Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Cancer Sci. 2013 May;104(5):647-50. doi: 10.1111/cas.12116. Epub 2013 Mar 10.
We report an adult T-cell leukemia/lymphoma patient suffering from Stevens-Johnson Syndrome (SJS) during mogamulizumab (humanized anti-CCR4 monoclonal antibody) treatment. There was a durable significant reduction of the CD4(+) CD25(high) FOXP3(+) regulatory T (Treg) cell subset in the patient's PBMC, and the affected inflamed skin almost completely lacked FOXP3-positive cells. This implies an association between reduction of the Treg subset by mogamulizimab and occurrence of SJS. The present case should contribute not only to our understanding of human pathology resulting from therapeutic depletion of Treg cells, but also alert us to the possibility of immune-related severe adverse events such as SJS when using mogamulizumab. We are currently conducting a clinical trial of mogamulizumab for CCR4-negative solid cancers (UMIN000010050), specifically aiming to deplete Treg cells.
我们报告了一例成人 T 细胞白血病/淋巴瘤患者在 mogamulizumab(人源化抗 CCR4 单克隆抗体)治疗期间发生 Stevens-Johnson 综合征(SJS)。患者的 PBMC 中 CD4(+) CD25(high) FOXP3(+) 调节性 T(Treg)细胞亚群出现持久且显著减少,受累的炎症皮肤几乎完全缺乏 FOXP3 阳性细胞。这表明 mogamulizimab 减少 Treg 亚群与 SJS 的发生之间存在关联。本病例不仅有助于我们理解治疗性耗竭 Treg 细胞导致的人类病理学,而且当使用 mogamulizumab 时,还可能引起我们对 SJS 等免疫相关严重不良事件的关注。我们目前正在开展一项针对 CCR4 阴性实体瘤的 mogamulizumab 临床试验(UMIN000010050),专门旨在耗竭 Treg 细胞。