Agis Hermine, Krauth Maria-Theresa, Böhm Alexandra, Mosberger Isabella, Müllauer Leonhard, Simonitsch-Klupp Ingrid, Walls Andrew F, Horny Hans-Peter, Valent Peter
Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Am J Clin Pathol. 2006 Feb;125(2):273-81. doi: 10.1309/M9FQ-MQGF-6616-7N2X.
In myeloproliferative disorders (MPDs), basophils typically increase in number in the bone marrow (BM) and blood. In chronic myeloid leukemia (CML), basophilia is a diagnostic and prognostic variable. However, no reliable approach for routine detection and enumeration of basophils in BM sections is available. We applied the antibasogranulin antibody BB1 on paraffin-embedded BM sections in 21 control samples (normal BM), 45 patients with CML, 9 with chronic idiopathic myelofibrosis, 11 with polycythemia vera, 19 with essential thrombocythemia, and 7 with indolent systemic mastocytosis. As assessed by immunostaining of serial BM sections, BB1+ cells coexpressed myeloperoxidase, histidine decarboxylase, and leukosialin but did not express B- or T-cell-restricted antigens. BB1+ BM cells were found to be highly elevated in patients with CML compared with normal BM or other MPDs, with maximum counts found in accelerated phase CML (median, 160 cells/mm(2)). In summary, BB1 (basogranulin) is a new immunohistochemical basophil marker that should allow quantification of basophils in CML at diagnosis and during therapy.
在骨髓增殖性疾病(MPD)中,嗜碱性粒细胞在骨髓(BM)和血液中的数量通常会增加。在慢性髓性白血病(CML)中,嗜碱性粒细胞增多是一个诊断和预后变量。然而,目前尚无用于常规检测和计数BM切片中嗜碱性粒细胞的可靠方法。我们将抗嗜碱粒细胞颗粒蛋白抗体BB1应用于21份对照样本(正常BM)、45例CML患者、9例慢性特发性骨髓纤维化患者、11例真性红细胞增多症患者、19例原发性血小板增多症患者以及7例惰性系统性肥大细胞增多症患者的石蜡包埋BM切片。通过对连续BM切片进行免疫染色评估,BB1+细胞共表达髓过氧化物酶、组氨酸脱羧酶和白细胞涎酸蛋白,但不表达B细胞或T细胞限制性抗原。与正常BM或其他MPD相比,发现CML患者的BB1+BM细胞高度升高,在CML加速期达到最高计数(中位数为160个细胞/mm²)。总之,BB1(嗜碱粒细胞颗粒蛋白)是一种新的免疫组化嗜碱性粒细胞标志物,可用于在CML诊断和治疗期间对嗜碱性粒细胞进行定量。