2022
DOI: 10.1007/978-3-031-08415-7_16
|View full text |Cite
|
Sign up to set email alerts
|

Delivery Vehicles for Self-amplifying RNA

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2022
2022
2025
2025

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(5 citation statements)
references
References 62 publications
0
5
0
Order By: Relevance
“…This method of vaccination provides a gateway to present complex antigenic composition to the immune system that may include T- and B-cell epitopes [ 22 , 72 ]. For testing the efficacy of these vaccines, several recombinant protein formats have been tested that are conceptually similar and undergo the introduction of HSV ORFs (complete or near complete), into bacterial or other vector systems [ 54 , 73 ].…”
Section: Resultsmentioning
confidence: 99%
“…This method of vaccination provides a gateway to present complex antigenic composition to the immune system that may include T- and B-cell epitopes [ 22 , 72 ]. For testing the efficacy of these vaccines, several recombinant protein formats have been tested that are conceptually similar and undergo the introduction of HSV ORFs (complete or near complete), into bacterial or other vector systems [ 54 , 73 ].…”
Section: Resultsmentioning
confidence: 99%
“…These RNAs based technology has already shown its targeted efficiency in various diseases in terms of high specificity, efficiency, low toxicity, and ease of formulation [83] , [84] . A diverse range of in silico experiments are in research annals for RNA-based inhibitor therapies against influenza virus infection, the need is to dictate these proposed candidates into clinical trials [85] , [86] .…”
Section: Modern Therapeutic Strategies Against Chronic and Seasonal I...mentioning
confidence: 99%
“…However, there are some issues associated with these immunologic preparations such as the need for long-term infusion and hospitalized supervision, high column dosages with the potential risk of excessive immune responses, and bloodborne pathogen development [ 54 , 79 ]. Similarly, they often make it impossible to apply other birth-associated vaccination drives such as against measles/mumps/rubella (MMR) vaccine or the smallpox vaccine [ 20 , 21 , 80 ]. Moreover, the issues of high cost and difficulty of manufacturing are also some issues challenges that need to be overcome for more profound immunoregulatory prophylaxis against RSV infection [ 20 , 21 ].…”
Section: Main Bodymentioning
confidence: 99%
“… Antiviral and Therapeutics Approach Candidates under Clinical Trials References 1. Viral cellular entity inhibitors Aptamers (nucleolin-binding agents) (G)-rich oligonucleotide (nucleolin inhibitor) [ 5 , 6 , 30 , 31 , 56 , 62 , 63 , 80 , 93 , 94 , 95 , 96 , 97 , 98 , 99 , 100 , 101 , 102 ] 2. Host virus fusion inhibitors GS-5806 (presatovir) VP-14637 (renamed to MDT-637and JNJ-2408068) ALX-0171 [ 9 , 11 , 23 , 29 , 48 , 70 , 100 , 103 , 104 , 105 , 106 , 107 ] 3.…”
Section: Main Bodymentioning
confidence: 99%