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作 者:蒋瑛[1] 万理萍[1] 王椿[1] 颜式可[1] 高彦荣[1] 姜杰玲[1] 杨隽[1] 蔡宇[1] 白海涛[1] 魏道林[1] 谢匡成[1]
机构地区:[1]上海交通大学附属第一人民医院血液科,200080
出 处:《中华血液学杂志》2008年第10期667-671,共5页Chinese Journal of Hematology
基 金:上海市科委重点项目(044119632)
摘 要:目的研究异基因造血干细胞移植(allo—HSCT)后各系细胞嵌合状态与移植物植人、急性移植物抗宿主病(aGVHD)、移植物被排斥和疾病复发的关系。方法对65例患者进行allo—HSCT,存移植后定期采集所有患者的外周m和骨髓。用流式细胞术分选了65例患者的CD3^+T淋巴细胞,52例分选了CD3^-CD56^+CD16^+NK细胞,32例分选了CD15^+粒细胞,20例分选了CD19^+B淋巴细胞。进行PCR扩增短串联重复序列检测各系细胞嵌合状态。结果移植后NK细胞早期植入比例(55.5%)最高,T细胞最晚(+21d)达到完全供者嵌合状态。+7dT淋巴细胞供者嵌合比例(DC)≥70%和+14dT淋巴细胞DC/〉95%属aGVHD发生的高危患者。除急性淋巴细胞白血病外,出现移植物被排斥的分子生物学征象者和疾病复发者,都以T淋巴细胞供者嵌合状态下降为主。在过继免疫治疗中,动态检测嵌合状态可以判断疗效和指导进一步的治疗。结论allo—HSCT后T淋巴细胞嵌合状态动态检测可以早期预测发生aGVHD的高危患者、判断移植物植入、发现移植物被排斥和疾病复发并指导免疫渊节治疗的时机和疗效。Objective To evaluate the relationship of chimerism status of cell subsets with engraftment, occurrence of acute graft versus host disease (aGVHD) , graft rejection and disease relapse after allogenieic hematopoietic stein cell transplantation (allo-HSCT). Methods Chimerism status in peripheral blood (PB) and bone marrow (BM) of 65 patients received allo-HSCT were monitored at regular intervals posttransplant. Fluorescence-activated cell sorter (FACS) was used to sort CD3 +T lymphoeytes in 65 cases, CD3^- CD56^ + CD16^ + NK cells in 52 cases, CD15 ^ + granulocytes in 32 cases and CD19^ + B lymphocytes in 20 cases post transplants. The ehilnerism status of different lineage cells was analyzed by polymerase chain reaction amplification of short tandem repeats (PCR-STR). Results On day + 7, NK-cells donor chimerism ( DC 55.5% ) was higher than other cell subsets. T lymphocyte was the latest one to reach complete donor chimerisin(CDC) with a median on day + 21. Patients whose T lymphoeytes donor chimerism was more than 70% on day +7 anti more than 95% on day + 14 had a high risk for acute aGVHD. In all cases except those with ALL, the decreased DC of T lymphoeytes were observed hefore molecular or hematological relapse occurred. Conclusion Serial anti quantitative T cell chimerism analysis provides a reliable and rapid screening method for the early detection of engraftment, graft rejection, disease relapse and occurrence of aGVHD, therefore, is a prognostic tool to identify patients at high risk of aGVHD and disease relapse following allo- HSCT.
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