Lymphocyte predominant cells of nodular lymphocyte predominant Hodgkin lymphoma interact with rosetting T cells in an immunological synapse

被引:21
作者
Bein, Julia [1 ]
Thurner, Lorenz [2 ,3 ]
Hansmann, Martin-Leo [1 ,4 ]
Hartmann, Sylvia [1 ]
机构
[1] Goethe Univ, Dr Senckenberg Inst Pathol, Frankfurt, Germany
[2] Saarland Univ, Med Sch, Dept Internal Med 1, Homburg, Germany
[3] Saarland Univ, Med Sch, Jose Carreras Ctr Immuno & Gene Therapy, Homburg, Germany
[4] Frankfurt Inst Adv Studies, Frankfurt, Germany
关键词
REED-STERNBERG CELLS; DISEASE; EXPRESSION; GENE; PATTERNS; FREQUENT; VARIANT; DIFFERENTIATION; LIGANDS; SUBSET;
D O I
10.1002/ajh.25972
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) is a subtype of Hodgkin lymphoma with a preserved B-cell phenotype and follicular T helper (T-FH) cells rosetting around the tumor cells, the lymphocyte-predominant (LP) cells. As we recently described reactivity of the B-cell receptors of LP cells of some NLPHL cases withMoraxellaspp. proteins, we hypothesized that LP cells could present peptides to rosetting T cells in a major histocompatibility complex class II (MHCII)-bound manner. Rosetting PD1(+)T cells were present in the majority of NLPHL cases, both in typical (17/20) and variant patterns (16/19). In most cases, T-cell rosettes were CD69(+)(typical NLPHL, 17/20; NLPHL variant, 14/19). Furthermore, both MHCII alpha and beta chains were expressed in the LP cells in 23/39 NLPHL. Proximity ligation assay and confocal laser imaging demonstrated interaction of the MHCII beta chain expressed by the LP cells and the T-cell receptor alpha chain expressed by rosetting T cells. We thus conclude that rosetting T cells in NLPHL express markers that are encountered after antigenic exposure, that MHCII is expressed by the LP cells, and that LP cells interact with rosetting T cells in an immunological synapse in a subset of cases. As they likely receive growth stimulatory signals in this way, blockade of this interaction, for example, by PD1-directed checkpoint inhibitors, could be a treatment option in a subset of cases in the future.
引用
收藏
页码:1495 / 1502
页数:8
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