Griffiths Owen R, Landon John, Morris R Keith, James Philip E, Adams Rachel A
Micropharm Ltd, Carmarthenshire, United Kingdom; Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom.
Micropharm Ltd, Carmarthenshire, United Kingdom.
Adv Protein Chem Struct Biol. 2022;129:189-213. doi: 10.1016/bs.apcsb.2021.11.009. Epub 2022 Feb 16.
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.
使用多克隆抗体的被动免疫疗法在预防和治疗抗原性及致病性疾病中发挥着重要作用。多克隆抗体用于治疗、诊断和研究目的,佐剂用于增强针对低抗原性蛋白质或自身抗原的免疫反应。本研究旨在通过评估新型佐剂CoVaccine HT™与已确立的弗氏佐剂相比,在产生针对促炎细胞因子人重组肿瘤坏死因子α(TNF-α)的绵羊多克隆抗体方面,优化当前的免疫方法。
对去势的雄性阿伯菲尔德杂交绵羊用CoVaccine HT™或弗氏佐剂中的TNF-α进行免疫。体外测定TNF-α抗体的结合效价和中和效价,以及通过简单的小规模亲和层析洗脱实验测定抗体结合强度。通过定期检查免疫部位反应监测动物福利,并根据反应大小进行分级。研究的第二部分观察了每4周或8周单独使用弗氏佐剂进行再免疫的情况。
弗氏佐剂产生的抗体结合效价比CoVaccine HT™显著更高,但在中和TNF-α方面效果较差,而TNF-α是功能效力的更好指标。CoVaccine HT™引起的免疫部位反应也较少,而抗体结合强度未观察到统计学差异。每4周和8周进行再免疫未显示统计学差异。
本研究提供的证据表明,在产生抗TNF-α抗体方面,CoVaccine HT™优于弗氏佐剂,并支持将这种替代佐剂用于临床和实验用途。通过本研究获得的结果适用于人和兽医学中产生多克隆抗体的被动和主动免疫疗法。