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Oncogene-induced TIM-3 ligand expression dictates susceptibility to anti–TIM-3 therapy in mice
Nana Talvard-Balland, … , Vijay K. Kuchroo, Robert Zeiser
Nana Talvard-Balland, … , Vijay K. Kuchroo, Robert Zeiser
Published June 25, 2024
Citation Information: J Clin Invest. 2024;134(16):e177460. https://doi.org/10.1172/JCI177460.
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Research Article

Oncogene-induced TIM-3 ligand expression dictates susceptibility to anti–TIM-3 therapy in mice

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Abstract

Leukemia relapse is a major cause of death after allogeneic hematopoietic cell transplantation (allo-HCT). We tested the potential of targeting T cell (Tc) immunoglobulin and mucin-containing molecule 3 (TIM-3) for improving graft-versus-leukemia (GVL) effects. We observed differential expression of TIM-3 ligands when hematopoietic stem cells overexpressed certain oncogenic-driver mutations. Anti–TIM-3 Ab treatment improved survival of mice bearing leukemia with oncogene-induced TIM-3 ligand expression. Conversely, leukemia cells with low ligand expression were anti–TIM-3 treatment resistant. In vitro, TIM-3 blockade or genetic deletion in CD8+ Tc enhanced Tc activation, proliferation, and IFN-γ production while enhancing GVL effects, preventing Tc exhaustion, and improving Tc cytotoxicity and glycolysis in vivo. Conversely, TIM-3 deletion in myeloid cells did not affect allogeneic Tc proliferation and activation in vitro, suggesting that anti–TIM-3 treatment–mediated GVL effects are Tc induced. In contrast to anti–programmed cell death protein 1 (anti–PD-1) and anti–cytotoxic T lymphocyte–associated protein 4 (anti–CTLA-4) treatment, anti–TIM-3-treatment did not enhance acute graft-versus-host disease (aGVHD). TIM-3 and its ligands were frequently expressed in acute myeloid leukemia (AML) cells of patients with post–allo-HCT relapse. We decipher the connections between oncogenic mutations found in AML and TIM-3 ligand expression and identify anti–TIM-3 treatment as a strategy for enhancing GVL effects via metabolic and transcriptional Tc reprogramming without exacerbation of aGVHD. Our findings support clinical testing of anti–TIM-3 Ab in patients with AML relapse after allo-HCT.

Authors

Nana Talvard-Balland, Lukas M. Braun, Karen O. Dixon, Melissa Zwick, Helena Engel, Alina Hartmann, Sandra Duquesne, Livius Penter, Geoffroy Andrieux, Lukas Rindlisbacher, Andrea Acerbis, Jule Ehmann, Christoph Köllerer, Michela Ansuinelli, Andres Rettig, Kevin Moschallski, Petya Apostolova, Tilman Brummer, Anna L. Illert, Markus A. Schramm, Yurong Cheng, Anna Köttgen, Justus Duyster, Hans D. Menssen, Jerome Ritz, Bruce R. Blazar, Melanie Boerries, Annette Schmitt-Gräff, Nurefsan Sariipek, Peter Van Galen, Joerg M. Buescher, Nina Cabezas-Wallscheid, Heike L. Pahl, Erika L. Pearce, Robert J. Soiffer, Catherine J. Wu, Luca Vago, Burkhard Becher, Natalie Köhler, Tobias Wertheimer, Vijay K. Kuchroo, Robert Zeiser

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Figure 4

Genetic TIM-3 deletion in CD8+ Tc enhances Tc activation, proliferation, and IFN-γ production as well as GVL effects.

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Genetic TIM-3 deletion in CD8+ Tc enhances Tc activation, proliferation,...
(A–E) Tc labeled with CTV (responders, C57BL/6) were cocultured for 6 days with allogeneic non-CD3 cells (stimulators, BALB/c). Responder cells were isolated from mice carrying TIM-3 deletion in CD8+ Tc (Havcr2fl/fl;E8icre/+) as described (23). (A) Proportion of proliferative cells was quantified at day 6 as the percentage of CTVlo cells in Havcr2fl/fl;E8icre/+ CD3+ responder Tc. (B) CD25 expression in proliferative CD3+ responder cells was quantified at day 6 by FC. (C) Representative staining of CD25 expression in Havcr2fl/fl (blue line) and in Havcr2fl/fl;E8icre/+ cells (red line). (D) CD69 expression in proliferative CD3+ responder cells was quantified at day 6 by FC. (E) Representative staining of CD69 expression in Havcr2fl/fl (blue line) and in Havcr2fl/fl;E8icre/+ cells (red line). (F and G) Production of IFN-γ in the supernatant of the culture analyzed at the indicated time points by ELISA. P values were calculated using an unpaired Student’s t test. (H and I) Kaplan-Meier plots showing survival of mice in the indicated groups. BALB/c recipient mice were injected i.v. with WEHI-3B AML cells (BALB/c background) and (H) allogeneic Havcr2fl/fl (n = 10) or Havcr2fl/fl;E8icre/+ (n = 10) BM and Tc or (I) allogeneic Havcr2fl/fl (n = 10) or Havcr2fl/fl;Cd4cre/+ (n = 10) BM and Tc. Data were pooled from 2 independent experiments, and P values were calculated using the 2-sided Mantel-Cox test. (J) Percentage of specific lysis of αCD3/CD28-activated Tc isolated from Havcr2cKO mice in contact with WEHI-3B cells. E:T (effector [Tc] to target [WEHI-3B cell]) ratio was titrated between 5:1 and 1:1, as indicated. Individual values are shown and mean ± SD of Havcr2fl/fl (n = 6) or Havcr2fl/fl;Cd4cre/+ (n = 6). P values were calculated using 2-way ANOVA followed by Šidák’s multiple-comparisons test.

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