Gouda Heba M, Abdel Mohsen Mohsen M
The Department of Clinical & Chemical Pathology, Cairo University, Egypt.
J Egypt Natl Canc Inst. 2009 Jun;21(2):93-9.
RHAMM/CD168 is a cell surface receptor for hyaluronan, a glycoaminoglycan that plays a fundamental role in cell growth, differentiation and motility. It is one of the leukemia-associated antigens (LAA) identified in patients with myeloid leukemias.
at studying the frequency of expression of RHAMM/CD168 in Egyptian patients with CML, both in chronic phase and accelerated/blastic phase, as a potential target structure for cellular immunotherapies, and to compare it with available western records.
RHAMM expression was tested by RT-PCR in peripheral blood mononuclear cells of 60 CML patients divided into 2 groups, group A: 44 chronic phase CML patients, group B: 16 accelerated/ blastic phase patients as well as 15 healthy volunteers.
Demonstrated that 14/44 (31.8%) of chronic CML patients showed positive RHAMM expression in contrast to 15/16 ( 93.7%) in the accelerated/blastic phase patients. Moreover within the chronic phase patients the RHAMM positive patients had a significantly higher level of bcr-abl/abl ratio. This highlighted the contribution of RHAMM expression with CML disease progression.
Our work demonstrated a similar proportion of RHAMM expression in both Egyptian and western CML patients. This may pave the way for subsequent studies suggesting the concomitant use of RHAMM R3 peptide vaccination with conventional CML therapy especially in accelerated phase, in order to achieve complete molecular remission for our patient.
RHAMM/CD168是透明质酸的细胞表面受体,透明质酸是一种糖胺聚糖,在细胞生长、分化和运动中起重要作用。它是在髓系白血病患者中鉴定出的白血病相关抗原(LAA)之一。
是研究RHAMM/CD168在埃及慢性粒细胞白血病(CML)患者慢性期和加速期/急变期的表达频率,作为细胞免疫治疗的潜在靶结构,并将其与现有的西方记录进行比较。
通过RT-PCR检测60例CML患者外周血单个核细胞中的RHAMM表达,这些患者分为2组,A组:44例慢性期CML患者,B组:16例加速期/急变期患者以及15名健康志愿者。
表明14/44(31.8%)的慢性CML患者RHAMM表达呈阳性,而加速期/急变期患者为15/16(93.7%)。此外,在慢性期患者中,RHAMM阳性患者的bcr-abl/abl比值明显更高。这突出了RHAMM表达对CML疾病进展的作用。
我们的研究表明埃及和西方CML患者中RHAMM表达比例相似。这可能为后续研究铺平道路,提示在常规CML治疗中,尤其是在加速期,同时使用RHAMM R3肽疫苗接种,以便使我们的患者实现完全分子缓解。