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Inflammasomes in lymphocytes as therapeutic targets.

作者信息

Albakova Zarema

机构信息

Department of Biology, Lomonosov Moscow State University, Moscow, Russia.

出版信息

Transl Oncol. 2025 Apr;54:102342. doi: 10.1016/j.tranon.2025.102342. Epub 2025 Mar 6.


DOI:10.1016/j.tranon.2025.102342
PMID:40054124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11928805/
Abstract

Inflammasomes are cytoplasmic macromolecular complexes playing an important role in sensing exogenous and endogenous stimuli. Inflammasome activation leads to IL-1β and IL-18 secretion and pyroptosis. The concept of non-self recognition triggering inflammasome activation has been well-established for myeloid cells. However, increasing evidence suggests the presence of functional inflammasome or inflammasome-related components in lymphocytes. Dysregulated expression of inflammasome contributes to the development of many diseases, including cardiovascular, infectious, neurodegenerative diseases and cancer. Multiple clinical trials are being conducted to assess drugs targeting various inflammasome components. This review discusses current knowledge on inflammasome activation in T, B and NK cells and explores their potential as therapeutic targets. Further understanding inflammasome and pyroptotic pathways in lymphocytes may have implications in the development of novel immunotherapeutic strategies.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/9acd7dd1745e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/a8515507d75a/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/43a66724aae2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/a48b1efa84ac/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/2e0a2e9f5dc8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/9acd7dd1745e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/a8515507d75a/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/43a66724aae2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/a48b1efa84ac/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/2e0a2e9f5dc8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b991/11928805/9acd7dd1745e/gr4.jpg

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本文引用的文献

[1]
FDA-approved disulfiram inhibits the NLRP3 inflammasome by regulating NLRP3 palmitoylation.

Cell Rep. 2024-8-27

[2]
Reprogramming the tumor immune microenvironment using engineered dual-drug loaded Salmonella.

Nat Commun. 2024-8-6

[3]
Swaying the advantage: multifaceted functions of inflammasomes in adaptive immunity.

FEBS J. 2025-4

[4]
Development of NK cell-based cancer immunotherapies through receptor engineering.

Cell Mol Immunol. 2024-4

[5]
Transmembrane protein 176B regulates amino acid metabolism through the PI3K-Akt-mTOR signaling pathway and promotes gastric cancer progression.

Cancer Cell Int. 2024-3-4

[6]
The CARD8 inflammasome dictates HIV/SIV pathogenesis and disease progression.

Cell. 2024-2-29

[7]
The role of inflammasomes in human diseases and their potential as therapeutic targets.

Signal Transduct Target Ther. 2024-1-5

[8]
immunotherapy engineered with highly efficient tumor antigen coating establishes antigen-specific CD8+ T cell immunity and increases in antitumor efficacy with type I interferon combination therapy.

Oncoimmunology. 2024

[9]
Dictionary of immune responses to cytokines at single-cell resolution.

Nature. 2024-1

[10]
Interplay between inflammasomes and PD-1/PD-L1 and their implications in cancer immunotherapy.

Carcinogenesis. 2023-12-30

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