Immunogenicity of HIV-1 Env-Gag VLP mRNA and Adenovirus Vector Vaccines in Mice

The results showed that the mRNA vaccines prime-adenovirus vector vaccines boost elicited higher cellular immune responses than those induced by homologous regimens at multiple time points, especially 8 weeks after the last immunization. Although the level of gp120 binding antibody in the combined immunization group is significantly lower than that of in the VLP mRNA vaccine group, a more balanced Th1/Th2 responses were induced in the combined immunization group, and significantly higher and longer-lasting neutralizing antibody levels were detected in this group making it a very promising HIV vaccine strategy.

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Publication Details

Journal
Vaccines
Published
2025-12-14
DOI
https://doi.org/10.3390/vaccines13121242
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
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article

Immunogenicity of HIV-1 Env-Gag VLP mRNA and Adenovirus Vector Vaccines in Mice

Hongxia Li, Yanzhe Hao, Xia Feng, Xiaoguang Zhang et al.
Vaccines
HIV Research and Treatment
article

Immunogenicity of HIV-1 Env-Gag VLP mRNA and Adenovirus Vector Vaccines in Mice

Hongxia Li, Yanzhe Hao, Xia Feng, Xiaoguang Zhang, Xiaozhou He, Qi Ma, Jing Yang
article en

Abstract

The results showed that the mRNA vaccines prime-adenovirus vector vaccines boost elicited higher cellular immune responses than those induced by homologous regimens at multiple time points, especially 8 weeks after the last immunization. Although the level of gp120 binding antibody in the combined immunization group is significantly lower than that of in the VLP mRNA vaccine group, a more balanced Th1/Th2 responses were induced in the combined immunization group, and significantly higher and longer-lasting neutralizing antibody levels were detected in this group making it a very promising HIV vaccine strategy.

VaccinesVol. 13(12)
National Institute for Viral Disease Control and Prevention (CN)
Openalex Percentile: Top 57%
HIV Research and Treatment
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