Bao Xiao-jing, He Jun, Chen Zi-xing, Wu De-pei, Yao Li, Yuan Xiao-ni, Cen Jian-nong, Qiu Qiao-cheng, Di Wen-ying, Zhang Hui, Zhang Jian, Zhou Xiao-hua, Xu Hui-xin
Jiangsu Institute of Hematology, First Affiliated Hospital of Soochow University, Suzhou, China.
Zhonghua Xue Ye Xue Za Zhi. 2007 Aug;28(8):510-3.
To study the biological function of killer cell immunoglobulin-like receptor (KIR) and the role of donor inhibitory KIR and recipient genetic background in HLA matched unrelated hematopoietic stem cell transplantation (HSCT).
HLA genotype of 51 patients (ALL 18 cases, CML 15 cases, AML 10 cases and others 8 cases) and their respective matched unrelated donors from Database of China Marrow Registration was determined by polymerase chain reaction sequence oligonucleotide probes (PCR-SSOP) and sequence specific primers (PCR-SSP). The KIR genotype was determined by PCR-SSP.
All the patients and the donors expressed KIR2DL1, KIR2DL2/L3, KIR2DL4, KIR3DL2 and KIR3DL3. 96.7% individuals expressed KIR3DL1. Among them, 21.57% of KIR was completely identical, while 78.43% was not. Of the non-identical KIRs, 25.49% were the recipient's KIR genotype containing the donor's ones, and 27.45% was the donor's containing the recipient's. 74.62% of donor's KIR2DL1 lacked recipient's C2 ligand, 5.91% of donor's KIR2DL2/L3 lacked recipient's C1 ligand, 19.74% of donor's KIR3DL1 lacked recipient's Bw4 ligand and 54.91% of donor's KIR3DL2 lacked recipient's A3, A11 ligand.
KIR genotype and HLA class I antigen are inherited independently. KIR2DLI and KIR3DL2 of donors may cause alloreactivity of NK cell. The mismatch of KIR/HLA in donor-recipient plays a very important role in matched unrelated allo-HSCT. The outcome of HSCT can be better predicted by the model of the presence of KIRs on the donor' sNK cells and the absence of corresponding KIR ligand in the recipient's HLA.
研究杀伤细胞免疫球蛋白样受体(KIR)的生物学功能以及供体抑制性KIR和受体遗传背景在人类白细胞抗原(HLA)相匹配的非血缘造血干细胞移植(HSCT)中的作用。
采用聚合酶链反应序列寡核苷酸探针(PCR-SSOP)和序列特异性引物(PCR-SSP)技术,对中国骨髓库中51例患者(急性淋巴细胞白血病18例、慢性粒细胞白血病15例、急性髓细胞白血病10例及其他8例)及其各自匹配的非血缘供体进行HLA基因分型,采用PCR-SSP技术进行KIR基因分型。
所有患者及供体均表达KIR2DL1、KIR2DL2/L3、KIR2DL4、KIR3DL2和KIR3DL3。96.7%的个体表达KIR3DL1。其中,21.57%的KIR完全相同,78.43%不同。在不同的KIR中,25.49%是受体的KIR基因型包含供体的,27.45%是供体的包含受体的。74.62%的供体KIR2DL1缺乏受体的C2配体,5.91%的供体KIR2DL2/L3缺乏受体的C1配体,19.74%的供体KIR3DL1缺乏受体的Bw4配体,54.91%的供体KIR3DL2缺乏受体的A3、A11配体。
KIR基因型与HLA I类抗原独立遗传。供体的KIR2DLI和KIR3DL2可能引起NK细胞的同种异体反应性。供受体间KIR/HLA错配在HLA相匹配的非血缘异基因HSCT中起非常重要的作用。通过供体NK细胞上KIR的存在及受体HLA中相应KIR配体缺失的模型可更好地预测HSCT的结局。