Ae. Jergens et al., IMMUNOHISTOCHEMICAL CHARACTERIZATION OF IMMUNOGLOBULIN-CONTAINING CELLS AND T-CELLS IN THE COLONIC MUCOSA OF HEALTHY DOGS, American journal of veterinary research, 59(5), 1998, pp. 552-556
Objectives-To quantitate numbers of immunoglobulin (Ig)-containing cel
ls (IgA, IgG, and IgM) and T cells (CD3+, CD4+, and CD8+) in the colon
ic mucosa of healthy dogs, and to determine whether mean cell numbers
differ among colonic regions. Animals-10 clinically normal young adult
mixed-breed dogs. Procedure-Endoscopically obtained specimens of asce
nding, transverse, and descending colonic mucosa were stained specific
ally for IgA, IgG, and IgM heavy chains and T-cell antigens, CD3+, CD4
+, and CD8+, using immunoperoxidase techniques. Morphometric analysis,
performed by light microscopy, was used to quantitate numbers in thes
e standardized areas of colonic mucosa. Data analysis allowed determin
ation of mean cell numbers in each colonic region, as well as comparis
on of mean cell numbers among colonic regions. Results-The CD3+ and CD
8+ T cells were the predominant immune cell types in ail colonic regio
ns. In the mucosa, CD3+ T cells were significantly (P < 0.05) more num
erous than CD8+ T cells, and CD8+ T cells were significantly (P < 0.05
) more numerous than CD4+ T cells. The IgA-containing cells were signi
ficantly (P < 0.05) more numerous than IgG-containing cells, whereas I
gM-containing cells were least numerous (P < 0.05). Differences in mea
n cell counts among colonic regions were not significant for Ig-contai
ning cells or T cells. Conclusions-Mean numbers of immune cells did no
t differ significantly among colonic regions in healthy dogs, although
differences existed in mean populations of T cells and Ig-containing
cells. The CD3+ and CD8+ T cells were the most numerous immune cell ty
pes in colonic mucosa. Clinical Relevance-These quantitative data prov
ide a basis for study of alterations in populations of mucosal immune
cells and their possible contribution to the pathogenesis of gastroint
estinal tract disease.