Immune and Hematological Reconstitution after Allogenic Bone Marrow Transplantation in Tunisian Pediatric Recipients: Prospective Study and Tunisian Experience Report

F. Jenhani, Z. Regaya, L. Berraies, F. Mellouli
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Abstract

AIM: A regular monitoring of the immune reconstitution mainly based on the quantitative determination of lymphocyte T subpopulation. This is prospective analysis for 1 year in Tunisian children treated with allogenic intrafamilial bone marrow transplantation. Methods: We conducted a prospective analysis for 1 year follow up enrolling 25 children treated with allogenic intrafamilial bone marrow transplantation among them two cases of Peripheral hematopoietic transplantation and placental cord blood transplantation including: aplastic anemia (6 cases), hemoglobinopathies (12 cases), myelodysplastic syndrome (1 case), 2 cases of Acute lymphocytic leukemia, a case of congenital amegacarycytosis and 3 cases of primary immunodeficiency with lack of expression of major MHC class II. All subjects received different conditioning regimens according to the indication. Our study consisted of a regular monitoring of the immune reconstitution mainly based on the quantitative determination of lymphocyte T subpopulation. So, these tests were routinely requested to 1 month, 2 months, 3 months, 6 months, 9 months and 12 months post- bone marrow transplantation. Results: The average time of engraftment was 18 days corresponding to neutrophil recovery (12-24). For the T cell recovery, a rate of CD4 + T lymphocytes > 200/ mm3 was provided within an average of 2.5 months (1-7). The average time to obtain CD8+ T lymphocytes >200 /mm3 was 2 months (1-5). The humoral immune reconstitution was made within an average of 2 months (1-4). A ratio of CD4+ / CD8+ T lymphocytes (>1) was obtained within 10 months and a half (1-24). Univaried analysis showed a significant correlation between the bone marrow sex matched and the faster reorganization of CD8 + T cells (p = 0.042). Moreover, a quantity of CD34 +> 6x 106/ kg was significantly associated with the recapture of a formula lymphocyte T CD4+ / CD8+ (> 1) (p=0.03). Conclusion: The immune recovery post bone marrow transplantation in children began with myeloid lineage then lymphoid B then lymphoid T. The inversion of the ratio CD4 +/CD8+ T lymphocytes, seemed to be influenced on the one hand by the high content of CD34 + cells in the graft as well as the type of conditioning on the other hand by the CMV infection since it accelerates significantly CD8+ T lymphocyte reconstitution. 
突尼斯儿童同种异体骨髓移植后的免疫和血液学重建:前瞻性研究和突尼斯经验报告
目的:以淋巴细胞T亚群的定量测定为基础,对免疫重建进行定期监测。这是突尼斯儿童接受同种异体家族内骨髓移植治疗1年的前瞻性分析。方法:我们对25例接受同种异体家族内骨髓移植治疗的儿童进行了1年的前瞻性分析,其中2例为外周造血移植和胎盘脐血移植,包括:再生障碍性贫血(6例)、血红蛋白病(12例)、骨髓增生异常综合征(1例),2例急性淋巴细胞白血病,1例先天性阿米巴细胞增多症,3例原发性免疫缺陷,主要MHC II类缺乏表达。所有受试者根据适应症接受不同的调理方案。我们的研究包括定期监测免疫重建,主要基于淋巴细胞T亚群的定量测定。因此,这些测试通常要求在骨髓移植后1个月、2个月、3个月、6个月、9个月和12个月进行。结果:平均植入时间为18天,相当于中性粒细胞的恢复时间(12-24)。对于T细胞的恢复,CD4+T淋巴细胞的比率>200/mm3在平均2.5个月内提供(1-7)。获得CD8+T淋巴细胞>200/mm3的平均时间为2个月(1-5)。体液免疫重建平均在2个月内完成(1-4)。CD4+/CD8+T淋巴细胞的比率在10个半月(1-24)内获得(>1)。单因素分析显示骨髓性别匹配与CD8+T细胞快速重组之间存在显著相关性(p=0.042),CD34+>6x106/kg与配方淋巴细胞T CD4+/CD8+(>1)的再捕获显著相关(p=0.03),似乎一方面受到移植物中高含量CD34+细胞的影响,另一方面受到CMV感染的调理类型的影响。
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