Ishii Tomohiro, Mazariegos George V, Bueno Javier, Ohwada Susumu, Reyes Jorge
Department of Transplant Surgery, Division of Pediatric Gastroenterology, Children's Hospital Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Pediatr Transplant. 2003 Jun;7(3):185-91. doi: 10.1034/j.1399-3046.2003.00063.x.
Graft rejection is the most significant cause of allograft failure after intestinal transplantation (ITx). Severity can vary and is based on histologic criteria, the most extreme form being exfoliation of the mucosa. We present the characteristics and outcome of children who developed exfoliative rejection (ER) after ITx.
Between June 1990 and March 2002, 88 patients received 92 ITx which included isolated small bowel (SB, n = 26), combined liver-small bowel (LSB, n = 54), and multivisceral MV n = 12) allografts performed under tacrolimus and steroid immunosuppresson. ER was diagnosed by endoscopy and confirmed by biopsy.
Thirteen (15%) of 88 patients developed 15 episodes of ER in 15 intestinal allografts, and included SB (n = 8), LSB (n = 5), and MV (n = 2). Time to ER after ITx ranged from 9 days to 45.5 months (median 22 days). Eight episodes of ER developed within 1 month after ITx. Ten episodes of ER were exacerbations of prior rejection. Five episodes occurred abruptly. All but one received OKT3. Fourteen of 15 allografts were lost; six patients underwent allograft enterectomy acutely as a salvage operation because of ER. The remainder of the allografts were either removed or lost to patient death as a consequence to infection or chronic rejection after resolution of ER. Retransplantation was performed in three patients, with subsequent recurrence of ER in two retransplanted allografts. Inclusion of a liver allograft was a protective factor toward decreasing the incidence of ER. The results of cross-matching, inclusion of a colonic segment, and simultaneous bone marrow infusion did not affect the incidence of ER. Infectious complications included post-transplant lymphoproliferative disease (n = 4), cytomegalovirus (n = 5), and adenovirus infection (n = 2).
Exfoliative rejection is associated with a high morbidity and mortality after ITx. Strategies to improve survival may include up front anti-lymphocyte antibody therapy and, when fail to respond promptly and satisfactorily, early intestinal allograft removal.
移植物排斥是肠道移植(ITx)后同种异体移植失败的最主要原因。其严重程度各异,基于组织学标准判断,最极端的形式是黏膜剥脱。我们呈现了ITx后发生剥脱性排斥(ER)的儿童的特征及结局。
1990年6月至2002年3月期间,88例患者接受了92次ITx,其中包括孤立小肠移植(SB,n = 26)、肝小肠联合移植(LSB,n = 54)和多脏器移植(MV,n = 12),均在使用他克莫司和类固醇进行免疫抑制的情况下进行。ER通过内镜诊断并经活检证实。
88例患者中有13例(15%)在15例肠道同种异体移植中发生了15次ER,包括SB移植(n = 8)、LSB移植(n = 5)和MV移植(n = 2)。ITx后发生ER的时间为9天至45.5个月(中位时间22天)。8次ER发生在ITx后1个月内。10次ER是先前排斥反应的加重。5次发作较为突然。除1例患者外,其余均接受了OKT3治疗。15例同种异体移植中有14例丢失;6例患者因ER作为挽救手术紧急接受了同种异体移植肠切除术。其余的同种异体移植要么被切除,要么因感染或ER缓解后的慢性排斥导致患者死亡而丢失。3例患者进行了再次移植,其中2例再次移植的同种异体移植中出现了ER复发。包含肝脏同种异体移植是降低ER发生率的一个保护因素。交叉配型的结果、包含结肠段以及同时进行骨髓输注均不影响ER的发生率。感染并发症包括移植后淋巴细胞增生性疾病(n = 4)、巨细胞病毒感染(n = 5)和腺病毒感染(n = )。
剥脱性排斥与ITx后的高发病率和死亡率相关。提高生存率的策略可能包括早期使用抗淋巴细胞抗体治疗,以及在对治疗无迅速且满意反应时,早期切除肠道同种异体移植。