MODE OF ACTION OF THE IGG INHIBITOR OF ERYTHROPOIESIS IN TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD

  • 1 January 1982
    • journal article
    • research article
    • Vol. 59  (1) , 114-123
Abstract
Twelve cases of transient erythroblastopenia (TEC) of childhood (TEC) were studied to evaluate their marrow cell erythropoiesis in vitro and the effect on it of their serum or IgG. The number of erythroid colony-forming units (CFU-E) and erythropoietic burst-forming units (BFU-E) in the bone marrow of 9 cases was extremely variable and did not allow any conclusion regarding the pathogenesis of this anemia. An IgG inhibitor of growth of erythroid colonies or bursts was detected in 8/12 cases. This IgG inhibitor had no effect on the growth of granulocyte-macrophage colonies. Further studies on its mode of action indicated that the IgG did not have antierythropoietin antibody properties and did not affect the mature erythroblasts, as shown by a lack of inhibition of their response to erythropoietin and by the lack of a cytotoxic effect on 59Fe-labeled erythroblasts. In 4 cases, preincubation studies demonstrated a direct effect of the IgG on the CFU-E, which was complement-mediated in 3 cases and complement-mediated in 3 cases and complement-independent in 1 case. In 2 other cases, the IgG suppressed the growth of normal BFU-E only without affecting the growth of CFU-E. The IgG inhibitor was no longer present after the erythroblastopenia had remitted. In the majority of cases of TEC, an IgG suppressor of erythropoiesis in vitro is apparently present. Its mode of action is heterogeneous regarding its requirement for complement. Its target cells are the earlier or later erythroid progenitors. BFU-E or CFU-E, but not the differentiated erythroblasts.