Pangault Céline, Amé-Thomas Patricia, Rossille Delphine, Dulong Joëlle, Caron Gersende, Nonn Céline, Chatonnet Fabrice, Desmots Fabienne, Launay Vincent, Lamy Thierry, Fest Thierry, Tarte Karin
UMR_S 1236, Univ Rennes, INSERM, Établissement Français du Sang (EFS) Bretagne, LabEx IGO, F-35000 Rennes, France.
Laboratoire Hématologie, Centre Hospitalier Universitaire de Rennes, F-35000 Rennes, France.
Cancers (Basel). 2020 Oct 5;12(10):2865. doi: 10.3390/cancers12102865.
Follicular lymphoma (FL), the most frequent indolent non-Hodgkin's B cell lymphoma, is considered as a prototypical centrocyte-derived lymphoma, dependent on a specific microenvironment mimicking the normal germinal center (GC). In agreement, several FL genetic alterations affect the crosstalk between malignant B cells and surrounding cells, including stromal cells and follicular helper T cells (Tfh). In our study, we sought to deconvolute this complex FL supportive synapse by comparing the transcriptomic profiles of GC B cells, Tfh, and stromal cells, isolated from normal versus FL tissues, in order to identify tumor-specific pathways. In particular, we highlighted a high expression of and in FL B cells that could favor the activation of FL Tfh overexpressing IFNG, able in turn to stimulate FL B cells without triggering MHC (major histocompatibility) class II expression. Moreover, the glycoprotein clusterin was found up-regulated in FL stromal cells and could promote FL B cell adhesion. Finally, besides its expression on Tfh, CD200 was found overexpressed on tumor B cells and could contribute to the induction of the immunosuppressive enzyme indoleamine-2,3 dioxygenase by CD200R-expressing dendritic cells. Altogether our findings led us to outline the contribution of major signals provided by the FL microenvironment and their interactions with malignant FL B cells.
滤泡性淋巴瘤(FL)是最常见的惰性非霍奇金B细胞淋巴瘤,被认为是一种典型的中心细胞来源的淋巴瘤,依赖于模仿正常生发中心(GC)的特定微环境。与此一致的是,一些FL基因改变影响恶性B细胞与周围细胞(包括基质细胞和滤泡辅助性T细胞(Tfh))之间的串扰。在我们的研究中,我们试图通过比较从正常组织与FL组织中分离出的GC B细胞、Tfh和基质细胞的转录组谱,来解构这种复杂的FL支持性突触,以便识别肿瘤特异性途径。特别是,我们强调了FL B细胞中 和 的高表达,这可能有利于过表达IFNG的FL Tfh的激活,而IFNG反过来又能够刺激FL B细胞而不触发主要组织相容性复合体(MHC)II类表达。此外,发现糖蛋白簇集素在FL基质细胞中上调,并可促进FL B细胞黏附。最后,除了在Tfh上表达外,还发现CD200在肿瘤B细胞上过表达,并且可能有助于表达CD200R的树突状细胞诱导免疫抑制酶吲哚胺-2,3-双加氧酶。总之,我们的研究结果使我们概述了FL微环境提供的主要信号的作用及其与恶性FL B细胞的相互作用。