Background Animal experimental data indicate a requirement for functionally
active T lymphocytes to allow optimal healing of dermal wounds. Little evi
dence exists to confirm that this is the case in humans. Lymphocyte involve
ment in regulation of healing is probably mediated by release of secreted c
ytokines/growth factors, and we hypothesize that the cytokine profile requi
rement will be modulated as healing progresses.
Objectives As this is likely to be reflected in lymphocyte subset changes o
ver the course of normal healing, we investigated the immunophenotype of ly
mphocyte subpopulations during wound healing.
Methods Sequential biopsies were taken over 42 days from the margin of 12 w
ounds healing by secondary intention after pilonidal sinus excision. Serial
biopsy sections were analysed by immunohistochemistry using lymphocyte-spe
cific monoclonal antibodies, and lymphocytes were counted microscopically.
Results Within 42 days, the mean decrease in wound volume was 87.5%. This w
as accompanied by significant changes in the wound margin lymphocyte popula
tion. Total numbers (mean +/- SEM) of T lymphocytes decreased from 36.8 +/-
9.8 cells per field at inclusion in the study to 25.9 +/- 3.0 immediately
prior to wound closure, with a concomitant increase in B lymphocytes from 1
+/- 0.4 to 9.5 +/- 3.6 cells per field. The CD4/CD8 T-lymphocyte ratio fel
l from an initial level of 3.6 +/- 0.3 to 2.1 +/- 0.3 (mean +/- SEM) prior
to closure.
Conclusions These data indicate that human wound-associated lymphocyte popu
lations are modulated during healing; the increase in numbers of CD8+ T-sup
pressor lymphocytes is in accordance with previous animal data, indicating
a role for these cells in downregulating healing as the wound closes. This
study also documents an associated increase in B lymphocytes and healing of
human wounds, with an as yet undefined role.