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- W2199758839 endingPage "188" @default.
- W2199758839 startingPage "143" @default.
- W2199758839 abstract "The unique nature of the mucosal immune system is exemplified by its ability to serve as a primary lymphoid area (in some animals) and by its ability to shield entirely separate cell populations from the systemic immune system. The available information supports the existence of not only distinct populations of isotype-specific T and B cells but also of cell subpopulations expressing unique receptor/idiotype repertoires within the mucosa. Few studies have examined changes within the mucosal immune system during aging or have compared these changes with those in the systemic immune system. It was found that while systemic IgM, IgG, and IgA plaque-forming cell (PFC) responses declined with age, mucosal PFC responses remained vigorous in cells bearing all three isotypes. This unimpaired mucosal response was also observed, and it was who found that IgA responses to the α(1-3) glucan determinant on dextran B1355 increased dramatically with age in the MLN. In the experiment described in the chapter, however, the splenic IgA immune response did not decline over the age span, but this may be a result of testing the BALB/c mice used up to only 17 months of age." @default.
- W2199758839 created "2016-06-24" @default.
- W2199758839 creator A5053078335 @default.
- W2199758839 creator A5074820357 @default.
- W2199758839 date "1984-01-01" @default.
- W2199758839 modified "2023-09-26" @default.
- W2199758839 title "Aging, Idiotype Repertoire Shifts, and Compartmentalization of the Mucosal-Associated Lymphoid System" @default.
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