🧬 Tumor Microenvironment β€” Jan 2026

β€’ Engineered CAR-T and TAM targeting reshape local immunity
β€’ Fibroblast checkpoints and macrophage signaling drive resistance
β€’ DNA sensing and pyroptosis pathways amplify immunotherapy response
β€’ Population-scale modeling refines immune stratification

https://pir.sh/9XygJPXd3w

#TumorMicroenvironment #CancerImmunology #Immunotherapy #TAMs #Biology

Tumor Microenvironment Research Summary January 2026 - Summarized Science

Summary of key Tumor Microenvironment publications highlighting major findings, clinical relevance, and emerging research trends.

🧬 Tumor Microenvironment - Dec 2025

β€’ Immune engineering boosts local antitumor activity
β€’ Tumor immunity mapped at scale with population-level models
β€’ Resistance linked to hypermutation, macrophages, and ECM remodeling

https://pir.sh/zZXgkeVd2M

#TumorMicroenvironment #CancerImmunology #Immunotherapy

Tumor Microenvironment Research Summary December 2025 - Summarized Science

Summary of key Tumor Microenvironment publications highlighting major findings, clinical relevance, and emerging research trends.

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'Single-cell sequencing reveals the expansion and diversity of T cell subsets in the bone marrow microenvironment of chronic myeloid leukemia' - a Genes & Diseases article on #ScienceOpen:

πŸ”Ž https://www.scienceopen.com/document?vid=a1a783a1-5180-487b-b736-d5d814a5fb75

#CancerImmunology #LeukemiaResearch #TCells #SingleCellSequencing

Single-cell sequencing reveals the expansion and diversity of T cell subsets in the bone marrow microenvironment of chronic myeloid leukemia

<p xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="first" dir="auto" id="d9200406e246">The immune microenvironment plays an important role in leukemia treatment. However, a specific single-cell profiling of the immune alteration in bone marrow of chronic myeloid leukemia (CML) patients is still lacking. We performed multi-level single-cell sequencing to systematically decipher the bone marrow T cell atlas of CML patients. The results exhibited extensive changes of T cells, including the decreased CD4 T cells and increased CD8 T cells in the CML bone marrow. Subpopulation analysis revealed a significant increase of CD8 terminal effector (TE) cells and a significant decrease of CD4 naΓ―ve T cells. T cell receptor sequencing showed that the overall diversity of the T cell receptor repertoire was reduced in CML, with the exception of the CD8 TE cell. In addition, CD8 TE cells were the main source of gene expression differences in CD8 T cells. Intercellular communication analysis revealed the altered interaction between CD8 TE and other non-T cells in CML, including neutrophil subtype, indicating the potential regulation of bone marrow microenvironment cells on CD8 TE dynamics. Collectively, our work characterises the alteration of T cell subsets in CML patients at multiple single-cell levels, providing a valuable resource for understanding the immune microenvironment and developing new immune strategies for CML therapy. </p>

ScienceOpen