Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA; Ph.D. Program in Translational and Molecular Medicine (DIMET), University of Milano-Bicocca, Monza.
Department of Data Science, Dana-Farber Cancer Institute, Harvard T H Chan School of Public Health, Boston, MA.
Haematologica. 2022 Nov 1;107(11):2617-2629. doi: 10.3324/haematol.2021.280444.
CD6 is a co-stimulatory receptor expressed on T cells that binds activated leukocyte cell adhesion molecule (ALCAM), expressed on antigen presenting cells, epithelial and endothelial tissues. The CD6-ALCAM pathway plays an integral role in modulating T-cell activation, proliferation, and trafficking. In this study we examined expression of CD6 by reconstituting T cells in 95 patients after allogeneic cell transplantation and evaluated the effects of itolizumab, an anti- CD6 monoclonal antibody, on T-cell activation. CD6 T cells reconstituted early after transplant with CD4 regulatory T cells (Treg)-expressing lower levels of CD6 compared to conventional CD4 T cells (Tcon) and CD8 T cells. After onset of acute graft-versus-host disease (aGvHD), CD6 expression was further reduced in Treg and CD8 T cells compared to healthy donors, while no difference was observed for Tcon. ALCAM expression was highest in plasmacytoid dendritic cells (pDC), lowest in myeloid dendritic cells (mDC) and intermediate in monocytes and was generally increased after aGvHD onset. Itolizumab inhibited CD4 and CD8 T-cell activation and proliferation in preGvHD samples, but inhibition was less prominent in samples collected after aGvHD onset, especially for CD8 T cells. Functional studies showed that itolizumab did not mediate direct cytolytic activity or antibody-dependent cytotoxicity in vitro. However, itolizumab efficiently abrogated the costimulatory activity of ALCAM on T-cell proliferation, activation and maturation. Our results identify the CD6-ALCAM pathway as a potential target for aGvHD control and a phase I/II study using itolizumab as first line treatment in combination with steroids for patients with aGvHD is currently ongoing (clinicaltrials gov. Identifier: NCT03763318).
CD6 是 T 细胞表面的共刺激受体,可与抗原呈递细胞、上皮细胞和内皮组织表面表达的活化白细胞细胞黏附分子(ALCAM)结合。CD6-ALCAM 通路在调节 T 细胞激活、增殖和归巢中起着重要作用。在这项研究中,我们在 95 例异基因细胞移植后的患者中重建 T 细胞,并检测了抗 CD6 单克隆抗体 itolizumab 对 T 细胞激活的影响,以研究 CD6 的表达。与常规 CD4 T 细胞(Tcon)和 CD8 T 细胞相比,移植后早期重建的 CD4 调节性 T 细胞(Treg)表达的 CD6 水平较低。发生急性移植物抗宿主病(aGvHD)后,与健康供体相比,Treg 和 CD8 T 细胞中的 CD6 表达进一步降低,而 Tcon 则没有差异。ALCAM 表达在浆细胞样树突状细胞(pDC)中最高,在髓样树突状细胞(mDC)中最低,在单核细胞中居中,在发生 aGvHD 后通常增加。Itolizumab 在 preGvHD 样本中抑制 CD4 和 CD8 T 细胞的激活和增殖,但在 aGvHD 发生后采集的样本中抑制作用不明显,尤其是 CD8 T 细胞。功能研究表明,Itolizumab 不能介导体外直接细胞溶解活性或抗体依赖性细胞毒性。然而,Itolizumab 可有效阻断 ALCAM 对 T 细胞增殖、激活和成熟的共刺激活性。我们的研究结果表明,CD6-ALCAM 通路可能是控制 aGvHD 的潜在靶点,一项使用 Itolizumab 作为一线治疗与类固醇联合治疗 aGvHD 患者的 I/II 期研究正在进行中(clinicaltrials.gov Identifier:NCT03763318)。