(ii) Retaining the ability of EBV- and CMV-specific CTLs to proliferate and produce IFN- [56]
(ii) Persistent CMV-specific T cells and IFN- response to CMV infection [56]
Suppressing
(i) Poor lymphocyte proliferative responses [57] (ii) Proliferation and IFN- production of CMV and influenza-specific T cells which were inhibited [58] (iii) Cytotoxicity of V9V2 T cells against influenza virus H1N1 which was inhibited [59]
(i) Decreasing survival of children treated with MSCs due to HAdV infection [54] (ii) An opportunistic viral infection developed in 3 of 6 patients receiving MSCs [60] (iii) VZV reactivation in VZV-seropositive patients [61]
MSCs, Mesenchymal Stromal Cells; CMV, cytomegalovirus; HAdV, human adenovirus; EBV, Epstein-Barr Virus; CTLs, cytotoxic T lymphocytes; IFN, interferon.