EBV-positive mucocutaneous ulcer arising in methotrexate-treated rheumatoid arthritis patients: a clinicopathological study of 12 cases with analysis of PD-L1 expression.

IF 0.9 Q4 HEMATOLOGY
Keisuke Sawada, Shuji Momose, Yosuke Iijima, Takumi Takahashi, Takahiro Kaneko, Wataru Yamamoto, Takahisa Yamashita, Morihiro Higashi, Masahiro Kizaki, Jun-Ichi Tamaru
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Abstract

Epstein-Barr virus-positive mucocutaneous ulcer (EBVMCU) is a newly recognized disease entity characterized by EBV-positive atypical B-cell proliferation. EBVMCU is a localized self-limited disease that affects mucosa and skin, especially the oral cavity. EBVMCU develops in immunosuppressive patients, such as those with methotrexate (MTX)-administrated rheumatoid arthritis (RA). Here we clinicopathologically analyzed 12 EBVMCU patients in a single institution. All cases were administrated MTX for RA, and five cases occurred in the oral cavity. All cases except one had demonstrated spontaneous regression after withdrawal of the immunosuppressive agent. We found 4 of 5 cases in the oral cavity had preceding traumatic events in the same site within a week before the onset of EBVMCU. Although there is no detailed and large study that has analyzed the trigger of EBVMCU, a traumatic event would indeed be a significant trigger for EBVMCU in the oral cavity. The cases were histologically classified; six cases were diffuse large B-cell lymphoma-type, five were polymorphous-type, and one was Hodgkin-like lesion type due to morphological appearance and immunophenotype. The PD-L1 expression was also examined by two antibodies for PD-L1 (E1J2J and SP142). Both antibodies revealed identical results for PD-L1 expression, and three cases were positive for PD-L1. The application of SP142 for evaluating the immune status of lymphomagenesis has also been proposed. Nine of 12 cases were negative for PD-L1, which implies that most EBVMCU cases may be caused by an immunodeficiency, rather than an immune-evasion, mechanism. However, as three cases were positive for PD-L1, immune escape may underly the pathogenesis in a subset of EBVMCU cases.

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甲氨蝶呤治疗的类风湿关节炎患者发生ebv阳性粘膜溃疡:12例PD-L1表达分析的临床病理研究
eb病毒阳性粘膜皮肤溃疡(EBVMCU)是一种以ebv阳性非典型b细胞增殖为特征的新认识的疾病实体。EBVMCU是一种局部自限性疾病,主要影响粘膜和皮肤,尤其是口腔。EBVMCU发展于免疫抑制患者,如甲氨蝶呤(MTX)给药类风湿性关节炎(RA)患者。在此,我们对同一医院的12例EBVMCU患者进行了临床病理分析。所有病例均给予甲氨蝶呤治疗RA,其中5例发生在口腔。除1例外,所有病例均在停用免疫抑制剂后表现出自发消退。我们发现5例口腔病例中有4例在EBVMCU发病前一周内在同一部位发生过创伤性事件。虽然目前还没有详细的大型研究分析EBVMCU的触发因素,但创伤事件确实是口腔EBVMCU的重要触发因素。对病例进行组织学分类;弥漫性大b细胞淋巴瘤型6例,多形型5例,霍奇金样病变型1例。用两种PD-L1抗体(E1J2J和SP142)检测PD-L1的表达。两种抗体对PD-L1的表达结果相同,其中3例PD-L1阳性。也有人提出应用SP142评价淋巴瘤发生的免疫状态。12例病例中有9例PD-L1阴性,这意味着大多数EBVMCU病例可能是由免疫缺陷引起的,而不是免疫逃避机制。然而,由于3例PD-L1阳性,免疫逃逸可能是部分EBVMCU病例发病机制的基础。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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