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Down-Regulates MHC Expression and Antigen Processing in a Human B Cell Line1
Department of Immunology, Windeyer Institute of Medical Sciences, University College London Medical School, London, United Kingdom
IFN-
is a crucial mediator in the induction of cell-mediated
Th1-type responses but is predominantly a negative regulator of B cell
differentiation and proliferation. This cytokine is therefore a key
factor in determining Th1 vs Th2 differentiation. This study
investigates the action of IFN-
in modulation of HLA-DR expression
and Ag presentation by EBV-transformed human B cell lines. In contrast
to its action on the monocyte/macrophage, IFN-
down-regulates
surface MHC expression on these B cells, and this regulation is
posttranscriptional. In parallel with MHC down-regulation, there is a
reduced capability to process and present exogenous protein and peptide
Ag to T cell hybridomas. IFN-
does not change the rates of fluid
phase endocytosis or exocytosis in this model system but correlates
with an up-regulation of the lysosomal enzymes cathepsins B and
D.
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