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Item Type: | Article |
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Title: | T helper cell 1-type CD4+ T cells, but not B cells, mediate colitis in interleukin 10-deficient mice |
Creators Name: | Davidson, N.J., Leach, M.W., Fort, M.M., Thompson-Snipes, L., Kühn, R., Müller, W., Berg, D.J. and Rennick, D.M. |
Abstract: | Mice rendered deficient in the production of interleukin 10 (IL-10-/-) develop a chronic inflammatory bowel disease (IBD) that predominates in the colon and shares histopathological features with human IBD. Our aim was to identify which cell type(s) can mediate colitis in IL-10-/- mice. We detected an influx of immunoglobulin-positive cells into the colon and the presence of colon-reactive antibodies in the serum of IL-10-/- mice. To assess a pathogenic role for B cells, we generated a B cell-deficient (B-/-) strain of IL-10-/- mice. B-/-IL-10-/- mice acquired a severe colitis analogous to that IL-10-/- mice, implying that B cells were not the primary mediator of IBD in this model. A series of cell transfer experiments was performed to assess a pathogenic role for T cells. When IL-10-/- T cell-enriched lamina propria lymphocytes (LPL) or intraepithelial lymphocytes (IEL) were transferred into immunodeficient recombinase-activating gene (RAG)-2-/- recipients, a mild to severe colitis developed, depending on the cell number transferred. Lymphocytes recovered from the colon of transplanted RAG-2-/- mice with colitis were predominantly alpha beta TCR+CD4+, including a large proportion of CD4+CD8 alpha + cells. These cells were also CD45RB-/low and CD44+, indicative of an activated/memory population. Individual populations of CD4+CD8 alpha-, CD4+CD8 alpha + and CD4-CD8 alpha + T cells were then isolated from the lamina propria compartment of IL-10-/- mice and transferred into RAG-2-/- recipients. Only IL-10-/- CD4-expressing LPL, including both the CD4+CD8 alpha- and CD4+CD8 alpha + populations, induced colitis in recipient mice. Interferon-gamma, but little to no IL-4, was produced by CD4+CD8 alpha- and CD4+CD8 alpha + LPL recovered from the inflamed colons of RAG-2-/- recipients implicating alpha T helper cell 1 (TH1)-mediated response. We thus conclude that colitis in IL-10-/- mice is predominantly mediated by TH1-type alpha beta TCR+ T cells expressing CD4 alone, or in combination with the CD8 alpha molecule. |
Keywords: | CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Colitis, Colon, Cytokines, DNA-Binding Proteins, Helper-Inducer T-Lymphocytes, Inflammatory Bowel Diseases, Interleukin-10, Passive Immunization, Proteins, T-Lymphocyte Subsets, alpha-beta T-Cell Antigen Receptors, Animals, Mice |
Source: | Journal of Experimental Medicine |
ISSN: | 0022-1007 |
Publisher: | Rockefeller University Press |
Volume: | 184 |
Number: | 1 |
Page Range: | 241-251 |
Date: | 1 July 1996 |
Official Publication: | https://doi.org/10.1084/jem.184.1.241 |
PubMed: | View item in PubMed |
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