Cross-Neutralization Activities of Antibodies against 18 Lyssavirus Glycoproteins

Some lyssaviruses, including the rabies virus (RABV), cause lethal neurological symptoms in humans. However, the efficacy of commercial vaccines has only been evaluated against RABV. To assess cross-reactivity among lyssaviruses, including RABV, sera from rabbits inoculated with human and animal RAB...

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Published inJapanese Journal of Infectious Diseases Vol. 77; no. 3; pp. 169 - 173
Main Authors Inoue, Yusuke, Kaku, Yoshihiro, Harada, Michiko, Ishijima, Keita, Kuroda, Yudai, Tatemoto, Kango, Virhuez-Mendoza, Milagros, Nishino, Ayano, Yamamoto, Tsukasa, Inoue, Satoshi, Matsuu, Aya, Maeda, Ken
Format Journal Article
LanguageEnglish
Published Japan National Institute of Infectious Diseases 31.05.2024
Japan Science and Technology Agency
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Summary:Some lyssaviruses, including the rabies virus (RABV), cause lethal neurological symptoms in humans. However, the efficacy of commercial vaccines has only been evaluated against RABV. To assess cross-reactivity among lyssaviruses, including RABV, sera from rabbits inoculated with human and animal RABV vaccines and polyclonal antibodies from rabbits immunized with expression plasmids of the glycoproteins of all 18 lyssaviruses were prepared, and cross-reactivity was evaluated via virus-neutralization tests using Duvenhage lyssavirus (DUVV), European bat lyssavirus-1 (EBLV-1), Mokola lyssavirus (MOKV), Lagos bat lyssavirus (LBV), and RABV. The sera from rabbits inoculated with RABV vaccines showed cross-reactivity with EBLV-1 and DUVV, both belonging to phylogroup I. However, reactivity with MOKV and LBV in phylogroup II was notably limited or below the detection level. Next, we compared the cross-reactivity of the polyclonal antibodies against all lyssavirus glycoproteins. Polyclonal antibodies had high virus-neutralization titers against the same phylogroup but not different phylogroups. Our findings indicate that a new vaccine should be developed for pre- and post-exposure prophylaxis against lyssaviral infections.
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ISSN:1344-6304
1884-2836
1884-2836
DOI:10.7883/yoken.JJID.2023.400