It has been demonstrated previously that chemical contact and respirat
ory allergens differ with respect to the quality of immune responses t
hey will provoke in mice. Trimellitic anhydride (TMA), a human respira
tory allergen, induces in mice responses consistent with the preferent
ial activation of Th2-type cells, resulting in the production ofIgE an
ti-hapten antibody and an increase in the serum concentration of IgE.
In contrast, oxazolone (OX), a potent contact allergen considered not
to cause respiratory hypersensitivity, induces instead Th1-type respon
ses in mice characterized by vigorous Igc2a antibody production and a
failure to elicit IgE. In the present study we have extended these inv
estigations and have examined the capacity of these chemicals to stimu
late inducible interleukin-4 (IL-4) production by draining lymph node
cells (LNC). IL-4 was measured in the supernatants of draining LNC cul
tured for various periods in the presence or absence of concanavalin A
(Con A). Following primary topical exposure to the chemical allergens
, Con A-stimulated LNC from OX-treated mice secreted significantly mor
e IL-4 than did LNC from mice exposed to trimellitic anhydride (TMA).
A different pattern of IL-4 secretion was observed following culture w
ith Con A of LNC prepared from lymph nodes draining the sites of secon
dary exposure to these chemicals. In this case significantly higher co
ncentrations of IL-4 were produced by TMA-treated mice. Detectable lev
els of IL-4 (> 300 pg/ml) were not found following culture of draining
LNC from sensitized mice in the absence of Con A or following culture
of LNC from naive mice with or without Con A. These data demonstrate
that chemical allergens of different types stimulate discrete and chan
ging patterns of inducible IL-4 synthesis consistent with the selectiv
e activation of Th-cell subpopulations.