Inhibition of Human Erythroid Colony-forming
نویسندگان
چکیده
We have previously reported that inhibition ofhuman CFU-erythroid (E) colony formation by tumor necrosis factor (TNF) is an indirect effect mediated by a soluble factor released from a fraction of marrow accessory cells which are predominantly stromal elements (Means, R. T., Jr., E. N. Dessypris, and S. B. Krantz. 1990. J. Clin. Invest. 86:538-541). Further studies reported here identify a mediator of this effect. The inhibitory effect of recombinant TNF on marrow CFUE is ablated by neutralizing antibodies to human #IFN, but not by antibodies to 'yIFN or IL-1. Anti-ftIFN also neutralizes the inhibitory effect of conditioned medium prepared from marrow cells exposed to TNF. Human ftIFN inhibits colony formation by unpurified marrow CFU-E as well as highly purified CFU-E generated from peripheral blood progenitors, and limiting dilution analysis shows that this is a direct inhibitory effect. TNF has been implicated in the pathogenesis of the anemia of chronic diseases since blood TNF levels are elevated in many patients with this syndrome, and since exposure to TNF produces a similar anemia in either humans or mice. The present study demonstrates that 8IFN is a required mediator of this inhibitory effect on erythropoiesis. (J. Clin. Invest. 1993. 91:416-419.)
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Inhibition of human erythroid colony-forming units by gamma interferon can be corrected by recombinant human erythropoietin.
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