Dual targeting of cancer metabolome and stress antigens affects transcriptomic heterogeneity and efficacy of engineered T cells.


Journal

Nature immunology
ISSN: 1529-2916
Titre abrégé: Nat Immunol
Pays: United States
ID NLM: 100941354

Informations de publication

Date de publication:
27 Nov 2023
Historique:
received: 29 12 2022
accepted: 29 09 2023
medline: 28 11 2023
pubmed: 28 11 2023
entrez: 27 11 2023
Statut: aheadofprint

Résumé

Few cancers can be targeted efficiently by engineered T cell strategies. Here, we show that γδ T cell antigen receptor (γδ TCR)-mediated cancer metabolome targeting can be combined with targeting of cancer-associated stress antigens (such as NKG2D ligands or CD277) through the addition of chimeric co-receptors. This strategy overcomes suboptimal γ9δ2 TCR engagement of αβ T cells engineered to express a defined γδ TCR (TEGs) and improves serial killing, proliferation and persistence of TEGs. In vivo, the NKG2D-CD28

Identifiants

pubmed: 38012415
doi: 10.1038/s41590-023-01665-0
pii: 10.1038/s41590-023-01665-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature America, Inc.

Références

Sebestyen, Z. et al. RhoB mediates phosphoantigen recognition by V
pubmed: 27210746 pmcid: 5035041 doi: 10.1016/j.celrep.2016.04.081
Rigau, M. et al. Butyrophilin 2A1 is essential for phosphoantigen reactivity by γδ T cells. Science 367, eaay5516 (2020).
pubmed: 31919129 doi: 10.1126/science.aay5516
Karunakaran, M. M. et al. Butyrophilin-2A1 directly binds germline-encoded regions of the V
pubmed: 32155411 pmcid: 7083227 doi: 10.1016/j.immuni.2020.02.014
Mamedov, M. R. et al. CRISPR screens decode cancer cell pathways that trigger γδ T cell detection. Nature 621, 188–195 (2023).
pubmed: 37648854 doi: 10.1038/s41586-023-06482-x
Harly, C. et al. Key implication of CD277/butyrophilin-3 (BTN3A) in cellular stress sensing by a major human γδ T-cell subset. Blood 120, 2269–2279 (2012).
pubmed: 22767497 pmcid: 3679641 doi: 10.1182/blood-2012-05-430470
Hsiao, C. C. et al. Ligand-induced interactions between butyrophilin 2A1 and 3A1 internal domains in the HMBPP receptor complex. Cell Chem. Biol. 29, 985–995 (2022).
pubmed: 35081362 doi: 10.1016/j.chembiol.2022.01.004
Yuan, L. et al. Phosphoantigens glue butyrophilin 3A1 and 2A1 to activate V
pubmed: 37674084 pmcid: 10533412 doi: 10.1038/s41586-023-06525-3
Vyborova, A. et al. γ9δ2T cell diversity and the receptor interface with tumor cells. J. Clin. Invest. 130, 4637–4651 (2020).
pubmed: 32484803 pmcid: 7456241 doi: 10.1172/JCI132489
Gründer, C. et al. γ9 and δ2CDR3 domains regulate functional avidity of T cells harboring γ9δ2TCRs. Blood 120, 5153–5162 (2012).
pubmed: 23018643 doi: 10.1182/blood-2012-05-432427
Straetemans, T. et al. Untouched GMP-ready purified engineered immune cells to treat cancer. Clin. Cancer Res. 21, 3957–3968 (2015).
pubmed: 25991821 doi: 10.1158/1078-0432.CCR-14-2860
de Witte, M. et al. First in human clinical responses and persistence data on TEG001: a next generation of engineered αβ T cells targeting AML and MM with a high affinity γ9δ2TCR. Blood 140, 12737–12739 (2022).
doi: 10.1182/blood-2022-158191
Dekkers, J. F. et al. Uncovering the mode of action of engineered T cells in patient cancer organoids. Nat. Biotechnol. 41, 60–69 (2022).
pubmed: 35879361 pmcid: 9849137 doi: 10.1038/s41587-022-01397-w
Fuertes, M. B., Domaica, C. I. & Zwirner, N. W. Leveraging NKG2D ligands in immuno-oncology. Front. Immunol. 12, 713158 (2021).
pubmed: 34394116 pmcid: 8358801 doi: 10.3389/fimmu.2021.713158
Marcu-Malina, V. et al. Redirecting αβ T cells against cancer cells by transfer of a broadly tumor-reactive γδ T-cell receptor. Blood 118, 50–59 (2011).
pubmed: 21566093 doi: 10.1182/blood-2010-12-325993
Benyamine, A. et al. BTN3A is a prognosis marker and a promising target for V
pubmed: 29296524 pmcid: 5739572 doi: 10.1080/2162402X.2017.1372080
Palakodeti, A. et al. The molecular basis for modulation of human V
pubmed: 22846996 pmcid: 3463320 doi: 10.1074/jbc.M112.384354
De Gassart, A. et al. Development of ICT01, a first-in-class, anti-BTN3A antibody for activating V
pubmed: 34669444 doi: 10.1126/scitranslmed.abj0835
Mansilla-Soto, J. et al. HLA-independent T cell receptors for targeting tumors with low antigen density. Nat. Med. 28, 345–352 (2022).
pubmed: 35027758 pmcid: 9469647 doi: 10.1038/s41591-021-01621-1
Oda, S. K. et al. A Fas-4-1BB fusion protein converts a death to a pro-survival signal and enhances T cell therapy. J. Exp. Med. 217, e20191166 (2020).
pubmed: 32860705 pmcid: 7953733 doi: 10.1084/jem.20191166
Liu, X. et al. A chimeric switch-receptor targeting PD1 augments the efficacy of second-generation CAR T cells in advanced solid tumors. Cancer Res. 76, 1578–1590 (2016).
pubmed: 26979791 pmcid: 4800826 doi: 10.1158/0008-5472.CAN-15-2524
Melenhorst, J. J. et al. Decade-long leukaemia remissions with persistence of CD4
pubmed: 35110735 pmcid: 9166916 doi: 10.1038/s41586-021-04390-6
Anderson, N. D. et al. Transcriptional signatures associated with persisting CD19 CAR-T cells in children with leukemia. Nat. Med. 29, 1700–1709 (2023).
pubmed: 37407840 pmcid: 10353931 doi: 10.1038/s41591-023-02415-3
Xia, A. et al. T cell dysfunction in cancer immunity and immunotherapy. Front. Immunol. 10, 1719 (2019).
pubmed: 31379886 pmcid: 6659036 doi: 10.3389/fimmu.2019.01719
Vandenberghe, P. et al. Ligation of the CD5 or CD28 molecules on resting human T cells induces expression of the early activation antigen CD69 by a calcium- and tyrosine kinase-dependent mechanism. Immunology 78, 210–217 (1993).
pubmed: 7682535 pmcid: 1421815
Kunzmann, V. et al. Stimulation of γδ T cells by aminobisphosphonates and induction of antiplasma cell activity in multiple myeloma. Blood 96, 384–392 (2000).
pubmed: 10887096 doi: 10.1182/blood.V96.2.384.013k07_384_392
Weinkove, R. et al. Selecting costimulatory domains for chimeric antigen receptors: functional and clinical considerations. Clin. Transl. Immunol. 8, e1049 (2019).
doi: 10.1002/cti2.1049
Kuball, J. et al. Cooperation of human tumor-reactive CD4
pubmed: 15664164 doi: 10.1016/j.immuni.2004.12.005
Braham, M. V. J. et al. Cellular immunotherapy on primary multiple myeloma expanded in a 3D bone marrow niche model. Oncoimmunology 7, e1434465 (2018).
pubmed: 29872571 pmcid: 5980416 doi: 10.1080/2162402X.2018.1434465
Eagle, R. A., Jafferji, I. & Barrow, A. D. Beyond stressed self: evidence for NKG2D ligand expression on healthy cells. Curr. Immunol. Rev. 5, 22–34 (2009).
pubmed: 19626129 pmcid: 2713595 doi: 10.2174/157339509787314369
Majzner, R. G. & Mackall, C. L. Clinical lessons learned from the first leg of the CAR T cell journey. Nat. Med. 25, 1341–1355 (2019).
pubmed: 31501612 doi: 10.1038/s41591-019-0564-6
Kawalekar, O. U. et al. Distinct signaling of coreceptors regulates specific metabolism pathways and impacts memory development in CAR T cells. Immunity 44, 380–390 (2016).
pubmed: 26885860 doi: 10.1016/j.immuni.2016.01.021
Philipson, B. I. et al. 4-1BB costimulation promotes CAR T cell survival through noncanonical NF-κB signaling. Sci. Signal. 13, eaay8248 (2020).
pubmed: 32234960 pmcid: 7883633 doi: 10.1126/scisignal.aay8248
Payne, K. K. et al. BTN3A1 governs antitumor responses by coordinating αβ and γδ T cells. Science 369, 942–949 (2020).
pubmed: 32820120 pmcid: 7646930 doi: 10.1126/science.aay2767
Qi, C. et al. Claudin18.2-specific CAR T cells in gastrointestinal cancers: phase 1 trial interim results. Nat. Med. 28, 1189–1198 (2022).
pubmed: 35534566 pmcid: 9205778 doi: 10.1038/s41591-022-01800-8
Majzner, R. G. et al. GD2-CAR T cell therapy for H3K27M-mutated diffuse midline gliomas. Nature 603, 934–941 (2022).
pubmed: 35130560 pmcid: 8967714 doi: 10.1038/s41586-022-04489-4
Guerra, N. & Lanier, L. L. Emerging concepts on the NKG2D receptor–ligand axis in health and diseases. Front. Immunol. 11, 562 (2020).
pubmed: 32318064 pmcid: 7155425 doi: 10.3389/fimmu.2020.00562
Gumber, D. & Wang, L. D. Improving CAR-T immunotherapy: overcoming the challenges of T cell exhaustion. EBioMedicine 77, 103941 (2022).
pubmed: 35301179 pmcid: 8927848 doi: 10.1016/j.ebiom.2022.103941
Deng, Q. et al. Characteristics of anti-CD19 CAR T cell infusion products associated with efficacy and toxicity in patients with large B cell lymphomas. Nat. Med. 26, 1878–1887 (2020).
pubmed: 33020644 pmcid: 8446909 doi: 10.1038/s41591-020-1061-7
Fraietta, J. A. et al. Determinants of response and resistance to CD19 chimeric antigen receptor (CAR) T cell therapy of chronic lymphocytic leukemia. Nat. Med. 24, 563–571 (2018).
pubmed: 29713085 pmcid: 6117613 doi: 10.1038/s41591-018-0010-1
Scott, A. C. et al. TOX is a critical regulator of tumour-specific T cell differentiation. Nature 571, 270–274 (2019).
pubmed: 31207604 pmcid: 7698992 doi: 10.1038/s41586-019-1324-y
Philip, M. & Schietinger, A. CD8
pubmed: 34253904 doi: 10.1038/s41577-021-00574-3
Lim, W. A. & June, C. H. The principles of engineering immune cells to treat cancer. Cell 168, 724–740 (2017).
pubmed: 28187291 pmcid: 5553442 doi: 10.1016/j.cell.2017.01.016
Peng, W. et al. PD-1 blockade enhances T-cell migration to tumors by elevating IFN-γ inducible chemokines. Cancer Res. 72, 5209–5218 (2012).
pubmed: 22915761 pmcid: 3476734 doi: 10.1158/0008-5472.CAN-12-1187
Oh, D. Y. & Fong, L. Cytotoxic CD4
pubmed: 34910940 pmcid: 8809482 doi: 10.1016/j.immuni.2021.11.015
Hashimoto, K. et al. Single-cell transcriptomics reveals expansion of cytotoxic CD4 T cells in supercentenarians. Proc. Natl Acad. Sci. USA 116, 24242–24251 (2019).
pubmed: 31719197 pmcid: 6883788 doi: 10.1073/pnas.1907883116
Li, G. et al. 4-1BB enhancement of CAR T function requires NF-κB and TRAFs. JCI Insight 3, e121322 (2018).
pubmed: 30232281 pmcid: 6237232 doi: 10.1172/jci.insight.121322
Hirabayashi, K. et al. Dual targeting CAR-T cells with optimal costimulation and metabolic fitness enhance antitumor activity and prevent escape in solid tumors. Nat. Cancer 2, 904–918 (2021).
pubmed: 34746799 pmcid: 8570569 doi: 10.1038/s43018-021-00244-2
Chen, S. et al. Prognostic and therapeutic significance of BTN3A proteins in tumors. J. Cancer 12, 4505–4512 (2021).
pubmed: 34149914 pmcid: 8210570 doi: 10.7150/jca.57831
Liang, F. et al. Comprehensive analysis of BTN3A1 in cancers: mining of omics data and validation in patient samples and cellular models. FEBS Open Bio. 11, 2586–2599 (2021).
pubmed: 34293829 pmcid: 8409294 doi: 10.1002/2211-5463.13256
Abramson, J. S. et al. Lisocabtagene maraleucel for patients with relapsed or refractory large B-cell lymphomas (TRANSCEND NHL 001): a multicentre seamless design study. Lancet 396, 839–852 (2020).
pubmed: 32888407 doi: 10.1016/S0140-6736(20)31366-0
Azangou-Khyavy, M. et al. CRISPR/Cas: from tumor gene editing to T cell-based immunotherapy of cancer. Front. Immunol. 11, 2062 (2020).
pubmed: 33117331 pmcid: 7553049 doi: 10.3389/fimmu.2020.02062
Textor, A. et al. CD28 co-stimulus achieves superior CAR T cell effector function against solid tumors than 4-1BB co-stimulus. Cancers 13, 1050 (2021).
pubmed: 33801448 pmcid: 7958604 doi: 10.3390/cancers13051050
Pichler, A. C. et al. TCR-independent CD137 (4-1BB) signaling promotes CD8
pubmed: 37392737 pmcid: 10649891 doi: 10.1016/j.immuni.2023.06.007
Driehuis, E., Kretzschmar, K. & Clevers, H. Establishment of patient-derived cancer organoids for drug-screening applications. Nat. Protoc. 15, 3380–3409 (2020).
pubmed: 32929210 doi: 10.1038/s41596-020-0379-4
Driehuis, E. et al. Oral mucosal organoids as a potential platform for personalized cancer therapy. Cancer Discov. 9, 852–871 (2019).
pubmed: 31053628 doi: 10.1158/2159-8290.CD-18-1522
Huch, M. et al. Long-term culture of genome-stable bipotent stem cells from adult human liver. Cell 160, 299–312 (2015).
pubmed: 25533785 pmcid: 4313365 doi: 10.1016/j.cell.2014.11.050
Saltsman, J. A. et al. A human organoid model of aggressive hepatoblastoma for disease modeling and drug testing. Cancers 12, 2668 (2020).
pubmed: 32962010 pmcid: 7563272 doi: 10.3390/cancers12092668
Miao, Y. et al. Next-generation surrogate Wnts support organoid growth and deconvolute Frizzled pleiotropy in vivo. Cell Stem Cell 27, 840–851 (2020).
pubmed: 32818433 pmcid: 7655723 doi: 10.1016/j.stem.2020.07.020
Jutz, S. et al. Assessment of costimulation and coinhibition in a triple parameter T cell reporter line: simultaneous measurement of NF-κB, NFAT and AP-1. J. Immunol. Methods 430, 10–20 (2016).
pubmed: 26780292 doi: 10.1016/j.jim.2016.01.007
Doench, J. G. et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR–Cas9. Nat. Biotechnol. 34, 184–191 (2016).
pubmed: 26780180 pmcid: 4744125 doi: 10.1038/nbt.3437
Muraro, M. J. et al. A single-cell transcriptome atlas of the human pancreas. Cell Syst. 3, 385–394 (2016).
pubmed: 27693023 pmcid: 5092539 doi: 10.1016/j.cels.2016.09.002
Wu, T. et al. clusterProfiler 4.0: a universal enrichment tool for interpreting omics data. Innovation 2, 100141 (2021).
pubmed: 34557778 pmcid: 8454663

Auteurs

Patricia Hernández-López (P)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Eline van Diest (E)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Peter Brazda (P)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Sabine Heijhuurs (S)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Angelo Meringa (A)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Lauren Hoorens van Heyningen (L)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Caterina Riillo (C)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Department of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.

Caroline Schwenzel (C)

Faculty of Biology, University of Freiburg, Freiburg, Germany.
Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Freiburg, Germany.
Center of Chronic Immunodeficiency (CCI) and Institute for Immunodeficiency, University Clinics and Medical Faculty, Freiburg, Germany.

Marina Zintchenko (M)

Faculty of Biology, University of Freiburg, Freiburg, Germany.
Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Freiburg, Germany.
Center of Chronic Immunodeficiency (CCI) and Institute for Immunodeficiency, University Clinics and Medical Faculty, Freiburg, Germany.

Inez Johanna (I)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Mara J T Nicolasen (MJT)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Astrid Cleven (A)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Thomas A Kluiver (TA)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Rosemary Millen (R)

Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW), Utrecht, the Netherlands.

Jiali Zheng (J)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Froso Karaiskaki (F)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Trudy Straetemans (T)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Hans Clevers (H)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW), Utrecht, the Netherlands.
Roche Pharmaceutical Research and Early Development, Basel, Switzerland.

Remco de Bree (R)

Department of Head and Neck Surgical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.

Hendrik G Stunnenberg (HG)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Weng Chuan Peng (WC)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Jeanine Roodhart (J)

Department of Medical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.

Susana Minguet (S)

Faculty of Biology, University of Freiburg, Freiburg, Germany.
Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Freiburg, Germany.
Center of Chronic Immunodeficiency (CCI) and Institute for Immunodeficiency, University Clinics and Medical Faculty, Freiburg, Germany.

Zsolt Sebestyén (Z)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Dennis X Beringer (DX)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Jürgen Kuball (J)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands. j.h.e.kuball@umcutrecht.nl.
Department of Hematology, University Medical Center Utrecht, Utrecht, the Netherlands. j.h.e.kuball@umcutrecht.nl.

Classifications MeSH