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作 者:张弦[1] 张艳玲[1] 王建玲[1] 童春容[1] 蔡鹏[1] 刘红星[1] 王静波[1] 曹星玉[1] 殷宇明[1] 吴彤[1]
机构地区:[1]北京市道培医院,100049
出 处:《中华血液学杂志》2011年第8期525-528,共4页Chinese Journal of Hematology
摘 要:目的分别探讨NK细胞中抑制性和激活性免疫球蛋白样受体(KIR)在亲缘半相合造血干细胞移植(HSCT)中的作用。方法检测47例亲缘半相合HSCT中的供者KIR基因型和患者HLA—c基因型,随访移植后2年总生存率、Ⅲ~Ⅳ度急性移植物抗宿主病(GVHD)发生率和复发率。结果①按供受者抑制性KIR与其配体HLA—C是否匹配分为两组,匹配组的2年总生存率明显高于不匹配组[分别为(87.5±8.3)%和(54.5±9.0)%,P=0.03];复发率明显降低[分别为0和(25.4±9.5)%,P=0.05]。将病例分为髓系白血病和淋巴细胞白血病,其中30例髓系白血病患者中匹配组复发率明显低于不匹配组[分别为0和(35.0±14.4)%,P=0.04]。其他项目差异无统计学意义。②常见的激活性KIR主要包括3个:KIR2DS1、KIR2DS2、KIR2DS3。分别按其供者是否表达进行单因素分析,其中KIR2DS1(+)组Ⅲ-Ⅳ度急性GVHD发生率比KITR2DS1(-)组低(分别为13%和28%,P〉0.05);KIR2DS2(+)组复发率低于KIR2DS2(-)组[分别为0和(17.3±7.1)%,P〉0.05];KIR2DS3(+)组Ⅲ~Ⅳ度急性GVHD发生率低于KIR2DS3(-)组(分别为11%和26%,P〉0.05);其他无明显差异。结论①亲缘半相合HSCT中,供者抑制性KIR与患者HLA—C匹配组较不匹配组总体生存率明显升高,复发率明显降低。特别在髓系白血病中,复发率明显降低。②对于激活性KIR受体中KIR2DS1或KIR2DS3的表达,可能降低急性重度GVHD的发生率;而KIR2DS2(+)组表达,可能降低复发率。Objective To investigate the effect of inhibitory and activating KIRs on a cohort of Chinese leukemia patients who received haplo-identieal hematopoietie stem cell transplantation (HSCT). Methods Donor' s inhibitory and activating KIRs and recipient' s HLA-C from 47 cases who received haplo-identical HSCT were tested by PCR-SSP. 2 year overall survival ( OS ) , incidence of severe ( grade Ⅲ to Ⅳ) acute GVHD (aGVHD) and relapse rate(RR) were analyzed. Results (1)According to Matched(M) vs Mis-Matched(MM) between donor' s inhibitory KIR and recipient' s HLA-C1/C2 subgroup, 2 year OS rate in M group [ (87.5 ± 8.3) % ] was significantly higher than that in MM group (54.5 ± 9.0) %, (P = 0.03 ). Lower incidence of relapse rate was seen in M group than in M/MM groups [ 0 vs ( 25.4 ± 9.5 ) % , P = 0.05 ]. In 30 cases of myeloid leukemia patients, there was lower RR in M group than in MM groups [ 0 vs (35.0 ± 14.4) % ,P =0.04]. (2)Aceording to the 3 activating KIR genes: KIR2DS1/KIR2DS2/KIR2DS3, lower incidence of grade HI - IV aGVHD was seen in KIR2DS1 ( + ) group than in KIR2DS1 ( - ) group (13% vs 28% , respectively, P 〉0.05) ; and so was done in KIR2DS3 ( + ) group( 11% vs 26% , respectively, P 〉 0.05 ). The RR was lower in KIR2DS2 ( + ) group [ 0% vs ( 17.3 + 7.1 ) %, respectively, P 〉 0.05 ]. Conclusions In our haplo-identical HSCT setting, match between donor' s inhibitory KIR and recipient' s HLA-C can significantly reduce the incidence of relapse rate and improve OS. Although lower incidences of severe aGVHD are noted in the donors with KIR2DS1 ( + ) or KIR2DS3 ( + ), and lower relapse rate is noted in the donors with KIR2DS2 ( + ) but without statistic difference, no remarkable effects of activating KIRs on OS have been found in our relatively small clinical series.
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