Cellular & Molecular Immunology
Cellular & Molecular Immunology(英文缩写 CELL MOL IMMUNOL),ISSN 1672-7681,eISSN 2042-0226 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-09-21 至 2026-09-21，按本站收录文献的发表日期统计。
指标来源：jcr_cas_ifqb
期刊简介
暂无简介。
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 22.100 | Q1 |
| 2022 | 24.100 | Q1 |
| 2023 | 21.800 | Q1 |
| 2024 | 19.800 | Q1 |
| 2025 | 23.900 | Q1 |
Cellular & Molecular Immunology 最新收录文献
※ 中文译文由 AI 辅助生成,仅供学术参考,请以英文原文为准。
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1. αTIGIT-guided IL-15 mimetics drive potent and safe antitumor immunity by restoring tumor-infiltrating T cells.
PMID:作者:日期:2026-09-11Cytokines are powerful modulators of antitumor immunity, but their clinical use is limited by structural instability, short half-life, poor drug-like properties, and severe systemic toxicity. Antibody-based cytokine mimetics have recently emerged to activate immune cells in vitro, but whether these …
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2. HnRNPK restrains memory precursor and plasma cell differentiation to control germinal center B-cell output.
PMID:作者:日期:2026-09-07Germinal center (GC) B cells are critical for the production of long-lived plasma cells and high-affinity antibodies. Upon exiting the GC reaction, B cells differentiate into either memory B (MB) cells or plasma cells depending on affinity signals and transcription factor profiles. However, the unde…
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3. p97-mediated proteostasis is a checkpoint for late-stage thymocyte positive selection.
PMID:作者:日期:2026-09-07AAA ATPase p97 is a central regulator of protein homeostasis, yet its role in late-stage thymocyte development remains undefined. Here, we demonstrate that T-cell-specific ablation of p97 in mice severely blocks the double-positive (DP) to single-positive (SP) transition, with a pronounced defect in…
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4. Targeting the FOXP3-T-bet interaction to restore Treg stability in IFN-γ-driven autoimmunity.
4. 靶向FOXP3-T-bet相互作用以恢复IFN-γ驱动的自身免疫中Treg的稳定性PMID:作者:日期:2026-09-03Regulatory T-cell (Treg) stability is maintained by dynamic remodeling of the FOXP3 transcriptional complex, and disruption of this complex leads to Treg dysfunction and immune dysregulation. However, how specific FOXP3 mutations alter the dynamic remodeling of the FOXP3 complex and thereby contribu…
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6. NADPH oxidases in immunometabolism and disease pathology: mechanistic networks, pollutant triggers, and therapeutic frontiers.
PMID:作者:日期:2026-09-01NADPH oxidases (NOXs) have emerged as central hubs that link environmental, metabolic, and immune cues through spatially organized redox signaling. However, their roles across tissues and disease states have not been comprehensively evaluated in an integrated manner. This review integrates recent ad…
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8. {"_":"Radiation-induced CD200 tumor-associated macrophages suppress eosinophil-mediated antitumor immunity through CD200R signaling in hepatocellular carcinoma.","sup":["+"]}
PMID:作者:日期:2026-09-01Radiotherapy elicits dual immunomodulatory effects in cancer, activating antitumor immunity while paradoxically inducing immunosuppression, which limits therapeutic efficacy. The molecular pathways mediating postradiation immune escape in hepatocellular carcinoma (HCC) remain poorly defined. Here, w…
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9. NLRC3 enhances antitumor immunity by specifically negatively regulating M-MDSCs in a STING-dependent manner.
PMID:作者:日期:2026-09-01NOD-like receptor (NLR) family CARD domain containing 3 (NLRC3), an intracellular member of the NLR family, is a negative regulator of both immune cell modulation and tumor cell proliferation. However, the role of NLRC3 and the mechanisms underlying its effect on the tumor immune microenvironment re…
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10. Tumor cell-released autophagosome (TRAP) programs inflammatory CAFs to drive the immune-excluded TIME through C3a.
PMID:作者:日期:2026-09-01The immune-excluded tumor immune microenvironment (TIME) limits responses to ICIs. Cancer-associated fibroblasts are the most abundant stromal population and key regulators of immune suppression; however, the upstream cues that program pathogenic CAF states and the mechanisms of the immune-excluded …