Abstract
Exogenous interferon-α (IFN-α) and interferon-β (IFN-β) (type I IFNs) are known to suppress the IFN-γ-dependent expression of class II MHC (Ia) antigens on macrophages (Mø). We report here that the endogenous type I IFNs produced by Mø in responser to IFN inducers regulate la expression of the Mø themselves. Coculture of Mø with IFN-γ and polyinosinic-polycytidylic acid [poly(I):poly(C)] resulted in the reduction of Ia expression in comparison with those cultured without poly(I):poly(C). Pretreatment of Mø with poly(I):poly(C) or a bacterial lipopolysaccharide (LPS), which is also a potent IFN inducer, in vitro or in vivo, before being exposed to IFN-γ was also effective in suppressing the Ia expression. Such suppression was abolished by the addition of anti-IFN-α/β antibodies to the Mø culture along with IFN-γ. Mø cultured with L-cell conditioned medium (LCM) containing M-CSF were less capable of expressing Ia antigens than those cultured without LCM. The Ia-expressing ability of LCM-treated Mø was also restored by the addition of anti-IFN-α/β antibodies. Mø in the early stage of sterile inflammation were less responsive to IFN-γ than those in the late stage. These results suggest that endogenous type I IFNs, which are produced in response to natural or synthetic IFN-inducers, regulate Mø Ia expression in an autocrinal manner.
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