ACCUMULATION OF IMMUNOGLOBULIN-CONTAINING CELLS IN THE GUT MUCOSA ANDPRESENCE OF FECAL IMMUNOGLOBULIN IN SEVERE COMBINED IMMUNODEFICIENT (SCID) MICE WITH T-CELL-INDUCED INFLAMMATORY BOWEL-DISEASE (IBD)
S. Bregenholt et al., ACCUMULATION OF IMMUNOGLOBULIN-CONTAINING CELLS IN THE GUT MUCOSA ANDPRESENCE OF FECAL IMMUNOGLOBULIN IN SEVERE COMBINED IMMUNODEFICIENT (SCID) MICE WITH T-CELL-INDUCED INFLAMMATORY BOWEL-DISEASE (IBD), Clinical and experimental immunology, 114(1), 1998, pp. 19-25
mice transplanted either with a gut wall graft or with low numbers of
purified CD4(+) T cells from immunocompetent syngeneic donor mice show
clinical signs of IBD 3-4 months post-transplantation. The disease is
mediated by mucosa-infiltrating CD4(+) TCR alpha beta(+) T cells. The
pathology of 52 individual colon segments obtained from 20 gut wall-
or CD4(+) T cell-transplanted diseased scid mice was evaluated by hist
ology and the numbers of infiltrating immunoglobulin-containing cells
were determined. In particular, cells positive for IgM, IgA and non-in
flammatory immunoglobulin isotypes such as IgG1 and IgC2b were found t
o accumulate in colon segments displaying the most severe histopatholo
gy, including inflammatory cellular infiltration, epithelial hyperplas
ia and ulcerative lesions. Compared with colon segments of normal C.B-
17 mice, the lesional scid colon shows increased levels of cells posit
ive for the IgG classes. Faecal extracts of the CD4(+) T cell-transpla
nted scid mice revealed the presence of all six murine immunoglobulin
isotypes. Disease progression was accompanied by an increased level of
excreted IgM and IgG3 and decreased levels of IgA. It is concluded th
at locally secreted immunoglobulins may play an immunomodulating role
in the pathological changes observed in the present model of T cell-in
duced inflammatory bowel disease.