Sharma Rahul Kumar, Purohit Abhishek, Somasundaram Venkatesan, Mishra Pravas Chandra, Kotru Mrinalini, Ranjan Ravi, Kumar Sunil, Sazawal Sudha, Pati Hara Prasad, Tyagi Seema, Saxena Renu
Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.
Blood Res. 2014 Dec;49(4):241-5. doi: 10.5045/br.2014.49.4.241. Epub 2014 Dec 23.
Aberrant myeloid antigen (MA) co-expression and high expression of CD34 antigen on the blasts of acute lymphoblastic leukemia (ALL) patients are independently reported to have a role in pathogenesis and prognosis. This study was conducted to determine whether these two parameters are related.
A total of 204 cases of ALL were included in an analysis of blast immunophenotypic data. CD34 expression was categorized as low when less than 50% of blasts were CD34-positive (CD34(low)) and as high when 50% or more were CD34-positive (CD34(high)).
Of 204 cases of ALL, 163 and 41 were of B-cell origin (B-ALL) and T-cell origin (T-ALL), respectively. Of all cases, 132 (64.7%) showed co-expression of MA and among these, 101 (76.51%) were CD34(high), while the remaining 31 (23.48%) were CD34(low). Of 72 cases without MA co-expression, 25 (34.72%) were CD34(high) and 47 (67.25%) were CD34(low). Furthermore, of 163 cases of B-ALL, 111 showed co-expression of MA and 84 of these were CD34(high). Of 52 cases of B-ALL without MA expression, 22 were CD34(high). Among 41 cases of T-ALL, 21 co-expressed MA, 17 of which were CD34(high). Moreover, all 20 cases of T-ALL without co-expression of MA were CD34(low). These differences were statistically significant.
We observed a strong correlation between aberrant MA expression and CD34(high) expression on the blasts of ALL. We hypothesize that these different patient subsets may represent unique prognostic characteristics.
急性淋巴细胞白血病(ALL)患者原始细胞异常共表达髓系抗原(MA)以及CD34抗原高表达,分别被独立报道在发病机制和预后中起作用。本研究旨在确定这两个参数是否相关。
共纳入204例ALL患者进行原始细胞免疫表型数据分析。当少于50%的原始细胞CD34呈阳性时,CD34表达被分类为低表达(CD34(低));当50%或更多原始细胞CD34呈阳性时,CD34表达被分类为高表达(CD34(高))。
204例ALL患者中,分别有163例和41例起源于B细胞(B-ALL)和T细胞(T-ALL)。在所有病例中,132例(64.7%)显示MA共表达,其中101例(76.51%)为CD34(高),其余31例(23.48%)为CD34(低)。在72例无MA共表达的病例中,25例(34.72%)为CD34(高),47例(67.25%)为CD34(低)。此外,在163例B-ALL病例中,111例显示MA共表达,其中84例为CD34(高)。在52例无MA表达的B-ALL病例中,22例为CD34(高)。在41例T-ALL病例中,21例共表达MA,其中17例为CD34(高)。此外,所有20例无MA共表达的T-ALL病例均为CD34(低)。这些差异具有统计学意义。
我们观察到ALL原始细胞中异常MA表达与CD34(高)表达之间存在强相关性。我们推测这些不同的患者亚组可能代表独特的预后特征。