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Echchannaoui, H.

Publications and source records attributed to Echchannaoui, H..

3 recordsLinked to original sources

A signaling-optimized TIGIT chimeric switch receptor promotes metabolic fitness and antitumor efficacy of TCR/CAR T cells

Adoptive T cell therapies have revolutionized the treatment of hematological malignancies, however, their efficacy against solid tumors often remains limited. Lack of activation and overabundance of immune checkpoint-mediated inhibitory signals from cancer cells drive T cell dysfunction and limit persistence. To circumvent this imbalance towards inhibitory factors, we engineered a chimeric switch receptor (CSR) that repurposes the immunosuppressive TIGIT extracellular domain by fusing it to a CD28-derived stimulatory signaling tail. Here we show that while the prototype CSR design enhances immediate cytolytic activity, it also induces premature proliferative arrest and terminal differentiation due to excessive tonic signaling. By introducing a strategic point mutation within the CD28 cytoplasmic domain, we "fine-tuned" the activation threshold of the CSR for optimal functional properties. Engineered T cells with 'fine-tuned' CSR exhibit superior mitochondrial bioenergetics and sustained metabolic flux in an in vitro system of chronic antigen exposure. In preclinical xenograft models, fine-tuned CSR-expressing T cells demonstrated robust expansion and durable persistence, leading to complete tumor eradication. These findings provide a scalable strategy to rewire inhibitory checkpoints into tailored costimulatory signals, offering a potent approach to enhance the metabolic fitness and persistence of therapeutic T cells, in suppressive tumor microenvironments, in particular.

immunology↗

Menin-Inhibition Sensitizes Acute Myeloid Leukemia to CLEC12A-Directed CAR Cell Therapy

Menin inhibitors targeting the Menin-KMT2A chromatin complex have emerged as highly selective therapies for KMT2A-rearranged (KMT2A-r) and NPM1-mutated (NPM1mut) acute myeloid leukemia (AML), with recent regulatory approval and increasing interest in combination strategies. In contrast, CAR cell therapies have not yet been successfully established for AML. Here, we show that menin-inhibition primes KMT2A-r and NPM1mut AML for CAR-based targeting by inducing robust and uniform expression of the myeloid antigen CLEC12A (CLL-1). Menin inhibitors did not impair T or NK cell viability, phenotype, or effector function. We engineered second-generation CLEC12A-directed CAR T cells that efficiently eliminated CLEC12A-positive AML. Across in vitro systems and xenograft models, the combination therapy consistently outperformed either monotherapy, resulting in profound disease control and significantly prolonged survival, with evidence of near-complete leukemia eradication in vivo. These findings support epigenetic priming with menin inhibitors to enhance CLEC12A-directed CAR cell-therapy in these AML subtypes. SignificanceMenin inhibitors, now approved for AML treatment, induce the immune target CLEC12A in NPM1mut and KMT2A-r AML subtypes and sensitize AML cells to CLEC12A-directed CAR T cells without compromising immune function. As CLEC12A-CARs are already in clinical testing, this combination is immediately actionable for clinical investigation.

cancer biology↗

DNMT/G9a Complex Inhibition Uncovers Epigenetic Vulnerabilities and Induces IFN-Response in Acute Myeloid Leukemia

Epigenetic dysregulation is a hallmark of Acute Myeloid Leukemia (AML), with mutations in DNA Methyltransferases (e.g., DNMT3A) being frequent and promising therapeutic targets. DNMTs form complexes with Histone Methyltransferases (HMTs), driving gene silencing loop via chromatin methylation crosstalk. However, potential connections between this DNMTs/HMTs cooperative activity and oncogenic requirements across the AML mutational spectrum remain poorly understood. Here, we demonstrate that AMLs carrying DNMT3A and Nucleophosmin (NPM1) mutations exhibit a specific epigenetic vulnerability toward a complex formed by DNMTs and G9a, a specific histone H3 Lysine 9 Methyltransferase (H3K9-HMT). Dual inhibition of DNMT/G9a restores differentiation, reduces tumor growth, and spares healthy progenitors compared to standard hypomethylating agents. Mechanistically, DNMT/G9a regulates NPM1 stability, inhibits HOXA9/MEIS1 activity, and triggers interferons (IFN) response via viral mimicry pathways by modulating hypermethylated retrotransposons. Collectively, our data unravel specific epigenetic vulnerabilities within the complex AML mutational landscape and provide a compelling rationale for the design of personalized epigenetic therapies with enhanced efficacy and safer clinical outcomes.

cancer biology↗