Author: Tzannou, Ifigeneia; Nicholas, Sarah K; Lulla, Premal; Aguayo-Hiraldo, Paibel I; Misra, Anisha; Martinez, Caridad A; Machado, Annette A; Orange, Jordan S; Piedra, Pedro A; Vera, Juan F; Leen, Ann M
                    Title: Immunologic Profiling of Human Metapneumovirus for the Development of Targeted Immunotherapy  Cord-id: s8t2udxj  Document date: 2017_7_25
                    ID: s8t2udxj
                    
                    Snippet: Human metapneumovirus (hMPV) is a respiratory virus detected in ≥9% of allogeneic hematopoietic stem cell transplant (HSCT) recipients, in whom it can cause significant morbidity and mortality. Given the lack of effective antivirals, we investigated the potential for immunotherapeutic intervention, using adoptively transferred T cells. Thus, we characterized the cellular immune response to the virus and identified F, N, M2-1, M, and P as immunodominant target antigens. Reactive T cells were po
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Human metapneumovirus (hMPV) is a respiratory virus detected in ≥9% of allogeneic hematopoietic stem cell transplant (HSCT) recipients, in whom it can cause significant morbidity and mortality. Given the lack of effective antivirals, we investigated the potential for immunotherapeutic intervention, using adoptively transferred T cells. Thus, we characterized the cellular immune response to the virus and identified F, N, M2-1, M, and P as immunodominant target antigens. Reactive T cells were polyclonal (ie, they expressed CD4 and CD8), T-helper type 1 polarized, and polyfunctional (ie, they produced interferon γ, tumor necrosis factor α, granulocyte-macrophage colony-stimulating factor, and granzyme B), and they were able to kill autologous antigen-loaded targets. The detection of hMPV-specific T cells in HSCT recipients who endogenously controlled active infections support the clinical importance of T-cell immunity in mediating protective antiviral effects. Our results demonstrate the feasibility of developing an immunotherapy for immunocompromised patients with uncontrolled infections.
 
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