Hansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, New York.
Department of Surgery, NYU Langone Health, New York, New York.
J Surg Res. 2021 Feb;258:17-22. doi: 10.1016/j.jss.2020.08.006. Epub 2020 Sep 23.
Authors have speculated that vascularized composite allotransplantation (VCA) recipients may require greater maintenance immunosuppression than solid organ transplant (SOT) recipients due to the higher antigenicity of skin. However, detailed comparisons of VCA and SOT immunosuppression regimens have been limited.
Hand and face VCA recipient immunosuppression data were collected through a systematic literature review. Kidney recipient data were obtained through a retrospective chart review of the authors' institution. Prednisone and mycophenolate mofetil (MMF) doses were compared between VCA and kidney recipients at predefined follow-up intervals (<1, 1-5, and >5 y). Tacrolimus target trough levels (TTTL) were compared at follow-up intervals of 1-5 and >5 y, and stratified into our institution's kidney transplant risk-based target ranges (4-6 ng/mL, 6-8 ng/mL) or higher (>8 ng/mL).
Immunosuppression data were available for 57 VCA and 98 kidney recipients. There were no significant differences in prednisone doses between groups at all follow-up intervals. VCA recipient mean MMF dose was significantly greater at <1-y (1.71 ± 0.58 versus 1.16 ± 0.55 gm/d; P = 0.01). For VCA recipients, there was a significant difference (P = 0.02) in TTTL distribution over the three predefined therapeutic ranges (4-6 ng/mL, 6-8 ng/mL, and >8 ng/mL) between 1 and 5 y (24.0%, 20.0%, 56.0%, respectively) and >5 y (28.6%, 42.9%, 28.6%).
At longer follow-up, VCA and kidney recipients receive comparable MMF/prednisone doses, and most VCA recipients are treated with TTTL similar to kidney recipients. Further research may improve our understanding of VCA's complex risk/benefit ratio, and enhance informed consent.
由于皮肤的抗原性较高,作者推测血管化复合组织移植(VCA)受者可能需要比实体器官移植(SOT)受者更大的维持性免疫抑制。然而,VCA 和 SOT 免疫抑制方案的详细比较受到限制。
通过系统文献回顾收集手部和面部 VCA 受者的免疫抑制数据。通过回顾作者机构的病历获得肾脏受者的数据。在预设的随访间隔(<1、1-5 和>5 年)比较 VCA 和肾脏受者的泼尼松和霉酚酸酯(MMF)剂量。在随访间隔为 1-5 年和>5 年时比较他克莫司目标谷浓度(TTTL),并分为我们机构的基于肾脏移植风险的目标范围(4-6ng/mL、6-8ng/mL)或更高(>8ng/mL)。
免疫抑制数据可用于 57 名 VCA 和 98 名肾脏受者。在所有随访间隔,两组之间的泼尼松剂量无显著差异。在<1 年时,VCA 受者的 MMF 剂量均值明显更高(1.71±0.58 与 1.16±0.55 g/d;P=0.01)。对于 VCA 受者,在 1 至 5 年和>5 年时,TTTL 在三个预设治疗范围内(4-6ng/mL、6-8ng/mL 和>8ng/mL)的分布存在显著差异(P=0.02)(分别为 24.0%、20.0%、56.0%和 28.6%、42.9%、28.6%)。
在较长的随访时间内,VCA 和肾脏受者接受类似的 MMF/泼尼松剂量,大多数 VCA 受者的 TTTL 与肾脏受者相似。进一步的研究可能会提高我们对 VCA 复杂风险/获益比的理解,并增强知情同意。