An IgE antibody targeting HER2 identified by clonal selection restricts breast cancer growth via immune-stimulating activities.

IF 12.8 1区 医学 Q1 ONCOLOGY Journal of Experimental & Clinical Cancer Research Pub Date : 2025-02-12 DOI:10.1186/s13046-025-03319-5
Lais C G F Palhares, Melanie Grandits, Katie Stoker, Jitesh Chauhan, Heng Sheng Sow, Gilbert O Fruhwirth, Sophia Tsoka, James Birtley, Leanne Partington, Tim Wilson, Elizabeth Hardaker, Sophia N Karagiannis, Heather J Bax, Kevin FitzGerald
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Abstract

Background: Tumor-targeting IgE antibodies have elicited potent tumor-restricting effects by recruiting immune effector mechanisms. However, a dedicated platform for the generation, selection and evaluation of novel IgEs based on target antigen recognition and functional profiles has not been reported.

Methods: By establishing an IgE class antibody therapeutic design platform to allow selection of lead candidates, we generated a panel of IgEs recognising the human epidermal growth factor receptor 2 (HER2), overexpressed in 15-20% of breast cancers. From 1840 phage display-generated variable region sequences panned against HER2, we engineered 30 full length IgE antibodies. We selected three clones based on biophysical properties, reactivity to HER2 + cancer cells, epitope reactivity and Fc-mediated anti-tumor profiles in vitro. Clones with cross-reactivity to rat HER2 were selected to allow functional evaluations in a fully immunocompetent syngeneic HER2 + rat breast cancer model.

Results: IgE antibodies induced degranulation and antibody-dependent cellular cytotoxicity against human and rat HER2-expressing tumor cells in vitro. IgE antibody 26 demonstrated anti-tumor activity in a syngeneic HER2 + rat model, and a human HER2 + breast cancer xenograft model in mice reconstituted with human immune cells. Treatment was associated with enhanced immune cell infiltration and pro-inflammatory immune signatures, and downregulated cancer progression signaling pathways, in the tumor microenvironment.

Conclusions: This study pioneers the design and generation of anti-HER2 IgE lead antibody candidates with immune-stimulating and tumor-restricting effects. The present work may pave the way for antibody engineering therapeutic opportunities for challenging-to-treat HER2-expressing cancers.

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克隆选择鉴定的靶向HER2的IgE抗体通过免疫刺激活性限制乳腺癌的生长。
背景:肿瘤靶向IgE抗体通过募集免疫效应机制引发了强有力的肿瘤限制作用。然而,基于靶抗原识别和功能谱的新型IgEs的生成、选择和评估的专用平台尚未报道。方法:通过建立一个IgE类抗体治疗设计平台,允许选择主要候选物,我们生成了一组识别人表皮生长因子受体2 (HER2)的IgE, HER2在15-20%的乳腺癌中过表达。从1840个噬菌体展示产生的针对HER2的可变区序列中,我们设计了30个全长IgE抗体。我们根据生物物理特性、对HER2 +癌细胞的反应性、表位反应性和fc介导的体外抗肿瘤特性选择了三个克隆。选择对大鼠HER2具有交叉反应性的克隆,在完全免疫活性的同基因HER2 +大鼠乳腺癌模型中进行功能评估。结果:IgE抗体对体外表达her2的人和大鼠肿瘤细胞具有脱颗粒和抗体依赖的细胞毒性。IgE抗体26在同基因HER2 +大鼠模型中显示出抗肿瘤活性,在人免疫细胞重建的小鼠HER2 +乳腺癌异种移植模型中显示出抗肿瘤活性。在肿瘤微环境中,治疗与增强免疫细胞浸润和促炎免疫特征以及下调癌症进展信号通路相关。结论:本研究开创了具有免疫刺激和肿瘤限制作用的抗her2 IgE先导抗体候选物的设计和产生。目前的工作可能为抗体工程治疗挑战治疗表达her2的癌症铺平道路。
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来源期刊
CiteScore
18.20
自引率
1.80%
发文量
333
审稿时长
1 months
期刊介绍: The Journal of Experimental & Clinical Cancer Research is an esteemed peer-reviewed publication that focuses on cancer research, encompassing everything from fundamental discoveries to practical applications. We welcome submissions that showcase groundbreaking advancements in the field of cancer research, especially those that bridge the gap between laboratory findings and clinical implementation. Our goal is to foster a deeper understanding of cancer, improve prevention and detection strategies, facilitate accurate diagnosis, and enhance treatment options. We are particularly interested in manuscripts that shed light on the mechanisms behind the development and progression of cancer, including metastasis. Additionally, we encourage submissions that explore molecular alterations or biomarkers that can help predict the efficacy of different treatments or identify drug resistance. Translational research related to targeted therapies, personalized medicine, tumor immunotherapy, and innovative approaches applicable to clinical investigations are also of great interest to us. We provide a platform for the dissemination of large-scale molecular characterizations of human tumors and encourage researchers to share their insights, discoveries, and methodologies with the wider scientific community. By publishing high-quality research articles, reviews, and commentaries, the Journal of Experimental & Clinical Cancer Research strives to contribute to the continuous improvement of cancer care and make a meaningful impact on patients' lives.
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