High endothelial venules (HEVs) in immunity, inflammation and cancer

[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.