Yadava Koshika, Bollyky Paul, Lawson Melissa A
Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Institute of Food Research, Norwich, Norfolk, UK.
Immunology. 2016 Nov;149(3):262-269. doi: 10.1111/imm.12649. Epub 2016 Aug 16.
Tertiary lymphoid follicles (TLFs) can develop in the respiratory tract in response to infections or chronic inflammation. However, their functional relevance remains unclear because they are implicated in both protective and pathological responses. In contrast to homeostatic conditions, external antigens and damage to the lung tissue may drive TLF formation in inflamed lungs, and once established, the presence of pulmonary TLFs may signal the progression of chronic lung disease. This novel concept will be discussed in light of recent work in chronic obstructive pulmonary disease and how changes in the pulmonary microbiota may drive and direct TLF formation and function. We will also discuss the cellularity of TLFs at the pulmonary mucosa, with emphasis on the potential roles of lymphoid tissue inducer cells, and B- and T-cell aggregates, and will examine the function of key chemokines and cytokines including CXCL13 and interleukin-17, in the formation and maintenance of pulmonary TLFs.
三级淋巴滤泡(TLFs)可在呼吸道中因感染或慢性炎症而形成。然而,它们的功能相关性仍不明确,因为它们与保护性反应和病理性反应均有关联。与稳态条件不同,外部抗原和肺组织损伤可能会促使炎症肺部形成TLFs,并且一旦形成,肺部TLFs的存在可能预示着慢性肺病的进展。将根据慢性阻塞性肺疾病的最新研究成果,以及肺部微生物群的变化如何驱动和指导TLFs的形成与功能来探讨这一新概念。我们还将讨论肺黏膜处TLFs的细胞构成,重点关注淋巴组织诱导细胞、B细胞和T细胞聚集体的潜在作用,并研究关键趋化因子和细胞因子(包括CXCL13和白细胞介素-17)在肺部TLFs形成和维持中的作用。