p24 HTLV3主要核心蛋白在LAS患者淋巴结中的分布。

C D Baroni, F Pezzella
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摘要

淋巴结病综合征(LAS)患者的淋巴结以两种主要的组织学模式为特征:增生反应性(H)和退行性(R)。在这两种情况下,副皮质(PC)因选择性Ia-1+高内皮小静脉的存在而显着激活。我们利用HTLV3主要核心蛋白p24的单克隆抗体,免疫组织化学方法测定了23例LAS患者HTLV3-ab血清学阳性患者淋巴结中p24+细胞的分布。11例显示P24 +细胞。对照节点为阴性。p24+细胞包括PC毛细血管后小静脉高内皮细胞、大血管周围细胞、PC和GC大单核或双核细胞以及少量淋巴细胞样细胞。我们的初步观察表明,大多数p24+细胞是高内皮细胞和辅助细胞,它们可能作为病毒库或作为抗原呈递细胞向T4淋巴细胞和GC B细胞。此外,高内皮细胞的p24阳性可能有助于解释其选择性Ia-1+。
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Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.

Lymph nodes of patients with lymphadenopathy syndrome (LAS) are characterized by two main histological patterns: hyperplastic reactive (H) and regressive (R). In both conditions, the paracortex (PC) is markedly activated with presence of selectively Ia-1+ high endothelial venules. Using a monoclonal antibody for p24, the major core protein of HTLV3, we have immunohistochemically determined the distribution of p24+ cells in lymph nodes from 23 LAS patients' HTLV3-ab serologically positive. p24+ cells were demonstrated in 11 cases. Control nodes were negative. p24+ cells included high endothelial cells of PC postcapillary venules, large perivenular cells, large mono- or binucleated cells in PC and in GC, and few lymphocytelike cells. Our preliminary observations indicate that the majority of p24+ cells are high endothelial and accessory cells that may act either as virus reservoir or as antigen-presenting cells to T4 lymphocytes and to GC B cells. In addition, the positivity of high endothelial cells for p24 might help to explain their selective Ia-1+.

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