Kawana Yuki, Suga Hiraku, Kamijo Hiroaki, Miyagaki Tomomitsu, Sugaya Makoto, Sato Shinichi
Department of Dermatology, Graduate School of Medicine, the University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Department of Dermatology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae-ku, Kanagawa 216-8511, Japan.
Int J Mol Sci. 2021 Nov 22;22(22):12576. doi: 10.3390/ijms222212576.
Mycosis fungoides (MF) and Sézary syndrome (SS), the most common types of cutaneous T-cell lymphoma (CTCL), are characterized by proliferation of mature CD4+ T-helper cells. Patients with advanced-stage MF and SS have poor prognosis, with 5-year survival rates of 52%. Although a variety of systemic therapies are currently available, there are no curative options for such patients except for stem cell transplantation, and thus the treatment of advanced MF and SS still remains challenging. Therefore, elucidation of the pathophysiology of MF/SS and development of medical treatments are desired. In this study, we focused on a molecule called OX40. We examined OX40 and OX40L expression and function using clinical samples of MF and SS and CTCL cell lines. OX40 and OX40L were co-expressed on tumor cells of MF and SS. OX40 and OX40L expression was increased and correlated with disease severity markers in MF/SS patients. Anti-OX40 antibody and anti-OX40L antibody suppressed the proliferation of CTCL cell lines both in vitro and in vivo. These results suggest that OX40-OX40L interactions could contribute to the proliferation of MF/SS tumor cells and that the disruption of OX40-OX40L interactions could become a new therapeutic strategy for the treatment of MF/SS.
蕈样肉芽肿(MF)和塞扎里综合征(SS)是皮肤T细胞淋巴瘤(CTCL)最常见的类型,其特征是成熟的CD4 +辅助性T细胞增殖。晚期MF和SS患者预后较差,5年生存率为52%。尽管目前有多种全身治疗方法,但除干细胞移植外,此类患者没有治愈方案,因此晚期MF和SS的治疗仍然具有挑战性。因此,阐明MF/SS的病理生理学并开发医学治疗方法是很有必要的。在本研究中,我们聚焦于一种名为OX40的分子。我们使用MF、SS的临床样本以及CTCL细胞系来检测OX40和OX40L的表达及功能。OX40和OX40L在MF和SS的肿瘤细胞上共表达。在MF/SS患者中,OX40和OX40L的表达增加且与疾病严重程度标志物相关。抗OX40抗体和抗OX40L抗体在体外和体内均抑制了CTCL细胞系的增殖。这些结果表明,OX40 - OX40L相互作用可能有助于MF/SS肿瘤细胞的增殖,并且破坏OX40 - OX40L相互作用可能成为治疗MF/SS的一种新的治疗策略。