scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Bart Lambrecht | Q18402373 |
Hamida Hammad | Q38329231 | ||
Frédéric Perros | Q56606126 | ||
Corine H. Geurts van Kessel | Q97423566 | ||
Katrijn Neyt | Q117274428 | ||
P2860 | cites work | A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 |
An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells | Q28235728 | ||
In situ diversification of the antibody repertoire in chronic Lyme arthritis synovium | Q28236584 | ||
Tyrosine kinase receptor RET is a key regulator of Peyer's patch organogenesis | Q28511182 | ||
Chemokine CXCL13 is essential for lymph node initiation and is induced by retinoic acid and neuronal stimulation | Q28585797 | ||
The nature of small-airway obstruction in chronic obstructive pulmonary disease | Q29618682 | ||
Antigen persistence and the control of local T cell memory by migrant respiratory dendritic cells after acute virus infection | Q30433900 | ||
Association of T-zone reticular networks and conduits with ectopic lymphoid tissues in mice and humans | Q30475578 | ||
Lymphotoxin beta receptor signaling promotes tertiary lymphoid organogenesis in the aorta adventitia of aged ApoE-/- mice | Q33399367 | ||
Inducible bronchus-associated lymphoid tissue elicited by a protein cage nanoparticle enhances protection in mice against diverse respiratory viruses | Q33506083 | ||
Bronchus-associated lymphoid tissue (BALT) and survival in a vaccine mouse model of tularemia | Q33618911 | ||
Necrotic and inflammatory changes in metal-on-metal resurfacing hip arthroplasties | Q33660778 | ||
Lymph node fibroblastic reticular cells directly present peripheral tissue antigen under steady-state and inflammatory conditions | Q33794995 | ||
Mouse aorta smooth muscle cells differentiate into lymphoid tissue organizer-like cells on combined tumor necrosis factor receptor-1/lymphotoxin beta-receptor NF-kappaB signaling | Q33869955 | ||
Ectopic expression of the murine chemokines CCL21a and CCL21b induces the formation of lymph node-like structures in pancreas, but not skin, of transgenic mice | Q34110300 | ||
The development of inducible bronchus-associated lymphoid tissue depends on IL-17. | Q34191942 | ||
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 | ||
Induced bronchus-associated lymphoid tissue serves as a general priming site for T cells and is maintained by dendritic cells. | Q35013206 | ||
In situ B cell-mediated immune responses and tubulointerstitial inflammation in human lupus nephritis | Q35070813 | ||
Type I interferon production by tertiary lymphoid tissue developing in response to 2,6,10,14-tetramethyl-pentadecane (pristane) | Q35088161 | ||
A critical role for dendritic cells in the formation of lymphatic vessels within tertiary lymphoid structures | Q35108664 | ||
Characterisation of mucosal lymphoid aggregates in ulcerative colitis: immune cell phenotype and TcR-gammadelta expression | Q35361010 | ||
Lymphotoxin beta receptor signaling is required for inflammatory lymphangiogenesis in the thyroid. | Q35691047 | ||
Lymphoid tissue homing chemokines are expressed in chronic inflammation | Q35810009 | ||
Pulmonary expression of CXC chemokine ligand 13, CC chemokine ligand 19, and CC chemokine ligand 21 is essential for local immunity to influenza | Q35973395 | ||
Th17 cells induce ectopic lymphoid follicles in central nervous system tissue inflammation | Q36174679 | ||
Chronic inflammation caused by lymphotoxin is lymphoid neogenesis | Q36366337 | ||
Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase | Q36370988 | ||
Dendritic cells induce autoimmune diabetes and maintain disease via de novo formation of local lymphoid tissue | Q36404280 | ||
Blockade of lymphotoxin-beta receptor signaling reduces aspects of Sjögren's syndrome in salivary glands of non-obese diabetic mice | Q37207114 | ||
CXCL13 blockade disrupts B lymphocyte organization in tertiary lymphoid structures without altering B cell receptor bias or preventing diabetes in nonobese diabetic mice | Q37299504 | ||
Omental milky spots develop in the absence of lymphoid tissue-inducer cells and support B and T cell responses to peritoneal antigens | Q37368320 | ||
Id2-, RORgammat-, and LTbetaR-independent initiation of lymphoid organogenesis in ocular immunity | Q37402415 | ||
New insights into the development of lymphoid tissues | Q37779724 | ||
Stromal cell-immune cell interactions | Q37809072 | ||
The stromal and haematopoietic antigen-presenting cells that reside in secondary lymphoid organs | Q37810779 | ||
Helicobacter-induced chronic active lymphoid aggregates have characteristics of tertiary lymphoid tissue | Q39755242 | ||
LTbetaR signaling induces cytokine expression and up-regulates lymphangiogenic factors in lymph node anlagen | Q39986041 | ||
Dendritic cells accumulate in human fibrotic interstitial lung disease. | Q40180589 | ||
Bacterial colonization of distal airways in healthy subjects and chronic lung disease: a bronchoscopic study | Q40895974 | ||
BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis. | Q41740089 | ||
Thyroid autoimmune disease: demonstration of thyroid antigen-specific B cells and recombination-activating gene expression in chemokine-containing active intrathyroidal germinal centers | Q41873772 | ||
Dendritic cells are crucial for maintenance of tertiary lymphoid structures in the lung of influenza virus-infected mice | Q42036256 | ||
The chemokine receptor CXCR5 is pivotal for ectopic mucosa-associated lymphoid tissue neogenesis in chronic Helicobacter pylori-induced inflammation | Q42202704 | ||
Th1-biased tertiary lymphoid tissue supported by CXC chemokine ligand 13-producing stromal network in chronic lesions of autoimmune gastritis. | Q42451126 | ||
Tertiary lymphoid structures in the pancreas promote selection of B lymphocytes in autoimmune diabetes | Q42617543 | ||
Mature follicular dendritic cell networks depend on expression of lymphotoxin beta receptor by radioresistant stromal cells and of lymphotoxin beta and tumor necrosis factor by B cells | Q42753323 | ||
Evolution of ectopic lymphoid neogenesis and in situ autoantibody production in autoimmune nonobese diabetic mice: cellular and molecular characterization of tertiary lymphoid structures in pancreatic islets | Q42936052 | ||
Role of inducible bronchus associated lymphoid tissue (iBALT) in respiratory immunity | Q45018410 | ||
The myasthenia gravis thymus: a rare source of human autoantibody-secreting plasma cells for testing potential therapeutics | Q46414452 | ||
Detection of ectopic B-cell follicles with germinal centers in the meninges of patients with secondary progressive multiple sclerosis. | Q47357498 | ||
Inflammation recapitulates the ontogeny of lymphoid stromal cells | Q47976120 | ||
Meningeal B-cell follicles in secondary progressive multiple sclerosis associate with early onset of disease and severe cortical pathology. | Q48200750 | ||
Pulmonary lymphoid neogenesis in idiopathic pulmonary arterial hypertension | Q49041508 | ||
Plasmacytoid dendritic cells in pulmonary lymphoid follicles of patients with COPD. | Q49108090 | ||
Role of lymphotoxin-alpha in cigarette smoke-induced inflammation and lymphoid neogenesis | Q49144536 | ||
Chemokine receptor CXCR5 supports solitary intestinal lymphoid tissue formation, B cell homing, and induction of intestinal IgA responses. | Q50056662 | ||
Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells. | Q50144852 | ||
Characterization of chemokines and adhesion molecules associated with T cell presence in tertiary lymphoid structures in human lung cancer. | Q50993488 | ||
Intracerebral expression of CXCL13 and BAFF is accompanied by formation of lymphoid follicle-like structures in the meninges of mice with relapsing experimental autoimmune encephalomyelitis. | Q51027456 | ||
Tertiary lymphoid tissues generate effector and memory T cells that lead to allograft rejection. | Q51976995 | ||
Cutting edge: ectopic expression of the chemokine TCA4/SLC is sufficient to trigger lymphoid neogenesis. | Q52022097 | ||
Lymphocyte-filled villi: comparison with other lymphoid aggregations in the mucosa of the human small intestine. | Q52036578 | ||
Induction of secondary and tertiary lymphoid structures in the skin. | Q52085787 | ||
Lymphoid tissue genesis induced by commensals through NOD1 regulates intestinal homeostasis. | Q52590127 | ||
Inhalation of diesel exhaust for three months affects major cytokine expression and induces bronchus-associated lymphoid tissue formation in murine lungs | Q54745717 | ||
Induction of BALT in the absence of IL-17 | Q57278729 | ||
Nodular lymphoid lesion of the liver: an immune-mediated disorder mimicking low-grade malignant lymphoma | Q57649393 | ||
Chronic Rejection Triggers the Development of an Aggressive Intragraft Immune Response through Recapitulation of Lymphoid Organogenesis | Q59387561 | ||
Sustained interleukin‐6 signalling leads to the development of lymphoid organ‐like structures in the lung | Q64377813 | ||
Lymphoid neogenesis in rheumatoid synovitis | Q74147962 | ||
Initiation of NALT organogenesis is independent of the IL-7R, LTbetaR, and NIK signaling pathways but requires the Id2 gene and CD3(-)CD4(+)CD45(+) cells | Q74548133 | ||
Persistence and responsiveness of immunologic memory in the absence of secondary lymphoid organs | Q79257160 | ||
Recruitment and activation of naive T cells in the islets by lymphotoxin beta receptor-dependent tertiary lymphoid structure | Q80171529 | ||
Inflammation and ectopic lymphoid structures in rheumatoid arthritis synovial tissues dissected by genomics technology: identification of the interleukin-7 signaling pathway in tissues with lymphoid neogenesis | Q80706974 | ||
CXCR5- and CCR7-dependent lymphoid neogenesis in a murine model of chronic antigen-induced arthritis | Q81377156 | ||
Lymphoid neogenesis in murine cardiac allografts undergoing chronic rejection | Q81395004 | ||
Adaptive immune responses are dispensable for isolated lymphoid follicle formation: antigen-naive, lymphotoxin-sufficient B lymphocytes drive the formation of mature isolated lymphoid follicles | Q81672214 | ||
Stromal activation and formation of lymphoid-like stroma in chronic lung allograft dysfunction | Q83930980 | ||
Persistent activation of dendritic cells after resolution of allergic airway inflammation breaks tolerance to inhaled allergens in mice | Q84077783 | ||
Antigen-dependent rescue of nose-associated lymphoid tissue (NALT) development independent of LTbetaR and CXCR5 signaling | Q84564792 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | autoimmunity | Q192360 |
tertiary lymphoid organ | Q108017266 | ||
P304 | page(s) | 297-305 | |
P577 | publication date | 2012-05-21 | |
2012-06-01 | |||
P1433 | published in | Trends in Immunology | Q15265730 |
P1476 | title | Tertiary lymphoid organs in infection and autoimmunity | |
P478 | volume | 33 |
Q33694988 | A Unique Cellular and Molecular Microenvironment Is Present in Tertiary Lymphoid Organs of Patients with Spontaneous Prostate Cancer Regression |
Q46225129 | A sphingosine-1-phosphate receptor 1 agonist inhibits tertiary lymphoid tissue reactivation and hypersensitivity in the lung |
Q37457716 | Activated dendritic cells delivered in tissue compatible biomatrices induce in-situ anti-tumor CTL responses leading to tumor regression |
Q49618396 | Active targeted delivery of immune therapeutics to lymph nodes |
Q89965511 | Advances in Targeting the Innate and Adaptive Immune Systems to Cure Chronic Hepatitis B Virus Infection |
Q35636731 | Adventitial Tertiary Lymphoid Organs as Potential Source of MicroRNA Biomarkers for Abdominal Aortic Aneurysm |
Q38242815 | Adventitial inflammation and its interaction with intimal atherosclerotic lesions |
Q89695246 | Aim2-mediated/IFN-β-independent regulation of gastric metaplastic lesions via CD8+ T cells |
Q38649554 | B cells as multi-functional players during Mycobacterium tuberculosis infection and disease. |
Q42539344 | B cells produce CXCL13 in lymphoid neogenesis during chronic obstructive pulmonary disease. The new kid on the block? |
Q35044819 | B-lymphocyte-mediated delayed cognitive impairment following stroke. |
Q48195816 | BAFF Induces Tertiary Lymphoid Structures and Positions T Cells within the Glomeruli during Lupus Nephritis. |
Q26739445 | Biosynthesis and Functional Significance of Peripheral Node Addressin in Cancer-Associated TLO |
Q35136409 | CCR7 directs the recruitment of T cells into inflamed pancreatic islets of nonobese diabetic (NOD) mice |
Q38751056 | CXCL13-producing TFH cells link immune suppression and adaptive memory in human breast cancer |
Q97546137 | Cancer systems immunology |
Q50755835 | Candidate Serum Markers in Early Crohn's Disease: Predictors of Disease Course. |
Q38070793 | Cellular immune reactions in the lung |
Q34105741 | Characterisation and prognostic value of tertiary lymphoid structures in oral squamous cell carcinoma |
Q27012852 | Characteristics of tertiary lymphoid structures in primary cancers |
Q50050297 | Characterization of mesenchymal stem/stromal cells with lymphoid tissue organizer cell potential in tonsils from children |
Q92538902 | Chronic Inflammation: A Common Promoter in Tertiary Lymphoid Organ Neogenesis |
Q37486824 | Chronic follicular bronchiolitis requires antigen-specific regulatory T cell control to prevent fatal disease progression |
Q38551796 | Compartmentalized intrathecal immunoglobulin synthesis during HIV infection - a model of chronic CNS inflammation? |
Q64999676 | Coordination of Immune-Stroma Crosstalk by IL-6 Family Cytokines. |
Q37046631 | Cross-platform comparison of independent datasets identifies an immune signature associated with improved survival in metastatic melanoma |
Q61811653 | Dendritic Cell Subsets and Effector Function in Idiopathic and Connective Tissue Disease-Associated Pulmonary Arterial Hypertension |
Q53166472 | Distinct Tertiary Lymphoid Structure Associations and Their Prognostic Relevance in HER2 Positive and Negative Breast Cancers. |
Q51634522 | Donor-Specific Antibodies Are Produced Locally in Ectopic Lymphoid Structures in Cardiac Allografts. |
Q38190588 | EBV and other viruses as triggers of tertiary lymphoid structures in primary Sjögren's syndrome. |
Q40557011 | Early IL-1 Signaling Promotes iBALT Induction after Influenza Virus Infection |
Q33755913 | Ectopic germinal center and megalin defect in primary Sjogren syndrome with renal Fanconi syndrome |
Q26778348 | Ectopic lymphoid follicles: inducible centres for generating antigen-specific immune responses within tissues |
Q38221815 | Ectopic lymphoid-like structures in infection, cancer and autoimmunity |
Q64067977 | Editorial: Immune Outposts on the Inflammatory Frontier: Tertiary Lymphoid Structures as Targets for Immunotherapy of Cancer and Autoimmunity |
Q34171463 | Emerging immune functions of non-hematopoietic stromal cells. |
Q41892066 | Endoscopic Findings of Gastric Extranodal Marginal Zone B-Cell Mucosa-Associated Lymphoid Tissue Lymphoma |
Q98196742 | Engineered immunological niches to monitor disease activity and treatment efficacy in relapsing multiple sclerosis |
Q89840605 | Existence of intratumoral tertiary lymphoid structures is associated with immune cells infiltration and predicts better prognosis in early-stage hepatocellular carcinoma |
Q93049095 | Fibroblastic reticular cells at the nexus of innate and adaptive immune responses |
Q36711018 | Flagellin is a strong vaginal adjuvant of a therapeutic vaccine for genital cancer. |
Q59384419 | Follicles, germinal centers, and immune mechanisms in primary biliary cirrhosis |
Q37512037 | Follicular B cells in thyroids of mice with spontaneous autoimmune thyroiditis contribute to disease pathogenesis and are targets of anti-CD20 antibody therapy |
Q89830523 | Graph-based description of tertiary lymphoid organs at single-cell level |
Q41377760 | Graves' disease TSHR-stimulating antibodies (TSAbs) induce the activation of immature thymocytes: a clue to the riddle of TSAbs generation? |
Q41161044 | Heterogeneous fibroblasts underlie age-dependent tertiary lymphoid tissues in the kidney |
Q48107857 | High endothelial venules associated with T cell subsets in the inflamed gut of newly diagnosed inflammatory bowel disease patients |
Q64988934 | Histopathological and microbiological findings in buffalo chronic mastitis: evidence of tertiary lymphoid structures. |
Q27015410 | Host immune response to infection and cancer: unexpected commonalities |
Q26742173 | How Follicular Dendritic Cells Shape the B-Cell Antigenome |
Q34562654 | IKKβ in myeloid cells controls the host response to lethal and sublethal Francisella tularensis LVS infection |
Q48172896 | IL-10 Paradoxically Promotes Autoimmune Neuropathy through S1PR1-Dependent CD4+ T Cell Migration |
Q41657985 | IRF5 is a novel regulator of CXCL13 expression in breast cancer that regulates CXCR5(+) B- and T-cell trafficking to tumor-conditioned media |
Q47195254 | Immune Cell Infiltration and Tertiary Lymphoid Structures as Determinants of Antitumor Immunity |
Q35658358 | Immunogenicity of infectious pathogens and vaccine antigens |
Q38133018 | Immunopathogenic mechanisms of systemic autoimmune disease |
Q40381617 | Induction and Analysis of Bronchus-Associated Lymphoid Tissue. |
Q38067055 | Intestinal stromal cells in mucosal immunity and homeostasis. |
Q50481833 | Intrahepatic myeloid-cell aggregates enable local proliferation of CD8(+) T cells and successful immunotherapy against chronic viral liver infection. |
Q35596407 | Intravascular staining for discrimination of vascular and tissue leukocytes. |
Q36637198 | Local T/B cooperation in inflamed tissues is supported by T follicular helper-like cells. |
Q30386823 | Long-Lasting Cross-Protection Against Influenza A by Neuraminidase and M2e-based immunization strategies |
Q89495110 | Lymphoid Aggregates in the CNS of Progressive Multiple Sclerosis Patients Lack Regulatory T Cells |
Q56369727 | Lymphoid aggregates in desmoplastic melanoma have features of tertiary lymphoid structures |
Q43238575 | Lymphoid neogenesis in melanoma: What does it tell us? |
Q48162719 | Lymphoid-Like Structures with Distinct B Cell Areas in Kidney Allografts are not Predictive for Graft Rejection. A Non-human Primate Study. |
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Q38201655 | Manipulation of tumour-infiltrating B cells and tertiary lymphoid structures: a novel anti-cancer treatment avenue? |
Q99707149 | Mapping Transplant Arteriosclerosis Cell-by-Cell: A Path to New Immune Insights |
Q52382940 | Maturation of tertiary lymphoid structures and recurrence of stage II and III colorectal cancer. |
Q92652833 | Mechanisms of Adverse Local Tissue Reactions to Hip Implants |
Q91763674 | Meningeal inflammation changes the balance of TNF signalling in cortical grey matter in multiple sclerosis |
Q55096337 | Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis. |
Q92424711 | Multiscale engineering of immune cells and lymphoid organs |
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