Follicular Dendritic Cell Meshwork in Angioimmunoblastic T-Cell Lymphoma Is Characterized by Accumulation of CXCL13<sup>+</sup> Cells

CXCL13型 血管免疫母细胞性T细胞淋巴瘤 生发中心 滤泡树突状细胞 CXCR5型 细胞 病理 B细胞 化学 癌症研究 细胞生物学 抗体 生物 免疫学 T细胞 医学 炎症 趋化因子 抗原提呈细胞 免疫系统 生物化学 趋化因子受体
作者
Haruo Ohtani,Takuya Komeno,Yoshiko Agatsuma,Motohiro Kobayashi,Masayuki Noguchi,Naoya Nakamura
出处
期刊:Journal of Clinical and Experimental Hematopathology [Japanese Society for Lymphoreticular Tissue Research]
卷期号:55 (2): 61-69 被引量:17
标识
DOI:10.3960/jslrt.55.61
摘要

Angioimmunoblastic T-cell lymphoma (AITL) is considered to originate from follicular helper T (TFH) cells. Currently, neoplastic cells in AITL are considered to express CXCL13 as a tumor marker. However, the identification of CXCL13+ cells remains unclear in terms of whether they are neoplastic cells (or TFH cells) or follicular dendritic cells (FDCs) in both AITL and normal germinal centers. Therefore, the exact identification of CXCL13+ cells was performed using 33 cases of AITL and normal germinal centers. Single-labeling immunohistochemistry and double-labeling immunofluorescent microscopy first confirmed that CXCL13 was expressed mainly in FDCs in the normal germinal centers. In 28 of 33 AITL cases, CXCL13 was expressed mainly in FDCs as a meshwork pattern, which was associated with CXCL13+ neoplastic cells. In the other five cases, CXCL13 was expressed mainly in neoplastic cells, which were densely distributed in and around the FDC meshwork. These findings indicate the abundance of CXCL13+ cells in the FDC meshwork irrespective of the cell type. Triple-labeling immunofluorescent microscopy showed that the CXCL13+ FDC meshwork in AITL harbored both neoplastic cells and B cells. CXCR5, the cognate receptor of CXCL13, was expressed in neoplastic cells in AITL. The present study suggests that neoplastic cells in AITL preserve a certain level of TFH-cell function since neoplastic cells and B cells are closely enmeshed in the CXCL13+ cell-rich FDC meshwork in a similar way as in normal germinal centers. [J Clin Exp Hematop 55(2) : 61-69, 2015]

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