Background The potential of colophony fumes from soldering flux to induce a
sthma has been known since the 1970s, however, no direct in vitro or in viv
o evidence has been reported. The present study investigated the potential
of colophony to stimulate human phagocytic cells to produce reactive oxygen
species.
Methods The human cell line HL-60 was differentiated to produce cells with
a monocyte-like and a neutrophil-like phenotypes. A number of procedures we
re used to confirm the phenotype of these differentiated cells including mo
rphology, esterase activity, flow cytometry and phagocytosis. The potential
of colophony to stimulate human phagocytic cells to produce reactive oxyge
n species was monitored using flow cytoenzymology.
Results We were able to show that intracellular peroxide levels were increa
sed in both monocyte-like and neutrophil-like cells, but not in undifferent
iated HL-60 cells following the addition of colophony.
Conclusions The resin acid epoxides and hydroperoxides which have been sugg
ested to be sensitizers in contact allergy, are degraded during the solderi
ng process. However, conditions for the oxidation of colophony may occur in
vivo as a result of the colophony-induced oxidative burst from neutrophils
and monocytes. These oxidation products may then interact with body protei
ns to further initiate immune responses. Therefore for the preparation of l
ow molecular weight chemical (LMWC)-protein conjugates, consideration must
be taken to determine whether the LMWC is undergoing a reaction in vivo bef
ore it is interacting with body proteins.