Selective inhibition of TGF-β1 produced by GARP-expressing Tregs overcomes resistance to PD-1/PD-L1 blockade in cancer

被引:112
作者
de Streel, Gregoire [1 ]
Bertrand, Charlotte [1 ]
Chalon, Nicolas [1 ]
Lienart, Stephanie [1 ]
Bricard, Orian [1 ]
Lecomte, Sara [1 ]
Devreux, Julien [1 ]
Gaignage, Melanie [1 ]
De Boeck, Gitte [2 ]
Marien, Lore [2 ]
Van de Walle, Inge [2 ]
van der Woning, Bas [2 ]
Saunders, Michael [2 ]
de Haard, Hans [2 ]
Vermeersch, Elien [3 ]
Maes, Wim [3 ]
Deckmyn, Hans [3 ]
Coulie, Pierre G. [1 ]
van Baren, Nicolas [1 ]
Lucas, Sophie [1 ]
机构
[1] Catholic Univ Louvain, de Duve Inst, B-1200 Brussels, Belgium
[2] Argenx, B-9052 Zwijnaarde, Belgium
[3] Katholieke Univ Leuven, IRF Life Sci, Lab Thrombosis Res, Campus Kulak Kortrijk, B-8500 Kortrijk, Belgium
基金
欧洲研究理事会;
关键词
REGULATORY T-CELLS; LATENT TGF-BETA; ANTITUMOR-ACTIVITY; PD-1; BLOCKADE; ANTIBODIES; GENE; RECEPTOR;
D O I
10.1038/s41467-020-17811-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
TGF-beta 1, beta 2 and beta 3 bind a common receptor to exert vastly diverse effects in cancer, supporting either tumor progression by favoring metastases and inhibiting anti-tumor immunity, or tumor suppression by inhibiting malignant cell proliferation. Global TGF-beta inhibition thus bears the risk of undesired tumor-promoting effects. We show that selective blockade of TGF-beta 1 production by Tregs with antibodies against GARP:TGF-beta 1 complexes induces regressions of mouse tumors otherwise resistant to anti-PD-1 immunotherapy. Effects of combined GARP:TGF-beta 1/PD-1 blockade are immune-mediated, do not require Fc gamma R-dependent functions and increase effector functions of anti-tumor CD8(+) T cells without augmenting immune cell infiltration or depleting Tregs within tumors. We find GARP-expressing Tregs and evidence that they produce TGF-beta 1 in one third of human melanoma metastases. Our results suggest that anti-GARP:TGF-beta 1 mAbs, by selectively blocking a single TGF-beta isoform emanating from a restricted cellular source exerting tumor-promoting activity, may overcome resistance to PD-1/PD-L1 blockade in patients with cancer.
引用
收藏
页数:15
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