Digital spatial profiling of CD4+ T cells in classic Hodgkin lymphoma

被引:5
作者
Takeuchi, Mai [1 ]
Miyoshi, Hiroaki [1 ]
Semba, Yuichiro [2 ]
Yamada, Kyohei [1 ]
Nakashima, Kazutaka [1 ]
Sato, Kensaku [1 ]
Furuta, Takuya [1 ]
Moritsubo, Mayuko [1 ]
Ogura, Yusuke [1 ]
Tanaka, Ken [1 ]
Imamoto, Teppei [1 ]
Arakawa, Fumiko [1 ]
Kohno, Kei [1 ]
Ohshima, Koichi [1 ]
机构
[1] Kurume Univ, Dept Pathol, Sch Med, Kurume, Fukuoka, Japan
[2] Kyushu Univ, Dept Med & Biosyst Sci, Fac Med, Fukuoka, Fukuoka, Japan
基金
日本学术振兴会;
关键词
Classic Hodgkin lymphoma; Hodgkin-Reed-Sternberg cells; CD4(+) T cell rosettes; Digital spatial profiling; Tumor microenvironment; ANALYSIS REVEALS; EXPRESSION; MICROENVIRONMENT; BLOCKADE; DISEASE;
D O I
10.1007/s00428-023-03562-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Classic Hodgkin lymphoma (CHL) harbors a small number of Hodgkin-Reed-Sternberg (HRS) cells scattered among numerous lymphocytes. HRS cells are surrounded by distinct CD4(+) T cells in a rosette-like manner. These CD4(+) T cell rosettes play an important role in the tumor microenvironment (TME) of CHL. To elucidate the interaction between HRS cells and CD4(+) T cell rosettes, we completed digital spatial profiling to compare the gene expression profiles of CD4(+) T cell rosettes and other CD4(+) T cells separated from the HRS cells. Immune checkpoint molecules including OX40, programed cell death-1 (PD-1), and cytotoxic T lymphocyte associated protein 4 (CTLA-4) expression was higher in CD4(+) T cell rosettes compared to other CD4(+) T cells. Immunohistochemistry confirmed variable PD-1, CTLA-4, and OX40 expression in the CD4(+) T cell rosettes. This study introduced a new pathological approach to study the CHL TME, and provided deeper insight into CD4(+) T cells in CHL.
引用
收藏
页码:255 / 260
页数:6
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