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-Structure paper
タイトル | Therapeutic antibody activation of the glucocorticoid-induced TNF receptor by a clustering mechanism. |
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ジャーナル・号・ページ | Sci Adv, Vol. 8, Issue 8, Page eabm4552, Year 2022 |
掲載日 | 2022年2月25日 |
著者 | Changhao He / Rachana R Maniyar / Yahel Avraham / Roberta Zappasodi / Radda Rusinova / Walter Newman / Heidi Heath / Jedd D Wolchok / Rony Dahan / Taha Merghoub / Joel R Meyerson / |
PubMed 要旨 | GITR is a TNF receptor, and its activation promotes immune responses and drives antitumor activity. The receptor is activated by the GITR ligand (GITRL), which is believed to cluster receptors into a ...GITR is a TNF receptor, and its activation promotes immune responses and drives antitumor activity. The receptor is activated by the GITR ligand (GITRL), which is believed to cluster receptors into a high-order array. Immunotherapeutic agonist antibodies also activate the receptor, but their mechanisms are not well characterized. We solved the structure of full-length mouse GITR bound to Fabs from the antibody DTA-1. The receptor is a dimer, and each subunit binds one Fab in an orientation suggesting that the antibody clusters receptors. Binding experiments with purified proteins show that DTA-1 IgG and GITRL both drive extensive clustering of GITR. Functional data reveal that DTA-1 and the anti-human GITR antibody TRX518 activate GITR in their IgG forms but not as Fabs. Thus, the divalent character of the IgG agonists confers an ability to mimic GITRL and cluster and activate GITR. These findings will inform the clinical development of this class of antibodies for immuno-oncology. |
リンク | Sci Adv / PubMed:35213218 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 4.4 Å |
構造データ | EMDB-24444, PDB-7rfp: |
由来 |
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キーワード | IMMUNE SYSTEM / Mouse glucocorticoid-induced tumor necrosis factor receptor / mGITR / TNF receptor / DTA-1 |