Kim Young Uk, Kim Byung-Seok, Lim Hoyong, Wetsel Rick A, Chung Yeonseok
Center for Immunology and Autoimmune Diseases, Institute of Molecular Medicine, The University of Texas Medical School, Houston, TX 77030, USA.
Laboratory of Immune Regulation, Research Institute of Pharmaceutical Science, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Biomol Ther (Seoul). 2017 Mar 1;25(2):130-139. doi: 10.4062/biomolther.2016.075.
CXCR5 T follicular helper (Tfh) cells are associated with aberrant autoantibody production in patients with antibody-mediated autoimmune diseases including lupus. Follicular regulatory T (Tfr) cells expressing CXCR5 and Bcl6 have been recently identified as a specialized subset of Foxp3 regulatory T (Treg) cells that control germinal center reactions. In this study, we show that retroviral transduction of gene in Foxp3 Treg cells induced a stable expression of functional CXCR5 on their surface. The -transduced Treg cells maintained the expression of Treg cell signature genes and the suppressive activity. The expression of CXCR5 as well as Foxp3 in the transduced Treg cells appeared to be stable in an adoptive transfer experiment. Moreover, -transduced Treg cells preferentially migrated toward the CXCL13 gradient, leading to an effective suppression of antibody production from B cells stimulated with Tfh cells. Therefore, our results demonstrate that enforced expression of CXCR5 onto Treg cells efficiently induces Tfr cell-like properties, which might be a promising cellular therapeutic approach for the treatment of antibody-mediated autoimmune diseases.
CXCR5滤泡辅助性T(Tfh)细胞与包括狼疮在内的抗体介导的自身免疫性疾病患者异常自身抗体产生有关。最近,表达CXCR5和Bcl6的滤泡调节性T(Tfr)细胞被鉴定为控制生发中心反应的Foxp3调节性T(Treg)细胞的一个特殊亚群。在本研究中,我们表明在Foxp3 Treg细胞中通过逆转录病毒转导基因可诱导其表面功能性CXCR5的稳定表达。转导的Treg细胞维持Treg细胞特征基因的表达和抑制活性。在过继转移实验中,转导的Treg细胞中CXCR5以及Foxp3的表达似乎是稳定的。此外,转导的Treg细胞优先向CXCL13梯度迁移,从而有效抑制由Tfh细胞刺激的B细胞产生抗体。因此,我们的结果表明,在Treg细胞上强制表达CXCR5可有效诱导Tfr细胞样特性,这可能是治疗抗体介导的自身免疫性疾病的一种有前景的细胞治疗方法。