Abstract
A specific antiviral cytotoxic immune response in vivo could be induced by the subcutaneous injection of the T-cell epitope of the lymphocytic choriomeningitis virus (LCMV) nucleoprotein as an unmodified free synthetic peptide (Arg-Pro-Gln-Ala-Ser-Gly-Val-Tyr-Met-Gly-Asn-Leu-Thr-Ala-Gln) emulsified in incomplete Freund's adjuvant. This immunization rendered mice into a LCMV-specific protective state as shown by the inhibition of LCMV replication in spleens of such mice. The protection level of these mice correlated with the ability to respond to the peptide challenge by CD8+ virus-specific cytotoxic T cells. This is a direct demonstration that peptide vaccines can be antivirally protective in vivo, thus encouraging further search for appropriate mixtures of stable peptides that may be used as T-cell vaccines.
MeSH Terms
Amino Acid Sequence
Animals
Lymphocytic Choriomeningitis/immunology,prevention & control
Lymphocytic choriomeningitis virus/drug effects,immunology,physiology
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Inbred ICR
Molecular Sequence Data
Nucleoproteins/immunology
Peptides/chemical synthesis,immunology
T-Lymphocytes, Cytotoxic/immunology
Vaccines, Synthetic/immunology
Viral Vaccines/immunology
Virus Replication/drug effects
Chemicals
Nucleoproteins
Peptides
Vaccines, Synthetic
Viral Vaccines
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schulz M
Institute of Pathology, University Hospital, Zürich, Switzerland.
Zinkernagel R M
Hengartner H
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