Interleukin‐33 is a Novel Immunosuppressor that Protects Cancer Cells from TIL Killing by a Macrophage‐Mediated Shedding Mechanism. Issue 21 (5th September 2021)
- Record Type:
- Journal Article
- Title:
- Interleukin‐33 is a Novel Immunosuppressor that Protects Cancer Cells from TIL Killing by a Macrophage‐Mediated Shedding Mechanism. Issue 21 (5th September 2021)
- Main Title:
- Interleukin‐33 is a Novel Immunosuppressor that Protects Cancer Cells from TIL Killing by a Macrophage‐Mediated Shedding Mechanism
- Authors:
- Wu, Jing
Chen, Ziqing
Wickström, Stina L.
Gao, Juan
He, Xingkang
Jing, Xu
Wu, Jieyu
Du, Qiqiao
Yang, Muyi
Chen, Yi
Zhang, Dingding
Yin, Xin
Guo, Ziheng
Jensen, Lasse
Yang, Yunlong
Tao, Wei
Lundqvist, Andreas
Kiessling, Rolf
Cao, Yihai - Abstract:
- Abstract: Recognition of specific antigens expressed in cancer cells is the initial process of cytolytic T cell‐mediated cancer killing. However, this process can be affected by other non‐cancerous cellular components in the tumor microenvironment. Here, it is shown that interleukin‐33 (IL‐33)‐activated macrophages protect melanoma cells from tumor‐infiltrating lymphocyte‐mediated killing. Mechanistically, IL‐33 markedly upregulates metalloprotease 9 (MMP‐9) expression in macrophages, which acts as a sheddase to trim NKG2D, an activating receptor expressed on the surface of natural killer (NK) cells, CD8+ T cells, subsets of CD4+ T cells, iNKT cells, and γδ T cells. Further, MMP‐9 also cleaves the MHC class I molecule, cell surface antigen‐presenting complex molecules, expressed in melanoma cells. Consequently, IL‐33‐induced macrophage MMP‐9 robustly mitigates the tumor killing‐effect by T cells. Genetic and pharmacological loss‐of‐function of MMP‐9 sheddase restore T cell‐mediated cancer killing. Together, these data provide compelling in vitro and in vivo evidence showing novel mechanisms underlying the IL‐33‐macrophage‐MMP‐9 axis‐mediated immune tolerance against cancer cells. Targeting each of these signaling components, including IL‐33 and MMP‐9 provides a new therapeutic paradigm for improving anticancer efficacy by immune therapy. Abstract : T cells execute specific killing effects on cancer cells through recognition of cell surface molecules expressed in both cells.Abstract: Recognition of specific antigens expressed in cancer cells is the initial process of cytolytic T cell‐mediated cancer killing. However, this process can be affected by other non‐cancerous cellular components in the tumor microenvironment. Here, it is shown that interleukin‐33 (IL‐33)‐activated macrophages protect melanoma cells from tumor‐infiltrating lymphocyte‐mediated killing. Mechanistically, IL‐33 markedly upregulates metalloprotease 9 (MMP‐9) expression in macrophages, which acts as a sheddase to trim NKG2D, an activating receptor expressed on the surface of natural killer (NK) cells, CD8+ T cells, subsets of CD4+ T cells, iNKT cells, and γδ T cells. Further, MMP‐9 also cleaves the MHC class I molecule, cell surface antigen‐presenting complex molecules, expressed in melanoma cells. Consequently, IL‐33‐induced macrophage MMP‐9 robustly mitigates the tumor killing‐effect by T cells. Genetic and pharmacological loss‐of‐function of MMP‐9 sheddase restore T cell‐mediated cancer killing. Together, these data provide compelling in vitro and in vivo evidence showing novel mechanisms underlying the IL‐33‐macrophage‐MMP‐9 axis‐mediated immune tolerance against cancer cells. Targeting each of these signaling components, including IL‐33 and MMP‐9 provides a new therapeutic paradigm for improving anticancer efficacy by immune therapy. Abstract : T cells execute specific killing effects on cancer cells through recognition of cell surface molecules expressed in both cells. This article shows that interleukin‐33‐stimulated macrophages produce MMP‐9 that eliminates cell surface molecules in immune cells and cancer cells. Through this mechanism, MMP‐9 debilitates the T cell‐medicated anticancer effects. … (more)
- Is Part Of:
- Advanced science. Volume 8:Issue 21(2021)
- Journal:
- Advanced science
- Issue:
- Volume 8:Issue 21(2021)
- Issue Display:
- Volume 8, Issue 21 (2021)
- Year:
- 2021
- Volume:
- 8
- Issue:
- 21
- Issue Sort Value:
- 2021-0008-0021-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-09-05
- Subjects:
- cancer cells -- cytolytic T cells -- interleukin‐33 -- metalloprotease -- T‐cell receptors
Science -- Periodicals
505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2198-3844 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/advs.202101029 ↗
- Languages:
- English
- ISSNs:
- 2198-3844
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26706.xml