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首页> 外文期刊>Tissue antigens. >Monoclonal antibody NU-B1 reacts with novel antigen on human B cells in mantle and marginal zones distinct from known CD molecules.
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Monoclonal antibody NU-B1 reacts with novel antigen on human B cells in mantle and marginal zones distinct from known CD molecules.

机译:单克隆抗体NU-B1与人类B细胞上新的抗原发生反应,位于不同于已知CD分子的地幔和边缘区域。

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摘要

To analyze the cellular antigens of human B-cell lineage, a monoclonal antibody, NU-B1, was raised using the acute lymphoblastic leukemia (ALL) cell line NALM-16 as the immunogen. NU-B1 reacted with 7.7+/-3.9% of the healthy adult peripheral blood mononuclear cells but not with neutrophils, monocytes, red blood cells or thymocytes. In order to distinguish the reaction specificity of NU-B1, two-color immunofluorescence staining using tonsillar cells was performed, and it was demonstrated that NU-B1-positive cells coexpressed CD20, which is a representative B-cell antigen. The expression of NU-B1 was highly restricted to cells of B-cell lineage when a panel of hematopoietic cell lines was examined. In a pathoimmunohistological study using human lymph node tissue, NU-B1-positive cells were localized in the mantle and marginal zones. In a clinical study, NU-B1 reacted specifically with leukemias/lymphomas of B-cell lineage: all 43 cases of ALL including common ALL and biphenotypic leukemia, all 4 cases of B-cell ALL, 6/7 B-cell type malignant lymphomas and 2/4 B-cell chronic lymphocytic leukemias. NU-B1 did not react with multiple myeloma, T-cell or myeloid leukemias/lymphomas. Immunoprecipitation of NU-B1 revealed two clear bands at 50 kDa and 42 kDa under either reducing or nonreducing conditions. Although anti-IgM treatment induced dramatic down modulation of CD79b, the NU-B1 antigen was also down modulated, but only slightly. However, crosslinking of NU-B1 did not induce tyrosine phosphorylation of intracellular proteins or the mobilization of calcium in NALM-16. The present results revealed that the antigenic determinant recognized by NU-B1 is not surface immunoglobulin chains, HLA-DR, a receptor for C3, Fc for immunoglobulin chains or any known CD molecule. We conclude that monoclonal antibody NU-B1 recognizes a novel human B-cell restricted antigen distinct from known CD molecules, and that it is a useful antibody in the immunophenotyping and classification of leukemias/lymphomas.
机译:为了分析人B细胞谱系的细胞抗原,使用急性淋巴细胞白血病(ALL)细胞系NALM-16作为免疫原,制备了单克隆抗体NU-B1。 NU-B1与健康成人外周血单核细胞的7.7 +/- 3.9%反应,但不与中性粒细胞,单核细胞,红细胞或胸腺细胞反应。为了区分NU-B1的反应特异性,使用扁桃体细胞进行了两色免疫荧光染色,并且证明了NU-B1阳性细胞共表达了代表性的B细胞抗原CD20。当检查一组造血细胞系时,NU-B1的表达高度限于B细胞系的细胞。在使用人类淋巴结组织进行的病理免疫组织学研究中,NU-B1阳性细胞位于地幔和边缘区。在一项临床研究中,NU-B1与B细胞谱系的白血病/淋巴瘤特异性反应:全部43例ALL包括普通ALL和双表型白血病,全部4例B细胞ALL,6/7 B细胞型恶性淋巴瘤和2/4 B细胞慢性淋巴细胞性白血病。 NU-B1与多发性骨髓瘤,T细胞或骨髓性白血病/淋巴瘤无反应。 NU-B1的免疫沉淀显示在还原或非还原条件下,在50 kDa和42 kDa处有两个清晰的条带。尽管抗IgM处理可诱导CD79b急剧下调,但NU-B1抗原也下调,但幅度很小。但是,NU-B1的交联不会诱导细胞内蛋白质的酪氨酸磷酸化或在NALM-16中钙的动员。目前的结果表明,NU-B1识别的抗原决定簇不是表面免疫球蛋白链,HLA-DR,C3受体,免疫球蛋白链的Fc或任何已知的CD分子。我们得出的结论是,单克隆抗体NU-B1识别不同于已知CD分子的新型人B细胞限制性抗原,并且它在白血病/淋巴瘤的免疫表型和分类中是有用的抗体。

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