Background: Hyperoxia has been reported to be protective against gut-derive
d sepsis, Although secretory immunoglobulin A (IgA) is primarily responsibl
e for humoral defense of mucosal surfaces, a potential synergistic effect,w
ith hyperoxia is unknown. An asanguineous cell monolayer system was used to
study these aspects in vitro.
Methods: MDCK cells were grown as polarized monolayers in a two-chamber cul
ture system. Apical chambers were inoculated with 10(8) Escherichia coli M1
4 with or,without polyclonal IgA and incubated in a 21 or 95% O-2 environme
nt. Basal medium,vas sampled at 90 and 180 minutes for bacterial translocat
ion, In a second experiment, MDCK cells were lysed at 90 minutes and intrac
ellular bacteria were quantitated,
Results: Bacterial translocation was decreased versus normoxia by the treat
ment groups IgA without hyperoxia or IgA with hyperoxia at 90 minutes. Bact
erial internalization at 90 minutes was reduced to the greatest extent by t
he combined effects of hyperoxia and IgA, Translocation data at 180 minutes
confirmed the additional protective effect of hyperoxia with IgA,
Conclusion: Hyperoxia exerts a significant protective effect on barrier fun
ction independent of enhanced leukocyte function. Hyperoxia has an added ef
fect to the mucosal defense provided by IgA.