CoVaccine HT™ adjuvant is superior to Freund's in eliciting ovine polyclonal antibodies against human tumor necrosis factor-alpha.

Adjuvant Anti-TNF-α CoVaccine HT™ Freund's Hyperimmunized serum Immunization Ovine Polyclonal antibodies Tumor necrosis factor-alpha

Journal

Advances in protein chemistry and structural biology
ISSN: 1876-1631
Titre abrégé: Adv Protein Chem Struct Biol
Pays: Netherlands
ID NLM: 101497281

Informations de publication

Date de publication:
2022
Historique:
entrez: 20 3 2022
pubmed: 21 3 2022
medline: 3 5 2022
Statut: ppublish

Résumé

Passive immunotherapy using polyclonal antibodies plays an important role in preventing and treating antigenic and pathogenic diseases. Polyclonal antibodies are used for therapeutic, diagnostic and investigational purposes, with adjuvants employed to enhance the immune response against proteins that are poorly antigenic or self-antigens. This study aimed to optimize current immunization methods by evaluating the novel adjuvant CoVaccine HT™ against the established Freund's at producing ovine polyclonal antibodies against pro-inflammatory cytokine human recombinant tumor necrosis factor alpha (TNF-α). Castrated male Aberfield cross sheep were immunized with TNF-α in CoVaccine HT™ or Freund's adjuvant. The binding titer of antibodies for TNF-α and neutralization titer were determined in vitro, as well as the strength of antibody binding by a simple small scale affinity chromatography elution experiment. Animal welfare was monitored through inspection of immunization site reactions at regular time points and graded according to reaction size. The second part of the study looked at re-immunization using Freund's adjuvant alone every 4- or 8-weeks. Freund's generated significantly higher antibody binding titers than CoVaccine HT™ but were less effective at neutralizing TNF-alpha which is a better indicator of functional potency. CoVaccine HT™ also caused fewer immunization site reactions, while no statistical difference was observed in the binding strength of antibodies. Re-immunization every 4- and 8-weeks showed no statistical difference. This study provides evidence that CoVaccine HT™ is superior to Freund's adjuvant for the production of antibodies to TNF-α, and supports the use of this alternative adjuvant for clinical and experimental use. The outcomes gained through this study are applicable to passive and active immunotherapy for the generation of polyclonal antibodies in human and veterinary medicine.

Identifiants

pubmed: 35305719
pii: S1876-1623(21)00090-0
doi: 10.1016/bs.apcsb.2021.11.009
pii:
doi:

Substances chimiques

Adjuvants, Immunologic 0
Immunoglobulin G 0
Tumor Necrosis Factor-alpha 0
Freund's Adjuvant 9007-81-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-213

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Competing interests No competing interests to declare.

Auteurs

Owen R Griffiths (OR)

Micropharm Ltd, Carmarthenshire, United Kingdom; Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom. Electronic address: owen.rees.griffiths@outlook.com.

John Landon (J)

Micropharm Ltd, Carmarthenshire, United Kingdom.

R Keith Morris (RK)

Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom.

Philip E James (PE)

Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom.

Rachel A Adams (RA)

Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom.

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Classifications MeSH