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PMID: 9456250 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Efficacy evaluation of prime-boost protocol: canarypoxvirus-based feline immunodeficiency virus (FIV) vaccine and inactivated FIV-infected cell vaccine against heterologous FIV challenge in cats.

AIDS (London, England) ·Vol. 12 ·No. 1 ·1998-01-01 ·页码 11-8

Tellier MC, Pu R, Pollock D, Vitsky A, Tartaglia J, Paoletti E, Yamamoto JK

Abstract

To evaluate the immunogenicity and prophylactic efficacy of immunization schemes employing a recombinant canarypoxvirus ('ALVAC')-based feline immunodeficiency virus (FIV) vaccine alone or in combination with an inactivated FIV-infected cell vaccine against homologous and heterologous FIV challenges in cats. Specific pathogen-free cats were given a total of three immunizations with subtype A vaccines and challenged 4 weeks after the final immunization with 50 median animal infectious doses (ID50) of FIV-Petaluma, a subtype A isolate. Following the initial challenge, protected cats received a second challenge with 75 ID50 of FIV-Bangston, a subtype B isolate. FIV-specific humoral and cell-mediated responses were measured to determine the immune correlates of protection. Two of three cats immunized with the ALVAC FIV recombinants alone were protected from homologous FIV challenge in the presence of FIV-specific cytotoxic T-lymphocyte (CTL) responses but in the absence of FIV-specific humoral responses. All three cats immunized with the ALVAC-FIV recombinant and boosted with FIV-infected cell vaccine were also protected from homologous FIV challenge in the presence of both FIV-specific CTL and humoral responses. Partial to full protection was observed in ALVAC-FIV/FIV-infected cell vaccine-immunized cats against a heterologous FIV challenge given 8 months after the initial challenge. Two out of three cats had transient infection and the remaining cat had no sign of FIV infection at a dose at which all three control cats were readily infected. Immunization schemes employing ALVAC-based FIV vaccines in combination with inactivated FIV-infected cell vaccine generate protective immune responses that can cross-react with FIV isolates that are genetically distinct from the vaccine strains.

MeSH 主题词
Animals Antibodies, Viral/analysis,immunology Avipoxvirus/genetics Bone Marrow Cells/virology Cats Cross Reactions/immunology Feline Acquired Immunodeficiency Syndrome/immunology,prevention & control Gene Products, gag/immunology Immunodeficiency Virus, Feline/genetics,immunology,metabolism Leukocytes, Mononuclear/virology Lymph Nodes/virology Neutralization Tests Pilot Projects Polymerase Chain Reaction RNA-Directed DNA Polymerase/metabolism Specific Pathogen-Free Organisms T-Lymphocytes, Cytotoxic/immunology Vaccines, Inactivated/administration & dosage,immunology Vaccines, Synthetic/administration & dosage,immunology Viral Envelope Proteins/immunology Viral Vaccines/administration & dosage,immunology
化学物质
Antibodies, Viral Gene Products, gag Vaccines, Inactivated Vaccines, Synthetic Viral Envelope Proteins Viral Vaccines RNA-Directed DNA Polymerase
作者与单位
共 7 位作者,点击展开单位 / ORCID
Tellier M C
Department of Pathobiology, School of Veterinary Medicine, University of Florida, Gainesville, USA.
Pu R
Pollock D
Vitsky A
Tartaglia J
Paoletti E
Yamamoto J K
Article Info
Journal
AIDS (London, England)
Abbr.
AIDS
ISSN
0269-9370
Published
1998-01-01
页码
11-8
Language
English
Country/Region
England
NLM ID
8710219
基金资助
NIAID NIH HHS · R01-AI30904 · United States
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