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抗药物抗体的分子特征揭示了 TNFα 拮抗剂治疗后免疫反应的机制。

Molecular Landscape of Anti-Drug Antibodies Reveals the Mechanism of the Immune Response Following Treatment With TNFα Antagonists.

机构信息

George S. Wise Faculty of Life Sciences, School of Molecular Cell Biology and Biotechnology, Tel Aviv University, Tel Aviv-Yafo, Israel.

Gastroenterology Department, Sheba Medical Center and Sackler School of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.

出版信息

Front Immunol. 2019 Dec 18;10:2921. doi: 10.3389/fimmu.2019.02921. eCollection 2019.

Abstract

Drugs formulated from monoclonal antibodies (mAbs) are clinically effective in various diseases. Repeated administration of mAbs, however, elicits an immune response in the form of anti-drug-antibodies (ADA), thereby reducing the drug's efficacy. Notwithstanding their importance, the molecular landscape of ADA and the mechanisms involved in their formation are not fully understood. Using a newly developed quantitative bio-immunoassay, we found that ADA concentrations specific to TNFα antagonists can exceed extreme concentrations of 1 mg/ml with a wide range of neutralization capacity. Our data further suggest a preferential use of the λ light chain in a subset of neutralizing ADA. Moreover, we show that administration of TNFα antagonists result in a vaccine-like response whereby ADA formation is governed by the extrafollicular T cell-independent immune response. Our bio-immunoassay coupled with insights on the nature of the immune response can be leveraged to improve mAb immunogenicity assessment and facilitate improvement in therapeutic intervention strategies.

摘要

单克隆抗体(mAbs)制成的药物在各种疾病的临床治疗中具有显著疗效。然而,mAbs 的重复给药会引发抗药物抗体(ADA)的免疫反应,从而降低药物的疗效。尽管它们很重要,但 ADA 的分子特征及其形成机制尚不完全清楚。我们使用新开发的定量生物免疫测定法发现,针对 TNFα 拮抗剂的 ADA 浓度可以超过 1mg/ml 的极端浓度,并具有广泛的中和能力。我们的数据进一步表明,在一组中和 ADA 中,λ 轻链优先使用。此外,我们还表明,TNFα 拮抗剂的给药会导致类似于疫苗的反应,ADA 的形成受滤泡外 T 细胞非依赖性免疫反应的控制。我们的生物免疫测定法结合对免疫反应性质的了解,可以用于提高 mAb 的免疫原性评估,并促进治疗干预策略的改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a6a/6930160/215c78a699eb/fimmu-10-02921-g0001.jpg

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