AGE-RELATED DIFFERENCES IN SUBSET COMPOSITION AND ACTIVATION RESPONSES OF INTESTINAL INTRAEPITHELIAL AND MESENTERIC LYMPH-NODE LYMPHOCYTES FROM NEONATAL SWINE

Citation
Mt. Whary et al., AGE-RELATED DIFFERENCES IN SUBSET COMPOSITION AND ACTIVATION RESPONSES OF INTESTINAL INTRAEPITHELIAL AND MESENTERIC LYMPH-NODE LYMPHOCYTES FROM NEONATAL SWINE, Cellular immunology, 163(2), 1995, pp. 215-221
Citations number
40
Categorie Soggetti
Cell Biology",Immunology
Journal title
ISSN journal
00088749
Volume
163
Issue
2
Year of publication
1995
Pages
215 - 221
Database
ISI
SICI code
0008-8749(1995)163:2<215:ADISCA>2.0.ZU;2-O
Abstract
Interesting differences were found in the phenotypes and functional re sponses of intestinal intraepithelial lymphocytes (IEL) and mesenteric lymph node lymphocytes (MLN) from neonatal swine aged 15 to 47 days. IEL and MLN differed significantly in their proliferative responses to the mitogens concanavalin A (Con A) and phorbol ester with ionophore (TPA/ionomycin) and to the cytokine, interleukin 2 (IL-2). IEL did not proliferate well in response to Con A, yet they were able to initiate a high proliferative response to exogenous IL-2, suggesting previous activation. In addition, the IEL response to TPA/ionomycin was very lo w unless the concentration of ionomycin was increased. With increasing age of the animals, response of the IEL increased. This IEL developme ntal response pattern was associated with a significant age-related ch ange in T cell phenotype from CD2(-)4(-)8(-) cells to CD2(+)4(-)8(-) c ells. In contrast to IEL, proliferation of MLN to Con A and TPA at a l ower ionomycin concentration was significant and not influenced by age . Unlike the IEL, MLN were unresponsive to exogenous IL-2. Similar to IEL, they produced very little IL-2 in response to Con A stimulation. Both lymphoid tissues contained 70% T cells and in the MLN more cells were CD4(+) or CD4(+)8(+) and fewer were CD4(-)8(-) compared to the IE L. These differences between IEL and MLN in neonatal swine may reflect differences not only in the state of cell. activation related to the in vivo microenvironment, but also the nature of responsive cell types in each lymphoid tissue. (C) 1995 Academic Press, Inc.