Vaca Alicia M, Ioannou Nikolaos, Sivina Mariela, Vlachonikola Elisavet, Clise-Dwyer Karen, Kim Ekaterina, Li Dan, Ma Qing, Ferrajoli Alessandra, Estrov Zeev, Wierda William G, Patten Piers E M, Ramsay Alan G, Burger Jan A
Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Leukemia. 2022 May;36(5):1324-1335. doi: 10.1038/s41375-022-01519-y. Epub 2022 Feb 11.
Interactions between chronic lymphocytic leukemia (CLL) cells and T-cell subsets in the lymph node microenvironment are thought to play a central role in disease biology. To study these interactions in a model of the CLL lymph node microenvironment, we characterized T-cell subsets in CLL nurselike cell (NLC) co-cultures. We focused on T-follicular helper (Tfh) cells, which are characterized by CXCR5 expression and localization to B-cell follicles. In co-cultures from 28 different CLL patients, we detected an expansion of Tfh cells based on PD-1, BCL6, and ICOS expression, with increased IL-21 and downmodulated CD40L surface expression. Regulatory T cells (Treg), which promote immune tolerance, also expanded in NLC co-cultures. T-cell receptor (TR) gene repertoire analyses confirmed the clonal expansion of CD4 T cells, with an enrichment of TR clonotypes commonly expanded also in primary CLL samples. Multicolor confocal microscopy revealed that Tfh, but not Treg co-localize with proliferating CLL cells in CLL lymph node sections. Collectively, these data provide new insight into the cellular and molecular cross-talk between CLL and T-cell subsets, resulting in clonal expansion of T-helper cells and interaction of Tfh cells with proliferating CLL cells which may open new avenues for therapeutic targeting.
慢性淋巴细胞白血病(CLL)细胞与淋巴结微环境中的T细胞亚群之间的相互作用被认为在疾病生物学中起着核心作用。为了在CLL淋巴结微环境模型中研究这些相互作用,我们对CLL滋养样细胞(NLC)共培养物中的T细胞亚群进行了表征。我们重点关注滤泡辅助性T(Tfh)细胞,其特征在于CXCR5表达以及定位于B细胞滤泡。在来自28例不同CLL患者的共培养物中,我们基于PD-1、BCL6和ICOS表达检测到Tfh细胞扩增,同时IL-21增加且CD40L表面表达下调。促进免疫耐受的调节性T细胞(Treg)在NLC共培养物中也有扩增。T细胞受体(TR)基因库分析证实了CD4 T细胞的克隆性扩增,原发性CLL样本中常见的TR克隆型也有富集。多色共聚焦显微镜显示,在CLL淋巴结切片中,Tfh而非Treg与增殖的CLL细胞共定位。总体而言,这些数据为CLL与T细胞亚群之间的细胞和分子相互作用提供了新见解,导致辅助性T细胞克隆性扩增以及Tfh细胞与增殖的CLL细胞相互作用,这可能为治疗靶点开辟新途径。