FTY720 Application Following Isolated Warm Liver Ischemia Improves Long-Term Survival and Organ Protection in a Mouse Model

2007 ◽  
Vol 39 (2) ◽  
pp. 493-498 ◽  
Author(s):  
C.P. Kaudel ◽  
M. Frink ◽  
M. van Griensven ◽  
U. Schmiddem ◽  
C. Probst ◽  
...  
2016 ◽  
Vol 139 (1) ◽  
pp. 194-204 ◽  
Author(s):  
Kelly Waldeck ◽  
Carleen Cullinane ◽  
Kerry Ardley ◽  
Jake Shortt ◽  
Ben Martin ◽  
...  

2019 ◽  
Vol 27 (8) ◽  
pp. 1436-1451
Author(s):  
Sabine Geiger ◽  
Emrah I. Ozay ◽  
Ulf Geumann ◽  
Marina K. Hereth ◽  
Terese Magnusson ◽  
...  

2020 ◽  
Vol 13 (10) ◽  
pp. 100826
Author(s):  
Takashi Higuchi ◽  
Norihiko Sugisawa ◽  
Jun Ho Park ◽  
Yu Sun ◽  
Guangwei Zhu ◽  
...  

2008 ◽  
Vol 17 (6) ◽  
pp. 619-629 ◽  
Author(s):  
Takashi Gunji ◽  
Takuro Saito ◽  
Yoshihiro Sato ◽  
Shinichi Matsuyama ◽  
Kazuya Ise ◽  
...  

Blood ◽  
2015 ◽  
Vol 125 (9) ◽  
pp. 1444-1451 ◽  
Author(s):  
Iris Appelmann ◽  
Cory D. Rillahan ◽  
Elisa de Stanchina ◽  
Gregory Carbonetti ◽  
Chong Chen ◽  
...  

Key Points In a Ph+ ALL mouse model, dasatinib inhibition of the BCR-ABL kinase resensitizes residual leukemic B cells to Janus kinase inhibition. Dasatinib, ruxolitinib, and dexamethasone together limit emergence of dasatinib-resistant BCR-ABL mutants and extend long-term survival.


Vaccines ◽  
2019 ◽  
Vol 7 (4) ◽  
pp. 196 ◽  
Author(s):  
Kei Amemiya ◽  
Jennifer L. Dankmeyer ◽  
Sergei S. Biryukov ◽  
Sylvia R. Treviño ◽  
Christopher P. Klimko ◽  
...  

Melioidosis is an emerging disease that is caused by the facultative intracellular pathogen Burkholderia pseudomallei. It is intrinsically resistant to many antibiotics and host risk factors play a major role in susceptibility to infection. Currently, there is no human or animal vaccine against melioidosis. In this study, multiple B. pseudomallei MSHR668 deletion mutants were evaluated as live attenuated vaccines in the sensitive BALB/c mouse model of melioidosis. The most efficacious vaccines after an intraperitoneal challenge with 50-fold over the 50% median lethal dose (MLD50) with B. pseudomallei K96243 were 668 ΔhisF and 668 ΔilvI. Both vaccines completely protected mice in the acute phase of infection and showed significant protection (50% survivors) during the chronic phase of infection. The spleens of the survivors that were examined were sterile. Splenocytes from mice vaccinated with 668 ΔhisF and 668 ΔilvI expressed higher amounts of IFN-γ after stimulation with B. pseudomallei antigens than splenocytes from mice vaccinated with less protective candidates. Finally, we demonstrate that 668 ΔhisF is nonlethal in immunocompromised NOD/SCID mice. Our results show that 668 ΔhisF and 668 ΔilvI provide protective cell-mediated immune responses in the acute phase of infection and promote long term survival in the sensitive BALB/c mouse model of melioidosis.


Oncotarget ◽  
2016 ◽  
Vol 7 (26) ◽  
pp. 39118-39135 ◽  
Author(s):  
Sylvie L. Lesuis ◽  
Herve Maurin ◽  
Peter Borghgraef ◽  
Paul J. Lucassen ◽  
Fred Van Leuven ◽  
...  

2000 ◽  
Vol 111 (1) ◽  
pp. 363-370 ◽  
Author(s):  
Katsuto Takenaka ◽  
Mine Harada ◽  
Tomoaki Fujisaki ◽  
Koji Nagafuji ◽  
Shinichi Mizuno ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A747-A748
Author(s):  
S DRESNER ◽  
A IMMMANUEL ◽  
P LAMB ◽  
S GRIFFIN

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