In vivo CAR T-cell therapy KLN-1010 achieved a 100% overall response rate in all 18 multiple myeloma patients in a Phase I trial.
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In vivo CAR T-cell therapy KLN-1010 achieved a 100% overall response rate in all 18 multiple myeloma patients in a Phase I trial.
China approves satricabtagene autoleucel, the first CAR T-cell therapy for solid tumors, showing promise in gastric and gastro-esophageal cancers with improved survival metrics.
In vivo CAR gene therapy shows promising clinical proof of concept with potential to overcome ex vivo manufacturing limitations.
Gut metabolites have opposing effects on CAR-T cell therapy outcomes, with valeric acid improving and indole metabolites impairing treatment efficacy.
γδ and αβ CAR-T cells show similar cytotoxicity but differ significantly in metabolic and signaling pathways, with γδ cells exhibiting lower glycolytic and oxidative capacities.
Arlocabtagene autoleucel achieves an 87% overall response rate with durable responses in heavily pretreated relapsed/refractory multiple myeloma patients.
CD19 CAR T-cell therapy without lymphodepletion shows promising safety and efficacy in pemphigus vulgaris patients, with significant disease improvement in all four cases.
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The ITCC-P4 platform developed 353 pediatric cancer PDX models, enabling preclinical testing and biomarker discovery for high-risk solid tumors.
TLR9 agonists enhance adoptive T cell therapy by activating a B cell-CD2 costimulatory pathway, leading to improved tumor control and T cell function.
Synthetic pH-responsive membranolytic peptide induces immunogenic cell death, boosting immune checkpoint therapy efficacy in tumors with 50% enhanced response.
CAR T cells targeting surface U5 snRNP200, an RNA-binding protein absent from normal hematopoietic precursors, effectively treat AML and B-cell ALL with improved safety.
CAR T cell therapy targeting CD19 can induce long-term remission of intestinal inflammation in ulcerative colitis, revealing a new therapeutic avenue for IBD.
Venetoclax-controlled DROP-CAR T cells effectively regulate tumor targeting and reduce off-tumor toxicity through dose-dependent cell-cell interaction modulation.
CAR-T cell therapies and cancer nanovaccines show promise but face distinct translational challenges, with recent advances highlighting their potential to reshape cancer treatment.
Intratumoral T cell activation can eradicate tumors without tumor-specific T cell receptors, relying on paracrine signaling and innate immune responses.
CytoVI enables comprehensive analysis of antibody-based single-cell data, accurately modeling 350 proteins and revealing disease-related immune cell states.
Harmonizing trial design and biomarker integration is essential to improve personalized treatment for large B-cell lymphoma patients.
Mucosal CAR-T cells persist and cause inflammatory remodeling in enterocolitis, with 10 patients showing severe mucosal dysregulation after BCMA CAR-T therapy.
mRNA-encoded CD19-targeting T cell engager achieves complete B cell depletion and durable platelet recovery in refractory immune thrombocytopenia with minimal safety concerns.
Heterobifunctional protein binders achieve cell-type-specific targeting with subnanomolar potency via FKBP12-dependent enrichment.
PreGame identifies tumour-reactive γδ T-cell receptors with broad reactivity, revealing potential for universal immunotherapy in multiple myeloma and other cancers.
Combining cyclophosphamide with immune checkpoint blockade expands effector CD8+ T cell clones, delaying tumor progression in multiple cancer models.
Elevated NF-κB activity in CD4 CAR-T cells predicts durable responses and improved survival in multiple myeloma patients treated with ide-cel.
CD4+CD25+FOXP3+ regulatory T cells significantly reduce graft-versus-host disease risk in allogeneic hematopoietic cell transplantation.
Localized PD-1 CAR T therapy effectively reprograms neuroinflammation, reducing CNS inflammation and improving outcomes in murine models of multiple sclerosis.
Arlocabtagene autoleucel achieves an 87% overall response rate with durable responses in heavily pretreated relapsed/refractory multiple myeloma patients.
Allogeneic BCMA CAR T cells armed with NKG2A receptor (CT0590) effectively resist host NK cell attacks and show durable responses in multiple myeloma patients.
CRISPR-Cas9 strategies enable precise reprogramming of immune responses to treat cancer and autoimmune diseases.
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