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免疫抑制受体 ILT3 在伴单核分化的急性髓系白血病中的表达。

Expression of immune inhibitory receptor ILT3 in acute myeloid leukemia with monocytic differentiation.

机构信息

Department of Pathology and Cell Biology, Columbia University Medical Center and New York Presbyterian Hospital, New York, New York, USA.

出版信息

Cytometry B Clin Cytom. 2013 Jan-Feb;84(1):21-9. doi: 10.1002/cyto.b.21050. Epub 2012 Oct 18.

DOI:10.1002/cyto.b.21050
PMID:23027709
Abstract

BACKGROUND

The diagnosis of AML with monocytic differentiation is limited by the lack of highly sensitive and specific monocytic markers. Immunoglobulin-like transcript 3 (ILT3) is an immune inhibitory receptor expressed by myelomonocytic cells and at high levels by tolerogenic dendritic cells.

METHODS

Using flow cytometry, we analyzed the expression of ILT3 in 37 patients with AML and 20 patients with no detectable disease.

RESULTS

We showed that ILT3 was expressed in all cases of AML displaying monocytic differentiation (FAB M4/M5; N = 18), but not in AML M1/M2 and M3 (N = 19; P < 0.0001). Co-expression of ILT3 and immature cell markers, such as CD34 and CD117, was observed in monoblastic leukemia. ILT3 expression was preserved after treatment in M4/M5 patients with refractory or relapsed disease. ILT3 expression was associated with the presence of cytogenetic abnormalities linked to an intermediate prognosis (P = 0.001). Rare CD45dimCD34+CD117+ILT3+ cells were identified in noninvolved bone marrow, suggesting that ILT3 expression is acquired at an early stage by normal myelomonocytic precursors.

CONCLUSIONS

ILT3 is a highly sensitive and specific marker which distinguishes AML with monocytic differentiation from other types of AML. Testing of ILT3 expression should be incorporated into the initial diagnostic work-up and monitoring of patients with AML.

摘要

背景

具有单核分化的 AML 的诊断受到缺乏高度敏感和特异的单核细胞标志物的限制。免疫球蛋白样转录物 3(ILT3)是一种表达于髓样单核细胞且高水平表达于耐受树突状细胞的免疫抑制受体。

方法

我们使用流式细胞术分析了 37 例 AML 患者和 20 例无明显疾病患者中 ILT3 的表达。

结果

我们发现,ILT3 在所有具有单核分化的 AML 病例中均有表达(FAB M4/M5;N = 18),但在 AML M1/M2 和 M3 中无表达(N = 19;P < 0.0001)。在单核白血病中观察到 ILT3 与未成熟细胞标志物如 CD34 和 CD117 的共表达。在难治性或复发性疾病的 M4/M5 患者中,经治疗后 ILT3 表达得以保留。ILT3 表达与与中等预后相关的细胞遗传学异常相关(P = 0.001)。在无累及骨髓中发现罕见的 CD45dimCD34+CD117+ILT3+细胞,提示 ILT3 表达是由正常髓样单核前体早期获得的。

结论

ILT3 是一种高度敏感和特异的标志物,可将具有单核分化的 AML 与其他类型的 AML 区分开来。ILT3 表达的检测应纳入 AML 患者的初始诊断和监测中。

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