Sanacore M, Zhang X, Brown S L, Connor K, Hilton S, Morris L E, Holland H K, Solomon S R, Bashey A
Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, USA.
Department of Mathematics and Statistics, Georgia State University, Atlanta, GA, USA.
Bone Marrow Transplant. 2015 Jun;50(6):829-33. doi: 10.1038/bmt.2015.41. Epub 2015 Mar 23.
Inadequate T-cell chimerism following reduced-intensity conditioning transplantation may contribute to graft rejection and disease relapse. Anti-thymocyte globulin (ATG) enhances early donor T-cell chimerism, but may also deplete donor T cells, increasing risks of infection and relapse. We prospectively tested administration of rabbit ATG (rATG) ⩾14 days before the infusion of the graft, followed by in vivo decay of active rATG levels, to selectively deplete host T cells. Twenty-three patients received rATG total dose 4.5 mg/kg on days -16 and -15, fludarabine 30 mg/m(2) per day on day -7 through -3, IV busulfan 130 mg/m(2) per day on days -4 and -3 and cyclophosphamide 1500 mg/m(2) on day -2. rATG levels were therapeutic in all patients on day -14, but were sub-therapeutic (<1 μg/mL) by day 0 in 82% of patients. Median donor T-cell chimerisms on days 30 and 180 were 100% (75-100%) and 100% (90-100%), respectively. Non-relapse mortality and relapse/progression at 48 months were 17 and 30%. Cumulative incidences of acute GvHD grades II-IV and III-IV were 39 and 9%. Median follow-up is 64 months (46-79 months). Survival and disease-free survival at 48 months were 70 and 52%. These data suggest that selective depletion of host T cells using this regimen is a feasible and effective strategy.
减低预处理强度移植后T细胞嵌合不足可能导致移植物排斥和疾病复发。抗胸腺细胞球蛋白(ATG)可增强早期供体T细胞嵌合,但也可能消耗供体T细胞,增加感染和复发风险。我们前瞻性地测试了在输注移植物前≥14天给予兔ATG(rATG),随后活性rATG水平在体内衰减,以选择性地消耗宿主T细胞。23例患者在第-16天和-15天接受rATG总剂量4.5mg/kg,在第-7天至-3天每天接受氟达拉滨30mg/m²,在第-4天和-3天每天接受静脉白消安130mg/m²,在第-2天接受环磷酰胺1500mg/m²。所有患者在第-14天rATG水平均具有治疗效果,但在第0天,82%的患者rATG水平低于治疗水平(<1μg/mL)。第30天和第180天供体T细胞嵌合率中位数分别为100%(75%-100%)和100%(90%-100%)。48个月时非复发死亡率和复发/进展率分别为17%和30%。急性移植物抗宿主病(GvHD)Ⅱ-Ⅳ级和Ⅲ-Ⅳ级的累积发生率分别为39%和9%。中位随访时间为64个月(46-79个月)。48个月时的生存率和无病生存率分别为70%和52%。这些数据表明,使用该方案选择性消耗宿主T细胞是一种可行且有效的策略。