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RUBY® - 一种具有优异功能性和 IgG 样稳定性、药理学和可开发性的四价(2+2)双特异性抗体形式。

RUBY® - a tetravalent (2+2) bispecific antibody format with excellent functionality and IgG-like stability, pharmacology and developability properties.

机构信息

Alligator Bioscience AB, Medicon Village, Lund, Sweden.

Faculty of Health and Society, Malmö University, Malmö, Sweden.

出版信息

MAbs. 2024 Jan-Dec;16(1):2330113. doi: 10.1080/19420862.2024.2330113. Epub 2024 Mar 25.

DOI:10.1080/19420862.2024.2330113
PMID:38527972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10965115/
Abstract

Despite the large number of existing bispecific antibody (bsAb) formats, the generation of novel bsAbs is still associated with development and bioprocessing challenges. Here, we present RUBY, a novel bispecific antibody format that allows rapid generation of bsAbs that fulfill key development criteria. The RUBY format has a 2 + 2 geometry, where two Fab fragments are linked via their light chains to the C-termini of an IgG, and carries mutations for optimal chain pairing. The unique design enables generation of bsAbs with mAb-like attributes. Our data demonstrate that RUBY bsAbs are compatible with small-scale production systems for screening purposes and can be produced at high yields (>3 g/L) from stable cell lines. The bsAbs produced are shown to, in general, contain low amounts of aggregates and display favorable solubility and stress endurance profiles. Further, compatibility with various IgG isotypes is shown and tailored Fc gamma receptor binding confirmed. Also, retained interaction with FcRn is demonstrated to translate into a pharmacokinetic profile in mice and non-human primates that is comparable to mAb controls. Functionality of conditional active RUBY bsAbs is confirmed in vitro. Anti-tumor effects in vivo have previously been demonstrated, and shown to be superior to a comparable mAb, and here it is further shown that RUBY bsAbs penetrate and localize to tumor tissue in vivo. In all, the RUBY format has attractive mAb-like attributes and offers the possibility to mitigate many of the development challenges linked to other bsAb formats, facilitating both high functionality and developability.

摘要

尽管已经存在大量的双特异性抗体(bsAb)形式,但新型 bsAb 的产生仍然与开发和生物加工挑战相关。在这里,我们提出了 RUBY,这是一种新型的双特异性抗体形式,可快速生成满足关键开发标准的 bsAb。RUBY 格式具有 2+2 几何形状,其中两个 Fab 片段通过其轻链连接到 IgG 的 C 末端,并携带优化链配对的突变。独特的设计使 bsAb 具有单抗样的属性。我们的数据表明,RUBY bsAb 与小规模生产系统兼容,可用于筛选目的,并且可以从稳定的细胞系中以高产量(>3g/L)生产。所产生的 bsAb 通常含有低量的聚集体,并显示出良好的溶解度和耐应激性。此外,还显示出与各种 IgG 同种型的兼容性,并证实了定制的 Fcγ受体结合。此外,保留与 FcRn 的相互作用被证明可转化为在小鼠和非人类灵长类动物中的药代动力学特征,与单抗对照相当。体外证实了条件活性 RUBY bsAb 的功能。先前已经证明了体内的抗肿瘤作用,并且优于可比的单抗,这里进一步表明 RUBY bsAb 能够穿透并在体内定位于肿瘤组织。总之,RUBY 格式具有吸引人的单抗样属性,并提供了减轻与其他 bsAb 形式相关的许多开发挑战的可能性,从而提高了功能和可开发性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/c78b76722ac3/KMAB_A_2330113_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/fa4fc46fe2e1/KMAB_A_2330113_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/d3a10762f39c/KMAB_A_2330113_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/8a98c113a192/KMAB_A_2330113_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/a7654b89af8b/KMAB_A_2330113_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/c78b76722ac3/KMAB_A_2330113_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/fa4fc46fe2e1/KMAB_A_2330113_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/d3a10762f39c/KMAB_A_2330113_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/8a98c113a192/KMAB_A_2330113_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/a7654b89af8b/KMAB_A_2330113_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59db/10965115/c78b76722ac3/KMAB_A_2330113_F0005_OC.jpg

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