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T细胞亚群剂量对去T细胞骨髓移植结果的影响。

Effect of T cell subset dose on outcome of T cell-depleted bone marrow transplantation.

作者信息

Kawanishi Y, Passweg J, Drobyski W R, Rowlings P, Cook-Craig A, Casper J, Pietryga D, Garbrecht F, Camitta B, Horowitz M, Juckett M, Margolis D, Flomenberg N, Keever-Taylor C A

机构信息

Bone Marrow Transplantation Program of the Medical College of Wisconsin, Milwaukee 53226, USA.

出版信息

Bone Marrow Transplant. 1997 Jun;19(11):1069-77. doi: 10.1038/sj.bmt.1700807.

Abstract

T cell depletion using the murine monoclonal antibody (moAb) T10B9 is unique in that the T cell receptor (TCR)gamma delta bearing subset is relatively spared compared to the TCR alpha beta + subset. We evaluated the probabilities of engraftment, acute and chronic graft-versus-host disease (GVHD), relapse, and survival in 273 recipients of marrow T cell depleted using T10B9. Sixty-two patients received marrow from an HLA-identical sibling, 54 patients received partially matched related donor marrow and 157 patients received unrelated donor marrow. Limiting dilution analysis (LDA) was used to estimate total clonable T cell dose in all patients and a modified LDA using moAb-coated immunomagnetic beads was used to estimate TCR alpha beta +, CD4+, and CD8+ T cells in a subset of patients. TCR gamma delta + cell dose was estimated by flow cytometry. Cox proportional hazards regression models were used to assess the impact of T cell subset dose/kg of body weight on outcome. We found a significant association of TCR gamma delta + T cell dose (P = 0.004), but not TCR alpha beta + T cell dose or total clonable T cell dose, with the probability of engraftment. TCR alpha beta +, CD4+, CD8+ and total clonable T cell dose were significantly associated (P < 0.001) with the risks of grade 2-4 acute GVHD in recipients of marrow from related donors but not in recipients of marrow from unrelated donors. Neither total clonable T cell dose nor any T cell subset dose was found to be significantly associated with chronic GVHD, relapse or survival. The results confirm preclinical studies showing TCR gamma delta + T cells promote engraftment. TCR gamma delta + T cells are not associated with an increased risk of acute GVHD while TCR alpha beta T cells are associated with acute GVHD but not engraftment in recipients of marrow grafts T cell depleted using T10B9. These findings support the hypothesis that T cell subsets differentially contribute to alloengraftment and GVHD.

摘要

使用鼠单克隆抗体(moAb)T10B9清除T细胞具有独特之处,即与TCRαβ +亚群相比,携带T细胞受体(TCR)γδ的亚群相对未受影响。我们评估了273例接受T10B9清除骨髓T细胞的受者的植入概率、急性和慢性移植物抗宿主病(GVHD)、复发率和生存率。62例患者接受了来自HLA相同同胞的骨髓,54例患者接受了部分匹配的相关供体骨髓,157例患者接受了无关供体骨髓。采用极限稀释分析(LDA)估计所有患者的可克隆T细胞总剂量,并使用包被有moAb的免疫磁珠的改良LDA估计一部分患者中的TCRαβ +、CD4 +和CD8 + T细胞。通过流式细胞术估计TCRγδ +细胞剂量。使用Cox比例风险回归模型评估每千克体重T细胞亚群剂量对结局的影响。我们发现TCRγδ + T细胞剂量(P = 0.004)与植入概率存在显著关联,但TCRαβ + T细胞剂量或可克隆T细胞总剂量与植入概率无此关联。TCRαβ +、CD4 +、CD8 +和可克隆T细胞总剂量与来自相关供体骨髓受者发生2 - 4级急性GVHD的风险显著相关(P < 0.001),但与来自无关供体骨髓受者发生急性GVHD的风险无关。未发现可克隆T细胞总剂量或任何T细胞亚群剂量与慢性GVHD、复发或生存存在显著关联。结果证实了临床前研究显示TCRγδ + T细胞促进植入。TCRγδ + T细胞与急性GVHD风险增加无关,而TCRαβ T细胞与急性GVHD有关,但与使用T10B9清除T细胞的骨髓移植受者的植入无关。这些发现支持了T细胞亚群对同种异体植入和GVHD有不同贡献的假说。

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