J. Hilton et al., SEROLOGICAL RESPONSES INDUCED IN MICE BY IMMUNOGENIC PROTEINS AND BY PROTEIN RESPIRATORY ALLERGENS, Toxicology letters, 73(1), 1994, pp. 43-53
It is known that a variety of materials, including both low molecular
weight chemicals and proteins, is able to induce occupational respirat
ory allergy. We have shown previously that exposure of mice to chemica
l respiratory sensitizers results in both a marked increase in the ser
um concentration of IgE and the appearance of specific IgE antibody. I
n the present study we have examined the characteristics of immune res
ponses induced in mice following intraperitoneal exposure to 3 protein
respiratory allergens, ovalbumin (OVA), a lipase from Aspergillus ory
zae (LP) and an amylase from Bacillus subtilis (AM) and to a fourth pr
otein, bovine serum albumin (BSA), which is considered usually not to
cause respiratory sensitization. Under conditions where all proteins p
rovoked IgE antibody responses, only OVA, LP and AM elicited specific
IgE antibody. As judged by passive cutaneous anaphylaxis (PCA) assay,
BSA failed to induce an IgE response. In contrast to chemical respirat
ory sensitizers, the protein allergens examined here failed to cause a
substantial increase in the serum concentration of IgE; OVA and AM in
duced no increase in serum IgE and LP only a comparatively modest incr
ease relative to control values. In conclusion, these data demonstrate
that while protein respiratory allergens are able to provoke specific
IgE antibody, they fail to cause a marked increase in the concentrati
on of this immunoglobulin in the sera of treated mice. It would appear
, therefore, that the mouse IgE test, which seeks to evaluate chemical
respiratory sensitization potential as a function of induced changes
in the concentration of serum IgE, will be inappropriate for the ident
ification of protein respiratory allergens. Nevertheless, identificati
on of protein allergens may be possible by exploiting the observations
reported here that such proteins induce in mice specific IgE antibody
responses.