The Progression of Mycosis Fungoides During Treatment with Mogamulizumab: A BIO-MUSE Case Study of the Tumor and Immune Response in Peripheral Blood and Tissue

被引:0
作者
Johansson, Angelica [1 ]
Kalliara, Eirini [1 ]
Belfrage, Emma [2 ]
Alling, Teodor [1 ]
Pyl, Paul Theodor [3 ]
Gerdtsson, Anna Sandstrom [1 ]
Gullberg, Urban [4 ]
Porwit, Anna [5 ]
Drott, Kristina [6 ]
Ek, Sara [1 ]
机构
[1] Lund Univ, Fac Engn LTH, Dept Immunotechnol, S-22363 Lund, Sweden
[2] Skane Univ Hosp SUS, Dept Dermatol & Venereol, S-20502 Lund, Sweden
[3] Lund Univ, Dept Lab Med, Sci Life Lab, Natl Bioinformat Infrastructure Sweden, S-22100 Lund, Sweden
[4] Lund Univ, Dept Lab Med, S-22100 Lund, Sweden
[5] Dept Clin Sci, Div Pathol, S-22100 Lund, Sweden
[6] Dept Clin Sci, Div Med Oncol, S-22100 Lund, Sweden
关键词
biomarker discovery; cutaneous T-cell lymphoma; mycosis fungoides; patient prognostication; personalized medicine; spatially resolved transcriptomics; scRNA-seq; TCR sequencing; LYMPHOMA TASK-FORCE; T-CELL; CUTANEOUS-LYMPHOMAS; INTERNATIONAL-SOCIETY; SEZARY-SYNDROME; EUROPEAN-ORGANIZATION; ASSOCIATION; EXPRESSION; MANAGEMENT;
D O I
10.3390/biomedicines13010186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background/objectives: Mycosis fungoides (MF) is a rare malignancy, with an indolent course in the early stages of the disease. However, due to major molecular and clinical heterogeneity, patients at an advanced stage of the disease have variable responses to treatment and considerably reduced life expectancy. Today, there is a lack of specific markers for the progression from early to advanced stages of the disease. To address these challenges, the non-interventional BIO-MUSE trial was initiated. Here, we report on a case study involving one patient, where combined omics analysis of tissue and blood was used to reveal the unique molecular features associated with the progression of the disease. Methods: We applied 10x genomics-based single-cell RNA sequencing to CD3+ peripheral T-cells, combined with T-cell receptor sequencing, to samples collected at multiple timepoints during the progression of the disease. In addition, GeoMx-based digital spatial profiling of T-helper (CD3+/CD8-), T-cytotoxic (CD3+/CD8+), and CD163+ cells was performed on skin biopsies. Results. The results pinpoint targets, such as transforming growth factor beta 1, as some of the mechanisms underlying disease progression, which may have the potential to improve patient prognostication and the development of precision medicine efforts. Conclusions: We propose that in patients with MF, the evolution of the malignant clone and the associated immune response need to be studied jointly to define relevant strategies for intervention.
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页数:29
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