The immune system in the elderly
- 1 December 1999
- journal article
- review article
- Published by Springer Nature in Immunologic Research
- Vol. 20 (3) , 117-126
- https://doi.org/10.1007/bf02786468
Abstract
The capability to cope with infectious agents and cancer cells resides not only in adaptive immune responses against specific antigens, mediated by T and B lymphocytes clonally distributed, but also in natural immune reactions. These innate defence mechanisms include chemotaxis, phagocytosis, natural cytotoxicity, cell interactions, and soluble mediators or cytokines. However, specific and natural immune mechanisms are always closely linked and interconnected, providing the primary defense against pathogens. The Authors discuss the main changes observed with advancing age in granulocytes and natural killer (NK) cell activity, in the expression and function of adhesion molecules, and in the pattern of cytokine production. Since phagocytic function is the primary mechanism through which the immune system eliminates most extracellular pathogenic microrganisms, analysis of this function is of clinical importance. Neutrophils from aged subjects often exhibit a diminished phagocytic capacity, as well as a depressed respiratory burst, notwithstanding an activated state. The activity of NK cells during aging has been studied extensively and different results have been reported. The most consistent data indicate an increase in cells with high NK activity with advancing age. Cells from healthy centenarians can efficiently kill target cells. This finding seems to suggest that innate immunity and in particualr NK cell activity, is not heavily deteriorated with age. Conversely, a low NK activity is a predictor of impending morbidity. Immunosenescence is associated with increased expression of several cell adhesion molecules (CAM) resulting in an augmented capacity to adhere. Finally, also the cytokine network, responsible for differentiation, proliferation, and survival of lymphoid cells, undergoes complex changes with age. The main findings are a Th1 to Th2 cytokine production shift and an increased production of proinflammatory cytokines, which could explain many aspects of age-associated pathological events, such as atherosclerosis and osteoporosis.Keywords
This publication has 77 references indexed in Scilit:
- Human TH1 and TH2 subsets: doubt no morePublished by Elsevier ,2004
- Cell Adhesion Molecules CD11a and CD18 in Blood Monocytes in Old Age and the Consequences for Immunological DysfunctionGerontology, 1995
- The immunology of exceptional individuals: the lesson of centenariansImmunology Today, 1995
- The Th1–Th2 hypothesis of HIV infection: new insightsImmunology Today, 1994
- Relationship between corticotropin‐releasing factor and interleukin‐2: Evolutionary evidenceFEBS Letters, 1994
- A possible role for bcl-2 in regulating T-cell memory - a ‘balancing act’ between cell death and survivalImmunology Today, 1993
- Aging: changes in cardiac α1-adrenoceptor responsiveness andEuropean Journal of Pharmacology: Molecular Pharmacology, 1991
- Extremely low frequency pulsed electromagnetic fields increase interleukin‐2 (IL‐2) utilization and IL‐2 receptor expression in mitogen‐stimulated human lymphocytes from old subjectsFEBS Letters, 1989
- Neutrophil chemotaxis, phagocytosis and parameters of reactive oxygen species in human aging: Cross-sectional and longitudinal studiesLife Sciences, 1989
- AGE DEPENDENT CHANGES IN SOME HUMAN LYMPHOCYTE SUB‐POPULATIONSActa Pathologica Microbiologica Scandinavica Section C Immunology, 1981