Publication | Open Access
Cutting Edge: Nonproliferating Mature Immune Cells Form a Novel Type of Organized Lymphoid Structure in Idiopathic Pulmonary Fibrosis
173
Citations
13
References
2006
Year
Inflammatory Lung DiseaseLung InflammationLymphocyte DevelopmentImmunologyPathologyImmunologic MechanismCd40 LigandImmune SystemMatrikinesNaive TLymphatic SystemFibrosisNovel TypeDc MaturationImmune SurveillancePulmonary FibrosisAutoimmunityCell BiologyLung CancerPulmonary DiseaseImmune Cell DevelopmentIdiopathic Pulmonary FibrosisMedicineOrganized Lymphoid Structure
Ectopic formation of secondary lymphoid tissue is initiated by the local attraction of naive T and B cells. In this study, we describe a novel type of organized lymphoid structure in the lung of human idiopathic pulmonary fibrosis, with key features of lymphoid neogenesis, including: 1) recently activated CD40 ligand (CD40L)+ T cells; 2) variable numbers of activated CD40+/CD40L+ B cells, sometimes organized in follicles; 3) fully mature dendritic cells (DC) expressing CD40, CD83, CD86, and DC-lysosome-associated membrane protein; 4) the expression of the chemokine CCL21; 5) the presence of vessels with characteristics of high endothelial venules; and 6) a dense network of follicular DC. Surprisingly, these structures are devoid of CCR7+ naive T cells, proliferating lymphocytes, and germinal centers, suggesting that newly recruited activated DC and Ag-experienced lymphocytes can drive lymphoid neogenesis and that factors present within the lymphoid aggregates, such as CD40L, are essential to induce DC maturation.
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