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Mild acute pancreatitis (AP) is a self-limiting disease, whereas severe AP has high mortality because of enhanced systemic inflammation and multiple organ failure. In experimental models of AP, infiltration of monocytes and activation of monocyte-derived macrophages largely determine the severity of the disease. Our previous studies have shown that CD11bLy-6C inflammatory monocytes were mobilized from bone marrow into peripheral blood and inflamed pancreas during the early stage of AP. However, the phenotype and characteristics of circulating monocytes in patients with AP are not well defined. Fifty patients with AP and nine age- and sex-matched healthy volunteers were enrolled in this study. Compared with those of healthy volunteers, the proportion of CD14CD16 monocytes and the level of myeloid-related cytokines/chemokines were increased in AP patients within 48 h after disease onset, especially in patients with a severe disease course. Moreover, the increased monocyte proportions were associated with decreased HLA-DR expression and a reduced T cell count. Notably, dynamic changes in circulating CD14CD16 monocytes and their HLA-DR expression, as well as in CD4 T cells, were obviously different between moderate severe AP and severe AP. Last, area under the receiver operating characteristic analysis showed that the combination of CD14CD16 monocyte proportions with their HLA-DR level had higher accuracy for predicting the severity of AP. Taken together, the ratio of CD14CD16 monocytes and their HLA-DR level might assist in predicting the severity of disease in AP patients at admission and in monitoring patients' clinical status during recovery.
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http://dx.doi.org/10.4049/jimmunol.1801194 | DOI Listing |
Sci Rep
August 2025
Department of Neuroscience, School of Translational Medicine, Faculty of Medicine, Nursing and Health Science, Monash University, Level 6 Alfred Centre, 99 Commercial Road, Melbourne, VIC, 3004, Australia.
Novel therapeutic targets are required to develop new treatments to lower the rates of drug-resistant epilepsy (DRE). This study assessed differences in plasma inflammatory biomarker concentrations and monocyte phenotype and function in patients with DRE versus psychogenic non-epileptic seizures (PNES). Luminex was used to analyse plasma samples from 21 DRE cases and 19 PNES controls for concentrations of selected cytokines and chitinase 3-like 1 (CHI3L1).
View Article and Find Full Text PDFInt Immunopharmacol
August 2025
Laboratory of Applied Molecular Biology and Immunology, W0414100, University of Tlemcen, 13000 Tlemcen, Algeria. Electronic address:
Background: Colorectal cancer (CRC) generates a complex tumor microenvironment (TME) known to profoundly alter the function and phenotype of immune cells, including monocytes. Key aspects of this environment can be mimicked by tumor-conditioned medium (TCM). Metformin has emerged as a promising candidate to counteract TCM-induced immune and inflammatory dysregulation.
View Article and Find Full Text PDFToxics
June 2025
Department of Otorhinolaryngology, University Hospital Schleswig-Holstein, 23538 Lübeck, Germany.
Tobacco smoking is closely associated with pro-inflammatory immunological alterations, whereas regular physical exercise is well known to lower systemic inflammations and related immune cell activities. The combined effects of smoking, nicotine pouch use, vaping, and exercise on individual immunological responses remain incompletely understood, especially in view of alternative nicotine delivery systems. In this study, we analyzed the immediate impact of different nicotine sources on exercise monocyte subsets in 16 human subjects using a four-arm cross-over design.
View Article and Find Full Text PDFAnticancer Res
May 2025
Department of Radiation Oncology, University of Luebeck, Luebeck, Germany;
Background/aim: Lung cancer remains one of the most prevalent cancers worldwide, with high morbidity and mortality rates. Besides established treatment options such as surgery and radio(chemo)therapy, advanced approaches such as anti-programmed death 1 (PD-1)/anti-programmed death ligand 1 (PD-L1) immune checkpoint inhibitors (ICIs) have been introduced as effective therapeutic options. In this context, PD-L1 expression on myeloid cells has been correlated with poor clinical outcomes in patients with cancer.
View Article and Find Full Text PDFCancers (Basel)
April 2025
Department of Pathology, Northwestern University Feinberg School of Medicine & Northwestern Memorial Hospital, Chicago, IL 60611, USA.
Background: Based on CD14/CD16 expression, monocytes can be divided into the following three functionally distinct subsets: classical (MO1, CD14++/CD16-), intermediate (MO2, CD14+/CD16+) and non-classical (MO3, CD14/CD16-). An expanded MO1 subset (cutoff, ≥94%) was found to be predictive of CMML. However, the utility of this test in routine practice has important limitations, with some reporting low sensitivity or a lack of correlation.
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