The beagle dog with naturally occurring periodontal disease is one of the m
ost widely used animal models in periodontal research for histological stud
ies on disease pathogenesis and on the effect of potential therapeutic regi
mens. However, previous studies were restricted to morphological assessment
of immunocompetent cells because of the lack of available cell-specific ma
rkers. In this study we systematically characterized the specificity and im
munoreactivity of a panel of anti-human antibodies for identification (ABC
method) of immunocompetent cells in formalin-fixed, EDTA-decalcified, paraf
fin-embedded inflamed periodontal tissues obtained from six beagle dogs. Ca
nine lymph nodes and a panel of different human tissues served as positive
controls. Polyclonal anti-CD3 immunolabeled canine T-lymphocytes specifical
ly. Anti-CD79 alpha (clone HM57) reacted with B-lymphocytes and plasma cell
s, and CD79 alpha (clone JCP117) showed no staining in canine tissues. Neut
rophils, monocytes, small macrophages, and keratinocytes reacted with an an
ti-myeloid/ histiocyte antibody (clone MAC387). Anti-CD68 (clones PG-M1 and
EBM11) immunolabeled large macrophages and plasma cells. Clone EBM11 also
stained osteoclasts and cementoclasts. With the exception of JCB117, all an
tibodies revealed similarly favorable immunolabeling of canine and human im
munocompetent cells. Long-term EDTA decalcification appeared to weaken immu
nostaining of plasma cells with HM57. MAC387 and CD68 can be used to distin
guish macrophages in different differentiation stages in canine periodontal
tissues.