New chemical method of viral inactivation for vaccine development based on membrane fusion inhibition
被引:5
作者:
Stauffer, Fausto
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Stauffer, Fausto
De Miranda, Joari
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
De Miranda, Joari
Schechter, Marcos C.
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Schechter, Marcos C.
Queiroz, Fernando A.
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Queiroz, Fernando A.
Santos, Nathalia O.
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Santos, Nathalia O.
Alves, Ada M. B.
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Alves, Ada M. B.
Da Poian, Andrea T.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, BrazilUniv Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
Da Poian, Andrea T.
[1
]
机构:
[1] Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
[2] Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Lab Imunopatol, BR-21040900 Rio De Janeiro, RJ, Brazil
Membrane fusion is an essential step in the entry of enveloped viruses into their host cells. This process is triggered by conformational changes in viral surface glycoproteins. We have demonstrated previously that modification of vesicular stomatitis virus (VSV) with diethylpyrocarbonate (DEPC abolished the conformational changes on VSV glycoprotein and the fusion reaction induced by the virus. Moreover, we observed that viral treatment with DEPC inactivates the virus, preserving the conformational integrity of its surface proteins. In the present work, we evaluated the potential use of DEPC as a viral inactivating chemical agent for the development of useful vaccines. Pathogenicity and viral replication in Balb/c mice were abolished by viral treatment with 0.5 mM DEPC. In addition, antibodies elicited in mice after intraperitoneal immunization with DEPC-inactivated VSV mixed with adjuvants were able to recognize and neutralize the native virus and efficiently protected animals against the challenge with lethal doses of VSV. These results together suggest that viral inactivation with DEPC seems to be a suitable method for the development of safe vaccines. (C) 2007 Elsevier Ltd. All rights reserved.