Development of an oral gut-targeted rabies virus-like particles (RVLPs) vaccine with mucosal immune adjuvant LTB via delivering of localized-release microparticles

Rabies, a fatal zoonotic infectious diseases caused by rabies virus (RABV) infection, still has a high incidence with no effective cure in many Asian countries, even though numerous commercial vaccines have been administered for decades. One of the most important reasons is the neglected that main reservoirs of RABV, such as many stray and wild animals, are inaccessible for effective vaccination, especially in natural wilderness environments. In this study, we developed a highly effective gut-targeted oral rabies vaccine (ORV), which containing the immunoadjuvant LTB by targeted administration of microparticles with local release in the intestine. Based on the virus like particles (RVLPs) were assembled by RABV glycoprotein (RVGP) and matrix protein (RVMP), the enterically released microparticles ELPGA MPs loaded with RVLPs and djuvant LTB (RVLPs + LTB/EPLGA MPs) were prepared and demonstrated the ability of intestinal targeting which released in a pH-dependent manner. Subsequently, <i>in vivo</i> immunoassay experiments showed that the levels of anti-RVLPs IgG, IFN-γ and IL-4 were significantly higher in the RVLPs + LTB/EPLGA MPs groups than in the normal saline group or positive control group (R group) after intragastric administration. Moreover, higher levels of CD4+/CD8+ T cells ratios in the peripheral blood and sIgA in the intestines and feces of mice indicated that RVLPs + LTB/EPLGA MPs group elicited a stronger cellular immune response and mucosal immunity. In short, the novel oral vaccine is exploring valuable strategies of oral gut-targeted vaccines and promising to effectively prevent the spread of RABV among terrestrial carnivorous animals and human populations.

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Publication Details

Journal
Emerging Microbes & Infections
Published
2025-06-06
DOI
https://doi.org/10.1080/22221751.2025.2515406
Citations
6
Primary Topic
Rabies epidemiology and control
Type
article
Field-Weighted Citation Impact
6.22

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article

Development of an oral gut-targeted rabies virus-like particles (RVLPs) vaccine with mucosal immune adjuvant LTB via delivering of localized-release microparticles

Jinping Niu, Zhangting Zhao, Wenyun Zheng, Shipo Li et al.
6 citations
Emerging Microbes & Infections
Rabies epidemiology and control
6.22
article

Development of an oral gut-targeted rabies virus-like particles (RVLPs) vaccine with mucosal immune adjuvant LTB via delivering of localized-release microparticles

Jinping Niu, Zhangting Zhao, Wenyun Zheng, Shipo Li, Linfeng Li, Tong Zhang, Qingwei Liu, Haipeng Liu, Xingyuan Ma, Hao Jia, Feng Yang, Liyao Huang, Seung Hun Yu
article en
6 citations

Abstract

Rabies, a fatal zoonotic infectious diseases caused by rabies virus (RABV) infection, still has a high incidence with no effective cure in many Asian countries, even though numerous commercial vaccines have been administered for decades. One of the most important reasons is the neglected that main reservoirs of RABV, such as many stray and wild animals, are inaccessible for effective vaccination, especially in natural wilderness environments. In this study, we developed a highly effective gut-targeted oral rabies vaccine (ORV), which containing the immunoadjuvant LTB by targeted administration of microparticles with local release in the intestine. Based on the virus like particles (RVLPs) were assembled by RABV glycoprotein (RVGP) and matrix protein (RVMP), the enterically released microparticles ELPGA MPs loaded with RVLPs and djuvant LTB (RVLPs + LTB/EPLGA MPs) were prepared and demonstrated the ability of intestinal targeting which released in a pH-dependent manner. Subsequently, <i>in vivo</i> immunoassay experiments showed that the levels of anti-RVLPs IgG, IFN-γ and IL-4 were significantly higher in the RVLPs + LTB/EPLGA MPs groups than in the normal saline group or positive control group (R group) after intragastric administration. Moreover, higher levels of CD4+/CD8+ T cells ratios in the peripheral blood and sIgA in the intestines and feces of mice indicated that RVLPs + LTB/EPLGA MPs group elicited a stronger cellular immune response and mucosal immunity. In short, the novel oral vaccine is exploring valuable strategies of oral gut-targeted vaccines and promising to effectively prevent the spread of RABV among terrestrial carnivorous animals and human populations.

Emerging Microbes & InfectionsVol. 14(1)
East China University of Science and Technology (CN), Shanghai Jiao Tong University (CN), Xiamen University (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 4%
Rabies epidemiology and control
6.22
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