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在接受Campath免疫抑制治疗的肠道移植受者中,淋巴浆细胞增生(可能为移植前淋巴细胞增生性疾病前期)具有多种表现和外观。

Lymphoplasmacytic hyperplasia (possibly pre-PTLD) has varied expression and appearance in intestinal transplant recipients receiving Campath immunosuppression.

作者信息

Ruiz P, Soares M F, Garcia M, Nicolas M, Kato T, Mittal N, Nishida S, Levi D, Selvaggi G, Madariaga J, Tzakis A

机构信息

Department of Pathology, University of Miami, Miami, Florida, USA.

出版信息

Transplant Proc. 2004 Mar;36(2):386-7. doi: 10.1016/j.transproceed.2004.01.094.

Abstract

Posttransplant lymphoproliferative disorders (PTLD) are a frequent complication in bowel transplant recipients. Histological changes in PTLD range from expansile lymphoplasmacytic (LP) hyperplasia to frank lymphoma. Small bowel allograft biopsies obtained in the first 250 days posttransplant were retrospectively graded after patients had received induction immunosuppression with either anti-CD52 (Campath) or anti-CD25 (Zenapax) monoclonal antibodies. The biopsies were analyzed with respect to the onset intensity of lymphoplasmacytic infiltrates and presence of in situ EBV hybridization (EBER) positivity. We observed that lymphoplasmacytic infiltrates were a frequent change in all bowel transplant patients over the examined period. Campath-treated patients developed earlier LP infiltrates of mild to moderate intensity between day 1 and 100 posttransplant, thereafter decreasing to mild. No EBER positivity was detected in this group. Zenapax-treated patients presented with LP infiltrates later of mild to moderate intensity through day 100 posttransplant. However, more persistent and intense LP infiltrates was observed after day 101 in this group, including a case of lymphoma and two cases of EBER positivity. We conclude that Campath immunosuppression results in an earlier appearance of LP lesions that are generally less intense than those evident with Zenapax. We attribute these findings to the more profound immunodeficiency and cell targeting following Campath treatment.

摘要

移植后淋巴细胞增生性疾病(PTLD)是肠移植受者常见的并发症。PTLD的组织学变化范围从扩张性淋巴浆细胞(LP)增生到明显的淋巴瘤。对移植后250天内获取的小肠同种异体移植活检标本进行回顾性分级,这些患者接受了抗CD52(Campath)或抗CD25(Zenapax)单克隆抗体诱导免疫抑制治疗。对活检标本分析淋巴细胞浸润的起始强度以及原位EBV杂交(EBER)阳性情况。我们观察到,在所研究期间,淋巴细胞浸润在所有肠移植患者中都是常见变化。接受Campath治疗的患者在移植后第1天至第100天出现轻度至中度强度的早期LP浸润,此后降至轻度。该组未检测到EBER阳性。接受Zenapax治疗的患者在移植后第100天内出现轻度至中度强度的较晚LP浸润。然而,该组在第101天后观察到更持久且强烈的LP浸润,包括1例淋巴瘤和2例EBER阳性。我们得出结论,Campath免疫抑制导致LP病变更早出现,其强度通常低于Zenapax治疗明显的病变强度。我们将这些发现归因于Campath治疗后更严重的免疫缺陷和细胞靶向作用。

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