Ioannidou Kalliopi, Ndiaye Daba-Rokhya, Noto Alessandra, Fenwick Craig, Fortis Sotirios P, Pantaleo Giuseppe, Petrovas Constantinos, de Leval Laurence
Department of Laboratory Medicine and Pathology, Institute of Pathology, Lausanne University Hospital and Lausanne University, Lausanne, Switzerland.
Service of Immunology and Allergy, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Front Immunol. 2021 Feb 3;11:607626. doi: 10.3389/fimmu.2020.607626. eCollection 2020.
Follicular helper CD4 T (Tfh) cells play an essential role in the formation of germinal centers (GCs), where mature B cells proliferate, differentiate, and provide long-term protective humoral responses. Despite the extensive phenotypic characterization and identification of human Tfh cell subsets, their spatial positioning at tissue level is not well understood. Here, we describe a quantitative multiplexed immunofluorescence approach allowing for the comprehensive characterization of Tfh cells in human tonsils and lymph nodes (LNs) from individuals with angioimmunoblastic T-cell lymphoma (AITL). We have developed eight multiplexed panels comprising a spectrum of Tfh cell markers, like PD-1, CXCR5, and ICOS, along with transcription factors (Bcl6, Tbet, GATA3), to assess their expression, frequencies, spatial distribution and co-localization in a quantitative manner. Combined analysis of relevant markers revealed the presence of several Tfh cell subsets at tissue level based on the differential expression of surface receptors, nuclear factors as well as their distinct localization within the follicular areas. Interestingly, we found a considerable amount of tonsillar Tfh cells expressing high levels of the Th2 regulator GATA3. The co-expression of GATA3, CXCR5, and BCL6, points to an important role of GATA3 for the generation of effector human Tfh cells. Furthermore, our data revealed significantly different Tfh cell profile signatures between health and disease. Therefore, our imaging platform generates meaningful information for the characterization of human Tfh cells and could provide the base for future studies aiming to a comprehensive understanding of Tfh cell tissue heterogeneity.
滤泡辅助性CD4 T(Tfh)细胞在生发中心(GC)的形成中起着至关重要的作用,在生发中心成熟B细胞增殖、分化并提供长期保护性体液反应。尽管对人类Tfh细胞亚群进行了广泛的表型特征分析和鉴定,但它们在组织水平上的空间定位仍未得到很好的理解。在这里,我们描述了一种定量多重免疫荧光方法,可全面表征来自血管免疫母细胞性T细胞淋巴瘤(AITL)患者的人类扁桃体和淋巴结(LN)中的Tfh细胞。我们开发了八个多重检测面板,其中包括一系列Tfh细胞标志物,如PD-1、CXCR5和ICOS,以及转录因子(Bcl6、Tbet、GATA3),以便以定量方式评估它们的表达、频率、空间分布和共定位。对相关标志物的联合分析揭示了基于表面受体、核因子的差异表达及其在滤泡区域内的不同定位,在组织水平上存在几个Tfh细胞亚群。有趣的是,我们发现大量扁桃体Tfh细胞表达高水平的Th2调节因子GATA3。GATA3、CXCR5和BCL6的共表达表明GATA3在效应性人类Tfh细胞的产生中起重要作用。此外,我们的数据揭示了健康与疾病之间Tfh细胞谱特征存在显著差异。因此,我们的成像平台为人类Tfh细胞的表征生成了有意义的信息,并可为未来旨在全面了解Tfh细胞组织异质性的研究提供基础。