As for BMY then I assume they might follow suit. Gritstone have created a heterologous prime-boost regime. With these types of vaccine you administer the same (neo)antigens differently. They will prime with a chimpanzee adenoviral vector and then boost using synthetic self replicating RNA. This has been shown to induce greater numbers of antigen specific T-cells and increases the quality of response by involving multiple subsets and cytokine profiles. With anti-CTLA4 in preclinical studies you get extremely high and sustained T-cell responses. This compares to T-cell numbers observed in successful ACT (adoptive cell transfer) http://cancerres.aacrjournals.org/content/78/13_Supplement/724