2021
DOI: 10.1016/j.vaccine.2021.01.047
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Recombinant lymphocytic choriomeningitis virus-based vaccine vector protects type I interferon receptor deficient mice from viral challenge

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Cited by 4 publications
(6 citation statements)
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“…are carried out in the cases of infectious outbreak. Reverse genetically engineered recombinant LCMV (rLCMV) is an important candidate for the development of vector-based vaccines [45]. Schmidt et al (2020) constructed a new vaccine TT1-E7E6 based on replicating attenuated LCMV [46].…”
Section: Lymphocytic Choriomeningitis Virus Infection-what Is Done An...mentioning
confidence: 99%
“…are carried out in the cases of infectious outbreak. Reverse genetically engineered recombinant LCMV (rLCMV) is an important candidate for the development of vector-based vaccines [45]. Schmidt et al (2020) constructed a new vaccine TT1-E7E6 based on replicating attenuated LCMV [46].…”
Section: Lymphocytic Choriomeningitis Virus Infection-what Is Done An...mentioning
confidence: 99%
“…Reverse genetically altered recombinant LCMV (rLCMV), in addition to serving as a significant research model in immunology, is a significant potential for the creation of vector-based vaccines. In immunosuppressed mice, who are deficient in a functioning type I IFN receptor, Krolik et al (2021) recently published the findings of a safety and effectiveness examination of a non-replicating rLCMV vector producing ovalbumin as a model antigen. When mice was immunised, this resulted in the development of multifunctional cytotoxic CD8+ T-cells and memory T-cells, which cleared the rLCMVovalbumin vector 7 days after vaccination (Krolik et al 2021).…”
Section: Vaccine Research In Lcmvmentioning
confidence: 99%
“…In immunosuppressed mice, who are deficient in a functioning type I IFN receptor, Krolik et al (2021) recently published the findings of a safety and effectiveness examination of a non-replicating rLCMV vector producing ovalbumin as a model antigen. When mice was immunised, this resulted in the development of multifunctional cytotoxic CD8+ T-cells and memory T-cells, which cleared the rLCMVovalbumin vector 7 days after vaccination (Krolik et al 2021). Non-replicating rLCMV-based vectors appear to be a good choice for vaccine development due to the rLCMV viral vector's outstanding safety profile and retained effectiveness in immunocompromised animals.…”
Section: Vaccine Research In Lcmvmentioning
confidence: 99%
“…In addition to an important role as a research model in immunology, reverse geneticallyengineered recombinant LCMV (rLCMV) is an important candidate in the development of vector-based vaccines. Krolik et al (2021) recently reported results of safety and efficacy analysis of a non-replicating rLCMV vector expressing ovalbumin as a model antigen in immunocompromised Ifnar−/− mice that lacks a functional type I IFN receptor. Immunization of Ifnar−/− mice induced differentiation of multifunctional cytotoxic CD8+ T-cells and memory T-cells, leading to the clearance of rLCMV-ovalbumin vector within 7 days post-vaccination [109].…”
Section: Lcmv In Vaccine Researchmentioning
confidence: 99%
“…Krolik et al (2021) recently reported results of safety and efficacy analysis of a non-replicating rLCMV vector expressing ovalbumin as a model antigen in immunocompromised Ifnar−/− mice that lacks a functional type I IFN receptor. Immunization of Ifnar−/− mice induced differentiation of multifunctional cytotoxic CD8+ T-cells and memory T-cells, leading to the clearance of rLCMV-ovalbumin vector within 7 days post-vaccination [109]. An excellent safety profile of the rLCMV viral vector derived from Clone 13 in combination with maintained efficacy in immunocompromised hosts suggest that non-replicating rLCMV-based vectors represent a promising candidate for vaccine development.…”
Section: Lcmv In Vaccine Researchmentioning
confidence: 99%