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

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.

Automated summary

By using digital spatial profiling, this study revealed the significant role of CD4(+) T cell rosettes in the tumor microenvironment of classic Hodgkin lymphoma (CHL). The expression of immune checkpoint molecules was found to be higher in CD4(+) T cell rosettes compared to other CD4(+) T cells.