IL-10 dampens antitumor immunity and promotes liver metastasis via PD-L1 induction

被引:57
作者
Shiri, Ahmad Mustafa [1 ,2 ]
Zhang, Tao [1 ,2 ]
Bedke, Tanja [1 ,2 ]
Zazara, Dimitra E. [3 ,4 ]
Zhao, Lilan [5 ]
Luecke, Joeran [1 ,2 ,5 ]
Sabihi, Morsal [1 ,2 ]
Fazio, Antonella [1 ,2 ]
Zhang, Siwen [1 ,2 ]
Tauriello, Daniele V. F. [6 ]
Batlle, Eduard [7 ,8 ,9 ]
Steglich, Babett [1 ,2 ]
Kempski, Jan [1 ,2 ,10 ]
Agalioti, Theodora [5 ]
Nawrocki, Mikolaj [1 ,2 ]
Xu, Yang [5 ]
Riecken, Kristoffer [11 ]
Liebold, Imke [1 ,2 ,12 ]
Brockmann, Leonie [1 ,2 ]
Konczalla, Leonie [5 ]
Bosurgi, Lidia [1 ,2 ,12 ]
Mercanoglu, Baris [5 ]
Seeger, Philipp [5 ]
Kuesters, Natalie [5 ]
Lykoudis, Panagis M. [13 ,14 ]
Heumann, Asmus [5 ]
Arck, Petra C. [4 ]
Fehse, Boris [11 ]
Busch, Philipp [5 ]
Grotelueschen, Rainer [5 ]
Mann, Oliver [5 ]
Izbicki, Jakob R. [5 ]
Hackert, Thilo [5 ]
Flavell, Richard A. [15 ,16 ]
Gagliani, Nicola [1 ,2 ,5 ]
Giannou, Anastasios D. [1 ,2 ,5 ,17 ]
Huber, Samuel [1 ,2 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Ctr Internal Med, I Dept Med, Sect Mol Immunol & Gastroenterol, Martinistr 52, D-20246 Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Hamburg Ctr Translat Immunol HCTI, D-20246 Hamburg, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Dept Obstet & Fetal Med, Div Expt Feto Maternal Med, Hamburg, Germany
[4] Univ Childrens Hosp, Univ Med Ctr Hamburg Eppendorf, Hamburg, Germany
[5] Univ Med Ctr Hamburg Eppendorf, Dept Gen Visceral & Thorac Surg, D-20246 Hamburg, Germany
[6] Univ Med Ctr, Dept Med Oncol, Erasmus MC, Rotterdam, Netherlands
[7] Barcelona Inst Sci & Technol BIST, Inst Res Biomed IRB Barcelona, Barcelona, Spain
[8] Ctr Invest Biomed Red Canc CIBERONC, Barcelona, Spain
[9] Institucio Catalana Recerca & Estudis Avancats ICR, Barcelona, Spain
[10] Univ Med Ctr Hamburg Eppendorf, Mildred Scheel Canc Career Ctr HaTriCS4, D-20246 Hamburg, Germany
[11] Univ Med Ctr Hamburg Eppendorf, Res Dept Cell & Gene Therapy, Dept Stem Cell Transplantat, D-20246 Hamburg, Germany
[12] Bernard Nocht Inst Trop Med, Protozoa Immunol, D-20359 Hamburg, Germany
[13] Natl & Kapodistrian Univ Athens, Dept Surg 3, Athens, Greece
[14] UCL, Div Surg & Intervent Sci, London, England
[15] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[16] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[17] Univ Med Ctr Hamburg Eppendorf, Dept Gen Visceral & Thorac Surg, D-20246 Hamburg, Germany
基金
欧洲研究理事会;
关键词
liver metastasis; IL-10; PD-L1; immunotherapy; immune cells; TGF-BETA; T-CELLS; INTERLEUKIN-10;
D O I
10.1016/j.jhep.2023.12.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The liver is one of the organs most commonly affected by metastasis. The presence of liver metastases has been reported to be responsible for an immunosuppressive microenvironment and diminished immunotherapy efficacy. Herein, we aimed to investigate the role of IL -10 in liver metastasis and to determine how its modulation could affect the efficacy of immunotherapy in vivo. Methods: To induce spontaneous or forced liver metastasis in mice, murine cancer cells (MC38) or colon tumor organoids were injected into the cecum or the spleen, respectively. Mice with complete and cell type -specific deletion of IL -10 and IL -10 receptor alpha were used to identify the source and the target of IL -10 during metastasis formation. Programmed death ligand 1 (PD -L1) -deficient mice were used to test the role of this checkpoint. Flow cytometry was applied to characterize the regulation of PD -L1 by IL -10. Results: We found that Il10 -deficient mice and mice treated with IL -10 receptor alpha antibodies were protected against liver metastasis formation. Furthermore, by using IL -10 reporter mice, we demonstrated that Foxp3+ regulatory T cells (Tregs) were the major cellular source of IL -10 in liver metastatic sites. Accordingly, deletion of IL -10 in Tregs, but not in myeloid cells, led to reduced liver metastasis. Mechanistically, IL -10 acted on Tregs in an autocrine manner, thereby further amplifying IL -10 production. Furthermore, IL -10 acted on myeloid cells, i.e . monocytes, and induced the upregulation of the immune checkpoint protein PD -L1. Finally, the PD-L1/PD-1 axis attenuated CD8-dependent cytotoxicity against metastatic lesions. Conclusions: Treg-derived IL -10 upregulates PD -L1 expression in monocytes, which in turn reduces CD8+ T -cell infiltration and related antitumor immunity in the context of colorectal cancer -derived liver metastases. These findings provide the basis for future monitoring and targeting of IL -10 in colorectal cancer -derived liver metastases . (c) 2023 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:634 / 644
页数:12
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