Nayar Saba, Campos Joana, Chung Ming May, Navarro-Núñez Leyre, Chachlani Menka, Steinthal Nathalie, Gardner David H, Rankin Philip, Cloake Thomas, Caamaño Jorge H, McGettrick Helen M, Watson Steve P, Luther Sanjiv, Buckley Christopher D, Barone Francesca
Rheumatology Research Group, Centre for Translational Inflammation Research, Institute of Inflammation and Ageing, University of Birmingham Research Laboratories, Queen Elizabeth Hospital, Birmingham B15 2WD, United Kingdom;
Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, United Kingdom;
J Immunol. 2016 Sep 1;197(5):1957-67. doi: 10.4049/jimmunol.1500686. Epub 2016 Jul 29.
Lymphangiogenesis associated with tertiary lymphoid structure (TLS) has been reported in numerous studies. However, the kinetics and dynamic changes occurring to the lymphatic vascular network during TLS development have not been studied. Using a viral-induced, resolving model of TLS formation in the salivary glands of adult mice we demonstrate that the expansion of the lymphatic vascular network is tightly regulated. Lymphatic vessel expansion occurs in two distinct phases. The first wave of expansion is dependent on IL-7. The second phase, responsible for leukocyte exit from the glands, is regulated by lymphotoxin (LT)βR signaling. These findings, while highlighting the tight regulation of the lymphatic response to inflammation, suggest that targeting the LTα1β2/LTβR pathway in TLS-associated pathologies might impair a natural proresolving mechanism for lymphocyte exit from the tissues and account for the failure of therapeutic strategies that target these molecules in diseases such as rheumatoid arthritis.
许多研究报道了与三级淋巴结构(TLS)相关的淋巴管生成。然而,TLS发育过程中淋巴管网络发生的动力学和动态变化尚未得到研究。利用成年小鼠唾液腺中病毒诱导的TLS形成的消退模型,我们证明淋巴管网络的扩张受到严格调控。淋巴管扩张发生在两个不同阶段。第一波扩张依赖于白细胞介素-7。第二阶段负责白细胞从腺体中流出,受淋巴毒素(LT)βR信号通路调控。这些发现虽然突出了淋巴管对炎症反应的严格调控,但表明在TLS相关疾病中靶向LTα1β2/LTβR通路可能会损害淋巴细胞从组织中流出的自然促消退机制,并解释了在类风湿性关节炎等疾病中靶向这些分子的治疗策略为何失败。