Author: Parra-Sánchez, Héctor; Bustamante-Córdova, Lorena; Reséndiz, Mónica; Mata-Haro, Verónica; Pinelli-Saavedra, Araceli; Hernández, Jesús
                    Title: Analysis of Swine Conventional Dendritic Cells, DEC205(+)CD172a(+/−)CADM1(+), from Blood and Spleen in Response to PRRSV and PEDV  Cord-id: zn9nagv9  Document date: 2019_10_31
                    ID: zn9nagv9
                    
                    Snippet: Conventional dendritic cells (cDCs) cannot be infected by porcine reproductive and respiratory syndrome virus (PRRSV) but respond to infection via cytokine production, indicating a possible role in initiation/regulation of the immune response against PRRSV. In this work, we evaluated the responses of splenic and blood cDCs, with DEC205(+)CADM1(+)CD172a(+/−) phenotype, as well as those of CD163(+) cells against PRRSV and porcine epidemic diarrhea virus (PEDV). Both populations were incubated in
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Conventional dendritic cells (cDCs) cannot be infected by porcine reproductive and respiratory syndrome virus (PRRSV) but respond to infection via cytokine production, indicating a possible role in initiation/regulation of the immune response against PRRSV. In this work, we evaluated the responses of splenic and blood cDCs, with DEC205(+)CADM1(+)CD172a(+/−) phenotype, as well as those of CD163(+) cells against PRRSV and porcine epidemic diarrhea virus (PEDV). Both populations were incubated in the presence of PRRSV or PEDV with and without naïve CD3(+) T cells, and cytokine responses were evaluated by qPCR and ELISA. Our results showed that cDCs, but not CD163(+) cells, produced IL-12 in response to PRRSV. PEDV did not induce IL-12 production. Cocultures of cDCs and autologous naïve CD3(+) cells resulted in decreased IL-12 production and low expression of IFN-γ transcripts in response to PRRSV. Interestingly, cDCs increased the proliferation of naïve T cells in the presence of PRRSV compared with that achieved with monocytes and peripheral blood mononuclear cells (PBMCs). Cocultures of CD163(+) cells induced IL-10 and IL-4 expression in the presence of PRRSV and PEDV, respectively. In conclusion, cDCs can selectively produce IL-12 in response to PRRSV but poorly participate in the activation of naïve T cells.
 
  Search related documents: 
                                Co phrase  search for related documents- absence presence and adaptive innate: 1, 2
  - absence presence and adaptive innate response: 1
  - absence presence and additional study: 1, 2, 3, 4
  - absence presence and low number: 1, 2, 3
  - absence presence and lymph node: 1, 2, 3, 4, 5
  - absence presence and lymphoid tissue: 1, 2, 3, 4
  - absence presence and lysis buffer: 1, 2, 3, 4, 5
  - acute infection and adaptive innate: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72
  - acute infection and adaptive innate response: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10
  - acute infection and additional study: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10
  - acute infection and low number: 1, 2, 3, 4, 5, 6, 7, 8, 9
  - acute infection and lymph node: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14
  - acute infection and lymph node cell: 1, 2, 3
  - acute infection and lymphoid blood: 1
  - acute infection and lymphoid tissue: 1, 2, 3, 4, 5, 6, 7, 8, 9
  - acute infection and lysis buffer: 1
  
 
                                Co phrase  search for related documents, hyperlinks ordered by date