ACTIVATION OF HUMAN BLOOD-LYMPHOCYTES BY HOUSE-DUST MITE PROTEIN AND MYCOBACTERIUM-TUBERCULOSIS PURIFIED PROTEIN DERIVATIVE - EFFECTS OF INTERFERON-GAMMA, INTERLEUKIN-4, DEXAMETHASONE AND CYCLOSPORINE-A
J. Storch et Rm. Cook, ACTIVATION OF HUMAN BLOOD-LYMPHOCYTES BY HOUSE-DUST MITE PROTEIN AND MYCOBACTERIUM-TUBERCULOSIS PURIFIED PROTEIN DERIVATIVE - EFFECTS OF INTERFERON-GAMMA, INTERLEUKIN-4, DEXAMETHASONE AND CYCLOSPORINE-A, International archives of allergy and immunology, 103(2), 1994, pp. 175-182
Peripheral blood mononuclear cells (PBMC) from nonatopic donors sensit
ive to Mycobacterium tuberculosis purified protein derivative (PPD) an
d from atopic donors sensitive to PPD and house dust mite antigen (HDM
), were stimulated in vitro to proliferate in response to exogenous IL
-2. In the presence of exogenous IFN-gamma, the response of cells from
atopic donors to PPD was either unaffected or slightly enhanced, wher
eas the response to HDM was inhibited in a dose-dependent manner. The
response of cells from nonatopic donors to PPD remained unchanged or w
as only slightly inhibited and this was not dose-dependent. Exogenous
IL-4 did not reverse the inhibitory effects of IFN-gamma and a neutral
izing antibody to IL-4 did not inhibit the proliferative response of c
ells to HDM and IL-2. Dexamethasone inhibited the IL-2-mediated respon
se of cells from atopic donors stimulated with HDM, whereas the IL-2-m
ediated response of cells induced by PPD was either unchanged or stimu
lated by dexamethasone. Cyclosporin A inhibited the response of cells
to both HDM and PPD. These results suggest that IFN-gamma can exert a
selective effect on the response of T lymphocytes to different antigen
s and that it is possible to identify compounds able to regulate this
activity.