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通过Ia同种异体抗原和补体受体对白血病细胞进行分类。细胞分化的表面探针。

Classification of leukemic cells by Ia alloantigens and complement receptors. Surface probes for cell differentiation.

作者信息

Barth P, Schunter F, Wilms K, Waller H D, Wernet P

出版信息

Bibl Haematol. 1978;45:124-30. doi: 10.1159/000402193.

Abstract

Of particular interest in the study of cell membrane markers of leukemic cells were cytotoxic and immunofluorescent results obtained in comparing Ia alloantigen and complement receptor (CR) expression on normal leukocytic and leukemic cell types. Using discontinuous Ficoll gradients, Ia alloantigens were found on varying numbers of leukemic myelo- and lymphoblasts, and on the early stages of normal melocytes. Ia alloantigens, however, were not detectable on mature polymorphonuclear cells. This establishes human Ia alloantigens as cell surface differentiation markers. The appearance of complement receptors was observed later than that of Ia alloantigens. CR1 (EAC1-4b) showed up later in the differentiation than CR2 (EAC1-3d). Thus, an immunological discrimination between AML blasts and CML blast crisis blasts appears to be possible: AML blasts are mostly Ia-positive but CR-negative, whilst CML blast crisis cells are only 20-30% Ia-positive and carry complement receptors in at least equal amounts. The AML blast cell would appear as the less-differentiated cell type when compared to the CML blast crisis cells. The picture, however, remains complex since in CML blast crisis at least three different types of blast cells can be identified: an Ia-positive and an Ia-negative myeloid blast as well as an Ia-positive lymphoid blast. The quantitative composition of these three elements within the myeloid differentiation profile can vary somewhat from patient to patient. Furthermore, these studies revealed a disturbed differentiation of leukemic cell types.

摘要

在白血病细胞细胞膜标志物的研究中,特别令人感兴趣的是在比较正常白细胞和白血病细胞类型上Ia同种异体抗原和补体受体(CR)表达时所获得的细胞毒性和免疫荧光结果。使用不连续的Ficoll梯度,发现不同数量的白血病髓母细胞和淋巴母细胞以及正常黑素细胞的早期阶段存在Ia同种异体抗原。然而,在成熟的多形核细胞上未检测到Ia同种异体抗原。这确立了人类Ia同种异体抗原作为细胞表面分化标志物。补体受体的出现比Ia同种异体抗原晚。CR1(EAC1-4b)在分化过程中比CR2(EAC1-3d)出现得更晚。因此,急性髓系白血病(AML)原始细胞和慢性髓系白血病(CML)急变期原始细胞之间的免疫学区分似乎是可能的:AML原始细胞大多为Ia阳性但CR阴性,而CML急变期细胞只有20%-30%为Ia阳性,且携带的补体受体数量至少相等。与CML急变期细胞相比,AML原始细胞似乎是分化程度较低的细胞类型。然而,情况仍然复杂,因为在CML急变期至少可以识别出三种不同类型的原始细胞:Ia阳性和Ia阴性髓系原始细胞以及Ia阳性淋巴系原始细胞。这三种成分在髓系分化谱中的定量组成在不同患者之间可能会有所不同。此外,这些研究揭示了白血病细胞类型的分化紊乱。

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