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6P4Y

Crystal Structure of anti-IL-7Ralpha 4A10 Fab

6P4Y の概要
エントリーDOI10.2210/pdb6p4y/pdb
分子名称4A10 Fab heavy chain, 4A10 Fab light chain (3 entities in total)
機能のキーワードantibody 4a10 fab fragment, protein polymer, immune system
由来する生物種Mus musculus (Mouse)
詳細
タンパク質・核酸の鎖数2
化学式量合計47966.46
構造登録者
Walsh, S.T.R.,Kashi, L.,Kohnhorst, C.L. (登録日: 2019-05-29, 公開日: 2019-09-04, 最終更新日: 2024-11-20)
主引用文献Hixon, J.A.,Andrews, C.,Kashi, L.,Kohnhorst, C.L.,Senkevitch, E.,Czarra, K.,Barata, J.T.,Li, W.,Schneider, J.P.,Walsh, S.T.R.,Durum, S.K.
New anti-IL-7R alpha monoclonal antibodies show efficacy against T cell acute lymphoblastic leukemia in pre-clinical models.
Leukemia, 34:35-49, 2020
Cited by
PubMed Abstract: Pediatric T cell acute lymphoblastic leukemia (T-ALL) cells frequently contain mutations in the interleukin-7 (IL-7) receptor pathway or respond to IL-7 itself. To target the IL-7 receptor on T-ALL cells, murine monoclonal antibodies (MAbs) were developed against the human IL-7Rα chain and chimerized with human IgG1 constant regions. Crystal structures demonstrate that the two MAbs bound different IL-7Rα epitopes. The MAbs mediated antibody-dependent cell-mediated cytotoxicity (ADCC) against patient-derived xenograft (PDX) T-ALL cells, which was improved by combining two MAbs. In vivo, the MAbs showed therapeutic efficacy via ADCC-dependent and independent mechanisms in minimal residual and established disease. PDX T-ALL cells that relapsed following a course of chemotherapy displayed elevated IL-7Rα, and MAb treatment is effective against relapsing disease, suggesting the use of anti-IL7Rα MAbs in relapsed T-ALL patients or patients that do not respond to chemotherapy.
PubMed: 31439943
DOI: 10.1038/s41375-019-0531-8
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.799 Å)
構造検証レポート
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件を2026-04-15に公開中

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