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Up to One-Third of Antibody Drugs Are Nonspecific, Study Shows

Up to One-Third of Antibody Drugs Are Nonspecific, Study Shows

研究顯示,多達三分之一的抗體藥物不具備特異性。
PR Newswire ·  09/17 20:09

Integral Molecular's Membrane Proteome Array Reveals Pervasive Binding of Antibody-Based Drugs to Unintended Targets

Integral Molecular的膜蛋白組陣列揭示了抗體藥物對非預期靶點的普遍結合

PHILADELPHIA, Sept. 17, 2024 /PRNewswire/ -- Integral Molecular, a leader in antibody discovery and characterization, has published new research in the journal mAbs, revealing that as many as one-third of antibody-based drugs exhibit nonspecific binding to unintended targets. A serious concern, off-target drug binding is a significant cause of adverse events in patients, with the potential to even cause death. Analysis of antibody off-target binding across different phases of clinical development suggests this to be a major cause of drug attrition. Early specificity testing could improve drug approvals and patient safety.

費城,2024年9月17日/ PRNewswire/-- Integral Molecular,一家抗體發現和特性研究領域的領先公司,已在期刊mAbs上發表新研究,揭示多達三分之一的抗體藥物在非特異性靶點上表現出結合。作爲一種嚴重的擔憂,離靶藥物結合是導致患者不良事件的重要原因,甚至可能導致死亡。對臨床開發不同階段的抗體離靶結合進行分析表明,這是藥物流失的主要原因之一。早期特異性測試可以改善藥物批准和患者安全性。

An Integral Molecular scientist screens antibody drugs for specificity using the Membrane Proteome Array, a high-throughput, cell-based, protein array technology.
Integral Molecular的科學家使用膜蛋白組陣列進行抗體藥物特異性篩選,這是一種高通量、基於細胞的蛋白質陣列技術。

Learn how antibody developers can use the Membrane Proteome Array to assess specificity and de-risk drug development

了解抗體開發人員如何使用膜蛋白組陣列來評估特異性並降低藥物開發的風險。

In this study, Norden et al. present the first empirical assessment of antibody specificity, quantifying the prevalence of off-target binding across the drug pipeline. They accomplished this through retrospective specificity analyses of leading antibody candidates from biopharmaceutical companies and a prospective study of clinically administered antibody drugs (including those that are given to patients in advanced clinical trials, FDA-approved, or withdrawn). The molecules were tested using the Membrane Proteome Array (MPA), a cell-based protein array representing the human membrane proteome, that was developed to test specificity and improve drug safety.

在這項研究中,Norden等人首次對抗體特異性進行了經驗評估,量化了藥物流程中離靶結合的普遍性。他們通過對生物製藥公司領先的抗體候選藥物進行回顧性特異性分析,以及對臨床給藥的抗體藥物進行前瞻性研究(包括那些在高級臨床試驗中給患者使用、FDA批准或撤回的藥物)。這些分子使用膜蛋白組陣列(MPA)進行測試,MPA是一種代表人類膜蛋白質組的基於細胞的蛋白質陣列,旨在測試特異性並提高藥物安全性。

Key Findings (Norden et al., mAbs)

主要發現(Norden et al., mAbs)

  • 18% of the 83 clinically administered antibody drugs tested showed off-target interactions.
  • 22% of the antibody drugs withdrawn from the market, often due to safety issues, showed nonspecific binding.
  • 33% of the 254 lead molecules tested showed nonspecific binding, a predictor of failure in future stages of development.
  • 83種臨床給藥的抗體藥物中有18%顯示出離靶相互作用。
  • 從市場上撤回的抗體藥物中,22%顯示出非特異性結合,通常是由於安全問題。
  • 經過測試的254個鉛分子中,有33%顯示出非特異性結合,這是未來研發階段失敗的預測指標。

These findings challenge the long-held belief in the absolute specificity of antibodies and underscore the critical need for more rigorous testing.

這些發現挑戰了長期以來對抗體絕對特異性的信念,並強調了對更嚴格測試的重要性。

"Nonspecific drug binding can lead to adverse events or even death," said Diana Norden, PhD, lead study author. "The presumption that every antibody confers absolute specificity is simply not accurate. New technologies like the MPA provide a detailed assessment of antibody specificity and can significantly de-risk drug development."

「非特異性藥物結合可能導致不良事件甚至死亡,」首席研究作者戴安娜·諾登博士說。「假設每個抗體都具有絕對特異性是不準確的。新技術如MPA能夠詳細評估抗體的特異性,並且能夠顯著降低藥物開發的風險。」

About the Membrane Proteome Array

關於膜蛋白組學陣列

Integral Molecular's Membrane Proteome Array is the industry-leading technology for antibody specificity testing used by hundreds of customers worldwide. The MPA assesses binding across ~6,000 proteins, representing the full human membrane proteome. Each protein within the array is individually presented in its biological conformation. MPA processes are ISO 9001 certified, and its specificity data has been accepted by regulatory bodies globally, including the FDA. The MPA is currently under review by the FDA for qualification as an accepted Drug Development Tool.

Integral Molecular的膜蛋白組學陣列是全球數百家客戶使用的抗體特異性測試領先技術。MPA評估約6,000種蛋白質的結合,代表完整的人類膜蛋白組學。陣列中的每個蛋白質都以其生物構象單獨呈現。MPA進程通過ISO 9001認證,並且其特異性數據已被全球監管機構(包括FDA)接受。MPA目前正在接受FDA審核,以獲得作爲可接受的藥物開發工具的資格。

About Integral Molecular

關於Integral Molecular

Integral Molecular (integralmolecular.com) is the industry leader in creating and commercializing transformative technologies that advance the discovery of therapeutics against difficult protein targets. With 20+ years of experience focused on membrane proteins, viruses, and antibodies, Integral Molecular's technologies have been integrated into the drug discovery pipelines of over 600 biotech and pharmaceutical companies to help discover new therapies for cancer, diabetes, autoimmune disorders, and viral threats such as SARS-CoV-2, Ebola, Zika, and dengue viruses.

Integral Molecular(integralmolecular.com)是在攻克難以治療的蛋白靶標方面創建和商業化變革性技術的行業領導者。憑藉20多年的膜蛋白質、病毒和抗體研究經驗,Integral Molecular的技術已經被超過600家生物技術和製藥公司整合到藥物發現流程中,以幫助發現治療癌症、糖尿病、自身免疫性疾病以及SARS-CoV-2、埃博拉、寨卡和登革病毒等病毒威脅的新療法。

Follow Integral Molecular on LinkedIn

在LinkedIn上關注Integral Molecular

Press Contact
Integral Molecular, Inc.
Soma Banik, PhD, Director of Public Relations
215-966-6061
[email protected]

新聞媒體聯繫人:
Integral Molecular, Inc.
Soma Banik, 博士, 公共關係董事
215-966-6061
[email protected]

SOURCE Integral Molecular

資訊來源:Integral Molecular

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