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真性红细胞增多症:疾病的干细胞起源及可能的克隆起源

Polycythemia vera: stem-cell and probable clonal origin of the disease.

作者信息

Adamson J W, Fialkow P J, Murphy S, Prchal J F, Steinmann L

出版信息

N Engl J Med. 1976 Oct 21;295(17):913-6. doi: 10.1056/NEJM197610212951702.

Abstract

Two women with polycythemia vera and heterozygosity (GdB/GdA) at the X-chromosome-linked locus for glucose-6-phosphate dehydrogenase were studied to determine the nature of the cellular origin of their polycythemia. In contrast to unaffected tissue, such as skin fibroblasts, which consisted of both B and A types, the glucose-6-phosphate dehydrogenase of the patients' erythrocytes, granulocytes and platelets was only of Type A. These results provide direct evidence for the stem-cell nature of polycythemia vera and strongly imply a clonal origin for this disease. The fact that no descendants of the presumed normal stem cells were found in circulation suggests that bone-marrow proliferation in this disorder is influenced by local (intramarrow) regulatory factors.

摘要

对两名患有真性红细胞增多症且在X染色体连锁的葡萄糖-6-磷酸脱氢酶位点呈杂合性(GdB/GdA)的女性进行了研究,以确定其红细胞增多症的细胞起源性质。与未受影响的组织(如由B型和A型细胞组成的皮肤成纤维细胞)不同,患者红细胞、粒细胞和血小板中的葡萄糖-6-磷酸脱氢酶仅为A型。这些结果为真性红细胞增多症的干细胞性质提供了直接证据,并强烈暗示该疾病起源于克隆。在循环中未发现推测的正常干细胞后代这一事实表明,该疾病中的骨髓增殖受局部(骨髓内)调节因子的影响。

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