Background and Objective: Late sepsis causes immunosuppression and is
associated with energy depletion in lymphocytes. Adjuvant treatment wi
th ATP-MgCL2 appears to improve cellular energetics and decrease morta
lity. Laser irradiation can promote cell proliferation and increase ce
llular ATP synthesis, which may improve the host immune response in se
psis. The purpose of this study was to determine whether laser irradia
tion (LII has a stimulatory effect on the immune response in sepsis us
ing an animal model. Study Deisgn/Materials and Methods: The cecal lig
ation and puncture (CLP) rat model was used. Thirty-six SD rats were d
ivided equally among four groups: control (nonoperative), sham operati
on, CLP treated with laser irradiation, and CLP without laser irradiat
ion. The peritoneal cavity of each animal in CLP/laser group was irrad
iated immediately after CLP using an Argon-dye laser at a wavelength o
f 630 nm and at a fluence of 5 J/cm(2). Some animals were euthanized 2
4 hr following CLP and were used to evaluate the immune response (lymp
hoctye proliferation). In a separate experiment, the survival of septi
c rats was observed for 60 days. Lymphocytes isolated from normal rat
spleens were used to observe far biostimulatory effects in vitro. Resu
lts: LI significantly improved ex-vivo lymphoctye proliferation of cel
ls from septic rats (179.7 +/- 17.2 vs. 129.5 +/- 7.8; P < 0.01) and e
nhanced survival in septic rats (79% vs. 42%; P < 0.001). LI significa
ntly stimulated lymphoctye proliferation in the presence of mitogenic
stimuli and enhanced lymphoctye ATP synthesis (P < 0.05). Conclusion:
LI improves the host inunune response and survival rate in sepsis in a
n animal model. Our studies suggest that LI may be useful as an adjuva
nt therapy for sepsis. (C) 1997 Wiley-Liss, Inc.