J Exp Med. 1996 Jul 1;184(1):241-51. Unique Identifier : AIDSLINE
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.
Animal Colitis/*IMMUNOLOGY Colon/IMMUNOLOGY Cytokines/BIOSYNTHESIS
CD4-Positive T-Lymphocytes/*IMMUNOLOGY CD8-Positive
T-Lymphocytes/IMMUNOLOGY Immunization, Passive Inflammatory Bowel
Diseases/GENETICS/*IMMUNOLOGY Interleukin-10/DEFICIENCY Mice Mice,
Inbred C57BL Mice, Knockout Proteins/PHYSIOLOGY Receptors, Antigen,
T-Cell, alpha-beta/ANALYSIS Support, Non-U.S. Gov't T-Lymphocyte
Subsets/IMMUNOLOGY T-Lymphocytes, Helper-Inducer/*IMMUNOLOGY JOURNAL
ARTICLE
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