Since it is too difficult to study aging of the organism as a whole, most investigators try to focus on a specific physiological system that exhibits age-dependent functional changes, in the hopes that elucidation (in biochemical and developmental terms) of the mechanism of senescent change will provide insight into the aging process itself. The immune system is among the most maleable of such models, in that well-defined cell types will produce well-defined molecules with predictable functions in vitro and in vivo. The increasing power of basic immunological science should, in the next decade, permit an increasingly fine appreciation of how aging leads to immune decline. This expanding conceptual framework will then suggest new ideas about the role of immunosenescence in degenerative, infectious, and neoplastic illnesses and may also generate increasingly rational strategies for therapeutic intervention. (Miller, 1991)
...In general, humoral immunity declines with age, and the onset can occur as early as when an individual reaches sexual maturity. The decline is due to changes in the immune cells and their milieu. Cell loss, shift in the proportion of subpopulations, and qualitative cellular changes have all been detected. The most prominent cellular target of aging appears to be T cells involved in the regulation of humoral response. Since the changes are closely associated with the involution and atrophy of the thymus, an understanding of its changes could be the key to understanding immunosenescence. ( Makinodan, 1980)
Here are some Reviews related to this topic
Further Information