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10.1111/imr.12138 http://scihub22266oqcxt.onion/10.1111/imr.12138 C3927231!3927231 !24517423     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\24517423 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Immunol+Rev 2014 ; 258 (1 ): 12-29 Nephropedia Template TP {{tp|p=24517423 |t=2014. Antiviral T-cell therapy |pdf=|usr=}}{{24517423 }} gab.com Text Antiviral T-cell therapy JO: Immunol Rev http://www.kidney.de/pget.php?&tw=1&pmid=24517423 #FOAvip Serious viral infections are a common cause of morbidity and mortality after allogeneic stem cell transplantation. They occur in the majority of allograft recipients and are fatal in 17-20%. These severe infections may be prolonged or recurrent and add substantially to the cost, both human and financial, of the procedure. Many features of allogeneic stem cell transplantation contribute to this high rate of viral disease. The cytotoxic and immunosuppressive drugs administered pretransplant to eliminate the host hematopoietic/immune system and any associated malignancy, the delay in recapitulating immune ontogeny post-transplant, the immunosuppressive drugs given to prevent graft versus host disease (GvHD), and the effects of GvHD itself, all serve to make stem cell transplant recipients vulnerable to disease from endogenous (latent) and exogenous (community) viruses, and to be incapable of controlling them as quickly and effectively as most normal individuals. Twit Text FOAVip Antiviral T-cell therapy ????Immunol Rev http://www.kidney.de/pget.php?&tw=1&pmid=24517423 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24517423 #FOAvip English Wikipedia <ref>{{Cite pmid|24517423 }}</ref> Antiviral T-cell therapy #MMPMID24517423 Leen AM ; Heslop HE ; Brenner MK Immunol Rev 2014[Mar]; 258 (1 ): 12-29 PMID24517423 show ga Serious viral infections are a common cause of morbidity and mortality after allogeneic stem cell transplantation. They occur in the majority of allograft recipients and are fatal in 17-20%. These severe infections may be prolonged or recurrent and add substantially to the cost, both human and financial, of the procedure. Many features of allogeneic stem cell transplantation contribute to this high rate of viral disease. The cytotoxic and immunosuppressive drugs administered pretransplant to eliminate the host hematopoietic/immune system and any associated malignancy, the delay in recapitulating immune ontogeny post-transplant, the immunosuppressive drugs given to prevent graft versus host disease (GvHD), and the effects of GvHD itself, all serve to make stem cell transplant recipients vulnerable to disease from endogenous (latent) and exogenous (community) viruses, and to be incapable of controlling them as quickly and effectively as most normal individuals. |Adoptive Transfer [MESH] |Animals [MESH] |Graft vs Host Disease/immunology/prevention & control [MESH] |Hematopoietic Stem Cell Transplantation/*adverse effects [MESH] |Humans [MESH] |Immunocompromised Host [MESH] |Immunosuppressive Agents/adverse effects [MESH] |Risk Factors [MESH] |T-Lymphocytes/immunology/*transplantation/virology [MESH] |Treatment Outcome [MESH]Antiviral T-cell therapy (epmc).pdf DeepDyve Pubget Overpricing