2022
DOI: 10.1016/j.cytogfr.2022.10.001
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Development of mRNA vaccines against respiratory syncytial virus (RSV)

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Cited by 39 publications
(31 citation statements)
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“…However, in contrast to preclinical testing in mice, in which potent CD4 + and CD8 + T cell responses were identified, 198 administration of mRNA‐1777 led to a cellular response predominated by the CD4 + T cell subset 197 . Further engineering and codon optimization has been undertaken to increase translation and improve immunogenicity resulting in an mRNA‐1345 vaccine candidate 199 . In phase 1 clinical trials, it has been tested in adults aged 18–75, demonstrating a good safety profile after single‐dose administration and leading to the generation of high titers of neutralizing antibodies for A and B type of RSV.…”
Section: Clinical Progress Of Mrna Candidates Beyond Covid‐19mentioning
confidence: 99%
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“…However, in contrast to preclinical testing in mice, in which potent CD4 + and CD8 + T cell responses were identified, 198 administration of mRNA‐1777 led to a cellular response predominated by the CD4 + T cell subset 197 . Further engineering and codon optimization has been undertaken to increase translation and improve immunogenicity resulting in an mRNA‐1345 vaccine candidate 199 . In phase 1 clinical trials, it has been tested in adults aged 18–75, demonstrating a good safety profile after single‐dose administration and leading to the generation of high titers of neutralizing antibodies for A and B type of RSV.…”
Section: Clinical Progress Of Mrna Candidates Beyond Covid‐19mentioning
confidence: 99%
“…In phase 1 clinical trials, it has been tested in adults aged 18–75, demonstrating a good safety profile after single‐dose administration and leading to the generation of high titers of neutralizing antibodies for A and B type of RSV. Compared to mRNA‐1777, approximately sevenfold higher antibody titers were observed 199 . Given these promising results, mRNA‐1345 was granted by the FDA a fast‐track designation that allowed it to enter the pivotal phase 2/3 clinical trial to establish the safety and efficacy of the mRNA‐1345 vaccine in adults ≥60 years 200 .…”
Section: Clinical Progress Of Mrna Candidates Beyond Covid‐19mentioning
confidence: 99%
“…Several RSV mRNA vaccines encoding the RSV stabilized prefusion F protein are in clinical trials among children and adults (Table 3) [52]. The mRNA-1777 vaccine was tested in adults aged 18–49 and 60–79 years at varying i.m.…”
Section: Mrna Vaccines Against Respiratory Syncytial Virusmentioning
confidence: 99%
“…Respiratory syncytial virus (RSV) is a nonsegmented, negative strand RNA virus that has caused severe lower respiratory tract infections of high mortality rates in infants and the elderly. 1,2 In recent years, the outbreak of RSV infection in China, Europe and the United States has brought serious burden to society. [3][4][5] Currently, there are approved RSV monoclonal antibodies designed for infants and children up to 2 years of age, 6 as well as two vaccines developed for older adults.…”
Section: Introductionmentioning
confidence: 99%