheading:9138976-CD4-Positive T-Lymphocytes, pubmed-meshheading:9138976-CD8-Positive T-Lymphocytes, pubmed-meshheading:9138976-Cell Division, pubmed-meshheading:9138976-Cross-Sectional Studies, pubmed-meshheading:9138976-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:9138976-Female, pubmed-meshheading:9138976-Flow Cytometry, pubmed-meshheading:9138976-Follow-Up Studies, pubmed-meshheading:9138976-Humans, pubmed-meshheading:9138976-Interleukin-2, pubmed-meshheading:9138976-Lymphocyte Count, pubmed-meshheading:9138976-Lymphocyte Subsets, pubmed-meshheading:9138976-Male, pubmed-meshheading:9138976-Middle Aged, pubmed-meshheading:9138976-Random Allocation, pubmed-meshheading:9138976-Receptors, Interleukin-2
pubmed:year
1996
pubmed:articleTitle
Changes in lymphocyte subsets, interleukin 2, and soluble interleukin 2 receptor in old and very old age.
pubmed:affiliation
Department of Geriatric Medicine, The Queen's University of Belfast, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't