An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease

Background: Respiratory syncytial virus (RSV) causes the most common type of severe lower respiratory tract infection worldwide, and the fusion (F) protein is a target for neutralizing antibodies and vaccine development. This study aimed to investigate the immunogenicity and efficacy of an mRNA-base...

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Main Authors: Jianglong Li, Haiyan Long, Shaoyi Chen, Zhendong Zhang, Shuang Li, Qi Liu, Jun Liu, Jiaru Cai, Liping Luo, Yucai Peng
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Vaccines
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Online Access:https://www.mdpi.com/2076-393X/13/1/52
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author Jianglong Li
Haiyan Long
Shaoyi Chen
Zhendong Zhang
Shuang Li
Qi Liu
Jun Liu
Jiaru Cai
Liping Luo
Yucai Peng
author_facet Jianglong Li
Haiyan Long
Shaoyi Chen
Zhendong Zhang
Shuang Li
Qi Liu
Jun Liu
Jiaru Cai
Liping Luo
Yucai Peng
author_sort Jianglong Li
collection DOAJ
description Background: Respiratory syncytial virus (RSV) causes the most common type of severe lower respiratory tract infection worldwide, and the fusion (F) protein is a target for neutralizing antibodies and vaccine development. This study aimed to investigate the immunogenicity and efficacy of an mRNA-based RSV vaccine with an F protein sequence. Methods: We designed an mRNA construct encoding a modified RSV F protein, which was further developed into an LNP-encapsulated mRNA vaccine (LVRNA007). LVRNA007 was administered to mice and cotton rats, followed by immunogenicity analysis and viral challenge studies. Protection of rodents from the viral infection was evaluated based on the presence of the virus in the lung and pathological examination of respiratory tissues. Results: LVRNA007 induced robust humoral and cellular immune responses in both mice and cotton rats, with neutralization antibody levels in the immunized animals maintained at high levels for over one year. Vaccination of LVRNA007 also protected the rodents from RSV challenge, judged by the much decreased virus titer and the pathological score in the lung tissue. In addition, no vaccine-enhanced disease (VED) phenomenon was observed with LVRNA007 vaccination. Conclusions: Based on the preclinical immunogenicity and efficacy data, LVRNA007 could be a potential promising vaccine for prophylaxis of RSV infection.
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issn 2076-393X
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spelling doaj-art-d099db11754a4cbdab92520222096c702025-01-24T13:51:47ZengMDPI AGVaccines2076-393X2025-01-011315210.3390/vaccines13010052An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory DiseaseJianglong Li0Haiyan Long1Shaoyi Chen2Zhendong Zhang3Shuang Li4Qi Liu5Jun Liu6Jiaru Cai7Liping Luo8Yucai Peng9Liverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaLiverna Therapeutics Inc., Zhuhai 519000, ChinaBackground: Respiratory syncytial virus (RSV) causes the most common type of severe lower respiratory tract infection worldwide, and the fusion (F) protein is a target for neutralizing antibodies and vaccine development. This study aimed to investigate the immunogenicity and efficacy of an mRNA-based RSV vaccine with an F protein sequence. Methods: We designed an mRNA construct encoding a modified RSV F protein, which was further developed into an LNP-encapsulated mRNA vaccine (LVRNA007). LVRNA007 was administered to mice and cotton rats, followed by immunogenicity analysis and viral challenge studies. Protection of rodents from the viral infection was evaluated based on the presence of the virus in the lung and pathological examination of respiratory tissues. Results: LVRNA007 induced robust humoral and cellular immune responses in both mice and cotton rats, with neutralization antibody levels in the immunized animals maintained at high levels for over one year. Vaccination of LVRNA007 also protected the rodents from RSV challenge, judged by the much decreased virus titer and the pathological score in the lung tissue. In addition, no vaccine-enhanced disease (VED) phenomenon was observed with LVRNA007 vaccination. Conclusions: Based on the preclinical immunogenicity and efficacy data, LVRNA007 could be a potential promising vaccine for prophylaxis of RSV infection.https://www.mdpi.com/2076-393X/13/1/52RSVmRNA vaccineF proteinLVRNA007viral challenge study
spellingShingle Jianglong Li
Haiyan Long
Shaoyi Chen
Zhendong Zhang
Shuang Li
Qi Liu
Jun Liu
Jiaru Cai
Liping Luo
Yucai Peng
An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
Vaccines
RSV
mRNA vaccine
F protein
LVRNA007
viral challenge study
title An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
title_full An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
title_fullStr An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
title_full_unstemmed An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
title_short An mRNA-Based Respiratory Syncytial Virus Vaccine Elicits Strong Neutralizing Antibody Responses and Protects Rodents Without Vaccine-Associated Enhanced Respiratory Disease
title_sort mrna based respiratory syncytial virus vaccine elicits strong neutralizing antibody responses and protects rodents without vaccine associated enhanced respiratory disease
topic RSV
mRNA vaccine
F protein
LVRNA007
viral challenge study
url https://www.mdpi.com/2076-393X/13/1/52
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