Boccadoro M, Van Acker A, Pileri A, Urbain J
Ann Immunol (Paris). 1981 Jan-Feb;132C(1):9-19. doi: 10.1016/0769-2625(81)90003-9.
We have studied seven human monoclonal gammopathies using anti-idiotypic sera. In benign and malignant gammopathies, we have observed a similar number of B lymphocytes bearing idiotypic specificities also found on the monoclonal protein. These observations suggest that the plasma cell population is only a phenotypic expression of a tumoral event occurring in a B lymphocytes precursor which can still completely differentiate. In four myeloma patients and one benign monoclonal gammopathy, we also observed T lymphocytes bearing receptors idiotypically cross-reactive with the monoclonal protein. The values ranged from 1.8 to 8.0% within the purified T-cell population. In a first hypothesis, these T lymphocytes can belong to the tumoral clone itself. The tumoral event must occur at the level of a common precursor not yet determined to B or T pathway of differentiation. In a second hypothesis, these T lymphocytes are not cancerous but are induced by a strong perturbation of the idiotypic network, due to the enormous amount of the idiotypic B-cell tumoral subset.
我们使用抗独特型血清研究了7种人类单克隆丙种球蛋白病。在良性和恶性丙种球蛋白病中,我们观察到携带与单克隆蛋白上相同独特型特异性的B淋巴细胞数量相似。这些观察结果表明,浆细胞群体只是B淋巴细胞前体中发生的肿瘤事件的一种表型表达,而该前体仍可完全分化。在4例骨髓瘤患者和1例良性单克隆丙种球蛋白病患者中,我们还观察到携带与单克隆蛋白独特型交叉反应受体的T淋巴细胞。在纯化的T细胞群体中,其比例范围为1.8%至8.0%。在第一种假设中,这些T淋巴细胞可能属于肿瘤克隆本身。肿瘤事件必定发生在尚未确定为B或T分化途径的共同前体水平。在第二种假设中,这些T淋巴细胞并非癌性的,而是由于独特型B细胞肿瘤亚群数量巨大导致独特型网络受到强烈干扰而被诱导产生的。