Nature reviews. Immunology, Journal Year: 2023, Volume and Issue: 24(5), P. 338 - 357
Published: Dec. 12, 2023
Language: Английский
Nature reviews. Immunology, Journal Year: 2023, Volume and Issue: 24(5), P. 338 - 357
Published: Dec. 12, 2023
Language: Английский
Journal of Hepatology, Journal Year: 2022, Volume and Issue: 77(4), P. 1136 - 1160
Published: June 22, 2022
Language: Английский
Citations
303Cellular and Molecular Immunology, Journal Year: 2023, Volume and Issue: 20(5), P. 432 - 447
Published: March 22, 2023
Abstract Dendritic cells (DCs) exhibit a specialized antigen-presenting function and play crucial roles in both innate adaptive immune responses. Due to their ability cross-present tumor cell-associated antigens naïve T cells, DCs are instrumental the generation of specific T-cell-mediated antitumor effector responses control growth cell dissemination. Within an immunosuppressive microenvironment, DC functions can, however, be severely impaired. In this review, we focus on mechanisms capture activation by role microenvironment shaping functions, taking advantage recent studies showing phenotype acquisition, transcriptional state functional programs revealed scRNA-seq analysis. The therapeutic potential DC-mediated antigen sensing priming immunity is also discussed.
Language: Английский
Citations
271Annual Review of Immunology, Journal Year: 2021, Volume and Issue: 39(1), P. 759 - 790
Published: March 12, 2021
As the professional antigen-presenting cells of immune system, dendritic (DCs) sense microenvironment and shape ensuing adaptive response. DCs can induce both activation tolerance according to peripheral cues. Recent work has established that comprise several phenotypically functionally heterogeneous subsets differentially regulate T lymphocyte differentiation. This review summarizes mouse human DC subset phenotypes, development, diversification, function. We focus on advances in our understanding how different distinct CD4+ helper (Th) cell differentiation outcomes, including Th1, Th2, Th17, follicular helper, regulatory cells. intrinsic properties, local tissue microenvironments, other together determine Th during homeostasis inflammation.
Language: Английский
Citations
264Nature Medicine, Journal Year: 2023, Volume and Issue: 29(6), P. 1389 - 1399
Published: June 1, 2023
Language: Английский
Citations
188Nature, Journal Year: 2022, Volume and Issue: 610(7933), P. 744 - 751
Published: Sept. 7, 2022
Language: Английский
Citations
181Nature, Journal Year: 2022, Volume and Issue: 606(7915), P. 776 - 784
Published: May 25, 2022
Language: Английский
Citations
176Nature, Journal Year: 2023, Volume and Issue: 618(7967), P. 1033 - 1040
Published: June 14, 2023
Most clinically applied cancer immunotherapies rely on the ability of CD8
Language: Английский
Citations
160Nature Medicine, Journal Year: 2021, Volume and Issue: 27(6), P. 1043 - 1054
Published: May 20, 2021
Language: Английский
Citations
145Nature Reviews Clinical Oncology, Journal Year: 2023, Volume and Issue: 20(11), P. 739 - 754
Published: Aug. 16, 2023
Language: Английский
Citations
134Nature, Journal Year: 2023, Volume and Issue: 620(7972), P. 200 - 208
Published: July 5, 2023
Abstract Cancer cells evade T cell-mediated killing through tumour–immune interactions whose mechanisms are not well understood 1,2 . Dendritic (DCs), especially type-1 conventional DCs (cDC1s), mediate cell priming and therapeutic efficacy against tumours 3 DC functions orchestrated by pattern recognition receptors 3–5 , although other signals involved remain incompletely defined. Nutrients emerging mediators of adaptive immunity 6–8 but whether nutrients affect function or communication between innate immune is largely unresolved. Here we establish glutamine as an intercellular metabolic checkpoint that dictates tumour–cDC1 crosstalk licenses cDC1 in activating cytotoxic cells. Intratumoral supplementation inhibits tumour growth augmenting cDC1-mediated CD8 + immunity, overcomes resistance to blockade immunotherapies. Mechanistically, cDC1s compete for uptake via the transporter SLC38A2 tune anti-tumour immunity. Nutrient screening integrative analyses show dominant amino acid promoting function. Further, signalling FLCN impinges on TFEB Loss selectively impairs vivo a TFEB-dependent manner phenocopies deficiency eliminating effect supplementation. Our findings glutamine-mediated underpins evasion, reveal acquisition limiting events activation putative targets cancer treatment.
Language: Английский
Citations
124