Construction and characterization of a replication-competent human adenovirus type 3-based vector as a live-vaccine candidate and a viral delivery vector

Vaccine ◽  
2009 ◽  
Vol 27 (8) ◽  
pp. 1145-1153 ◽  
Author(s):  
Qiwei Zhang ◽  
Xiaobo Su ◽  
Donald Seto ◽  
Bo-jian Zheng ◽  
Xingui Tian ◽  
...  
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Haitao Li ◽  
Rong Zhou ◽  
Jingxian Chen ◽  
Xingui Tian ◽  
Qiwei Zhang ◽  
...  

2014 ◽  
Vol 183 ◽  
pp. 67-74 ◽  
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Chunyan Xue ◽  
Xingui Tian ◽  
Xiao Li ◽  
Zhichao Zhou ◽  
Xiaobo Su ◽  
...  

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Vol 177 (2) ◽  
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Xingui Tian ◽  
Chenyang Li ◽  
Chunyan Xue ◽  
Xiao Li ◽  
Zhichao Zhou ◽  
...  

2012 ◽  
Vol 157 (9) ◽  
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Tianhua Zhong ◽  
Xiao Li ◽  
Zhichao Zhou ◽  
Ting Li ◽  
Xingui Tian ◽  
...  

Gene ◽  
1994 ◽  
Vol 146 (2) ◽  
pp. 257-259 ◽  
Author(s):  
Alain Cuzange ◽  
Jadwiga Chroboczek ◽  
Bernard Jacrot

1988 ◽  
Vol 16 (23) ◽  
pp. 11374-11374 ◽  
Author(s):  
Alain Houde ◽  
Joseph M. Weber

2002 ◽  
Vol 83 (1) ◽  
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Christopher J. Cohen ◽  
Zhi Quan Xiang ◽  
Guang-Ping Gao ◽  
Hildegund C. J. Ertl ◽  
James M. Wilson ◽  
...  

A replication-defective form of chimpanzee adenovirus type 68 (C68) has been developed to circumvent problems posed by widespread preexisting immunity to common human adenovirus vectors. To investigate the determinants of C68 tropism, its interaction with the coxsackievirus and adenovirus receptor (CAR) was studied. Although CHO cells were resistant to transduction by C68 as well as by adenovirus type 5 (Ad5), CHO cells expressing either human or murine CAR were transduced readily. C68 transduction, like Ad5 transduction, was blocked when cells were exposed to anti-CAR antibody or when virus was exposed to a soluble form of the CAR extracellular domain. These results indicate that gene delivery by C68 occurs by a CAR-dependent mechanism.


Gene ◽  
1994 ◽  
Vol 142 (2) ◽  
pp. 309-310
Author(s):  
Pei Pei Smith ◽  
Surendra Dheer ◽  
Alan Davis ◽  
Paul P. Hung ◽  
Shaw-Guang Lee

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