Plug and play virus-like particles for the generation of anti-toxin antibodies

Snakebite is a major global health concern, for which antivenom remains the only approved treatment to neutralise the harmful effects of the toxins. However, some medically important toxins are poorly immunogenic, resulting in reduced efficacy of the final product. Boosting the immunogenicity of these toxins in the commercial antivenom immunising mixtures could be an effective strategy to improve the final dose efficacy, and displaying snake antigens on Virus-like particles (VLPs) is one method for this. However, despite some applications in the field of snakebite, VLPs have yet to be explored in methods that could be practical at an antivenom manufacturing scale. Here we describe the utilisation of a "plug and play" VLP system to display immunogenic linear peptide epitopes from three finger toxins (3FTxs) and generate anti-toxin antibodies. Rabbits were immunised with VLPs displaying individual consensus linear epitopes and their antibody responses were characterised by immunoassay. Of the three experimental consensus sequences, two produced antibodies capable of recognising the consensus peptides, whilst only one of these could also recognise native whole toxins. Further characterisation of antibodies raised against this peptide demonstrated a sub-class specific response, and that these were able to elicit partially neutralising antibody responses, resulting in increased survival times in a murine snakebite envenoming model.

Authors

Institutions

Publication Details

Journal
Toxicon X
Published
2024-08-26
DOI
https://doi.org/10.1016/j.toxcx.2024.100204
Citations
3
Primary Topic
Venomous Animal Envenomation and Studies
Type
article
Field-Weighted Citation Impact
1.65

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Plug and play virus-like particles for the generation of anti-toxin antibodies

Amy E. Marriott, Mark C. Wilkinson, Julien Slagboom, Lloyd D. W. King et al.
3 citations
Toxicon X
Venomous Animal Envenomation and Studies
1.65
article

Plug and play virus-like particles for the generation of anti-toxin antibodies

Amy E. Marriott, Mark C. Wilkinson, Julien Slagboom, Lloyd D. W. King, Simon J. Draper, Choo Hock Tan, Rohit N. Patel, Kavi Ratanabanangkoon, Rebecca J. Edge, Stuart Ainsworth, Emma Stars
article en
3 citations

Abstract

Snakebite is a major global health concern, for which antivenom remains the only approved treatment to neutralise the harmful effects of the toxins. However, some medically important toxins are poorly immunogenic, resulting in reduced efficacy of the final product. Boosting the immunogenicity of these toxins in the commercial antivenom immunising mixtures could be an effective strategy to improve the final dose efficacy, and displaying snake antigens on Virus-like particles (VLPs) is one method for this. However, despite some applications in the field of snakebite, VLPs have yet to be explored in methods that could be practical at an antivenom manufacturing scale. Here we describe the utilisation of a "plug and play" VLP system to display immunogenic linear peptide epitopes from three finger toxins (3FTxs) and generate anti-toxin antibodies. Rabbits were immunised with VLPs displaying individual consensus linear epitopes and their antibody responses were characterised by immunoassay. Of the three experimental consensus sequences, two produced antibodies capable of recognising the consensus peptides, whilst only one of these could also recognise native whole toxins. Further characterisation of antibodies raised against this peptide demonstrated a sub-class specific response, and that these were able to elicit partially neutralising antibody responses, resulting in increased survival times in a murine snakebite envenoming model.

Toxicon XVol. 23
University of Liverpool (GB), Liverpool School of Tropical Medicine (GB), Mahidol University (TH), National Tsing Hua University (TW), University of Malaya (MY), University of Oxford (GB), Vrije Universiteit Amsterdam (NL)
UK Research and Innovation, University of Liverpool, National Centre for the Replacement, Refinement and Reduction of Animals in Research, National Centre for the Replacement Refinement and Reduction of Animals in Research, Medical Research Council
Openalex Percentile: Top 15%
Venomous Animal Envenomation and Studies
1.65
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.