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The Immunobiology of Nipah Virus
被引:22
|作者:
Liew, Yvonne Jing Mei
[1
,2
]
Ibrahim, Puteri Ainaa S.
[1
]
Ong, Hui Ming
[1
]
Chong, Chee Ning
[1
]
Tan, Chong Tin
[3
]
Schee, Jie Ping
[3
]
Roman, Raul Gomez
[4
]
Cherian, Neil George
[4
]
Wong, Won Fen
[1
]
Chang, Li-Yen
[1
]
机构:
[1] Univ Malaya, Fac Med, Dept Med Microbiol, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Deputy Vice Chancellors Off Res & Innovat, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Fac Med, Dept Med, Div Neurol, Kuala Lumpur 50603, Malaysia
[4] Coalit Epidem Preparedness Innovat CEPI, Vaccine Res & Dev, Askekroken 11, N-0277 Oslo, Norway
关键词:
henipavirus infections;
encephalitis;
chiroptera;
innate immunity;
humoral immunity;
cellular immunity;
interferon type I;
animal models;
medical countermeasures;
TO-PERSON TRANSMISSION;
DATE PALM SAP;
HENDRA VIRUS;
CELL-DEATH;
V-PROTEIN;
ATTACHMENT GLYCOPROTEIN;
CLINICAL-FEATURES;
RECEPTOR-BINDING;
HAMSTER MODEL;
PIG-FARMERS;
D O I:
10.3390/microorganisms10061162
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Nipah virus (NiV) is a highly lethal zoonotic paramyxovirus that emerged in Malaysia in 1998. It is a human pathogen capable of causing severe respiratory infection and encephalitis. The natural reservoir of NiV, Pteropus fruit bats, remains a continuous virus source for future outbreaks, although infection in the bats is largely asymptomatic. NiV provokes serious disease in various mammalian species. In the recent human NiV outbreaks in Bangladesh and India, both bats-to-human and human-to-human transmissions have been observed. NiV has been demonstrated to interfere with the innate immune response via interferon type I signaling, promoting viral dissemination and preventing antiviral response. Studies of humoral immunity in infected NiV patients and animal models have shown that NiV-specific antibodies were produced upon infection and were protective. Studies on cellular immunity response to NiV infection in human and animal models also found that the adaptive immune response, specifically CD4+ and CD8+ T cells, was stimulated upon NiV infection. The experimental vaccines and therapeutic strategies developed have provided insights into the immunological requirements for the development of successful medical countermeasures against NiV. This review summarizes the current understanding of NiV pathogenesis and innate and adaptive immune responses induced upon infection.
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