Old T Cells Cripple Immune Function In The Elderly
- Date:
- December 21, 2004
- Source:
- Journal Of Experimental Medicine
- Summary:
- T cells are the weakest link in the immune systems of older people, based on a report by Eaton and colleagues in the December 20 issue of The Journal of Experimental Medicine. The authors show that old CD4 "helper" T cells cannot provide the stimulatory signals to B cells that prompt them to make antibodies. Old and young B cells, however, are equally effective if helped by young CD4 T cells. The authors think this may help explain why immunizations are less effective in the elderly.
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T cells are the weakest link in the immune systems of older people, based on a report by Eaton and colleagues in the December 20 issue of The Journal of Experimental Medicine. The authors show that old CD4 "helper" T cells cannot provide the stimulatory signals to B cells that prompt them to make antibodies. Old and young B cells, however, are equally effective if helped by young CD4 T cells. The authors think this may help explain why immunizations are less effective in the elderly.
B cell activation and antibody production are known to be impaired with age in both mice and humans, but it was not clear whether this defect is intrinsic to B cells or is a by-product of declining CD4 T cell helper functions.
Eaton and colleagues transferred young or old CD4 T cells into mice lacking their own CD4 T cells to determine which cells are responsible for the age-related decline in B cell function. They show that B cell activation and antibody production can be restored in old mice if they are infused with young CD4 T cells prior to immunization. On the flip side, young mice infused with old CD4 T cells developed antibody defects, even though their B cells were young. In other words, old B cells function like young ones if provided with signals from young helper T cells. While the mechanism is not completely clear, the authors show that old T cells can travel to the right location in the spleen of the mice, but have fewer of the surface proteins that send stimulatory signals to B cells.
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