H. Yamamoto et al., BURN INJURY INDUCES A BIPHASIC IMMUNOGLOBULIN-M RESPONSE TO BACTERIAL-ANTIGEN, The journal of trauma, injury, infection, and critical care, 39(2), 1995, pp. 279-284
We studied 75 BALB/c mice to examine the role of impaired imunnoglobul
in M (IgM) synthesis in the increased risk of bacterial infection afte
r burn injury by investigating the kinetics of IgM synthesis to peptid
oglycan polysaccharide (PGPS), a ubiquitous bacterial antigen. Splenoc
ytes were isolated 1, 5, and 8 days postburn (PBD) and cultured with l
ipopolysaccharide for 5 days. Culture supernatant was collected and an
ti-PGPS IgM and total IgM levels were measured by ELISA. Total IgM-sec
reting cells were measured by ELISPOT assay. Total IgM and anti-PGPS I
gM per IgM-secreting cell were calculated. On PBD 1, anti-PGPS IgM syn
thesis but not total IgM synthesis is increased in burned animals. By
PBD 5, total IgM and anti-PGPS IgM synthesis in the burn group start t
o fall and by PBD 8, both are significantly decreased. The early incre
ase in anti-PGPS IgM synthesis represents a positive response to bacte
rial challenge. However, the late nonspecific decrease in total IgM an
d anti-POPS IgM synthesis suggests a potential mechanism for increased
susceptibility to bacterial infection 5 to 10 days after burn injury.