T cell apoptosis is critical to development and homeostasis of the immune system. The most salient feature of apoptosis is the lack of an attendant inflammatory response or tissue damage. Here, we present evidence that apoptotic T cells release TGF-β, thereby contributing to an immunosuppressive milieu. Apoptotic T cells released not only latent but also bio-active TGF-β. Nonetheless, TGF-β transcription was not upregulated, suggesting release of existing rather than synthesis of new TGF-β. Localized within the intracellular membrane-bound compartment, which includes mitochondria, TGF-β was redistributed into the cytosol following loss of mitochondrial membrane potential. TGF-β secreted from apoptotic T cells inhibited proinflammatory cytokine production by activated macrophages to foster immune suppression. These findings broaden the potential mechanisms whereby induction of immune tolerance or deficiency occurs through T cell deletion.