Immune-related alterations in aged gut-associated lymphoid tissues in mice.

Abstract

To study whether senescence-induced changes in the gut-associated lymphoid tissue (GALT) are mainly quantitative, several parameters were examined in three age groups of BALB/c mice (1-2, 12-14, and 24-28 months old). A substantial senescence-associated decline in the number of lymphoid cells was found in the mesenteric lymph nodes (MLN) and spleen (SPN), and especially in the Peyer's patches (PP), but not in the lamina propria (LP). The distribution of lymphocyte subsets in these tissues was also altered with an absolute reduction of T cells--in particular, a L3T4+ helper/inducer T-cell marker-bearing subset. These changes were most remarkable in PP, followed by MLN. The in vitro proliferative reactivity and the production of each isotype-specific immunoglobulin (Ig) by PP, MLN, and SPN were profoundly affected when T-cell-dependent (Td) B-cell mitogens were used, but minimally affected when T-cell-independent (Ti) B-cell mitogens were used. The isotype-specific Ig content of small-intestinal perfusates was also influenced by aging, but only to a minor extent, as exemplified by a decrease in IgA levels in the fasting condition. Thus, despite the defects in the quantity and distribution of lymphocytes in aged PP and MLN, the finding of little change in the total amount of secreted IgA in aged intestine suggests that gut IgA-mediated luminal immune responses could remain nearly unaltered with senescence. The constancy of intraluminal IgA levels could be of physiological significance in host defense at the gut mucosal surface in aged mice.