Flavivirus-induced antibody cross-reactivity

被引:195
|
作者
Mansfield, Karen L. [1 ,2 ]
Horton, Daniel L. [1 ,3 ]
Johnson, Nicholas [1 ]
Li, Li [4 ]
Barrett, Alan D. T. [4 ]
Smith, Derek J. [3 ]
Galbraith, Sareen E. [2 ]
Solomon, Tom [2 ]
Fooks, Anthony R. [1 ,5 ]
机构
[1] Anim Hlth & Vet Labs Agcy, Wildlife Zoonoses & Vector Borne Dis Res Grp, Addlestone KT15 3NB, Surrey, England
[2] Univ Liverpool, Brain Infect Grp, Liverpool L69 3BX, Merseyside, England
[3] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
[4] Univ Texas Galveston, Med Branch, Dept Pathol, Galveston, TX 77550 USA
[5] Univ Liverpool, Natl Ctr Zoonoses Res, Liverpool L69 3BX, Merseyside, England
来源
关键词
WEST-NILE-VIRUS; JAPANESE ENCEPHALITIS-VIRUS; PROTEIN-DOMAIN-III; ANTIGENIC RELATIONSHIPS; MONOCLONAL-ANTIBODIES; GENETIC EVOLUTION; INFECTION; IMMUNITY; VACCINE; FEVER;
D O I
10.1099/vir.0.031641-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dengue viruses (DENV) cause countless human deaths each year, whilst West Nile virus (WNV) has re-emerged as an important human pathogen. There are currently no WNV or DENV vaccines licensed for human use, yet vaccines exist against other flaviviruses. To investigate flavivirus cross-reactivity, sera from a human cohort with a history of vaccination against tick-borne encephalitis virus (TBEV), Japanese encephalitis virus (JEV) and yellow fever virus (YFV) were tested for antibodies by plaque reduction neutralization test. Neutralization of louping ill virus (LIV) occurred, but no significant neutralization of Murray Valley encephalitis virus was observed. Sera from some individuals vaccinated against TBEV and JEV neutralized WNV, which was enhanced by YFV vaccination in some recipients. Similarly, some individuals neutralized DENV-2, but this was not significantly influenced by YFV vaccination. Antigenic cartography techniques were used to generate a geometric illustration of the neutralization titres of selected sera against WNV, TBEV, JEV, LIV, YFV and DENV-2. This demonstrated the individual variation in antibody responses. Most sera had detectable titres against LIV and some had titres against WNV and DENV-2. Generally, LIV titres were similar to titres against TBEV, confirming the close antigenic relationship between TBEV and LIV. JEV was also antigenically closer to TBEV than WNV, using these sera. The use of sera from individuals vaccinated against multiple pathogens is unique relative to previous applications of antigenic cartography techniques. It is evident from these data that notable differences exist between amino acid sequence identity and mapped antigenic relationships within the family Flaviviridae.
引用
收藏
页码:2821 / 2829
页数:9
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