Normal view
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Molecular Therapy Advances
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Clinical Immunogenicity in rAAV Gene Therapy: Insights and Implications
Recombinant AAV gene therapies deliver durable clinical benefit but face immune-mediated challenges that vary by vector, dose, route, and patient. Gulve and colleagues synthesize the clinical manifestations, temporal patterns, and mechanisms of rAAV immunogenicity, highlighting risk assessment and emerging mitigation strategies to support safer, more effective gene therapy development.
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Molecular Therapy
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C-terminal CD28 phosphorylation, pY218, modulates IL-2 secretion and therapeutic effect of CAR-T cells
This study identifies the interleukin-2-inducible T cell Kinase (ITK)-mediated phosphorylation of Y218 in the CD28 cytoplasmic domain as key for CAR-T cell function and demonstrates that engineering a synthetic ITK-binding motif into the CAR enhances IL-2 production and antitumor efficacy in vivo.
C-terminal CD28 phosphorylation, pY218, modulates IL-2 secretion and therapeutic effect of CAR-T cells
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Molecular Therapy
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ACC1 inhibition enhances BCG-induced trained immunity by reprogramming acetyl-CoA metabolism
The efficacy of vaccines remains suboptimal in many settings, underscoring the need for new strategies. Baydemir and colleagues show that modulation of acetyl-CoA metabolism reshapes metabolic and epigenetic programs underlying Bacille Calmette-Guérin-induced trained immunity, enhancing cellular innate immune responses and identifying immunometabolic targeting as a promising approach to improve vaccine efficacy.
ACC1 inhibition enhances BCG-induced trained immunity by reprogramming acetyl-CoA metabolism
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Molecular Therapy
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Advanced iPSC-based modelling of LMNA-related congenital muscular dystrophy enables development of genetic therapies for muscle laminopathies
LMNA-related congenital muscular dystrophy (L-CMD) is a devastating early-onset muscle disease caused by dysfunctional nuclear lamina. Current models fail to capture the complexity of human muscle pathology, limiting translational progress. This study overcomes this limitation by establishing a robust, human iPSC-based platform for modelling L-CMD and testing gene editing strategies.
Advanced iPSC-based modelling of LMNA-related congenital muscular dystrophy enables development of genetic therapies for muscle laminopathies
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Molecular Therapy
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Integrin α7 defines a profibrotic adipose stromal population targeted for nanoparticle PAI-1 gene silencing in obesity
Obesity expands a pathogenic ITGA7high adipose stromal cell population that promotes fibrosis. We engineered ITGA7-targeted lipid-coated mesoporous silica nanoparticles to selectively deliver plasminogen activator inhibitor-1 small interfering RNA, suppress profibrotic signaling, and restore a healthier adipose microenvironment.
Integrin α7 defines a profibrotic adipose stromal population targeted for nanoparticle PAI-1 gene silencing in obesity
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Molecular Therapy
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Triple-AAV intein-mediated gene therapy ameliorates dystrophic phenotype in MDC1A mice
To overcome the strict packaging limits of AAV vectors, this study utilizes a triple-AAV system paired with orthogonal split inteins to reconstitute the exceptionally large LAMA2 protein. This scarless, multi-vector approach successfully rescues the dystrophic phenotype in vivo, offering a scalable platform for large-gene therapies.
Triple-AAV intein-mediated gene therapy ameliorates dystrophic phenotype in MDC1A mice
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Molecular Therapy
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Repurposing base editors for targeted knockin and simultaneous multiplex knockouts to generate allo-CAR T cells with minimal translocations
Wagner and colleagues develop BEKI (Base Editor-mediated Knock-In), a non-viral platform that combines targeted transgene insertion with simultaneous gene knockouts in a single step. BEKI-engineered CAR T cells show markedly reduced chromosomal rearrangements compared with conventional nuclease-based approaches, advancing safer manufacturing of multiplex-edited cell therapies for cancer and autoimmune diseases.
Repurposing base editors for targeted knockin and simultaneous multiplex knockouts to generate allo-CAR T cells with minimal translocations
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Molecular Therapy
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Repurposing triamterene as chloride intracellular channel 1 inhibitor via ligand-based approach for glioblastoma
Currently no effective therapies are available for glioblastoma. Florio and colleagues identified, via computational screening, triamterene as a CLIC1 blocker that suppresses human glioblastoma stem cell proliferation, invasiveness, and tumor growth. Triamterene also enhances temozolomide and radio-chemotherapy efficacy, making it a repurposed therapeutic candidate for glioblastoma treatment in future clinical applications.
Repurposing triamterene as chloride intracellular channel 1 inhibitor via ligand-based approach for glioblastoma
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Molecular Therapy
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Targeted antisense oligonucleotide therapy rescues PRPF31 expression in retinitis pigmentosa caused by a splicing mutation
Stanek and colleagues uncover a novel PRPF31 intronic mutation that disrupts splicing and lowers protein levels. Targeted antisense oligonucleotides restore normal splicing and boost PRPF31 expression in patient-derived RPE, highlighting a potential therapeutic strategy for retinitis pigmentosa.
Targeted antisense oligonucleotide therapy rescues PRPF31 expression in retinitis pigmentosa caused by a splicing mutation
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cs.AI, q-bio.NC updates on arXiv.org
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Albedo Estimation via Latent Bridge Matching
arXiv:2609.09884v1 Announce Type: cross Abstract: Recent advances in Intrinsic Image Decomposition (IID) have increasingly relied on generative models. However, progress remains limited by three key challenges: (a) insufficient physical consistency, (b) high computational cost at inference time, and (c) limited generalization capabilities. In this work, we show that latent bridge matching (LBM) effectively addresses these limitations for albedo estimation. We introduce a novel LBM-based archite
Albedo Estimation via Latent Bridge Matching
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cs.AI, q-bio.NC updates on arXiv.org
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Context operations to architecture modelling output from large language models and evaluation criteria for their use in systems engineering design
arXiv:2609.10132v1 Announce Type: cross Abstract: The development of generative artificial intelligence resources enables opportunities of speeding up systems and engineering design work. This contribution introduces a framework of formal operations for assembling context in LLM-based engineering design. This framework involves the assembly of modular context units, including policy prompts, reference units with persistence, and user questions with prompt vectoring. This approach enables the sy
Context operations to architecture modelling output from large language models and evaluation criteria for their use in systems engineering design
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cs.AI, q-bio.NC updates on arXiv.org
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EVA-Bench: A New End-to-end Framework for Evaluating Voice Agents
arXiv:2605.13841v3 Announce Type: replace-cross Abstract: Voice agents are increasingly deployed across enterprise applications. However, no existing benchmark jointly addresses realistic conversation simulation and comprehensive voice-specific evaluation. We present EVA-Bench, an end-to-end evaluation framework that addresses both. On the simulation side, EVA-Bench orchestrates dynamic bot-to-bot audio conversations with automatic simulation validation that detects user simulator error and app
EVA-Bench: A New End-to-end Framework for Evaluating Voice Agents
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cs.AI, q-bio.NC updates on arXiv.org
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PRIME-SVR: Physics-infoRmed Implicit Multi-Echo Slice-to-Volume Reconstruction for Fetal T2 mapping
arXiv:2607.20136v2 Announce Type: replace-cross Abstract: Slice-to-volume reconstruction (SVR) is the standard method for obtaining high-resolution (HR) 3D fetal brain volumes from motion-corrupted 2D MRI slice stacks acquired in multiple orientations. Existing SVR methods are optimized and validated only for clinical-range echo times (TEs), limiting their use at non-clinical TEs and making them incompatible with quantitative T2 mapping, a protocol- and center-independent biomarker of fetal bra
PRIME-SVR: Physics-infoRmed Implicit Multi-Echo Slice-to-Volume Reconstruction for Fetal T2 mapping
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TechCrunch
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AI research startup Listen Labs scrubbed a $1.5B funding round for Salesforce talks
Listen Labs walked away from a signed Series C term sheet from Menlo Ventures, sources say.
AI research startup Listen Labs scrubbed a $1.5B funding round for Salesforce talks
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Journal of Medical Internet Research
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Smartphone-Based Monitoring of Quality of Life and Adverse Events After Neurosurgery: Prospective Cohort Study
Background: Postoperative outcome assessment is often based on discrete follow-up visits, limiting characterization of individual recovery trajectories, and the timely identification of adverse events (AEs). Longitudinal smartphone-based monitoring may overcome these limitations by enabling frequent, resource-efficient collection of patient-reported outcomes and complications throughout recovery. Such data may provide a more patient-centered understanding of the postoperative course and compleme
Smartphone-Based Monitoring of Quality of Life and Adverse Events After Neurosurgery: Prospective Cohort Study
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STAT

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STAT+: ARPA-H to invest $62 million to develop FDA-authorized AI to help treat heart failure
ARPA-H, the government agency that funds cutting-edge health research, plans to commit $62.7 million to develop artificial intelligence bots that direct treatment of heart failure. Among the goals of the program, called ADVOCATE, is to produce partially autonomous AI devices authorized by the Food and Drug Administration to help treat patients, including assessing symptom severity, prescribing drugs, and ordering lab tests. ARPA-H on Wednesday announced the first batch of awards to health te
STAT+: ARPA-H to invest $62 million to develop FDA-authorized AI to help treat heart failure
ARPA-H, the government agency that funds cutting-edge health research, plans to commit $62.7 million to develop artificial intelligence bots that direct treatment of heart failure. Among the goals of the program, called ADVOCATE, is to produce partially autonomous AI devices authorized by the Food and Drug Administration to help treat patients, including assessing symptom severity, prescribing drugs, and ordering lab tests.
ARPA-H on Wednesday announced the first batch of awards to health tech companies Atman Health, UpDoc, Tempus AI, and teams from Stanford University, Duke University, and the Kaiser Permanente health system. ARPA-H may still fund additional teams. The amount committed for the first year is $33.7 million, and the remainder may be renegotiated up or down.
Many of the 6.7 million Americans with heart failure don’t get optimal treatment because of difficulty accessing specialists, and the hope is that AI agents developed with ARPA-H funding can help address the gap, especially in rural and other underserved settings.
Continue to STAT+ to read the full story…


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Journal of Medical Internet Research
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“Small” Large Language Models in the Hospital: Evaluation Study on Real-World Data in a Resource-Constrained Setting
Background: Large language models (LLMs) are increasingly being deployed in health care, but their use and deployment in many real-world hospital environments pose significant challenges and concerns. In particular, state-of-the-art commercial models store or process data externally, which is often in conflict with ensuring patient data protection. At the same time, using LLMs locally is limited by the lack of available computing infrastructure. Small open-source LLMs that do not require substan
“Small” Large Language Models in the Hospital: Evaluation Study on Real-World Data in a Resource-Constrained Setting
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Nature - Issue - nature.com science feeds
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Highly efficient base editing at <i>PCSK9</i> and normal human embryo development
Nature, Published online: 09 September 2026; doi:10.1038/s41586-026-11118-xHighly efficient base editing at PCSK9 and normal human embryo development
Highly efficient base editing at <i>PCSK9</i> and normal human embryo development
Nature, Published online: 09 September 2026; doi:10.1038/s41586-026-11118-x
Highly efficient base editing at PCSK9 and normal human embryo development-
Nature - Issue - nature.com science feeds
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Integrated signatures define mutational processes in prostate cancer
Nature, Published online: 09 September 2026; doi:10.1038/s41586-026-10468-wEight integrated mutational footprints collectively explain the mutational processes in 85% of primary prostate cancer genomes.
Integrated signatures define mutational processes in prostate cancer
Nature, Published online: 09 September 2026; doi:10.1038/s41586-026-10468-w
Eight integrated mutational footprints collectively explain the mutational processes in 85% of primary prostate cancer genomes.-
npj Digital Medicine
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A global framework for artificial intelligence education in medicine: international working group recommendations
npj Digital Medicine, Published online: 09 September 2026; doi:10.1038/s41746-026-03197-xA global framework for artificial intelligence education in medicine: international working group recommendations
A global framework for artificial intelligence education in medicine: international working group recommendations
npj Digital Medicine, Published online: 09 September 2026; doi:10.1038/s41746-026-03197-x
A global framework for artificial intelligence education in medicine: international working group recommendations