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一种选择性抑制膜CD73的新型抗CD73抗体具有抗肿瘤活性并诱导肿瘤免疫逃逸。

A Novel Anti-CD73 Antibody That Selectively Inhibits Membrane CD73 Shows Antitumor Activity and Induces Tumor Immune Escape.

作者信息

Kellner Markus, von Neubeck Bettina, Czogalla Bastian, Feederle Regina, Vick Binje, Jeremias Irmela, Zeidler Reinhard

机构信息

Research Group Therapeutic Antibodies, Helmholtz Zentrum München German Research Center for Environmental Health, Feodor-Lynen-Str. 21, 81377 Munich, Germany.

Department of Obstetrics and Gynecology, University Hospital, Ludwig Maximilian Universität, 81377 Munich, Germany.

出版信息

Biomedicines. 2022 Mar 31;10(4):825. doi: 10.3390/biomedicines10040825.

Abstract

CD73 catalyzes the conversion of ATP to adenosine, which is involved in various physiological and pathological processes, including tumor immune escape. Because CD73 expression and activity are particularly high on cancer cells and contribute to the immunosuppressive properties of the tumor environment, it is considered an attractive target molecule for specific cancer therapies. In line, several studies demonstrated that CD73 inhibition has a significant antitumor effect. However, complete blocking of CD73 activity can evoke autoimmune phenomena and adverse side effects. We developed a CD73-specific antibody, 22E6, that specifically inhibits the enzymatic activity of membrane-tethered CD73 present in high concentrations on cancer cells and cancer cell-derived extracellular vesicles but has no inhibitory effect on soluble CD73. Inhibition of CD73 on tumor cells with 22E6 resulted in multiple effects on tumor cells in vitro, including increased apoptosis and interference with chemoresistance. Intriguingly, in a xenograft mouse model of acute lymphocytic leukemia (ALL), 22E6 treatment resulted in an initial tumor growth delay in some animals, followed by a complete loss of CD73 expression on ALL cells in all 22E6 treated animals, indicating tumor immune escape. Taken together, 22E6 shows great potential for cancer therapy, favorably in combination with other drugs.

摘要

CD73催化ATP转化为腺苷,这一过程参与包括肿瘤免疫逃逸在内的各种生理和病理过程。由于CD73在癌细胞上的表达和活性特别高,并有助于肿瘤环境的免疫抑制特性,因此它被认为是特异性癌症治疗的一个有吸引力的靶分子。相应地,多项研究表明CD73抑制具有显著的抗肿瘤作用。然而,完全阻断CD73活性会引发自身免疫现象和不良副作用。我们开发了一种CD73特异性抗体22E6,它能特异性抑制癌细胞和癌细胞衍生的细胞外囊泡中高浓度存在的膜结合型CD73的酶活性,但对可溶性CD73没有抑制作用。用22E6抑制肿瘤细胞上的CD73在体外对肿瘤细胞产生了多种影响,包括增加细胞凋亡和干扰化疗耐药性。有趣的是,在急性淋巴细胞白血病(ALL)的异种移植小鼠模型中,22E6治疗在一些动物中导致了最初的肿瘤生长延迟,随后在所有接受22E6治疗的动物中ALL细胞上的CD73表达完全丧失,表明肿瘤免疫逃逸。综上所述,22E6在癌症治疗中显示出巨大潜力,与其他药物联合使用效果更佳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09ef/9031174/4e2ef5a88c2a/biomedicines-10-00825-g001.jpg

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