6FIB

Structure of human 4-1BB ligand

6FIB の概要

• エントリーDOI: 10.2210/pdb6fib/pdb
• 分子名称: Tumor necrosis factor ligand superfamily member 9, Tumor necrosis factor ligand superfamily member 9,4-1BBL -CH/CL fusion, Tumor necrosis factor ligand superfamily member 9,Uncharacterized protein, ... (4 entities in total)
• 機能のキーワード: cytokine, signal anchor, tnf family
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 82496.89

構造登録者

Joseph, C.,Claus, C.,Ferrara, C.,von Hirschheydt, T.,Prince, C.,Funk, D.,Klein, C.,Benz, J. (登録日: 2018-01-17, 公開日: 2019-03-13, 最終更新日: 2024-01-17)

主引用文献

Claus, C.,Ferrara, C.,Xu, W.,Sam, J.,Lang, S.,Uhlenbrock, F.,Albrecht, R.,Herter, S.,Schlenker, R.,Husser, T.,Diggelmann, S.,Challier, J.,Mossner, E.,Hosse, R.J.,Hofer, T.,Brunker, P.,Joseph, C.,Benz, J.,Ringler, P.,Stahlberg, H.,Lauer, M.,Perro, M.,Chen, S.,Kuttel, C.,Bhavani Mohan, P.L.,Nicolini, V.,Birk, M.C.,Ongaro, A.,Prince, C.,Gianotti, R.,Dugan, G.,Whitlow, C.T.,Solingapuram Sai, K.K.,Caudell, D.L.,Burgos-Rodriguez, A.G.,Cline, J.M.,Hettich, M.,Ceppi, M.,Giusti, A.M.,Crameri, F.,Driessen, W.,Morcos, P.N.,Freimoser-Grundschober, A.,Levitsky, V.,Amann, M.,Grau-Richards, S.,von Hirschheydt, T.,Tournaviti, S.,Molhoj, M.,Fauti, T.,Heinzelmann-Schwarz, V.,Teichgraber, V.,Colombetti, S.,Bacac, M.,Zippelius, A.,Klein, C.,Umana, P.
Tumor-targeted 4-1BB agonists for combination with T cell bispecific antibodies as off-the-shelf therapy.
Sci Transl Med, 11:-, 2019

PubMed Abstract: Endogenous costimulatory molecules on T cells such as 4-1BB (CD137) can be leveraged for cancer immunotherapy. Systemic administration of agonistic anti-4-1BB antibodies, although effective preclinically, has not advanced to phase 3 trials because they have been hampered by both dependency on Fcγ receptor-mediated hyperclustering and hepatotoxicity. To overcome these issues, we engineered proteins simultaneously targeting 4-1BB and a tumor stroma or tumor antigen: FAP-4-1BBL (RG7826) and CD19-4-1BBL. In the presence of a T cell receptor signal, they provide potent T cell costimulation strictly dependent on tumor antigen-mediated hyperclustering without systemic activation by FcγR binding. We could show targeting of FAP-4-1BBL to FAP-expressing tumor stroma and lymph nodes in a colorectal cancer-bearing rhesus monkey. Combination of FAP-4-1BBL with tumor antigen-targeted T cell bispecific (TCB) molecules in human tumor samples led to increased IFN-γ and granzyme B secretion. Further, combination of FAP- or CD19-4-1BBL with CEA-TCB (RG7802) or CD20-TCB (RG6026), respectively, resulted in tumor remission in mouse models, accompanied by intratumoral accumulation of activated effector CD8 T cells. FAP- and CD19-4-1BBL thus represent an off-the-shelf combination immunotherapy without requiring genetic modification of effector cells for the treatment of solid and hematological malignancies.

PubMed: 31189721
DOI: 10.1126/scitranslmed.aav5989

実験手法

X-RAY DIFFRACTION (2.7 Å)