Hao Xiong, Huitao Zhang, Wenting Tie, Yongqiang Wang, Yijun Dong, Li Zhang, Yanhong Li, Jun Bai, Jinping Zhang, Yuxian Wang, Liansheng Zhang, Lijuan Li
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引用次数: 0
Abstract
Disorder of the immune microenvironment plays an important role in the occurrence and development of multiple myeloma in patients. While bone marrow SUVmax on 18F-FDG PET/CT correlates with MM disease characteristics, its association with the immune microenvironment remains unclear. This study analyzed 49 newly diagnosed MM patients, dividing them into high and low SUVmax groups based on bone marrow 18F-FDG uptake. Differences in clinical characteristics, laboratory indicators, lymphocyte subsets, and cytokines were examined. Additionally, the correlation between SUVmax and these parameters was assessed. Results showed that patients with high SUVmax had a heavier disease burden, including a greater proportion of advanced-stage disease, more pathological fractures, and increased bone marrow plasma cell percentage. The high SUVmax group also exhibited a more immunosuppressive microenvironment, with a reduced proportion of CD4+ T cells and increased levels of regulatory T cells (Tregs) and cytokines such as IL-4 and IL-10. Correlation analysis indicated that the SUVmax of 18F-FDG uptake was positively correlated with the proportion of Treg cells and the concentrations of cytokines such as IL-4, IL-6, and IL-10, while negatively correlated with the proportion of CD4+ T cells.After adjustment for bone marrow plasma cell percentage, high SUVmax remained associated with decreased CD4+ T cells and increased Treg cells. This study suggests that bone marrow SUVmax is associated with both disease burden and immune microenvironment status in MM patients, which may provide valuable insights for disease assessment and treatment.
期刊介绍:
IMMUNOLOGIC RESEARCH represents a unique medium for the presentation, interpretation, and clarification of complex scientific data. Information is presented in the form of interpretive synthesis reviews, original research articles, symposia, editorials, and theoretical essays. The scope of coverage extends to cellular immunology, immunogenetics, molecular and structural immunology, immunoregulation and autoimmunity, immunopathology, tumor immunology, host defense and microbial immunity, including viral immunology, immunohematology, mucosal immunity, complement, transplantation immunology, clinical immunology, neuroimmunology, immunoendocrinology, immunotoxicology, translational immunology, and history of immunology.