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血红蛋白病中羟基脲对胎儿血红蛋白生成和γ-信使核糖核酸表达的体外和体内反应比较

Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in Hemoglobinopathies.

作者信息

Italia Khushnooma, Jijina Farah, Merchant Rashid, Swaminathan Suchitra, Nadkarni Anita, Gupta Maya, Ghosh Kanjaksha, Colah Roshan

机构信息

National Institute of Immunohematology, Hematogenetics, 13 Floor, K.E.M. Hospital Campus, Parel, Mumbai, India.

出版信息

Indian J Hum Genet. 2013 Apr;19(2):251-8. doi: 10.4103/0971-6866.116128.

Abstract

BACKGROUND

Hydroxyurea, which induces Fetal hemoglobin (HbF) synthesis, is the only drug widely used in different hemoglobinopathies; however, the response is very variable. We compared the efficacy of hydroxyurea in-vitro in erythroid cultures and in-vivo in the same patients with different hemoglobinopathies to induce HbF production and enhance γ-messenger RNA expression.

MATERIALS AND METHODS

A total of 24-patients with different Hemoglobinopathies were given hydroxyurea and their response was studied in-vivo and in-vitro on mononuclear cells collected from them simultaneously.

RESULTS

A total of 57.7% of patients (responders) showed no further crisis or transfusion requirements after hydroxyurea therapy with a mean increase in fetal cells (F-cells) of 63.8 ± 59.1% and γ-mRNA expression of 205.5 ± 120.8%. In-vitro results also showed a mean increase in F-cells of 27.2 ± 24.7% and γ-mRNA expression of 119.6% ± 65.4% among the treated cells. Nearly 19.0% of the partial-responders reduced their transfusion requirements by 50% with a mean increase in F-cells of 61.2 ± 25.0% and 28.4 ± 25.3% and γ-mRNA-expression of 21.0% ± 1.4% and 80.0% ± 14.1% in-vivo and in-vitro respectively. The non-responders (15.3%) showed no change in their clinical status and there was no significant increase in F-cells levels and γ-mRNA expression in-vivo or in-vitro.

CONCLUSION

Thus, this method may help to predict the in-vivo response to hydroxyurea therapy; however, a much larger study is required.

摘要

背景

羟基脲可诱导胎儿血红蛋白(HbF)合成,是唯一广泛用于治疗不同血红蛋白病的药物;然而,其疗效差异很大。我们比较了羟基脲在患有不同血红蛋白病的同一患者的红细胞培养物中的体外疗效以及体内疗效,以诱导HbF产生并增强γ-信使核糖核酸表达。

材料与方法

共24例患有不同血红蛋白病的患者接受了羟基脲治疗,并同时对从他们身上采集的单核细胞进行了体内和体外反应研究。

结果

共有57.7%的患者(反应者)在接受羟基脲治疗后不再出现危机或有输血需求,胎儿细胞(F细胞)平均增加63.8±59.1%,γ-信使核糖核酸表达增加205.5±120.8%。体外结果还显示,在处理过的细胞中,F细胞平均增加27.2±24.7%,γ-信使核糖核酸表达增加119.6%±65.4%。近19.0%的部分反应者输血需求减少了50%,体内和体外F细胞平均分别增加61.2±25.0%和28.4±25.3%,γ-信使核糖核酸表达分别增加21.0%±1.4%和80.0%±14.1%。无反应者(15.3%)的临床状态没有变化,体内或体外F细胞水平和γ-信使核糖核酸表达均无显著增加。

结论

因此,该方法可能有助于预测羟基脲治疗的体内反应;然而,需要进行更大规模的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a84/3758735/11a8c5d6a2e8/IJHG-19-251-g004.jpg

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