Biberfeld P, Porwit-Ksiazek A, Böttiger B, Morfeldt-Månsson L, Biberfeld G
Cancer Res. 1985 Sep;45(9 Suppl):4665s-4670s.
Lymph node biopsies from 43 male homosexuals with persistent generalized lymphadenopathy and from ten acquired immunodeficiency syndrome patients, all with serum antibodies to human T-cell leukemia virus III, were studied with regard to histopathology, immunohistology, and T-cell subsets in cell suspensions. All acquired immunodeficiency syndrome biopsies except one with Kaposi's sarcoma had the same histopathological pattern of follicular depletion, whereas the persistent generalized lymphadenopathy nodes showed a spectrum of changes characterized as follicular hyperplasia, involution with follicular fragmentation, or involution with follicular atrophy. Immunohistology showed a temporal and structural relation between follicular involution, disappearance of follicular dendritic reticulum cells, and follicular invasion by T-cells. These observations suggest elimination of dendritic reticulum cells as part of a pathogenic mechanism in follicular involution. Angiogenesis measured by staining of endothelial cells with antibodies to Factor VIII was increased in many biopsies in stages of involution and depletion. Our observations indicate the occurrence of marked changes not only in T-cells but also in the B-cell compartment of patients with persistent generalized lymphadenopathy or acquired immunodeficiency syndrome. The possibility of staging lymph nodes of these patients by combined histopathology and immunohistology is indicated. This might improve the evaluation of prognosis in these patients. A possible importance of angiogenesis for the tumorigenesis of Kaposi's sarcoma is suggested.
对43名患有持续性全身性淋巴结病的男性同性恋者以及10名获得性免疫缺陷综合征患者的淋巴结活检组织进行了研究,所有患者血清中均含有针对人类T细胞白血病病毒III的抗体,研究内容包括组织病理学、免疫组织学以及细胞悬液中的T细胞亚群。除1例伴有卡波西肉瘤的获得性免疫缺陷综合征活检组织外,其余所有活检组织均呈现相同的滤泡耗竭组织病理学模式,而持续性全身性淋巴结病的淋巴结则表现出一系列变化,其特征为滤泡增生、伴有滤泡破碎的退化或伴有滤泡萎缩的退化。免疫组织学显示滤泡退化、滤泡树突状网状细胞消失以及T细胞对滤泡的浸润之间存在时间和结构上的关系。这些观察结果表明,作为滤泡退化致病机制的一部分,树突状网状细胞被清除。通过用抗VIII因子抗体对内皮细胞进行染色来测量的血管生成,在许多处于退化和耗竭阶段的活检组织中有所增加。我们的观察结果表明,患有持续性全身性淋巴结病或获得性免疫缺陷综合征的患者不仅T细胞发生了显著变化,B细胞区室也发生了显著变化。提示通过联合组织病理学和免疫组织学对这些患者进行淋巴结分期的可能性。这可能会改善对这些患者预后的评估。提示血管生成对卡波西肉瘤肿瘤发生可能具有重要意义。