Literature DB >> 1083861

Immunobiology of aging.

T Makinodan.   

Abstract

Normal immune functions can begin to decline shortly after an individual reaches sexual maturity. Although changes in cellular environment are partially responsible, the decline is due primarily to changes within the cells, especially the T cells and to some extent the stem cells. This is reflected in their inability to proliferate and differentiate efficiently. What needs to be resolved is whether the altered properties of T cells and stem cells are permanent or reversible and, if permanent, whether they are due to a stochastic or genetically programmed event. The decline with age in certain normal immune functions is associated with an increase in the frequency of autoimmune and immune complex diseases, certain types of cancer, and viral and fungal infections. These diseases, compromise normal immune functions in short-lived strains of mice. In long-lived mice and in humans, however, the decline in immune functions to threshold levels seems to predispose in individuals to illness.

Entities:  

Mesh:

Year:  1976        PMID: 1083861     DOI: 10.1111/j.1532-5415.1976.tb03299.x

Source DB:  PubMed          Journal:  J Am Geriatr Soc        ISSN: 0002-8614            Impact factor:   5.562


  4 in total

Review 1.  Temperature and host defense.

Authors:  N J Roberts
Journal:  Microbiol Rev       Date:  1979-06

2.  Age-related decline in the resistance of mice to infection with intracellular pathogens.

Authors:  I D Gardner; J S Remington
Journal:  Infect Immun       Date:  1977-05       Impact factor: 3.441

3.  Aging is associated with a numerical and functional decline in plasmacytoid dendritic cells, whereas myeloid dendritic cells are relatively unaltered in human peripheral blood.

Authors:  Yu Jing; Elias Shaheen; Richard R Drake; Nianyong Chen; Stefan Gravenstein; Yuping Deng
Journal:  Hum Immunol       Date:  2009-07-23       Impact factor: 2.850

4.  Age-related effects on the number of human lymphocytes in culture initially responding to an antigenic stimulus.

Authors:  P G Sohnle; C Collins-Lech; K E Huhta
Journal:  Clin Exp Immunol       Date:  1982-01       Impact factor: 4.330

  4 in total

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