Although not significant, a clear trend toward restoration of proliferation for CD8 + T cells when compared to direct contact TGF-β MSCs was observed ( Figure 5 B).
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TGF-β1-Licensed Murine MSCs Show Superior Therapeutic Efficacy in Modulating Corneal Allograft Immune Rejection In Vivo.
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The same trend was observed for CD8 + activated effector T cells; however, differences failed to reach statistical significance in the lungs and spleens of transplanted, treated mice ( Figure 8 E).