High endothelial venules (HEVs) in immunity, inflammation and cancer
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[1] Hae-Chul Park,et al. Dual role of endothelial Myct1 in tumor angiogenesis and tumor immunity , 2021, Science Translational Medicine.
[2] M. Péoc'h,et al. High endothelial venules are present in pharyngeal and laryngeal carcinomas and they are associated with better prognosis. , 2021, Pathology, research and practice.
[3] Jennifer L. Taylor,et al. STING agonist-based treatment promotes vascular normalization and tertiary lymphoid structure formation in the therapeutic melanoma microenvironment , 2021, Journal for ImmunoTherapy of Cancer.
[4] N. Annabi,et al. Simultaneous targeting of primary tumor, draining lymph node, and distant metastases through high endothelial venule-targeted delivery. , 2021, Nano today.
[5] F. Wärnberg,et al. Remodeling of the Lymph Node High Endothelial Venules Reflects Tumor Invasiveness in Breast Cancer and is Associated with Dysregulation of Perivascular Stromal Cells , 2021, Cancers.
[6] G. Altan-Bonnet,et al. Stem-like CD8 T cells mediate response of adoptive cell immunotherapy against human cancer , 2020, Science.
[7] D. Baeten,et al. Anti-IL-17A treatment reduces serum inflammatory, angiogenic and tissue remodeling biomarkers accompanied by less synovial high endothelial venules in peripheral spondyloarthritis , 2020, Scientific Reports.
[8] A. Copik,et al. High endothelial venules accelerate naive T cell recruitment by tumor necrosis factor-mediated R-Ras up-regulation. , 2020, The American journal of pathology.
[9] V. Engelhard,et al. Insights into Tumor-Associated Tertiary Lymphoid Structures: Novel Targets for Antitumor Immunity and Cancer Immunotherapy , 2020, Cancer Immunology Research.
[10] M. Heikenwalder,et al. Amelioration of Murine Autoimmune Pancreatitis by Targeted LTβR Inhibition and Anti-CD20 Treatment , 2020, ImmunoHorizons.
[11] J. Abe,et al. The Dual Role of High Endothelial Venules in Cancer Progression versus Immunity , 2020, Trends in cancer.
[12] W. Curran,et al. Tumor-draining lymph node is important for a robust abscopal effect stimulated by radiotherapy , 2020, Journal for ImmunoTherapy of Cancer.
[13] C. Fiala,et al. Densities of decidual high endothelial venules correlate with T-cell influx in healthy pregnancies and idiopathic recurrent pregnancy losses. , 2020, Human reproduction.
[14] Juan Fang,et al. Prognostic value of tertiary lymphoid structure and tumour infiltrating lymphocytes in oral squamous cell carcinoma , 2020, International Journal of Oral Science.
[15] C. Fenton,et al. Kidney tertiary lymphoid structures in Lupus Nephritis develop into large interconnected networks and resemble lymph nodes in gene signature. , 2020, The American journal of pathology.
[16] Min Kyoon Kim,et al. High Endothelial Venule with Concomitant High CD8+ Tumor-Infiltrating Lymphocytes Is Associated with a Favorable Prognosis in Resected Gastric Cancer , 2020, Journal of clinical medicine.
[17] K. Red-Horse,et al. A molecular map of murine lymph node blood vascular endothelium at single cell resolution , 2020, Nature Communications.
[18] L. Aqrawi,et al. Expression of NGAL-specific cells and mRNA levels correlate with inflammation in the salivary gland, and its overexpression in the saliva, of patients with primary Sjögren’s syndrome , 2020, Autoimmunity.
[19] Motohiro Kobayashi,et al. Induction of High Endothelial Venule–like Vessels in Oral and Cutaneous Lichen Planus: A Comparative Study , 2020, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[20] G. Mills,et al. Verteporfin Inhibits PD-L1 through Autophagy and the STAT1–IRF1–TRIM28 Signaling Axis, Exerting Antitumor Efficacy , 2020, Cancer Immunology Research.
[21] S. Turley,et al. Lymph node stromal cells: cartographers of the immune system , 2020, Nature Immunology.
[22] S. Brunak,et al. Immune Profiling of Human Gut-Associated Lymphoid Tissue Identifies a Role for Isolated Lymphoid Follicles in Priming of Region-Specific Immunity. , 2020, Immunity.
[23] Thomas D. Wu,et al. Peripheral T cell expansion predicts tumour infiltration and clinical response , 2020, Nature.
[24] Shanshan Liu,et al. Dual-mechanism based CTLs infiltration enhancement initiated by Nano-sapper potentiates immunotherapy against immune-excluded tumors , 2020, Nature Communications.
[25] J. Hamzah,et al. Remodeling of Metastatic Vasculature Reduces Lung Colonization and Sensitizes Overt Metastases to Immunotherapy. , 2020, Cell reports.
[26] Jeffrey E. Lee,et al. B cells and tertiary lymphoid structures promote immunotherapy response , 2020, Nature.
[27] J. Wargo,et al. B cells are associated with survival and immunotherapy response in sarcoma , 2020, Nature.
[28] Huanming Yang,et al. An Integrated Gene Expression Landscape Profiling Approach to Identify Lung Tumor Endothelial Cell Heterogeneity and Angiogenic Candidates. , 2020, Cancer cell.
[29] D. Schadendorf,et al. Tertiary lymphoid structures improve immunotherapy and survival in melanoma , 2020, Nature.
[30] P. Gaulard,et al. Exclusive B‐cell phenotype of primary prostatic lymphomas: a potential role of chronic prostatitis , 2019, Histopathology.
[31] A. Kamphorst,et al. An intra-tumoral niche maintains and differentiates stem-like CD8 T cells , 2019, Nature.
[32] M. Ishii,et al. High-endothelial cell-derived S1P regulates dendritic cell localization and vascular integrity in the lymph node , 2019, eLife.
[33] Brandy E. Olin,et al. CytoMAP: A Spatial Analysis Toolbox Reveals Features of Myeloid Cell Organization in Lymphoid Tissues , 2019, bioRxiv.
[34] M. Kloor,et al. High endothelial venules are associated with microsatellite instability, hereditary background and immune evasion in colorectal cancer , 2019, British Journal of Cancer.
[35] O. Kamenyeva,et al. In Vivo F-Actin Filament Organization during Lymphocyte Transendothelial and Interstitial Migration Revealed by Intravital Microscopy , 2019, iScience.
[36] Howard Y. Chang,et al. Clonal replacement of tumor-specific T cells following PD-1 blockade , 2019, bioRxiv.
[37] C. Sautès-Fridman,et al. Tertiary lymphoid structures in the era of cancer immunotherapy , 2019, Nature Reviews Cancer.
[38] M. Bajénoff,et al. Remodeling of reactive lymph nodes: Dynamics of stromal cells and underlying chemokine signaling , 2019, Immunological reviews.
[39] S. Fujieda,et al. Induction of peripheral lymph node addressin in human nasal mucosa with eosinophilic chronic rhinosinusitis. , 2019, Pathology.
[40] J. Girard,et al. Single-Cell Analysis Reveals Heterogeneity of High Endothelial Venules and Different Regulation of Genes Controlling Lymphocyte Entry to Lymph Nodes. , 2019, Cell reports.
[41] F. Hodi,et al. Subsets of exhausted CD8+ T cells differentially mediate tumor control and respond to checkpoint blockade , 2019, Nature Immunology.
[42] Daniel E. Speiser,et al. Intratumoral Tcf1+PD‐1+CD8+ T Cells with Stem‐like Properties Promote Tumor Control in Response to Vaccination and Checkpoint Blockade Immunotherapy , 2019, Immunity.
[43] M. Kneilling,et al. Tumor-draining lymph nodes are pivotal in PD-1/PD-L1 checkpoint therapy. , 2018, JCI insight.
[44] N. Annabi,et al. Ectopic high endothelial venules in pancreatic ductal adenocarcinoma: A unique site for targeted delivery , 2018, EBioMedicine.
[45] Paul J. Hoover,et al. Defining T Cell States Associated with Response to Checkpoint Immunotherapy in Melanoma , 2018, Cell.
[46] C. Sautès-Fridman,et al. Association of IL-36γ with tertiary lymphoid structures and inflammatory immune infiltrates in human colorectal cancer , 2018, Cancer Immunology, Immunotherapy.
[47] M. Genovese,et al. Clinical Efficacy and Safety of Baminercept, a Lymphotoxin &bgr; Receptor Fusion Protein, in Primary Sjögren's Syndrome: Results From a Phase II Randomized, Double‐Blind, Placebo‐Controlled Trial , 2018, Arthritis & rheumatology.
[48] G. Liszkay,et al. Correlation with lymphocyte infiltration, but lack of prognostic significance of MECA-79-positive high endothelial venules in primary malignant melanoma , 2018, Melanoma research.
[49] J. Mulé,et al. Induction of Tertiary Lymphoid Structures With Antitumor Function by a Lymph Node-Derived Stromal Cell Line , 2018, Front. Immunol..
[50] M. Fernández-Figueras,et al. Expression of Peripheral Node Addressins by Plasmacytic Plaque of Children, APACHE, TRAPP, and Primary Cutaneous Angioplasmacellular Hyperplasia , 2018, Applied immunohistochemistry & molecular morphology : AIMM.
[51] G. Bergers,et al. Vascular targeting of LIGHT normalizes blood vessels in primary brain cancer and induces intratumoural high endothelial venules , 2018, The Journal of pathology.
[52] Z. Bago-Horvath,et al. Lymph node blood vessels provide exit routes for metastatic tumor cell dissemination in mice , 2018, Science.
[53] Eelco F. J. Meijer,et al. Lymph node metastases can invade local blood vessels, exit the node, and colonize distant organs in mice , 2018, Science.
[54] Jedd D. Wolchok,et al. Cancer immunotherapy using checkpoint blockade , 2018, Science.
[55] O. Ichii,et al. Histopathological Correlations between Mediastinal Fat-Associated Lymphoid Clusters and the Development of Lung Inflammation and Fibrosis following Bleomycin Administration in Mice , 2018, Front. Immunol..
[56] S. Steigen,et al. Presence of high-endothelial venules correlates with a favorable immune microenvironment in oral squamous cell carcinoma , 2018, Modern Pathology.
[57] P. Kubes,et al. Neutrophils recruited through high endothelial venules of the lymph nodes via PNAd intercept disseminating Staphylococcus aureus , 2018, Proceedings of the National Academy of Sciences.
[58] V. Engelhard,et al. Immune Cell Infiltration and Tertiary Lymphoid Structures as Determinants of Antitumor Immunity , 2018, The Journal of Immunology.
[59] J. Girard,et al. Interleukin‐33 (IL‐33): A nuclear cytokine from the IL‐1 family , 2018, Immunological reviews.
[60] A. Gallimore,et al. Tertiary Lymphoid Structures in Cancer: Drivers of Antitumor Immunity, Immunosuppression, or Bystander Sentinels in Disease? , 2017, Front. Immunol..
[61] G. Tse,et al. Distinct Tertiary Lymphoid Structure Associations and Their Prognostic Relevance in HER2 Positive and Negative Breast Cancers. , 2017, The oncologist.
[62] D. Berman,et al. Tertiary Lymphoid Structures Associate with Tumour Stage in Urothelial Bladder Cancer , 2017, Bladder cancer.
[63] C. Ware,et al. Treg Depletion Licenses T Cell–Driven HEV Neogenesis and Promotes Tumor Destruction , 2017, Cancer Immunology Research.
[64] R. Ganss,et al. De novo induction of intratumoral lymphoid structures and vessel normalization enhances immunotherapy in resistant tumors , 2017, Nature Immunology.
[65] H. Wanibuchi,et al. B cells in tertiary lymphoid structures are associated with favorable prognosis in gastric cancer. , 2017, The Journal of surgical research.
[66] Shao-Cong Sun,et al. The non-canonical NF-κB pathway in immunity and inflammation , 2017, Nature Reviews Immunology.
[67] Simon C Watkins,et al. Tbet and IL-36γ cooperate in therapeutic DC-mediated promotion of ectopic lymphoid organogenesis in the tumor microenvironment , 2017, Oncoimmunology.
[68] K. Ley,et al. Differential DARC/ACKR1 expression distinguishes venular from non-venular endothelial cells in murine tissues , 2017, BMC Biology.
[69] J. Rangel-Moreno,et al. A Unique Cellular and Molecular Microenvironment Is Present in Tertiary Lymphoid Organs of Patients with Spontaneous Prostate Cancer Regression , 2017, Front. Immunol..
[70] D. Hanahan,et al. Combined antiangiogenic and anti–PD-L1 therapy stimulates tumor immunity through HEV formation , 2017, Science Translational Medicine.
[71] M. Groenen,et al. High endothelial venules associated with T cell subsets in the inflamed gut of newly diagnosed inflammatory bowel disease patients , 2017, Clinical and experimental immunology.
[72] Motohiro Kobayashi,et al. Appearance of High Endothelial Venule‐Like Vessels in Benign Prostatic Hyperplasia is Associated With Lower Urinary tract Symptoms , 2017, The Prostate.
[73] A. Ager. High Endothelial Venules and Other Blood Vessels: Critical Regulators of Lymphoid Organ Development and Function , 2017, Front. Immunol..
[74] I. Mellman,et al. Elements of cancer immunity and the cancer–immune set point , 2017, Nature.
[75] S. Albelda,et al. CAR T Cell Therapy for Solid Tumors. , 2017, Annual review of medicine.
[76] I. Cremer,et al. Immune contexture and histological response after neoadjuvant chemotherapy predict clinical outcome of lung cancer patients , 2016, Oncoimmunology.
[77] M. Hirokawa,et al. High endothelial venule-like vessels and lymphocyte recruitment in diffuse sclerosing variant of papillary thyroid carcinoma. , 2016, Pathology.
[78] S. Wienert,et al. Clonal Proliferation and Stochastic Pruning Orchestrate Lymph Node Vasculature Remodeling. , 2016, Immunity.
[79] H. Lee,et al. Predictive Value of Tertiary Lymphoid Structures Assessed by High Endothelial Venule Counts in the Neoadjuvant Setting of Triple-Negative Breast Cancer , 2016, Cancer research and treatment : official journal of Korean Cancer Association.
[80] Fabio Grizzi,et al. Spatial distribution of B cells predicts prognosis in human pancreatic adenocarcinoma , 2016, Oncoimmunology.
[81] Xiaoxiao Wang,et al. Facilitating T Cell Infiltration in Tumor Microenvironment Overcomes Resistance to PD-L1 Blockade. , 2016, Cancer cell.
[82] T. Mayadas,et al. Protection from septic peritonitis by rapid neutrophil recruitment through omental high endothelial venules , 2016, Nature Communications.
[83] Yan Shi,et al. Peripheral Lymphoid Volume Expansion and Maintenance Are Controlled by Gut Microbiota via RALDH+ Dendritic Cells. , 2016, Immunity.
[84] J. Soria,et al. Immune-related adverse events with immune checkpoint blockade: a comprehensive review. , 2016, European journal of cancer.
[85] R. Boidot,et al. Tumor infiltration by Tbet+ effector T cells and CD20+ B cells is associated with survival in gastric cancer patients , 2016, Oncoimmunology.
[86] S. Steigen,et al. Presence of tumour high-endothelial venules is an independent positive prognostic factor and stratifies patients with advanced-stage oral squamous cell carcinoma , 2016, Tumor Biology.
[87] B. Nelson,et al. Tumor-Infiltrating Plasma Cells Are Associated with Tertiary Lymphoid Structures, Cytolytic T-Cell Responses, and Superior Prognosis in Ovarian Cancer , 2016, Clinical Cancer Research.
[88] T. Abe,et al. Lysophosphatidic acid receptors LPA4 and LPA6 differentially promote lymphocyte transmigration across high endothelial venules in lymph nodes , 2015, International immunology.
[89] D. Vestweber,et al. How leukocytes cross the vascular endothelium , 2015, Nature Reviews Immunology.
[90] K. Rajewsky,et al. Ectopic lymphoid structures function as microniches for tumor progenitor cells in hepatocellular carcinoma , 2015, Nature Immunology.
[91] Nikhil S. Joshi,et al. Regulatory T Cells in Tumor-Associated Tertiary Lymphoid Structures Suppress Anti-tumor T Cell Responses. , 2015, Immunity.
[92] Y. Sakai,et al. Lymphocyte ‘homing’ and chronic inflammation , 2015, Pathology international.
[93] M. May,et al. Understanding high endothelial venules: Lessons for cancer immunology , 2015, Oncoimmunology.
[94] Y. Kanai,et al. Intratumoral tertiary lymphoid organ is a favourable prognosticator in patients with pancreatic cancer , 2015, British Journal of Cancer.
[95] J. Caamaño,et al. Stromal cells in chronic inflammation and tertiary lymphoid organ formation. , 2015, Annual review of immunology.
[96] V. Engelhard,et al. Effector lymphocyte-induced lymph node-like vasculature enables naïve T-cell entry into tumors and enhanced anti-tumor immunity , 2015, Nature Communications.
[97] P. Sharma,et al. The future of immune checkpoint therapy , 2015, Science.
[98] S. Rosenberg,et al. Adoptive cell transfer as personalized immunotherapy for human cancer , 2015, Science.
[99] T. Schumacher,et al. Neoantigens in cancer immunotherapy , 2015, Science.
[100] J. Kabat,et al. Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus , 2015, PLoS pathogens.
[101] S. Fismen,et al. Tertiary lymphoid structures are associated with higher tumor grade in primary operable breast cancer patients , 2015, BMC Cancer.
[102] Geraint T. Williams,et al. High endothelial venules are rare in colorectal cancers but accumulate in extra-tumoral areas with disease progression , 2015, Oncoimmunology.
[103] G. Freeman,et al. Orchestration and Prognostic Significance of Immune Checkpoints in the Microenvironment of Primary and Metastatic Renal Cell Cancer , 2015, Clinical Cancer Research.
[104] E. Tanaka,et al. Superficially located enlarged lymphoid follicles characterise nodular gastritis , 2015, Pathology.
[105] J. Bienkowska,et al. Lymphotoxin-LIGHT Pathway Regulates the Interferon Signature in Rheumatoid Arthritis , 2014, PloS one.
[106] C. Sautès-Fridman,et al. Tertiary lymphoid structures in cancer and beyond. , 2014, Trends in immunology.
[107] R. Emerson,et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance , 2014, Nature.
[108] E. Butcher,et al. Transcriptional programs of lymphoid tissue capillary and high endothelium reveal control mechanisms for lymphocyte homing , 2014, Nature Immunology.
[109] Simon A. Jones,et al. Ectopic lymphoid-like structures in infection, cancer and autoimmunity , 2014, Nature Reviews Immunology.
[110] Yong Song,et al. Alterations of high endothelial venules in primary and metastatic tumors are correlated with lymph node metastasis of oral and pharyngeal carcinoma , 2014, Cancer biology & therapy.
[111] R. Kitazawa,et al. High endothelial venule‐like vessels and lymphocyte recruitment in testicular seminoma , 2014, Andrology.
[112] P. Allavena,et al. Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers , 2014, Clinical Cancer Research.
[113] Pierre Validire,et al. Dendritic cells in tumor-associated tertiary lymphoid structures signal a Th1 cytotoxic immune contexture and license the positive prognostic value of infiltrating CD8+ T cells. , 2014, Cancer research.
[114] C. Monteagudo,et al. Correlation between High Endothelial Vessels and Histopathological Features of Different Pigmented Lesions , 2013, Current health sciences journal.
[115] C. Monteagudo,et al. The density and type of MECA‐79‐positive high endothelial venules correlate with lymphocytic infiltration and tumour regression in primary cutaneous melanoma , 2013, Histopathology.
[116] J. Girard,et al. Regulation of tumor-associated high-endothelial venules by dendritic cells , 2013, Oncoimmunology.
[117] S. Coughlin,et al. Podoplanin maintains high endothelial venule integrity by interacting with platelet CLEC-2 , 2013, Nature.
[118] P. Rochaix,et al. High Endothelial Venule Blood Vessels for Tumor-Infiltrating Lymphocytes Are Associated with Lymphotoxin β–Producing Dendritic Cells in Human Breast Cancer , 2013, The Journal of Immunology.
[119] I. Mellman,et al. Oncology meets immunology: the cancer-immunity cycle. , 2013, Immunity.
[120] M. Fukuda,et al. Role of High Endothelial Venule–Expressed Heparan Sulfate in Chemokine Presentation and Lymphocyte Homing , 2013, The Journal of Immunology.
[121] C. Sautès-Fridman,et al. Characteristics and Clinical Impacts of the Immune Environments in Colorectal and Renal Cell Carcinoma Lung Metastases: Influence of Tumor Origin , 2013, Clinical Cancer Research.
[122] B. Ludewig,et al. Endothelial cell–specific lymphotoxin-β receptor signaling is critical for lymph node and high endothelial venule formation , 2013, The Journal of experimental medicine.
[123] Ayumi Ohya,et al. Lymphocyte recruitment via high endothelial venules in lymphoid stroma of Warthin's tumour , 2013, Pathology.
[124] T. Morohoshi,et al. Periductal Induction of High Endothelial Venule-Like Vessels in Type 1 Autoimmune Pancreatitis , 2013, Pancreas.
[125] A. Aguzzi,et al. Lymphotoxin β receptor signaling promotes development of autoimmune pancreatitis. , 2012, Gastroenterology.
[126] K. Ladell,et al. T-cell trafficking facilitated by high endothelial venules is required for tumor control after regulatory T-cell depletion. , 2012, Cancer research.
[127] Yi-Chun Chen,et al. Autotaxin through Lysophosphatidic Acid Stimulates Polarization, Motility, and Transendothelial Migration of Naive T Cells , 2012, The Journal of Immunology.
[128] Swe Swe Myint,et al. Changes in specialized blood vessels in lymph nodes and their role in cancer metastasis , 2012, Journal of Translational Medicine.
[129] G. Proctor,et al. Inducible Tertiary Lymphoid Structures, Autoimmunity, and Exocrine Dysfunction in a Novel Model of Salivary Gland Inflammation in C57BL/6 Mice , 2012, The Journal of Immunology.
[130] Reinhold Förster,et al. HEVs, lymphatics and homeostatic immune cell trafficking in lymph nodes , 2012, Nature Reviews Immunology.
[131] J. V. Stein,et al. Optical projection tomography reveals dynamics of HEV growth after immunization with protein plus CFA and features shared with HEVs in acute autoinflammatory lymphadenopathy , 2012, Front. Immun..
[132] P. Rochaix,et al. High endothelial venules (HEVs) in human melanoma lesions , 2012, Oncoimmunology.
[133] H. Hammad,et al. Pulmonary lymphoid neogenesis in idiopathic pulmonary arterial hypertension. , 2012, American journal of respiratory and critical care medicine.
[134] J. J. van den Oord,et al. Neogenesis of lymphoid structures and antibody responses occur in human melanoma metastases. , 2012, Cancer research.
[135] J. Marth,et al. Coordinated roles of ST3Gal-VI and ST3Gal-IV sialyltransferases in the synthesis of selectin ligands. , 2012, Blood.
[136] H. Hammad,et al. Tertiary lymphoid organs in infection and autoimmunity , 2012, Trends in Immunology.
[137] I. Do,et al. Lymphatic Vessels and High Endothelial Venules are Increased in the Sentinel Lymph Nodes of Patients with Oral Squamous Cell Carcinoma Before the Arrival of Tumor Cells , 2012, Annals of Surgical Oncology.
[138] C. Sautès-Fridman,et al. The immune contexture in human tumours: impact on clinical outcome , 2012, Nature Reviews Cancer.
[139] Michael D. Davis,et al. Lymph node B lymphocyte trafficking is constrained by anatomy and highly dependent upon chemoattractant desensitization. , 2012, Blood.
[140] M. Goddard,et al. Blocking lymphotoxin signaling abrogates the development of ectopic lymphoid tissue within cardiac allografts and inhibits effector antibody responses , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[141] E. Kremmer,et al. Lymph node T cell homeostasis relies on steady state homing of dendritic cells. , 2011, Immunity.
[142] M. Lipp,et al. Coordinated Regulation of Lymph Node Vascular–Stromal Growth First by CD11c+ Cells and Then by T and B Cells , 2011, The Journal of Immunology.
[143] Ronald N Germain,et al. High endothelial venules as traffic control points maintaining lymphocyte population homeostasis in lymph nodes. , 2011, Blood.
[144] J. Girard,et al. Dendritic cells control lymphocyte entry to lymph nodes through high endothelial venules , 2011, Nature.
[145] A. Bolstad,et al. Lymphotoxin-beta receptor blockade reduces CXCL13 in lacrimal glands and improves corneal integrity in the NOD model of Sjögren's syndrome , 2011, Arthritis research & therapy.
[146] P. Validire,et al. Characterization of chemokines and adhesion molecules associated with T cell presence in tertiary lymphoid structures in human lung cancer. , 2011, Cancer research.
[147] Thomas Filleron,et al. Human solid tumors contain high endothelial venules: association with T- and B-lymphocyte infiltration and favorable prognosis in breast cancer. , 2011, Cancer research.
[148] J. Kolls,et al. The development of inducible Bronchus Associated Lymphoid Tissue (iBALT) is dependent on IL-17 , 2011, Nature Immunology.
[149] M. Fukuda,et al. Essential role of peripheral node addressin in lymphocyte homing to nasal-associated lymphoid tissues and allergic immune responses , 2011, The Journal of experimental medicine.
[150] K. Khoo,et al. Prominent expression of sialyl Lewis X‐capped core 2‐branched O‐glycans on high endothelial venule‐like vessels in gastric MALT lymphoma , 2011, The Journal of pathology.
[151] W. Muller,et al. Mechanisms of leukocyte transendothelial migration. , 2011, Annual review of pathology.
[152] U. V. von Andrian,et al. Endothelial heparan sulfate controls chemokine presentation in recruitment of lymphocytes and dendritic cells to lymph nodes. , 2010, Immunity.
[153] Kaori Sato,et al. Novel Anti-carbohydrate Antibodies Reveal the Cooperative Function of Sulfated N- and O-Glycans in Lymphocyte Homing*♦ , 2010, The Journal of Biological Chemistry.
[154] T. Meyer,et al. The chemokine receptor CXCR5 is pivotal for ectopic mucosa-associated lymphoid tissue neogenesis in chronic Helicobacter pylori-induced inflammation , 2010, Journal of Molecular Medicine.
[155] B. Engelhardt,et al. Immunobiology: Comprehensive analysis of lymph node stroma-expressed Ig superfamily members reveals redundant and nonredundant roles for ICAM-1, ICAM-2, and VCAM-1 in lymphocyte homing , 2012 .
[156] V. Engelhard,et al. Tumor masses support naive T cell infiltration, activation, and differentiation into effectors , 2010, The Journal of experimental medicine.
[157] R. Écochard,et al. Chronic Rejection Triggers the Development of an Aggressive Intragraft Immune Response through Recapitulation of Lymphoid Organogenesis , 2010, The Journal of Immunology.
[158] Yoshinori Fukui,et al. Global lymphoid tissue remodeling during a viral infection is orchestrated by a B cell-lymphotoxin-dependent pathway. , 2010, Blood.
[159] Melody A. Swartz,et al. Induction of Lymphoidlike Stroma and Immune Escape by Tumors That Express the Chemokine CCL21 , 2010, Science.
[160] Takashi Ito,et al. B Cell-Derived Vascular Endothelial Growth Factor A Promotes Lymphangiogenesis and High Endothelial Venule Expansion in Lymph Nodes , 2010, The Journal of Immunology.
[161] V. Guaiquil,et al. CD11chi Dendritic Cells Regulate the Re-establishment of Vascular Quiescence and Stabilization after Immune Stimulation of Lymph Nodes , 2010, The Journal of Immunology.
[162] M. Shimaoka,et al. Distinct roles for LFA-1 affinity regulation during T-cell adhesion, diapedesis, and interstitial migration in lymph nodes. , 2010, Blood.
[163] S. Akira,et al. Id2-, RORγt-, and LTβR-independent initiation of lymphoid organogenesis in ocular immunity , 2009, The Journal of experimental medicine.
[164] S. Keshavjee,et al. The Role of Intrapulmonary De Novo Lymphoid Tissue in Obliterative Bronchiolitis after Lung Transplantation1 , 2009, The Journal of Immunology.
[165] Kim L Kusser,et al. Omental milky spots develop in the absence of lymphoid tissue-inducer cells and support B and T cell responses to peritoneal antigens. , 2009, Immunity.
[166] P. Muranski,et al. Wnt signaling arrests effector T cell differentiation and generates CD8+ memory stem cells , 2009, Nature Medicine.
[167] K. Suzawa,et al. GlcNAc6ST‐1‐mediated decoration of MAdCAM‐1 protein with L‐selectin ligand carbohydrates directs disease activity of ulcerative colitis , 2009, Inflammatory bowel diseases.
[168] A. Bolstad,et al. Blockade of lymphotoxin-beta receptor signaling reduces aspects of Sjögren's syndrome in salivary glands of non-obese diabetic mice , 2009, Arthritis research & therapy.
[169] G. Getz,et al. Lymphotoxin β receptor signaling promotes tertiary lymphoid organogenesis in the aorta adventitia of aged ApoE−/− mice , 2009, The Journal of experimental medicine.
[170] Stephen Kelly,et al. Ectopic Lymphoid Structures Support Ongoing Production of Class-Switched Autoantibodies in Rheumatoid Synovium , 2009, PLoS medicine.
[171] T. Tsuruo,et al. Involvement of the lysophosphatidic acid-generating enzyme autotaxin in lymphocyte-endothelial cell interactions. , 2008, The American journal of pathology.
[172] F. Sallusto,et al. CD40L+ CD4+ memory T cells migrate in a CD62P-dependent fashion into reactive lymph nodes and license dendritic cells for T cell priming , 2008, The Journal of experimental medicine.
[173] Burkhard Ludewig,et al. Form follows function: lymphoid tissue microarchitecture in antimicrobial immune defence , 2008, Nature Reviews Immunology.
[174] R. Medzhitov. Origin and physiological roles of inflammation , 2008, Nature.
[175] W. Leonard,et al. IL-2 and IL-21 confer opposing differentiation programs to CD8+ T cells for adoptive immunotherapy. , 2008, Blood.
[176] yang-xin fu,et al. Targeting tumors with LIGHT to generate metastasis-clearing immunity. , 2008, Cytokine & growth factor reviews.
[177] S. Marsal,et al. Clinical significance of synovial lymphoid neogenesis and its reversal after anti-tumour necrosis factor α therapy in rheumatoid arthritis , 2008, Annals of the rheumatic diseases.
[178] Antal Rot,et al. CCR7 and its ligands: balancing immunity and tolerance , 2008, Nature Reviews Immunology.
[179] M. Gunn,et al. Autotaxin, an ectoenzyme that produces lysophosphatidic acid, promotes the entry of lymphocytes into secondary lymphoid organs , 2008, Nature Immunology.
[180] D. Jackson,et al. CCL21 expression pattern of human secondary lymphoid organ stroma is conserved in inflammatory lesions with lymphoid neogenesis. , 2007, The American journal of pathology.
[181] M. McGurk,et al. 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 Sjögren’s Syndrome1 , 2007, The Journal of Immunology.
[182] K. Suzawa,et al. Preferential Induction of Peripheral Lymph Node Addressin on High Endothelial Venule-Like Vessels in the Active Phase of Ulcerative Colitis , 2007, The American Journal of Gastroenterology.
[183] Kim L Kusser,et al. Pulmonary expression of CXC chemokine ligand 13, CC chemokine ligand 19, and CC chemokine ligand 21 is essential for local immunity to influenza , 2007, Proceedings of the National Academy of Sciences.
[184] Ronald N Germain,et al. L-selectin-negative CCR7− effector and memory CD8+ T cells enter reactive lymph nodes and kill dendritic cells , 2007, Nature Immunology.
[185] J. Marth,et al. Critical functions of N-glycans in L-selectin-mediated lymphocyte homing and recruitment , 2007, Nature Immunology.
[186] M. Skobe,et al. Lymphotoxin β receptor signaling is required for inflammatory lymphangiogenesis in the thyroid , 2007, Proceedings of the National Academy of Sciences.
[187] B. Teh,et al. Prospects for Vasculature Reorganization in Sentinel Lymph Nodes , 2007, Cell cycle.
[188] D. Baeten,et al. Published Online First , 2007 .
[189] Delphine A. Lacorre,et al. IL-33, the IL-1-like cytokine ligand for ST2 receptor, is a chromatin-associated nuclear factor in vivo , 2007, Proceedings of the National Academy of Sciences.
[190] M. Di Nicola,et al. Quilty Effect Has the Features of Lymphoid Neogenesis and Shares CXCL13–CXCR5 Pathway With Recurrent Acute Cardiac Rejections , 2007, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[191] Ronald N Germain,et al. Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes. , 2006, Immunity.
[192] B. Berghuis,et al. Preparing the "soil": the primary tumor induces vasculature reorganization in the sentinel lymph node before the arrival of metastatic cancer cells. , 2006, Cancer research.
[193] S. Lira,et al. Interaction of mature CD3+CD4+ T cells with dendritic cells triggers the development of tertiary lymphoid structures in the thyroid. , 2006, The Journal of clinical investigation.
[194] Z. Trajanoski,et al. Type, Density, and Location of Immune Cells Within Human Colorectal Tumors Predict Clinical Outcome , 2006, Science.
[195] S. Liao,et al. Synchrony of High Endothelial Venules and Lymphatic Vessels Revealed by Immunization1 , 2006, The Journal of Immunology.
[196] E. Ekland,et al. Regulation of lymph node vascular growth by dendritic cells , 2006, The Journal of experimental medicine.
[197] S. Hemmerich,et al. Induction of PNAd and N-acetylglucosamine 6-O-sulfotransferases 1 and 2 in mouse collagen-induced arthritis , 2006, BMC Immunology.
[198] Y. Kuroda,et al. Type I interferon production by tertiary lymphoid tissue developing in response to 2,6,10,14-tetramethyl-pentadecane (pristane). , 2006, The American journal of pathology.
[199] S. Liao,et al. Lymphoid organ development: from ontogeny to neogenesis , 2006, Nature Immunology.
[200] F. Aloisi,et al. Lymphoid neogenesis in chronic inflammatory diseases , 2006, Nature Reviews Immunology.
[201] F. Ginhoux,et al. B cell-driven lymphangiogenesis in inflamed lymph nodes enhances dendritic cell mobilization. , 2006, Immunity.
[202] F. Amalric,et al. Cancer cells regulate lymphocyte recruitment and leukocyte-endothelium interactions in the tumor-draining lymph node. , 2005, Cancer research.
[203] Akiko Iwasaki,et al. Innate control of adaptive immunity via remodeling of lymph node feed arteriole. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[204] S. Perrin,et al. Lymphotoxin-β Receptor Signaling Is Required for the Homeostatic Control of HEV Differentiation and Function , 2005 .
[205] M. Fukuda,et al. N-acetylglucosamine-6-O-sulfotransferases 1 and 2 cooperatively control lymphocyte homing through L-selectin ligand biosynthesis in high endothelial venules , 2005, Nature Immunology.
[206] R. Kannagi,et al. A major class of L-selectin ligands is eliminated in mice deficient in two sulfotransferases expressed in high endothelial venules , 2005, Nature Immunology.
[207] J. V. Stein,et al. Chemokine control of lymphocyte trafficking: a general overview , 2005, Immunology.
[208] E. S. Baekkevold,et al. Disparate lymphoid chemokine expression in mice and men: no evidence of CCL21 synthesis by human high endothelial venules. , 2005, Blood.
[209] T. Waldmann,et al. Central memory self/tumor-reactive CD8+ T cells confer superior antitumor immunity compared with effector memory T cells. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[210] J. Reimund,et al. A comparative study of endothelial cell markers expressed in chronically inflamed human tissues: MECA‐79, Duffy antigen receptor for chemokines, von Willebrand factor, CD31, CD34, CD105 and CD146 , 2005, The Journal of pathology.
[211] T. Torkkeli,et al. Endothelial L-selectin ligands in sinus mucosa during chronic maxillary rhinosinusitis. , 2005, American Journal of Respiratory and Critical Care Medicine.
[212] G. Valesini,et al. Association of CXCL13 and CCL21 expression with the progressive organization of lymphoid-like structures in Sjögren's syndrome. , 2005, Arthritis and rheumatism.
[213] B. Bresnihan,et al. Systematic microanatomical analysis of CXCL13 and CCL21 in situ production and progressive lymphoid organization in rheumatoid synovitis , 2005, European journal of immunology.
[214] Waldemar Kolanus,et al. Lymphocyte arrest requires instantaneous induction of an extended LFA-1 conformation mediated by endothelium-bound chemokines , 2005, Nature Immunology.
[215] J. Pablos,et al. A HEV-restricted sulfotransferase is expressed in rheumatoid arthritis synovium and is induced by lymphotoxin-α/β and TNF-α in cultured endothelial cells , 2005, BMC Immunology.
[216] S. Hemmerich,et al. Therapeutic targeting of endothelial ligands for L-selectin (PNAd) in a sheep model of asthma. , 2005, The American journal of pathology.
[217] Fadi G Lakkis,et al. Lymphoid Neogenesis in Murine Cardiac Allografts Undergoing Chronic Rejection , 2005, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[218] M. Fukuda,et al. Induction of peripheral lymph node addressin in human gastric mucosa infected by Helicobacter pylori. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[219] M. Karin,et al. IκB Kinase Complex α Kinase Activity Controls Chemokine and High Endothelial Venule Gene Expression in Lymph Nodes and Nasal-Associated Lymphoid Tissue1 , 2004, The Journal of Immunology.
[220] T. Cupedo,et al. Induction of secondary and tertiary lymphoid structures in the skin. , 2004, Immunity.
[221] P. Frenette,et al. A Novel Model for Lymphocytic Infiltration of the Thyroid Gland Generated by Transgenic Expression of the CC Chemokine CCL211 , 2004, The Journal of Immunology.
[222] J. Caamaño,et al. A Stroma-Derived Defect in NF-κB2−/− Mice Causes Impaired Lymph Node Development and Lymphocyte Recruitment1 , 2004, The Journal of Immunology.
[223] Kim L Kusser,et al. Role of inducible bronchus associated lymphoid tissue (iBALT) in respiratory immunity , 2004, Nature Medicine.
[224] K. Matsushima,et al. Evidence for recruitment of plasmacytoid dendritic cell precursors to inflamed lymph nodes through high endothelial venules. , 2004, International immunology.
[225] Delphine A. Lacorre,et al. Plasticity of endothelial cells: rapid dedifferentiation of freshly isolated high endothelial venule endothelial cells outside the lymphoid tissue microenvironment. , 2004, Blood.
[226] J. Cyster,et al. Detection of a sulfotransferase (HEC-GlcNAc6ST) in high endothelial venules of lymph nodes and in high endothelial venule-like vessels within ectopic lymphoid aggregates: relationship to the MECA-79 epitope. , 2004, The American journal of pathology.
[227] S. Hemmerich,et al. Differential gene expression profile of human tonsil high endothelial cells: implications for lymphocyte trafficking , 2004, Journal of leukocyte biology.
[228] M. Miyasaka,et al. Lymphocyte trafficking across high endothelial venules: dogmas and enigmas , 2004, Nature Reviews Immunology.
[229] U. V. von Andrian,et al. CXCL12 Mediates CCR7-independent Homing of Central Memory Cells, But Not Naive T Cells, in Peripheral Lymph Nodes , 2004, The Journal of experimental medicine.
[230] C. Berek,et al. Establishment of Early Lymphoid Organ Infrastructure in Transplanted Tumors Mediated by Local Production of Lymphotoxin α and in the Combined Absence of Functional B and T Cells1 , 2004, The Journal of Immunology.
[231] S. Rosen. Ligands for L-selectin: homing, inflammation, and beyond. , 2004, Annual review of immunology.
[232] R. Schreiber,et al. The three Es of cancer immunoediting. , 2004, Annual review of immunology.
[233] S. Henrickson,et al. T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases , 2004, Nature.
[234] Youjin Lee,et al. Priming of naive T cells inside tumors leads to eradication of established tumors , 2004, Nature Immunology.
[235] Ulrich H. von Andrian,et al. Homing and cellular traffic in lymph nodes , 2003, Nature Reviews Immunology.
[236] T. Hara,et al. Th1-Biased Tertiary Lymphoid Tissue Supported by CXC Chemokine Ligand 13-Producing Stromal Network in Chronic Lesions of Autoimmune Gastritis 1 , 2003, The Journal of Immunology.
[237] S. Granjeaud,et al. The Strategy of T Cell Antigen-presenting Cell Encounter in Antigen-draining Lymph Nodes Revealed by Imaging of Initial T Cell Activation , 2003, The Journal of experimental medicine.
[238] S. Akira,et al. Cutting Edge: The B Cell Chemokine CXC Chemokine Ligand 13/B Lymphocyte Chemoattractant Is Expressed in the High Endothelial Venules of Lymph Nodes and Peyer’s Patches and Affects B Cell Trafficking Across High Endothelial Venules1 , 2003, The Journal of Immunology.
[239] S. Nathanson,et al. Insights into the mechanisms of lymph node metastasis , 2003, Cancer.
[240] E. S. Baekkevold,et al. Molecular characterization of NF-HEV, a nuclear factor preferentially expressed in human high endothelial venules. , 2003, The American journal of pathology.
[241] J. Fox,et al. Helicobacter-Induced Chronic Active Lymphoid Aggregates Have Characteristics of Tertiary Lymphoid Tissue , 2003, Infection and Immunity.
[242] Baohui Xu,et al. Lymphocyte Homing to Bronchus-associated Lymphoid Tissue (BALT) Is Mediated by L-selectin/PNAd, α4β1 Integrin/VCAM-1, and LFA-1 Adhesion Pathways , 2003, The Journal of experimental medicine.
[243] W. Lesslauer,et al. Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase , 2003, The Journal of experimental medicine.
[244] U. V. von Andrian,et al. Naive T Cell Recruitment to Nonlymphoid Tissues: A Role for Endothelium-Expressed CC Chemokine Ligand 21 in Autoimmune Disease and Lymphoid Neogenesis1 , 2003, The Journal of Immunology.
[245] R. Mebius. Organogenesis of lymphoid tissues , 2003, Nature reviews. Immunology.
[246] George Coukos,et al. Intratumoral T cells, recurrence, and survival in epithelial ovarian cancer. , 2003, The New England journal of medicine.
[247] R. Schreiber,et al. Cancer immunoediting: from immunosurveillance to tumor escape , 2002, Nature Immunology.
[248] T. Paavonen,et al. Hydrocortisone reduced in vivo, inflammation-induced slow rolling of leukocytes and their extravasation into human conjunctiva. , 2002, Blood.
[249] T. Paavonen,et al. Glycosylation might provide endothelial zip codes for organ-specific leukocyte traffic into inflammatory sites. , 2002, The American journal of pathology.
[250] J. Cyster,et al. Differing Activities of Homeostatic Chemokines CCL19, CCL21, and CXCL12 in Lymphocyte and Dendritic Cell Recruitment and Lymphoid Neogenesis1 , 2002, The Journal of Immunology.
[251] S. Fukuyama,et al. 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. , 2002, Immunity.
[252] J. Cyster,et al. Chemokine Requirements for B Cell Entry to Lymph Nodes and Peyer's Patches , 2002, The Journal of experimental medicine.
[253] T. Wada,et al. High Endothelial Venule-Like Vessels in the Interstitial Lesions of Human Glomerulonephritis , 2002, American Journal of Nephrology.
[254] S. Lira,et al. 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 , 2002, The Journal of Immunology.
[255] J. Sedgwick,et al. Tumor Necrosis Factor–dependent Segmental Control of MIG Expression by High Endothelial Venules in Inflamed Lymph Nodes Regulates Monocyte Recruitment , 2001, The Journal of experimental medicine.
[256] Steffen Jung,et al. Inflammatory Chemokine Transport and Presentation in HEV , 2001, The Journal of experimental medicine.
[257] S. Hemmerich,et al. Sulfation of L-selectin ligands by an HEV-restricted sulfotransferase regulates lymphocyte homing to lymph nodes. , 2001, Immunity.
[258] S. Michie,et al. Lymphocyte migration to inflamed lacrimal glands is mediated by vascular cell adhesion molecule-1/alpha(4)beta(1) integrin, peripheral node addressin/l-selectin, and lymphocyte function-associated antigen-1 adhesion pathways. , 2001, The American journal of pathology.
[259] F. Lund-Johansen,et al. Plasmacytoid dendritic cells (natural interferon- alpha/beta-producing cells) accumulate in cutaneous lupus erythematosus lesions. , 2001, The American journal of pathology.
[260] J. Marth,et al. Novel Sulfated Lymphocyte Homing Receptors and Their Control by a Core1 Extension β1,3-N-Acetylglucosaminyltransferase , 2001, Cell.
[261] F. Reinholt,et al. The Ccr7 Ligand ELC (Ccl19) Is Transcytosed in High Endothelial Venules and Mediates T Cell Recruitment , 2001, The Journal of experimental medicine.
[262] J. Becker,et al. Targeting of lymphotoxin-alpha to the tumor elicits an efficient immune response associated with induction of peripheral lymphoid-like tissue. , 2001, Immunity.
[263] K. Matsushima,et al. Regulation by Chemokines of Circulating Dendritic Cell Precursors, and the Formation of Portal Tract–Associated Lymphoid Tissue, in a Granulomatous Liver Disease , 2001, The Journal of experimental medicine.
[264] T. Paavonen,et al. De novo induction of endothelial L-selectin ligands during kidney allograft rejection. , 2000, Journal of the American Society of Nephrology : JASN.
[265] Stephen Shaw,et al. Lymph-Borne Chemokines and Other Low Molecular Weight Molecules Reach High Endothelial Venules via Specialized Conduits While a Functional Barrier Limits Access to the Lymphocyte Microenvironments in Lymph Node Cortex , 2000, The Journal of experimental medicine.
[266] F. Lund-Johansen,et al. Experimentally Induced Recruitment of Plasmacytoid (CD123high) Dendritic Cells in Human Nasal Allergy1 , 2000, The Journal of Immunology.
[267] T. Paavonen,et al. Endothelial sulfated sialyl Lewis x glycans, putative L-selectin ligands, are preferentially expressed in bronchial asthma but not in other chronic inflammatory lung diseases. , 2000, American journal of respiratory cell and molecular biology.
[268] D. Hanahan,et al. BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis. , 2000, Immunity.
[269] M. Dorf,et al. Cutting Edge: Ectopic Expression of the Chemokine TCA4/SLC Is Sufficient to Trigger Lymphoid Neogenesis1 , 2000, The Journal of Immunology.
[270] U. V. von Andrian,et al. The Cc Chemokine Thymus-Derived Chemotactic Agent 4 (Tca-4, Secondary Lymphoid Tissue Chemokine, 6ckine, Exodus-2) Triggers Lymphocyte Function–Associated Antigen 1–Mediated Arrest of Rolling T Lymphocytes in Peripheral Lymph Node High Endothelial Venules , 2000, The Journal of experimental medicine.
[271] K. Okubo,et al. Expression profile of active genes in mouse lymph node high endothelial cells. , 1999, International immunology.
[272] E. S. Baekkevold,et al. Heterogeneity of endothelial cells: the specialized phenotype of human high endothelial venules characterized by suppression subtractive hybridization. , 1999, The American journal of pathology.
[273] M. Nieminen,et al. Endothelial L-selectin ligands are likely to recruit lymphocytes into rejecting human heart transplants. , 1999, The American journal of pathology.
[274] K. Wolff,et al. Peripheral lymph node addressins are expressed on skin endothelial cells. , 1999, The Journal of investigative dermatology.
[275] S. Tsuboi,et al. A novel, high endothelial venule-specific sulfotransferase expresses 6-sulfo sialyl Lewis(x), an L-selectin ligand displayed by CD34. , 1999, Immunity.
[276] C. Collett,et al. Selective Induction of Endothelial L-selectin Ligand Human Lung Inflammation , 1999, The Histochemical Journal.
[277] R. Zinkernagel,et al. Dendritic Cells Induce Autoimmune Diabetes and Maintain Disease via De Novo Formation of Local Lymphoid Tissue , 1998, The Journal of experimental medicine.
[278] D. Hanahan,et al. Tumor microenvironment can restrict the effectiveness of activated antitumor lymphocytes. , 1998, Cancer research.
[279] J. Lowe,et al. Regulation of fucosyltransferase‐VII expression in peripheral lymph node high endothelial venules , 1998, European journal of immunology.
[280] R. Kannagi,et al. Identification of a Major Carbohydrate Capping Group of the L-selectin Ligand on High Endothelial Venules in Human Lymph Nodes as 6-Sulfo Sialyl Lewis X* , 1998, The Journal of Biological Chemistry.
[281] E. Butcher,et al. Molecular Mechanisms of Lymphocyte Homing to Peripheral Lymph Nodes , 1998, The Journal of experimental medicine.
[282] J. Cyster,et al. A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[283] P. Isaacson,et al. Expression of lymphocyte homing receptors and vascular addressins in low-grade gastric B-cell lymphomas of mucosa-associated lymphoid tissue. , 1997, The American journal of pathology.
[284] C. Mackay,et al. Human mucosal addressin cell adhesion molecule-1 is preferentially expressed in intestinal tract and associated lymphoid tissue. , 1997, The American journal of pathology.
[285] S. Jalkanen,et al. Homing of mucosal leukocytes to joints. Distinct endothelial ligands in synovium mediate leukocyte-subtype specific adhesion. , 1997, The Journal of clinical investigation.
[286] I. Weissman,et al. A developmental switch in lymphocyte homing receptor and endothelial vascular addressin expression regulates lymphocyte homing and permits CD4+ CD3- cells to colonize lymph nodes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[287] U. Andrian. Intravital Microscopy of the Peripheral Lymph Node Microcirculation in Mice , 1996 .
[288] Petr Malý,et al. The α(1,3)Fucosyltransferase Fuc-TVII Controls Leukocyte Trafficking through an Essential Role in L-, E-, and P-selectin Ligand Biosynthesis , 1996, Cell.
[289] E. Butcher,et al. Peripheral lymphoid tissue-like adhesion molecule expression in nodular infiltrates in inflammatory myopathies , 1996, Neuromuscular Disorders.
[290] L. Picker,et al. Lymphocyte Homing and Homeostasis , 1996, Science.
[291] A. Campos-Neto,et al. Chronic inflammation caused by lymphotoxin is lymphoid neogenesis , 1996, The Journal of experimental medicine.
[292] C. Berek,et al. Differentiation of B cells in the nonlymphoid tissue of the synovial membrane of patients with rheumatoid arthritis. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[293] T. Springer,et al. High endothelial venules (HEVs): specialized endothelium for lymphocyte migration. , 1995, Immunology today.
[294] P. Pizcueta,et al. L-selectin-deficient mice have impaired leukocyte recruitment into inflammatory sites , 1995, The Journal of experimental medicine.
[295] S. Watson,et al. Selective modulation of the expression of L-selectin ligands by an immune response , 1995, Current Biology.
[296] S. Rosen,et al. Localization of ligands for L-selectin in mouse peripheral lymph node high endothelial cells by colloidal gold conjugates. , 1994, Blood.
[297] F. Lepault,et al. Expression of homing and adhesion molecules in infiltrated islets of Langerhans and salivary glands of nonobese diabetic mice. , 1994, Journal of immunology.
[298] R. Macdermott,et al. Aberrant binding of lamina propria lymphocytes to vascular endothelium in inflammatory bowel diseases. , 1994, Gastroenterology.
[299] S. Watson,et al. Expression of GlyCAM-1, an endothelial ligand for L-selectin, is affected by afferent lymphatic flow. , 1993, Journal of immunology.
[300] L. Picker,et al. The human peripheral lymph node vascular addressin. An inducible endothelial antigen involved in lymphocyte homing. , 1993, The American journal of pathology.
[301] R. Tisch,et al. Inhibition of insulitis and prevention of diabetes in nonobese diabetic mice by blocking L-selectin and very late antigen 4 adhesion receptors. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[302] O. Simell,et al. Vascular addressins are induced on islet vessels during insulitis in nonobese diabetic mice and are involved in lymphoid cell binding to islet endothelium. , 1993, The Journal of clinical investigation.
[303] S. Hemmerich,et al. Binding of L-selectin to the vascular sialomucin CD34. , 1993, Science.
[304] S. Shaw,et al. T cell adhesion to endothelium: the FRC conduit system and other anatomic and molecular features which facilitate the adhesion cascade in lymph node. , 1993, Seminars in immunology.
[305] P. Streeter,et al. The influence of afferent lymphatic vessel interruption on vascular addressin expression , 1991, The Journal of cell biology.
[306] E. Butcher,et al. Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodes , 1988, The Journal of cell biology.
[307] A. Freemont. Functional and biosynthetic changes in endothelial cells of vessels in chronically inflamed tissues: Evidence for endothelial control of lymphocyte entry into diseased tissues , 1988, The Journal of pathology.
[308] Eugene C. Butcher,et al. A tissue-specific endothelial cell molecule involved in lymphocyte homing , 1988, Nature.
[309] A. Freemont. Molecules controlling lymphocyte-endothelial interactions in lymph nodes are produced in vessels of inflamed synovium. , 1987, Annals of the rheumatic diseases.
[310] D. Hanahan,et al. Non-tolerance and autoantibodies to a transgenic self antigen expressed in pancreatic β cells , 1987, Nature.
[311] A. Steere,et al. A distinct endothelial cell recognition system that controls lymphocyte traffic into inflamed synovium. , 1986, Science.
[312] M. Ziff,et al. Electron microscopic study of rheumatoid synovial vasculature. Intimate relationship between tall endothelium and lymphoid aggregation. , 1986, The Journal of clinical investigation.
[313] A. Freemont,et al. Changes in vascular endothelium related to lymphocyte collections in diseased synovia. , 1983, Arthritis and rheumatism.
[314] A. Freemont. A possible route for lymphocyte migration into diseased tissues , 1983, Journal of clinical pathology.
[315] A. Freemont. The small blood vessels in areas of lymphocytic infiltration around malignant neoplasms. , 1982, British Journal of Cancer.
[316] A. Anderson,et al. Lymphocyte emigration from high endothelial venules in rat lymph nodes. , 1976, Immunology.
[317] A. Anderson,et al. Studies on the structure and permeability of the microvasculature in normal rat lymph nodes. , 1975, The American journal of pathology.
[318] B. Deurs,et al. The postnatal development of high‐endothelial venules in lymph nodes of mice , 1975 .
[319] E. Reith,et al. The ultrastructure of mouse lymph node venules and the passage of lymphocytes across their walls. , 1974, Journal of ultrastructure research.
[320] Schoefl Gi. The migration of lymphocytes across the vascular endothelium in lymphoid tissue. A reexamination. , 1972 .
[321] E. J. Knight,et al. The route of re-circulation of lymphocytes in the rat , 1964, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[322] V. Marchesi,et al. The migration of lymphocytes through the endothelium of venules in lymph nodes: an electron microscope study , 1964, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[323] S. Schumacher. Ueber Phagocytose und die Abfuhrwege der Leucocyten in den Lymphdrüsen , 1899 .
[324] Holger Moch,et al. Germinal Centers Determine the Prognostic Relevance of Tertiary Lymphoid Structures and Are Impaired by Corticosteroids in Lung Squamous Cell Carcinoma. , 2018, Cancer research.
[325] S. Hemmerich,et al. Functional contributions of N- and O-glycans to L-selectin ligands in murine and human lymphoid organs. , 2011, The American journal of pathology.
[326] J. Becker,et al. Immunological tumor destruction in a murine melanoma model by targeted LTα independent of secondary lymphoid tissue , 2007, Cancer Immunology, Immunotherapy.
[327] Kee Chan,et al. Lymphotoxin plays a crucial role in the development and function of nasal-associated lymphoid tissue through regulation of chemokines and peripheral node addressin. , 2005, The American journal of pathology.
[328] S. Perrin,et al. Lymphotoxin-beta receptor signaling is required for the homeostatic control of HEV differentiation and function. , 2005, Immunity.
[329] M. Karin,et al. I kappa B kinase complex alpha kinase activity controls chemokine and high endothelial venule gene expression in lymph nodes and nasal-associated lymphoid tissue. , 2004, Journal of Immunology.
[330] R. Dixon,et al. Selectin blockade prevents antigen-induced late bronchial responses and airway hyperresponsiveness in allergic sheep. , 1999, American journal of respiratory and critical care medicine.
[331] N. Ruddle. Lymphoid neo-organogenesis: lymphotoxin's role in inflammation and development. , 1999, Immunologic research.
[332] W. Lesslauer,et al. Differential activities of secreted lymphotoxin-alpha3 and membrane lymphotoxin-alpha1beta2 in lymphotoxin-induced inflammation: critical role of TNF receptor 1 signaling. , 1998, Journal of immunology.
[333] D. Hanahan,et al. Modulation of L-selectin ligand expression during an immune response accompanying tumorigenesis in transgenic mice. , 1996, The Journal of clinical investigation.
[334] U. V. von Andrian. Intravital microscopy of the peripheral lymph node microcirculation in mice. , 1996, Microcirculation.
[335] T. Springer,et al. Cloning from purified high endothelial venule cells of hevin, a close relative of the antiadhesive extracellular matrix protein SPARC. , 1995, Immunity.
[336] E. Butcher,et al. L-selectin and alpha 4 beta 7 integrin homing receptor pathways mediate peripheral lymphocyte traffic to AKR mouse hyperplastic thymus. , 1995, The American journal of pathology.
[337] L. Lasky,et al. Global vascular expression of murine CD34, a sialomucin-like endothelial ligand for L-selectin. , 1994, Blood.
[338] G. Kraal,et al. Rapid decrease in lymphocyte adherence to high endothelial venules in lymph nodes deprived of afferent lymphatic vessels , 1987, European journal of immunology.
[339] I. L. Eestermans,et al. Disappearance and reappearance of high endothelial venules and immigrating lymphocytes in lymph nodes deprived of afferent lymphatic vessels: a possible regulatory role of macrophages in lymphocyte migration , 1983, European journal of immunology.