Cs. Hultman et al., EARLY BUT NOT LATE BURN WOUND EXCISION PARTIALLY RESTORES VIRAL-SPECIFIC T-LYMPHOCYTE CYTOTOXICITY, The journal of trauma, injury, infection, and critical care, 43(3), 1997, pp. 441-447
Objective: Early burn wound excision restores immunocompetence and imp
roves patient survival, but the exact mechanisms have not yet been def
ined, Burn injury impairs cytotoxic T lymphocyte (CTL) activity as a f
unction of burn size, increasing the risk of infection, The purpose of
this study was to determine if early wound excision improved viral-sp
ecific CTL function. Methods: Anesthetized C57BL/6 mice (n = 20) recei
ved 0%, 20%, or 40% total body surface area full-thickness contact bur
ns and were inoculated 3 days later with intraperitoneal lymphocytic c
horiomeningitis virus, Eight days after infection, or 11 days after bu
rn, CTL effectors (E) were harvested and tested against infected, radi
olabeled L-D-b targets (T) in a Cr-51-release assay, at varied E:T rat
ios, Dilution curves of CTL activity were compared by analysis of vari
ance, In the second experiment, mice n = 18) underwent a 30% burn that
was totally excised and grafted on postburn days (PBDs) 0, 3, and 7,
Control groups included sham burn and no excision of a 30% burn. In th
e third experiment, mice (n = 22) received a 30% burn that was partial
ly, completely, or not excised on PBD 3, Control groups included sham
burn with and without excision, All groups were infected with intraper
itoneal lymphocytic choriomeningitis virus on PBD 3, Viral-specific CT
L activity was determined on PBD 11. Results: Both 20% and 40% burn in
jury impaired viral-specific CTL function, Wound excision on PBDs 0 an
d 3, but not on PBD 7, partially restored CTL function, Total excision
of the 30% burn improved CTL activity to a greater extent than did pa
rtial excision. Conclusion: Burn injury inhibits viral-specific CTL ac
tivity, Early, complete mound excision augments CTL function. Improved
CTL activity after burn may reduce the risk of infection, providing a
n immunologic rationale for expeditious wound excision.