The aim of this study was to investigate the contribution of lymphocytes an
d macrophages to keloid scarring by morphologically characterising inflamma
tory cell subpopulations in keloid scars in comparison with normal skin. We
took 3 min punch biopsies from the anterior forearms of eight normal healt
hy volunteers. Eight keloid scars were excised using an intralesional techn
ique. All tissue was snap frozen in liquid nitrogen and serial sections wer
e stained with a panel of anti-inflammatory cell monoclonal antibodies. The
numbers of macrophages and lymphocytes and the proportions of the subpopul
ations were compared. Higher numbers of both macrophages and lymphocytes we
re found in keloid dermis (P = 0.01 and P = 0.02, respectively (Mann-Whitne
y U-test)). There was no significant increase in the expression of the lymp
hocyte activation markers, CD25 and CD27. However, there was a significantl
y higher CD4(+): CD8(+) (Th: Ts) ratio (P = 0.046) in keloid tissue. This s
uggests that an imbalance in these inflammatory cell subpopulations may con
tribute to keloid scarring in man. (C) 2001 The British Association of Plas
tic Surgeons.