Leger-Ravet M B, Peuchmaur M, Devergne O, Audouin J, Raphael M, Van Damme J, Galanaud P, Diebold J, Emilie D
INSERM U131, Clamart, France.
Blood. 1991 Dec 1;78(11):2923-30.
Defined by histological criteria, Castleman's disease (CD) is a clinically and histologically heterogeneous syndrome. The functional status of immune cells in affected tissues may vary between the different forms of the disease. To address this question, the expression of cytokine genes in eight CD lymph nodes was analyzed by in situ hybridization. Two lymph nodes were taken from patients with a localized form of the disease associated with systemic manifestations, two from patients with a localized form without systemic symptoms, and four from patients with a multicentric form. Five lymph nodes exhibiting a benign follicular hyperplasia were used as controls. The interleukin-6 (IL-6) gene was expressed at a very high level in two cases: the two localized forms of CD associated with systemic manifestations. IL-6 gene overexpression occurred inside follicles of these lymph nodes. The morphology of follicular cells hybridizing with the IL-6 probe or labeled with an anti-IL-6 monoclonal antibody suggested that follicular dendritic cells expressed the IL-6 gene. In contrast, no IL-6 gene expression was detected inside follicles of the six other CD lymph nodes or of the five control lymph nodes. In interfollicular areas, IL-6 gene-expressing cells were detected in all lymph nodes by both in situ hybridization and immunohistochemistry. In CD lymph nodes, positive cells were located outside sinuses, in close contact with blood vessels and plasma cells. This distribution was clearly different from that observed in control lymph nodes, in which IL-6 gene-expressing cells were present inside sinuses. A similar difference between CD and control lymph nodes was observed for the distribution of IL-1 beta and IL-1 alpha gene-expressing cells in interfollicular areas. The morphology of interfollicular IL-6-producing cells was heterogeneous, consistent with that of macrophages, interdigitating cells, lymphocytes, and endothelial cells, and different from that of plasma cells. Taken together these results show that CD is consistently associated with a particular pattern of IL-6 gene expression in interfollicular areas whereas elevated IL-6 gene expression inside follicles only occurs in the localized form of the disease associated with systemic manifestations. The variable pattern of IL-6 gene expression as well as the clinical and histologic heterogeneity of CD indicate that different immune mechanisms may be involved in the different forms of this disease.
根据组织学标准定义,卡斯特曼病(CD)是一种临床和组织学上异质性的综合征。在受影响组织中免疫细胞的功能状态在该疾病的不同形式之间可能有所不同。为了解决这个问题,通过原位杂交分析了8个CD淋巴结中细胞因子基因的表达。从患有与全身表现相关的局限性疾病形式的患者中获取了2个淋巴结,从没有全身症状的局限性疾病形式的患者中获取了2个淋巴结,从多中心性疾病形式的患者中获取了4个淋巴结。将5个表现为良性滤泡性增生的淋巴结用作对照。白细胞介素-6(IL-6)基因在2例中表达水平非常高:与全身表现相关的两种局限性CD形式。IL-6基因过表达发生在这些淋巴结的滤泡内。与IL-6探针杂交或用抗IL-6单克隆抗体标记的滤泡细胞形态表明滤泡树突状细胞表达IL-6基因。相比之下,在其他6个CD淋巴结或5个对照淋巴结的滤泡内未检测到IL-6基因表达。在滤泡间区域,通过原位杂交和免疫组织化学在所有淋巴结中均检测到表达IL-6基因的细胞。在CD淋巴结中,阳性细胞位于窦外,与血管和浆细胞紧密接触。这种分布与在对照淋巴结中观察到的明显不同,在对照淋巴结中,表达IL-6基因的细胞存在于窦内。在滤泡间区域中,对于表达IL-1β和IL-1α基因的细胞的分布,在CD和对照淋巴结之间也观察到了类似的差异。滤泡间产生IL-6的细胞形态是异质性的,与巨噬细胞、交错突细胞、淋巴细胞和内皮细胞的形态一致,与浆细胞的形态不同。综上所述,这些结果表明,CD始终与滤泡间区域中特定的IL-6基因表达模式相关,而滤泡内IL-6基因表达升高仅发生在与全身表现相关的局限性疾病形式中。IL-6基因表达的可变模式以及CD的临床和组织学异质性表明,不同的免疫机制可能参与了该疾病的不同形式。