scholarly journals Fusion toxin protein inhibits CMV infection

2015 ◽  
Vol 14 (8) ◽  
pp. 528-528
Author(s):  
Sarah Crunkhorn
2019 ◽  
Vol 131 (1) ◽  
pp. 5-17 ◽  
Author(s):  
B A Krishna ◽  
M R Wills ◽  
J H Sinclair

Abstract Background Human cytomegalovirus (HCMV) is a threat to immunologically weak patients. HCMV cannot yet be eliminated with a vaccine, despite recent advances. Sources of data Sources of data are recently published research papers and reviews about HCMV treatments. Areas of agreement Current antivirals target the UL54 DNA polymerase and are limited by nephrotoxicity and viral resistance. Promisingly, letermovir targets the HCMV terminase complex and has been recently approved by the FDA and EMA. Areas of controversy Should we screen newborns for HCMV, and use antivirals to treat sensorineural hearing loss after congenital HCMV infection? Growing points Growing points are developing drugs against latently infected cells. In addition to small molecule inhibitors, a chemokine-based fusion toxin protein, F49A-FTP, has shown promise in killing both lytically and latently infected cells. Areas timely for developing research We need to understand what immune responses are required to control HCMV, and how best to raise these immune responses with a vaccine.


2020 ◽  
Vol 39 (4) ◽  
pp. S83
Author(s):  
R. VP Ribeiro ◽  
T. Ku ◽  
V.H. Ferreira ◽  
M. Galasso ◽  
S. Moshkelgosha ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
B. A. Krishna ◽  
K. Spiess ◽  
E. L. Poole ◽  
B. Lau ◽  
S. Voigt ◽  
...  
Keyword(s):  

2016 ◽  
Vol 04 (01) ◽  
pp. 4-10

AbstractImmunosuppression permits graft survival after transplantation and consequently a longer and better life. On the other hand, it increases the risk of infection, for instance with cytomegalovirus (CMV). However, the various available immunosuppressive therapies differ in this regard. One of the first clinical trials using de novo everolimus after kidney transplantation [1] already revealed a considerably lower incidence of CMV infection in the everolimus arms than in the mycophenolate mofetil (MMF) arm. This result was repeatedly confirmed in later studies [2–4]. Everolimus is now considered a substance with antiviral properties. This article is based on the expert meeting “Posttransplant CMV infection and the role of immunosuppression”. The expert panel called for a paradigm shift: In a CMV prevention strategy the targeted selection of the immunosuppressive therapy is also a key element. For patients with elevated risk of CMV, mTOR inhibitor-based immunosuppression is advantageous as it is associated with a significantly lower incidence of CMV events.


2020 ◽  
Author(s):  
Keyword(s):  

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