首页> 美国卫生研究院文献>Case Reports in Dermatology >A Case of Erythema Multiforme Major Developed after Sequential Use of Two Immune Checkpoint Inhibitors Nivolumab and Ipilimumab for Advanced Melanoma: Possible Implication of Synergistic and/or Complementary Immunomodulatory Effects
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A Case of Erythema Multiforme Major Developed after Sequential Use of Two Immune Checkpoint Inhibitors Nivolumab and Ipilimumab for Advanced Melanoma: Possible Implication of Synergistic and/or Complementary Immunomodulatory Effects

机译:顺序使用两种免疫检查点抑制剂Nivolumab和Ipilimumab治疗晚期黑素瘤后出现多形性大红斑的病例:可能具有协同和/或互补的免疫调节作用

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摘要

Immune checkpoint inhibitors, such as ipilimumab and nivolumab, reverse the imbalance of antitumor self-tolerance and enhance T-cell responses. Currently, ipilimumab and nivolumab have a reported therapeutic impact on unresectable or metastatic melanomas; however, they also induce immune-related adverse events (irAEs). Ipilimumab-induced cutaneous irAEs are mostly low grade and manageable, although all-grade rash may occur in approximately 45% of all patients. We here report the case of a young woman with erythema multiforme major, which developed after sequential use of these 2 immune checkpoint inhibitors for advanced melanoma of the scalp. Initially, she received 12 cycles of nivolumab monotherapy followed by ipilimumab. A week later, multiple erythematous papulo-erythemas appeared on almost her entire body, with high-grade fever, mucosal involvements, and dyspnea. Immunohistochemistry using the lesioned skin revealed lymphocytic infiltration predominantly positive for CD8, contrasting with those for CD4 and Foxp3. Ipilimumab was stopped but she continued to receive empirical antibiotics; additionally, she was treated with intravenous steroid pulse therapy and immunoglobulin, followed by oral prednisolone. Her symptoms subsided rapidly, allowing a restart of nivolumab monotherapy alone. In our case, the long-standing preceding nivolumab monotherapy may synergistically and/or complementary have contributed to – in combination with the later administration of ipilimumab – recover antigen-responsive T-cell immunity, which is similar to the concept of immune reconstitution inflammatory syndrome, resulting in the establishment of an underlying immunopathology of erythema multiforme and life-threatening airway obstruction.
机译:免疫检查点抑制剂,例如ipilimumab和nivolumab,可逆转抗肿瘤自身耐受性的失衡并增强T细胞反应。目前,据报道,ipilimumab和nivolumab对无法切除或转移的黑色素瘤具有治疗作用;然而,它们也诱导免疫相关的不良事件(irAE)。伊匹木单抗诱导的皮肤irAE大多为低度且可控制,尽管所有患者中约有45%可能发生全等级皮疹。我们在这里报告了一名年轻女子,患有多形性红斑的情况,该妇女在连续使用这两种免疫检查点抑制剂治疗头皮晚期黑色素瘤后出现发展。最初,她接受了nivolumab单药治疗的12个周期,随后是ipilimumab。一周后,她的全身几乎出现多处红斑丘疹性红斑,伴有高烧,粘膜受累和呼吸困难。使用病变皮肤的免疫组织化学分析显示,CD8的淋巴细胞浸润主要为阳性,而CD4和Foxp3则为淋巴细胞浸润。伊匹木单抗已停止使用,但她仍继续接受经验性抗生素。此外,还接受了静脉类固醇脉冲疗法和免疫球蛋白治疗,随后口服泼尼松龙。她的症状迅速消退,仅允许重新开始尼伏单抗单药治疗。在我们的案例中,长期使用的以前的诺和单抗可能协同作用和/或互补作用–结合以后的ipilimumab给药–恢复了抗原反应性T细胞免疫,这类似于免疫重建炎症综合征的概念,导致建立了多形性红斑和威胁生命的气道阻塞的潜在免疫病理学。

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