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Preclinical evaluation of an ALVAC (canarypox)-human cytomegalovirus glycoprotein B vaccine candidate

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Tartalom: http://real.mtak.hu/6360/
Archívum: MTA Könyvtár
Gyűjtemény: Status = Published


Type = Article
Cím:
Preclinical evaluation of an ALVAC (canarypox)-human cytomegalovirus glycoprotein B vaccine candidate
Létrehozó:
Gönczöl, Éva
Berencsi, K.
Pincus, S.
Endrész, Valéria
Kiadó:
Elsevier
Dátum:
1995
Téma:
QR180 Immunology / immunológia
RZ Other systems of medicine / orvostudomány egyéb területei
Tartalmi leírás:
Successful vaccination against the human cytomegalovirus (HCMV) requires induction. of both neutralizing antibody and cytotoxic T lymphocyte (CTL) responses. The HCMV glycoprotein B (gB, UL55) would be one of the most important immunogens to induce neutralizing antibodies. We tested the immunogenicity of art ALVAC (canarypox)-HCPAV-gB (ALVAC-gB) recombinant in mice and guinea pigs in order to provide preclinical data for a phase I clinical trial of a HCMV vaccine candidate, AL VAC is an attenuated vaccine strain of canarypox virus which replicates productively in avian species but abortively in mammalian cells, The ALVAC-gB recombinant inoculated subcutaneously in mice and intramuscularly in guinea pigs induced HCMV-specific neutralizing antibodies and gB-specific CTL responses. Ultraviolet irradiation of the ALVAC-gB recombinant before immunization diminished CTL responses, indicating that intracellular expression and processing of gB-protein were necessary for CTL induction. Prior immunity to vaccinia virus did Plot decrease immunogenicity of the ALVAC-gB recombinant in mice. Thus, despite its host range restriction, ALVAC-gB is potentially capable of inducing both humoral and cell-mediated immune responses to HCMV in both vaccinia-immune and non-immune individuals.
Típus:
Article
PeerReviewed
Formátum:
text
Azonosító:
Gönczöl, Éva and Berencsi, K. and Pincus, S. and Endrész, Valéria (1995) Preclinical evaluation of an ALVAC (canarypox)-human cytomegalovirus glycoprotein B vaccine candidate. VACCINE, 13 (12). pp. 1080-1085. ISSN 0264-410X
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