Takahashi H, Furukawa T, Hashimoto S, Suzuki N, Kuroha T, Yamazaki F, Inano K, Takahashi M, Aizawa Y, Koike T
First Department of Internal Medicine, College of Biochemical Technology, Niigata University School of Medicine, Japan.
Bone Marrow Transplant. 2000 Dec;26(12):1317-23. doi: 10.1038/sj.bmt.1702724.
Some cytokines are believed to play a role in the development of acute and chronic GVHD after allo-hematopoietic stem cell transplantation. It has been reported that TNF-alpha and IL-10 gene polymorphisms are associated with the production of those cytokines and the development of graft failure after organ transplantation and systemic lupus erythematosus. We examined whether TNF-alpha and IL-10 gene polymorphisms affect the severity of acute GVHD (aGVHD) and chronic GVHD (cGVHD). Sixty-two and 54 patients were available for the analysis of aGVHD and cGVHD, respectively. We analyzed the gene polymorphisms derived from pre- and post-transplant blood cells. Donor-derived TNF2 allele (A) was more frequently detected in patients with aGVHD III/IV than those aGVHD 0-II (2/6 vs 2/56) (P = 0.04). The donors of the patients with cGVHD more frequently possessed a greater number of alleles (allele 13 or more which contain 26 or more CA repeats) in IL-10.G than those without (13/26 vs 5/28) (P = 0.02), and the patients with cGVHD had more CA repeats in donor-derived IL-10.G than those without (mean = 25.2 vs 23.4) (P = 0.01). Donor-derived TNF-308 and IL-10.G alleles may contribute to severe aGVHD and cGVHD, respectively, and will help us distinguish those patients at high risk for GVHD.
一些细胞因子被认为在异基因造血干细胞移植后的急性和慢性移植物抗宿主病(GVHD)发展中起作用。据报道,肿瘤坏死因子-α(TNF-α)和白细胞介素-10(IL-10)基因多态性与这些细胞因子的产生以及器官移植和系统性红斑狼疮后移植物失败的发展有关。我们研究了TNF-α和IL-10基因多态性是否会影响急性移植物抗宿主病(aGVHD)和慢性移植物抗宿主病(cGVHD)的严重程度。分别有62例和54例患者可用于aGVHD和cGVHD的分析。我们分析了移植前后血细胞的基因多态性。与aGVHD 0-II级患者相比,aGVHD III/IV级患者中更频繁地检测到供体来源的TNF2等位基因(A)(2/6 vs 2/56)(P = 0.04)。cGVHD患者的供体在IL-10.G中比无cGVHD的供体更频繁地拥有更多数量的等位基因(等位基因13个或更多,其中包含26个或更多CA重复序列)(13/26 vs 5/28)(P = 0.02),并且cGVHD患者供体来源的IL-10.G中的CA重复序列比无cGVHD的患者更多(平均值 = 25.2 vs 23.4)(P = 0.01)。供体来源的TNF - 308和IL-10.G等位基因可能分别导致严重的aGVHD和cGVHD,并将有助于我们区分那些GVHD高风险患者。