Reference
Reference TypeLiterature
TitleDelayed infection after immunization with a peptide from the transmembrane glycoprotein of the feline immunodeficiency virus.
AuthorsJ Richardson; A Moraillon; F Crespeau; S Baud; P Sonigo; G Pancino
AffiliationsGénétique des Virus (ICGM-CNRS UPR 0415), Institut Cochin de Génétique Moléculaire, Paris, France.
JournalJ Virol
Year1998
AbstractRecent advances in the quantitative assessment of viral burden, by permitting the extension of criteria applied to assess the efficacy of vaccines from all-or-none protection to diminution of the viral burden, may allow the identification of original immunogens of value in combined vaccines. Peptides corresponding to three domains of the envelope glycoproteins of feline immunodeficiency virus that are recognized during natural infection were used to immunize cats. After challenge with a primary isolate of feline immunodeficiency virus, the development of acute infection was monitored by quantitative assessment of the viral burden in plasma and tissues by competitive reverse transcription-PCR, by measurement of the humoral response developed to viral components, and by lymphocyte subset analysis. Whereas immunization with two peptides derived from the surface glycoprotein had no effect on the early course of infection, immunization with a peptide derived from the transmembrane glycoprotein delayed infection, as reflected by a diminished viral burden in the early phase of primary infection and delayed seroconversion. This peptide, located in the membrane-proximal region of the extracellular domain, has homology to an epitope of human immunodeficiency virus type 1 recognized by a broadly neutralizing monoclonal antibody. These results suggest that lentivirus transmembrane glycoproteins share a determinant in the juxtamembrane ectodomain which could be of importance in the design of vaccines against AIDS.
Curation Last Updated2023-08-18 20:27:50
Epitope
Epitope ID87755
Chemical TypeLinear peptide
Linear SequenceQVVKQPDYLVVPGEVMEYKPRR
Source Molecule NameEnvelope glycoprotein gp150
Source OrganismFeline immunodeficiency virus (isolate wo)
Starting Position586
Ending Position607
Epitope Reference Details
Epitope Structure DefinesEpitope containing region/antigenic site
Epitope NameSU5
Reference Starting Position586
Reference Ending Position607
Location of Data in ReferenceMaterials and Methods
Immunization
Host OrganismFelis catus (cat)
Host Details
Age4 month old
1st In Vivo Process
In Vivo Process TypeAdministration in vivo to prevent or reduce disease
1st In Vivo Process Administration Details
AdjuvantsFreund's complete;VO:0000139
Routesubcutaneous
Dose Schedule5 doses of 120 μg of FIV peptide (approximately 250 μg of KLH-coupled peptide)
1st Immunogen
Epitope RelationEpitope
Chemical TypeLinear peptide
Linear SequenceQVVKQPDYLVVPGEVMEYKPRR
Source Molecule NameEnvelope glycoprotein gp150
Source OrganismFeline immunodeficiency virus (isolate wo)
Starting Position586
Ending Position607
Immunization Comments
Immunization CommentsImmunogen carrier: Peptide conjugate: Keyhole limpet hemocyanin (Megathura crenulata). Four booster injections were administered subcutaneously in incomplete Freund´s adjuvant, at intervals of 2 to 3 weeks for the 1st, 2nd and 3rd, and 7 weeks for the 4th. A cysteine residue was added at the N-terminus of the peptide for coupling to KLH.
B Cell Assay
Qualitative MeasurementPositive-Low
Method/Techniquein vivo assay
Measurement ofprotection from pathogen challenge
Measurement Details
Number of Subjects Tested4
Number of Subjects Responded1
Response Frequency (%)25
Antigen
Epitope RelationSource Organism
Object TypeOrganism
OrganismFeline immunodeficiency virus (isolate wo)
Assay Reference Details
Assay Comments by IEDB CuratorCats were challenged 1 week after the final immunization by intraperitoneal inoculation of 10 50% cat infectious doses (CID50) of the Wo isolate of FIV. The kinetics of appearance of viral RNA in plasma were delayed in one cat compared to control cats. Levels of viral RNA in axillary lymph nodes, spleen and thymus were similar to those in control cats.
Location of Assay Data in ReferenceFigures 3 and 4