In vivo, activated T cells can be propagated from endomyocardial biopsy (EMB) samples of cardiac allografts in cultures containing recombinant interleukin-2 (rIL-2). However, T cells are sometimes not propagated in such cultures, even when rejection is present, and at other times the yield of lymphocytes is too small to allow further studies of these graft-infiltrating cells. The current study investigated the effects of the addition of recombinant interleukin-4 (rIL-4) to the culture environment.
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