| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Francesca Barone | Q48321559 |
| Sanjiv A Luther | Q51797070 | ||
| Christopher D Buckley | Q87865766 | ||
| Saba Nayar | Q109774294 | ||
| P2093 | author name string | David H Gardner | |
| Nathalie Steinthal | |||
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| Rorγt+ innate lymphocytes and γδ T cells initiate psoriasiform plaque formation in mice | Q36005413 | ||
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| Viral targeting of fibroblastic reticular cells contributes to immunosuppression and persistence during chronic infection | Q36024206 | ||
| IL-22 regulates lymphoid chemokine production and assembly of tertiary lymphoid organs | Q36055624 | ||
| Serum levels of CXCL13 are associated with ultrasonographic synovitis and predict power Doppler persistence in early rheumatoid arthritis treated with non-biological disease-modifying anti-rheumatic drugs | Q36085027 | ||
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| Therapy of gastric mucosa-associated lymphoid tissue lymphoma | Q36847291 | ||
| Limited tumor infiltration by activated T effector cells restricts the therapeutic activity of regulatory T cell depletion against established melanoma | Q36853440 | ||
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| Follicular dendritic cells emerge from ubiquitous perivascular precursors | Q36991851 | ||
| Maternal retinoids control type 3 innate lymphoid cells and set the offspring immunity. | Q37064773 | ||
| Mesenchymal Cells of the Intestinal Lamina Propria | Q37125569 | ||
| Bimodal Expansion of the Lymphatic Vessels Is Regulated by the Sequential Expression of IL-7 and Lymphotoxin α1β2 in Newly Formed Tertiary Lymphoid Structures | Q37189681 | ||
| The role and therapeutic implications of fibroblast-like synoviocytes in inflammation and cartilage erosion in rheumatoid arthritis | Q37211275 | ||
| B cells promote resistance to heterosubtypic strains of influenza via multiple mechanisms. | Q37267195 | ||
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| Specific fibroblastic niches in secondary lymphoid organs orchestrate distinct Notch-regulated immune responses | Q34375200 | ||
| B cell homeostasis and follicle confines are governed by fibroblastic reticular cells | Q34383642 | ||
| Tissue injury and hypoxia promote malignant progression of prostate cancer by inducing CXCL13 expression in tumor myofibroblasts | Q34383988 | ||
| Lymphotoxin alpha/beta and tumor necrosis factor are required for stromal cell expression of homing chemokines in B and T cell areas of the spleen | Q34488105 | ||
| Microbiota-induced tertiary lymphoid tissues aggravate inflammatory disease in the absence of RORgamma t and LTi cells | Q34501407 | ||
| Interaction of mature CD3+CD4+ T cells with dendritic cells triggers the development of tertiary lymphoid structures in the thyroid. | Q34568588 | ||
| Inducible bronchus-associated lymphoid tissue (iBALT) in patients with pulmonary complications of rheumatoid arthritis. | Q34586903 | ||
| Human blood CXCR5(+)CD4(+) T cells are counterparts of T follicular cells and contain specific subsets that differentially support antibody secretion | Q34615273 | ||
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| Development of secondary lymphoid organs | Q34764895 | ||
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| Identification of a new stromal cell type involved in the regulation of inflamed B cell follicles | Q35017978 | ||
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| Lymphotoxin plays a crucial role in the development and function of nasal-associated lymphoid tissue through regulation of chemokines and peripheral node addressin | Q35083503 | ||
| Organogenesis of lymphoid tissues | Q35096187 | ||
| Deciphering the stromal and hematopoietic cell network of the adventitia from non-aneurysmal and aneurysmal human aorta | Q35108490 | ||
| A critical role for dendritic cells in the formation of lymphatic vessels within tertiary lymphoid structures | Q35108664 | ||
| Circulating T follicular regulatory and helper cells have memory-like properties | Q35145397 | ||
| Foxp3+ follicular regulatory T cells control the germinal center response. | Q35239023 | ||
| Coordinated regulation of lymph node vascular-stromal growth first by CD11c+ cells and then by T and B cells. | Q35566574 | ||
| Fibroblast activation protein is expressed by rheumatoid myofibroblast-like synoviocytes | Q35630052 | ||
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| Innate lymphoid cells. Innate lymphoid cells: a new paradigm in immunology | Q35638915 | ||
| Follicular dendritic cells help establish follicle identity and promote B cell retention in germinal centers | Q35669109 | ||
| Lymphotoxin beta receptor signaling is required for inflammatory lymphangiogenesis in the thyroid. | Q35691047 | ||
| Inflammation, Innate Immunity, and the Intestinal Stromal Cell Niche: Opportunities and Challenges | Q35754092 | ||
| Interleukin-23-Independent IL-17 Production Regulates Intestinal Epithelial Permeability | Q35797634 | ||
| Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis | Q35834582 | ||
| Reproducible isolation of lymph node stromal cells reveals site-dependent differences in fibroblastic reticular cells | Q35927606 | ||
| Pulmonary expression of CXC chemokine ligand 13, CC chemokine ligand 19, and CC chemokine ligand 21 is essential for local immunity to influenza | Q35973395 | ||
| Cellular interactions in lymph node development | Q35990072 | ||
| Trapping of naive lymphocytes triggers rapid growth and remodeling of the fibroblast network in reactive murine lymph nodes | Q37475213 | ||
| Role of the Lymphotoxin/LIGHT System in the Development and Maintenance of Reticular Networks and Vasculature in Lymphoid Tissues | Q37576573 | ||
| Lymphatic vessels and tertiary lymphoid organs | Q37602241 | ||
| New insights into the development of lymphoid tissues | Q37779724 | ||
| Cellular and Molecular Requirements in Lymph Node and Peyer's Patch Development | Q37783746 | ||
| Stromal cell-immune cell interactions | Q37809072 | ||
| Why does chronic inflammation persist: An unexpected role for fibroblasts | Q37844776 | ||
| Evolution of lymphoid tissues | Q38000791 | ||
| Tertiary lymphoid organs in infection and autoimmunity | Q38012568 | ||
| Control of dichotomic innate and adaptive immune responses by artery tertiary lymphoid organs in atherosclerosis. | Q38025388 | ||
| Intestinal stromal cells in mucosal immunity and homeostasis. | Q38067055 | ||
| Mesenchymal cell differentiation during lymph node organogenesis | Q38068182 | ||
| The role of non-hematopoietic stromal cells in the persistence of inflammation | Q38075556 | ||
| Insight into lymphoid tissue morphogenesis. | Q38129702 | ||
| Ectopic lymphoid-like structures in infection, cancer and autoimmunity | Q38221815 | ||
| T follicular helper cell differentiation, function, and roles in disease | Q38264816 | ||
| Tertiary lymphoid structures in cancer and beyond | Q38274486 | ||
| Stromal infrastructure of the lymph node and coordination of immunity | Q38286890 | ||
| Maturation of lymph node fibroblastic reticular cells from myofibroblastic precursors is critical for antiviral immunity | Q38408658 | ||
| Stromal cells in chronic inflammation and tertiary lymphoid organ formation | Q38415281 | ||
| IL-17 increases cadherin-11 expression in a model of autoimmune experimental arthritis and in rheumatoid arthritis | Q38471885 | ||
| Immunological hallmarks of stromal cells in the tumour microenvironment | Q38608340 | ||
| IL-17-induced CXCL12 recruits B cells and induces follicle formation in BALT in the absence of differentiated FDCs | Q38641655 | ||
| IL-23 is required for long-term control of Mycobacterium tuberculosis and B cell follicle formation in the infected lung | Q38939468 | ||
| CLEC-2 is required for development and maintenance of lymph nodes. | Q39675353 | ||
| Interleukin (IL) 4 and IL-13 act on human lung fibroblasts. Implication in asthma. | Q39804205 | ||
| Organizer-like reticular stromal cell layer common to adult secondary lymphoid organs | Q39926763 | ||
| LTbetaR signaling induces cytokine expression and up-regulates lymphangiogenic factors in lymph node anlagen | Q39986041 | ||
| Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells | Q40068378 | ||
| Tumor evasion of the immune system by converting CD4+CD25- T cells into CD4+CD25+ T regulatory cells: role of tumor-derived TGF-beta | Q40168787 | ||
| Generation of a synthetic lymphoid tissue-like organoid in mice | Q40487229 | ||
| The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways | Q40696432 | ||
| Central Nervous System Stromal Cells Control Local CD8(+) T Cell Responses during Virus-Induced Neuroinflammation | Q40775503 | ||
| Functional effects of TNF and lymphotoxin alpha1beta2 on FDC-like cells. | Q40852544 | ||
| Conduits mediate transport of low-molecular-weight antigen to lymph node follicles | Q41291427 | ||
| T-cell trafficking facilitated by high endothelial venules is required for tumor control after regulatory T-cell depletion | Q41400520 | ||
| Expression of surface lymphotoxin and tumor necrosis factor on activated T, B, and natural killer cells | Q41589815 | ||
| BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis. | Q41740089 | ||
| Lymph sacs are not required for the initiation of lymph node formation | Q41985446 | ||
| Dendritic cells are crucial for maintenance of tertiary lymphoid structures in the lung of influenza virus-infected mice | Q42036256 | ||
| Lymph node stromal cells constrain immunity via MHC class II self-antigen presentation. | Q42095379 | ||
| Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 | ||
| The chemokine receptor CXCR5 is pivotal for ectopic mucosa-associated lymphoid tissue neogenesis in chronic Helicobacter pylori-induced inflammation | Q42202704 | ||
| Lymphotoxin a-dependent and -independent signals regulate stromal organizer cell homeostasis during lymph node organogenesis. | Q51984858 | ||
| Presumptive lymph node organizers are differentially represented in developing mesenteric and peripheral nodes. | Q52087999 | ||
| Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization. | Q52528591 | ||
| Lymphoid tissue genesis induced by commensals through NOD1 regulates intestinal homeostasis. | Q52590127 | ||
| Control of the T follicular helper-germinal center B-cell axis by CD8⁺ regulatory T cells limits atherosclerosis and tertiary lymphoid organ development. | Q52656274 | ||
| IL-22 capacitates dermal fibroblast responses to TNF in scleroderma. | Q52911127 | ||
| Mycobacterium tuberculosis triggers formation of lymphoid structure in murine lungs. | Q52928677 | ||
| Loss of IL-22 inhibits autoantibody formation in collagen-induced arthritis in mice. | Q53148065 | ||
| Prenatal blockage of lymphotoxin beta receptor and TNF receptor p55 signaling cascade resulted in the acceleration of tissue genesis for isolated lymphoid follicles in the large intestine. | Q53624871 | ||
| Tissue-Specific Function of Lymph Node Fibroblastic Reticulum Cells | Q57556772 | ||
| Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma | Q58003719 | ||
| Expression of the B cell-attracting chemokine CXCL13 in the target organ and autoantibody production in ectopic lymphoid tissue in the chronic inflammatory disease Sjögren's syndrome | Q60548220 | ||
| Ultrasonographic and MRI characterisation of the palindromic phase of rheumatoid arthritis | Q60622647 | ||
| Involvement of subchondral bone marrow in rheumatoid arthritis: Lymphoid neogenesis and in situ relationship to subchondral bone marrow osteoclast recruitment | Q60622664 | ||
| CXCL13, CCL21, and CXCL12 Expression in Salivary Glands of Patients with Sjogren's Syndrome and MALT Lymphoma: Association with Reactive and Malignant Areas of Lymphoid Organization | Q60810847 | ||
| Activation-Induced Cytidine Deaminase Expression in Follicular Dendritic Cell Networks and Interfollicular Large B Cells Supports Functionality of Ectopic Lymphoid Neogenesis in Autoimmune Sialoadenitis and MALT Lymphoma in Sjogren's Syndrome | Q60810867 | ||
| Association of CXCL13 and CCL21 expression with the progressive organization of lymphoid-like structures in Sjögren's syndrome | Q60810881 | ||
| Systematic microanatomical analysis of CXCL13 and CCL21in situ production and progressive lymphoid organization in rheumatoid synovitis | Q60810884 | ||
| Clinical significance of synovial lymphoid neogenesis and its reversal after anti-tumour necrosis factor therapy in rheumatoid arthritis | Q60915160 | ||
| RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation | Q61051808 | ||
| Sustained interleukin‐6 signalling leads to the development of lymphoid organ‐like structures in the lung | Q64377813 | ||
| Fetal and neonatal development of human spleen: an immunohistological study | Q68154646 | ||
| Role of lymphotoxin and the type I TNF receptor in the formation of germinal centers | Q71095987 | ||
| Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin beta receptor, and TNF receptor I function | Q73419615 | ||
| Targeting of lymphotoxin-alpha to the tumor elicits an efficient immune response associated with induction of peripheral lymphoid-like tissue | Q73588426 | ||
| MAdCAM-1 expressed in chronic inflammatory liver disease supports mucosal lymphocyte adhesion to hepatic endothelium (MAdCAM-1 in chronic inflammatory liver disease) | Q73851577 | ||
| Priming of naive T cells inside tumors leads to eradication of established tumors | Q75221014 | ||
| Different cytokines induce surface lymphotoxin-alphabeta on IL-7 receptor-alpha cells that differentially engender lymph nodes and Peyer's patches | Q78651212 | ||
| Persistence and responsiveness of immunologic memory in the absence of secondary lymphoid organs | Q79257160 | ||
| Mature antigen-experienced T helper cells synthesize and secrete the B cell chemoattractant CXCL13 in the inflammatory environment of the rheumatoid joint | Q79765411 | ||
| Recruitment and activation of naive T cells in the islets by lymphotoxin beta receptor-dependent tertiary lymphoid structure | Q80171529 | ||
| Cutting edge: regulatory T cells induce CD4+CD25-Foxp3- T cells or are self-induced to become Th17 cells in the absence of exogenous TGF-beta | Q80358435 | ||
| CXCR5- and CCR7-dependent lymphoid neogenesis in a murine model of chronic antigen-induced arthritis | Q81377156 | ||
| Epidermal CCR6+ γδ T cells are major producers of IL-22 and IL-17 in a murine model of psoriasiform dermatitis | Q85067559 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | inflammation | Q101991 |
| tertiary lymphoid structure | Q54928327 | ||
| P304 | page(s) | 477 | |
| P577 | publication date | 2016-11-08 | |
| P1433 | published in | Frontiers in Immunology | Q27723748 |
| P1476 | title | Stromal Fibroblasts in Tertiary Lymphoid Structures: A Novel Target in Chronic Inflammation | |
| P478 | volume | 7 |
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