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使用单克隆抗体和异种抗体对大细胞淋巴瘤进行分析。

Analysis of large-cell lymphomas using monoclonal and heterologous antibodies.

作者信息

van der Valk P, van den Besselaar-Dingjan G, Daha M R, Meijer C J

出版信息

J Clin Pathol. 1983 Jan;36(1):44-50. doi: 10.1136/jcp.36.1.44.

DOI:10.1136/jcp.36.1.44
PMID:6337190
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC498103/
Abstract

Fifteen cases of large-cell lymphoma, diagnosed as centroblastic (5), B-immunoblastic (5) or true histiocytic (5). lymphoma and one case of malignant histiocytosis were studied with monoclonal antibodies. Each diagnosis was based on morphological as well as marker studies. A panel of monoclonal and heterologous antibodies against T lymphocyte differentiation antigens (Leul, Leu2a, Leu3a, OKT4, OKT8, TA1), B lymphocyte subsets (BA1, BA2, HLA-DR, alpha C3b receptor antiserum, surface immunoglobulins), the common acute lymphoblastic leukaemia antigen (CALLA), monocytes/macrophages (OKM1, anti-human monocyte 1, TA1, Mac1, HLA-DR, anti-C3b receptor), myeloid cells (VIM-D5, elastase, OKM1) and the cells of the Langerhans cell/interdigitating reticulum cell series (OKT6, NA1/34). The results show a specific staining pattern for true histiocytic lymphoma (histiocytic sarcoma). Centroblastic and B-immunoblastic lymphomas showed gradual differences with mostly strong staining for HLA-DR and weak with anti C3b receptor for B-immunoblastic lymphomas in contrast to centroblastic lymphomas. Staining with BA1 and BA2 indicated immunological heterogeneity in these lymphomas. The number of admixed cells was usually low with few B cells and a shift in the ratio helper/inducer to suppressor/cytotoxic T cells in favour of the suppressor/cytotoxic subset.

摘要

对15例大细胞淋巴瘤(诊断为中心母细胞性5例、B免疫母细胞性5例或真性组织细胞性5例)及1例恶性组织细胞增多症患者进行了单克隆抗体研究。每项诊断均基于形态学及标志物研究。使用了一组针对T淋巴细胞分化抗原(Leul、Leu2a、Leu3a、OKT4、OKT8、TA1)、B淋巴细胞亚群(BA1、BA2、HLA - DR、αC3b受体抗血清、表面免疫球蛋白)、常见急性淋巴细胞白血病抗原(CALLA)、单核细胞/巨噬细胞(OKM1、抗人单核细胞1、TA1、Mac1、HLA - DR、抗C3b受体)、髓样细胞(VIM - D5、弹性蛋白酶、OKM1)以及朗格汉斯细胞/交错突网状细胞系列细胞(OKT6、NA1/34)的单克隆和异源抗体。结果显示真性组织细胞性淋巴瘤(组织细胞肉瘤)有特定的染色模式。中心母细胞性和B免疫母细胞性淋巴瘤表现出逐渐的差异,B免疫母细胞性淋巴瘤大多对HLA - DR呈强染色,而与中心母细胞性淋巴瘤相比,对抗C3b受体呈弱染色。用BA1和BA2染色表明这些淋巴瘤存在免疫异质性。混合细胞数量通常较少,B细胞很少,辅助/诱导性T细胞与抑制/细胞毒性T细胞的比例发生偏移,有利于抑制/细胞毒性亚群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/0d8e7f166de2/jclinpath00506-0058-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/7f4260d85ab4/jclinpath00506-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/4a1f8186bcb5/jclinpath00506-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/0d8e7f166de2/jclinpath00506-0058-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/7f4260d85ab4/jclinpath00506-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/4a1f8186bcb5/jclinpath00506-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f058/498103/0d8e7f166de2/jclinpath00506-0058-b.jpg

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本文引用的文献

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Am J Clin Pathol. 1957 Jan;27(1):13-23. doi: 10.1093/ajcp/27.1.13.
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Malignant lymphoma of true histiocytic origin: histiocytic sarcoma. A morphological, ultrastructural, immunological, cytochemical and clinical study of 10 cases.真性组织细胞起源的恶性淋巴瘤:组织细胞肉瘤。10例的形态学、超微结构、免疫学、细胞化学及临床研究
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