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Protective immunity spectrum induced by immunization with a vaccine from the TBEV strain Sofjin.
Chernokhaeva, L L; Rogova, Yu V; Vorovitch, M F; Romanova, L Iu; Kozlovskaya, L I; Maikova, G B; Kholodilov, I S; Karganova, G G.
Affiliation
  • Chernokhaeva LL; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Rogova YV; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Vorovitch MF; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Romanova LIu; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Kozlovskaya LI; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Maikova GB; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Kholodilov IS; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia.
  • Karganova GG; Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow 142782 Russia. Electronic address: karganova@bk.ru.
Vaccine ; 34(20): 2354-61, 2016 Apr 29.
Article in En | MEDLINE | ID: mdl-27013433
Tick-borne encephalitis (TBE) circulates widely in the territory of Eurasia with up to 10,000 cases registered annually. The TBE virus (TBEV) includes three main subtypes: European, Siberian and Far-Eastern, and two new Asiatic variants, phylogenetically distant from the others. The inactivated antigen of European or Far-Eastern strains is used in commercial TBE vaccines. A set of 14 TBEV strains, isolated in 1937-2008, with different passage histories, representing all subtypes and variants, was used in this work. The chosen set covers almost all the TBE area. Sera of mice, immunized with the TBE vaccine Moscow, prepared from the TBEV strain Sofjin, were studied in a plaque neutralization test against the set of TBEV strains. The vaccine induced antibodies at a protective titer against all TBEV strains and Omsk hemorrhagic fever virus (OHFV) with Е protein amino acid distances of 0.008-0.069, but not against Powassan virus. We showed that after a course of two immunizations, factors such as the period between vaccinations (1-4 weeks), the challenging virus dose (30-1000 LD50) and terms of challenge (1-4 weeks after the last immunization) did not significantly affect the assessment of protective efficacy of the vaccine in vivo. The protective effect of the TBE vaccine Moscow against the set of TBEV strains and the OHFV was demonstrated in in vivo experiments. TBE vaccine Moscow did not protect mice against 10 LD50 of the Powassan virus. We showed that this range of Е protein amino acid distances between the vaccine strain and challenging virus do not have a decisive impact on the TBE vaccine protective effect in vitro and in vivo. Moreover, the TBE vaccine Moscow induces an immune response protective against a wide range of TBEV variants.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Vaccines / Encephalitis, Tick-Borne / Cross Protection Limits: Animals Language: En Journal: Vaccine Year: 2016 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Vaccines / Encephalitis, Tick-Borne / Cross Protection Limits: Animals Language: En Journal: Vaccine Year: 2016 Document type: Article Country of publication: Netherlands