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T cells

Prognostic Significance of TIM-3 Expression Pattern at Diagnosis in Patients with t(8; 21) Acute Myeloid Leukemia

[Leukemia & Lymphoma] The authors investigated the prognostic significance of T cell immunoglobulin and mucin domain-containing protein 3 (TIM-3) in t(8;21) acute myeloid leukemia (AML). A total of 47 t(8;21) AML patients were tested for TIM-3 expression by multi-parameter flow cytometry at diagnosis.

Cancer Stem Cell-Targeted Chimeric Antigen Receptor (CAR)-T Cell Therapy: Challenges and Prospects

[Acta Pharmaceutica Sinica B] CAR-T cell therapy has shown more efficiency in cancer treatment, particularly regarding blood cancers. The expression of specific markers such as TAAs on CSCs in varied cancer types makes them as potent tools for CAR-T cell therapy.

Immunomodulation Effect of Mesenchymal Stem Cells in Islet Transplantation

[Biomedicine & Pharmacotherapy] The authors highlight the interactions between mesenchymal stem cells (MSCs) and different immune cells to mediate immunomodulatory functions along with the importance of MSCs therapy for the successful islet transplantation.

Single-Cell Evaluation Reveals Shifts in the Tumor-Immune Niches That Shape and Maintain Aggressive Lesions in the Breast

[Nature Communications] Single-cell transcriptomics and multiparametric imaging applied to a mouse model of breast cancer reveals that the aggressive tumor niche was characterized by an expanded basal-like population, specialization of tumor subpopulations, and mixed-lineage tumor cells potentially serving as a transition state between luminal and basal phenotypes.

Stromal Cell-Derived DEL-1 Inhibits Tfh Cell Activation and Inflammatory Arthritis

[Journal of Clinical Investigation] Scientists mice with endothelial-specific overexpression of DEL-1 were protected from arthritis relative to WT controls, while arthritis was exacerbated in DEL-1-deficient mice.

Targeted T Cell Receptor Gene Editing Provides Predictable T Cell Product Function for Immunotherapy

[Cell Reports Medicine] By studying 51 different T cell receptors (TCRs), scientists showed that conventional genetic engineering by viral transduction led to variable TCR expression and functionality as a result of variable transgene copy numbers and untargeted transgene integration.

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