Asou N, Suzushima H, Hattori T, Nishikawa K, Wang J X, Okubo T, Oura K, Sato M, Kawano F, Shido T
Second Department of Internal Medicine, Kumamoto University Medical School, Japan.
Leukemia. 1991 Apr;5(4):293-9.
To analyze the development pathways of early hematopoietic cells, we studied the rearrangement and expression of the immunoglobulin (Ig) and T-cell receptor (TCR) genes in 12 patients with acute unclassified leukemia (AUL). Leukemia cells from these patients were negative for myeloperoxidase staining and failed to express B-cell, T-cell, or megakaryocyte associated antigens. The expression of the CD7 antigen, myeloid associated antigens, or both was detected in three patients each. Ig and/or TCR gene rearrangements were detected in seven of the 12 patients, and five had rearrangement of both the Ig and TCR genes. Full length mature TCR gene transcripts were not demonstrated in most of the patients showing TCR gene rearrangements. In contrast, cells from two patients with germline configurations of the Ig and TCR genes tested expressed truncated forms of both Ig and TCR genes. These results suggest that AUL may generally originate from undifferentiated cells with an aberrant rearrangement and/or expression of the Ig and TCR genes.
为分析早期造血细胞的发育途径,我们研究了12例急性未分类白血病(AUL)患者免疫球蛋白(Ig)和T细胞受体(TCR)基因的重排及表达情况。这些患者的白血病细胞髓过氧化物酶染色呈阴性,且不表达B细胞、T细胞或巨核细胞相关抗原。分别有3例患者检测到CD7抗原、髓系相关抗原或两者均表达。12例患者中有7例检测到Ig和/或TCR基因重排,其中5例Ig和TCR基因均发生重排。大多数显示TCR基因重排的患者未检测到全长成熟TCR基因转录本。相反,检测的2例Ig和TCR基因呈种系构型的患者的细胞表达了截短形式的Ig和TCR基因。这些结果表明,AUL通常可能起源于具有Ig和TCR基因异常重排和/或表达的未分化细胞。