Journals of Gerontology Series A: Biological Sciences and Medical Sciences Large Type Edition
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The Journals of Gerontology Series A: Biological Sciences and Medical Sciences 56:B218-B223 (2001)
© 2001 The Gerontological Society of America

Effect of Age on the Gastrointestinal-Associated Mucosal Immune Response of Humans

Alison A. Beharkaa, Sergio Paivab,c, Lynette S. Lekaa, Judy D. Ribaya-Mercadob, Robert M. Russellb and Simin Nikbin Meydania

a Nutritional Immunology, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts
b Gastrointestinal Nutrition Laboratories, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts
c Faculdade de Medicina de Botucatu, UNESP, San Paolo, Brazil

Correspondence: Simin Nikbin Meydani, Nutritional Immunology Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, 711 Washington Street, Boston, MA 02111 E-mail: smeydani{at}HNRC.Tufts.edu.

Decision Editor: John A. Faulkner, PhD

Age-related changes in gastrointestinal-associated mucosal immune response have not been well studied. Thus, we investigated the effect of age on this response and compared these responses to those of peripheral immune cells. Saliva, blood, and intestinal biopsies were collected from young and old healthy subjects to determine immunoglobulin (Ig) levels and to isolate peripheral blood mononuclear cells, intraepithelial lymphocytes (IELs), and lamina propria lymphocytes (LPLs). Although subject age did not influence the level of total IgA found in saliva, IgA levels in serum increased (p < .05) with age. Older subjects' peripheral blood mononuclear cell proliferation and IL-2 production were significantly lower than those of young subjects. LPLs from older subjects produced significantly less IL-2 in response to all stimuli than did that from the young. IEL's ability to proliferate and produce IL-2 was not affected by subject age. Thus, LPL but not IEL demonstrated an age-related decline in immune function similar to that seen in peripheral lymphocytes.




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