With the aid of monoclonal antibodies, macrophages can be split into f
unctionally distinct subpopulations on the basis of their phenotype. A
bsence of macrophage subtypes has been noted in chronic inflammatory p
rocesses, e.g. posttraumatic osteomyelitis, rheumatoid arthritis and s
arcoidosis. In the inflammatory focus of acute septic arthritis (n = 1
3 patients) however, macrophages constitute the majority of immunocomp
etent cells. The inflammatory macrophage subtype 27E10 was clearly pre
sent in increased numbers in 11 of 13 biopsies from the inflammatory f
oci, showing the effector task of this subtype in synovial resistance.
The anti-inflammatory macrophage subset RM3/1 was present in increase
d numbers in biopsies of infected tissue and the surrounding soft tiss
ue. The occurrence of 25F9-positive macrophages, typical of the late p
hase of inflammation, varied widely in the biopsies.