Harris N L, Bhan A K
Hum Pathol. 1985 Aug;16(8):829-37. doi: 10.1016/s0046-8177(85)80255-0.
The relation between chronic lymphocytic leukemia (CLL, lymphocytic lymphoma (SL), plasmacytoid lymphocytic lymphoma (LP), plasmacytoma (PL), and multiple myeloma (MM) was investigated with cryostat sections stained with antibodies to immunoglobulin heavy and light chains and the B-cell differentiation antigens B1, B2, Ia, T1, and CALLA. Neoplasms were subclassified according to plasmacytoid features, leukemia (CLL) site of involvement (nodal or extranodal), serum monoclonal immunoglobulin, or clinical evidence of MM. The results defined two groups of lymphocytic lymphomas without plasmacytoid features (16 cases). Ten of these lymphomas were associated with CLL. Nine involved lymph nodes, all expressed IgM, five expressed IgD, nine were B2-positive, eight were T1-positive, and all were B1- and Ia-positive. Six of the lymphomas were not associated with CLL. Five of these tumors were extranodal, all were T1- B1+ B2- Ia+, five expressed IgM without IgD, and one contained IgG. These differences in clinical and immunologic phenotypes suggest that CLL and SL without CLL may be related to different stages of B-cell differentiation. T1 appeared to be a marker for CLL, since all T1-positive neoplasms were leukemic. Lymphomas with plasmacytoid features (ten cases) were more often extranodal, and none was leukemic. The immunologic phenotypes were heterogeneous: all of these lymphomas were T1-negative, most were IgM+ IgD-, three were B2-positive, and all were Ia-positive. The plasma cells in five lymphomas with marked plasmacytoid features were B1-negative; they were Ia-positive in four and Ia-negative in one. These data suggest that LP is a heterogeneous group, reflecting B cells at diverse stages of differentiation. Ten plasmacytomas, nine of which were associated with MM, differed from LP in showing heavy chain class switching; all were T1- B1- B2-, and all but one were Ia-negative. These results are consistent with the existence of two pathways or stages of B-cell differentiation: one that generates IgM-producing plasma cells, as seen in the primary immune response or in response to pokeweed mitogen, and one that generates IgG- or IgA-positive plasma cells, as seen in the late primary or secondary immune response. Plasmacytoid lymphocytic lymphoma reflects the first, while PL/MM reflects the second pathway. B1 appears to be lost before Ia in terminal plasma cell differentiation.
利用冷冻切片,用针对免疫球蛋白重链和轻链以及B细胞分化抗原B1、B2、Ia、T1和CALLA的抗体进行染色,研究了慢性淋巴细胞白血病(CLL)、小淋巴细胞淋巴瘤(SL)、浆细胞样淋巴细胞淋巴瘤(LP)、浆细胞瘤(PL)和多发性骨髓瘤(MM)之间的关系。根据浆细胞样特征、白血病(CLL)的受累部位(淋巴结或结外)、血清单克隆免疫球蛋白或MM的临床证据对肿瘤进行亚分类。结果确定了两组无浆细胞样特征的淋巴细胞淋巴瘤(16例)。其中10例淋巴瘤与CLL相关。9例累及淋巴结,均表达IgM,5例表达IgD,9例B2阳性,8例T1阳性,均为B1和Ia阳性。6例淋巴瘤与CLL无关。其中5例肿瘤为结外病变,均为T1 - B1 + B2 - Ia +,5例表达IgM而无IgD,1例含有IgG。这些临床和免疫表型的差异表明,CLL和无CLL的SL可能与B细胞分化的不同阶段有关。T1似乎是CLL的一个标志物,因为所有T1阳性肿瘤均为白血病性。具有浆细胞样特征的淋巴瘤(10例)更常为结外病变,且无一例为白血病性。免疫表型是异质性的:所有这些淋巴瘤均为T1阴性,大多数为IgM + IgD -,3例为B2阳性,均为Ia阳性。5例具有明显浆细胞样特征的淋巴瘤中的浆细胞为B1阴性;其中4例Ia阳性,1例Ia阴性。这些数据表明,LP是一个异质性群体,反映了B细胞在不同分化阶段的情况。10例浆细胞瘤中,9例与MM相关,与LP不同的是表现出重链类别转换;均为T1 - B1 - B2 -,除1例外在均为Ia阴性。这些结果与B细胞分化存在两条途径或阶段一致:一条途径产生产生IgM的浆细胞,如在初次免疫反应或对商陆有丝分裂原反应中所见;另一条途径产生IgG或IgA阳性浆细胞,如在初次或二次免疫反应后期所见。浆细胞样淋巴细胞淋巴瘤反映了第一条途径,而PL/MM反映了第二条途径。在终末浆细胞分化过程中,B1似乎在Ia之前丢失。