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A Molecularly Cloned Schwarz Strain of Measles Virus Vaccine Induces Strong Immune Responses in Macaques and Transgenic Mice
- Source :
- Journal of Virology, Journal of Virology, 2003, 77 (21), pp.11546-11554. ⟨10.1128/jvi.77.21.11546-11554.2003⟩, Journal of Virology, American Society for Microbiology, 2003, 77 (21), pp.11546-11554. ⟨10.1128/jvi.77.21.11546-11554.2003⟩
- Publication Year :
- 2003
- Publisher :
- American Society for Microbiology, 2003.
-
Abstract
- Live attenuated RNA viruses make highly efficient vaccines. Among them, measles virus (MV) vaccine has been given to a very large number of children and has been shown to be highly efficacious and safe. Therefore, this vaccine might be a very promising vector to immunize children against both measles and other infectious agents, such as human immunodeficiency virus. A vector was previously derived from the Edmonston B strain of MV, a vaccine strain abandoned 25 years ago. Sequence analysis revealed that the genome of this vector diverges from Edmonston B by 10 amino acid substitutions not related to any Edmonston subgroup. Here we describe an infectious cDNA for the Schwarz/Moraten strain, a widely used MV vaccine. This cDNA was constructed from a batch of commercial vaccine. The extremities of the cDNA were engineered in order to maximize virus yield during rescue. A previously described helper cell-based rescue system was adapted by cocultivating transfected cells on primary chicken embryo fibroblasts, the cells used to produce the Schwarz/Moraten vaccine. After two passages the sequence of the rescued virus was identical to that of the cDNA and of the published Schwarz/Moraten sequence. Two additional transcription units were introduced in the cDNA for cloning foreign genetic material. The immunogenicity of rescued virus was studied in macaques and in mice transgenic for the CD46 MV receptor. Antibody titers and T-cell responses (ELISpot) in animals inoculated with low doses of rescued virus were identical to those obtained with commercial Schwarz MV vaccine. In contrast, the immunogenicity of the previously described Edmonston B strain-derived MV clone was much lower. This new molecular clone will allow for the production of MV vaccine without having to rely on seed stocks. The additional transcription units allow expressing heterologous antigens, thereby providing polyvalent vaccines based on an approved, safe, and efficient MV vaccine strain that is used worldwide.
- Subjects :
- DNA, Complementary
[SDV]Life Sciences [q-bio]
Measles Vaccine
Molecular Sequence Data
Immunology
Mice, Transgenic
Chick Embryo
Biology
Antibodies, Viral
Microbiology
Virus
Membrane Cofactor Protein
Measles virus
Mice
03 medical and health sciences
Antigen
Antigens, CD
Virology
Complementary DNA
Chlorocebus aethiops
Vaccines and Antiviral Agents
Animals
Humans
Amino Acid Sequence
Cloning, Molecular
Vero Cells
030304 developmental biology
Recombination, Genetic
0303 health sciences
Membrane Glycoproteins
Base Sequence
030306 microbiology
CD46
Immunogenicity
Sequence Analysis, DNA
biology.organism_classification
3. Good health
Insect Science
biology.protein
Macaca
Immunization
Measles vaccine
Antibody
Measles
Subjects
Details
- ISSN :
- 10985514 and 0022538X
- Volume :
- 77
- Database :
- OpenAIRE
- Journal :
- Journal of Virology
- Accession number :
- edsair.doi.dedup.....5b5b665deceee2e459470fec8e4e1a34