ArticleFrontiers in oncology2025
Development of a novel prognostic model for mantle cell lymphoma based on quantitative detection of CD3 by quantitative dot blot.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- A novel immune model predicts the prognosis of mantle cell lymphoma.Frontiers in medicine · 2026Article
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7 authors.
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Abstract
Background: The Mantle Cell Lymphoma International Prognostic Index (MIPI) is the standard risk stratification model, but it primarily relies on clinical parameters and does not incorporate molecular markers. Studies suggest that CD3+ T cells, as a key component of the tumor microenvironment (TME), play a crucial role in mantle cell lymphoma (MCL) progression and prognosis. However, conventional immunohistochemistry (IHC) has limitations in quantifying CD3 expression due to its subjectivity and variability. Quantitative Dot Blot (QDB) is an emerging high-throughput protein quantification technique that allows for precise measurement of CD3+ T cells. This study aimed to evaluate the prognostic significance of CD3+ T cells quantified using QDB and IHC in MCL patients and to introduce the MIPI/CD3 model to enhance risk stratification and improve prognostic accuracy. Methods: A retrospective analysis of 120 newly diagnosed MCL patients from four hospitals between 2008 and 2020. The CD3 expression was assessed using both IHC and QDB. Patients were classified into CD3 Results: CD3 quantification by IHC was correlated with OS (p=0.47), whereas QDB-based CD3 quantification showed a significant association with OS (p=0.0051), with the CD3 Conclusion: CD3+ T cells are an important prognostic biomarker in MCL, with high expression indicating a better prognosis. Integrating CD3 into the MIPI model enhances risk stratification accuracy. Compared to traditional IHC, QDB provides a more precise and reliable method for measuring CD3+ T cells. However, further validation in larger MCL cohorts is necessary to confirm its clinical utility. Future research should integrate immune and molecular biomarkers to further refine MCL risk models and advance personalized treatment.
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