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混合IgE-IgG1抗体(IgEG):一种结合了IgE和IgG功能的新型抗体类别。

Hybrid IgE-IgG1 antibodies (IgEG): a new antibody class that combines IgE and IgG functionality.

作者信息

Grandits Melanie, Palhares Lais C G F, Macleod Olivia, Devlin John, Amin Oliver E, Birtley James, Partington Leanne, Wilson Tim, Hardaker Elizabeth, Karagiannis Sophia N, Bax Heather J, FitzGerald Kevin

机构信息

St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, UK.

Epsilogen Ltd, Waterfront, ARC West London, London, UK.

出版信息

MAbs. 2025 Dec;17(1):2502673. doi: 10.1080/19420862.2025.2502673. Epub 2025 May 16.

DOI:10.1080/19420862.2025.2502673
PMID:40377029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12087487/
Abstract

IgG-based anti-cancer therapies have achieved promising clinical outcomes, but, especially for patients with solid tumors, response rates vary. IgE antibodies promote distinct immune responses compared to IgG and have shown anti-tumoral pre-clinical activity and preliminary efficacy and safety profile in clinical testing. To improve potency further, we engineered a hybrid IgE-IgG1 antibody (IgEG), to combine the functions of both isotypes. Two IgEGs were generated with variable regions taken from trastuzumab (Tras IgEG) and from a novel anti-HER2 IgE (26 IgEG). Both IgEGs expressed well in mammalian cells and demonstrated IgE-like stability. IgEGs demonstrated both IgE and IgG1 functionality . A lack of type I hypersensitivity associated with IgEG incubation with human blood is suggestive of acceptable safety. , IgEGs exhibited distinct pharmacokinetic profiles and produced anti-tumoral efficacy comparable to IgE. These findings highlight the potential of IgEG as a new therapeutic modality in oncology.

摘要

基于IgG的抗癌疗法已取得了令人鼓舞的临床效果,但特别是对于实体瘤患者,缓解率各不相同。与IgG相比,IgE抗体可促进不同的免疫反应,并且在临床前试验中已显示出抗肿瘤活性,在临床试验中也展现出初步的疗效和安全性。为进一步提高效力,我们构建了一种杂合IgE-IgG1抗体(IgEG),以结合两种同种型的功能。通过取自曲妥珠单抗(Tras IgEG)和一种新型抗HER2 IgE(26 IgEG)的可变区,产生了两种IgEG。两种IgEG在哺乳动物细胞中均表达良好,并表现出类似IgE的稳定性。IgEG表现出IgE和IgG1的功能。与用人类血液孵育IgEG相关的I型超敏反应的缺乏表明其安全性是可接受的。此外,IgEG表现出独特的药代动力学特征,并产生了与IgE相当的抗肿瘤疗效。这些发现突出了IgEG作为肿瘤学新治疗方式的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/d6cf35553ea1/KMAB_A_2502673_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/9774c615f139/KMAB_A_2502673_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/953811e46347/KMAB_A_2502673_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/acbe8b7a55f6/KMAB_A_2502673_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/f6cdff1abb1d/KMAB_A_2502673_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/d6cf35553ea1/KMAB_A_2502673_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/9774c615f139/KMAB_A_2502673_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/953811e46347/KMAB_A_2502673_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/acbe8b7a55f6/KMAB_A_2502673_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/f6cdff1abb1d/KMAB_A_2502673_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b8/12087487/d6cf35553ea1/KMAB_A_2502673_F0005_OC.jpg

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Nat Commun. 2025 Apr 10;16(1):2903. doi: 10.1038/s41467-025-57870-y.
2
Fc-mediated immune stimulating, pro-inflammatory and antitumor effects of anti-HER2 IgE against HER2-expressing and trastuzumab-resistant tumors.抗HER2 IgE对HER2表达且对曲妥珠单抗耐药肿瘤的Fc介导免疫刺激、促炎和抗肿瘤作用。
J Immunother Cancer. 2025 Mar 12;13(3):e010945. doi: 10.1136/jitc-2024-010945.
3
An IgE antibody targeting HER2 identified by clonal selection restricts breast cancer growth via immune-stimulating activities.
通过克隆选择鉴定出的一种靶向HER2的IgE抗体通过免疫刺激活性限制乳腺癌生长。
J Exp Clin Cancer Res. 2025 Feb 12;44(1):49. doi: 10.1186/s13046-025-03319-5.
4
The Immunosuppressive Receptor CD32b Regulation of Macrophage Polarization and Its Implications in Tumor Progression.CD32b 免疫抑制受体对巨噬细胞极化的调节及其在肿瘤进展中的意义。
Int J Mol Sci. 2024 Sep 9;25(17):9737. doi: 10.3390/ijms25179737.
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Cancer therapy with antibodies.抗体癌症疗法。
Nat Rev Cancer. 2024 Jun;24(6):399-426. doi: 10.1038/s41568-024-00690-x. Epub 2024 May 13.
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NK cell exhaustion in the tumor microenvironment.肿瘤微环境中的 NK 细胞耗竭。
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