Lymphatic function and immune regulation in health and disease

Myeloid-derived-suppressor cells as regulators of the immune system

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Molecular regulation of vessel maturation

Jain, R. K. (2003) · Nature Medicine · doi:10.1038/nm0603-685 · Cited by 2,515 · see citing works

A Randomized Comparison of Sentinel-Node Biopsy with Routine Axillary Dissection in Breast Cancer

Veronesi, U., Paganelli, G., Viale, G., Luini, A., Zurrida, S., Galimberti, V. E., Intra, M., Veronesi, P., Robertson, C., Maisonneuve, P., et al. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa012782 · Cited by 2,204 · see citing works

Sentinel-Node Biopsy or Nodal Observation in Melanoma

Morton, D. L., Thompson, J. F., Cochran, A. J., Mozzillo, N., Elashoff, R. M., Essner, R., Nieweg, O. E., Roses, D. F., Hoekstra, H. J., Karakousis, C. P., et al. (2006) · New England Journal of Medicine · doi:10.1056/nejmoa060992 · Cited by 1,817 · see citing works

T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases

Mempel, T. R., Henrickson, S. E., & von Andrian, U. H. (2004) · Nature · doi:10.1038/nature02238 · Cited by 1,720 · see citing works

The role of myeloid cells in the promotion of tumour angiogenesis

Murdoch, C., Muthana, M., Coffelt, S. B., & Lewis, C. E. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2444 · Cited by 1,642 · see citing works

Lymphangiogenesis: Molecular Mechanisms and Future Promise

Tammela, T., & Alitalo, K. K. (2010) · Cell · doi:10.1016/j.cell.2010.01.045 · Cited by 1,443 · see citing works

Consequences of Cell Death

Sauter, B., Albert, M. L., Francisco, L. M., Larsson, M., Somersan, S., & Bhardwaj, N. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.3.423 · Cited by 1,357 · see citing works

Lymphangiogenesis in development and human disease

Alitalo, K. K., Tammela, T., & Petrova, T. V. (2005) · Nature · doi:10.1038/nature04480 · Cited by 1,287 · see citing works

Homing and cellular traffic in lymph nodes

von Andrian, U. H., & Mempel, T. R. (2003) · Nature reviews. Immunology · doi:10.1038/nri1222 · Cited by 1,271 · see citing works

The role of nitric oxide in tumour progression

Fukumura, D., Kashiwagi, S., & Jain, R. K. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1910 · Cited by 1,260 · see citing works

Immature Dendritic Cells Phagocytose Apoptotic Cells via αvβ5 and CD36, and Cross-present Antigens to Cytotoxic T Lymphocytes

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Dendritic-cell trafficking to lymph nodes through lymphatic vessels

Randolph, G. J., Angeli, V., & Swartz, M. A. (2005) · Nature Reviews Immunology · doi:10.1038/nri1670 · Cited by 1,111 · see citing works

The Neutrophil-Activating Protein (NAP-1) Is Also Chemotactic for T Lymphocytes

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Functionally specialized junctions between endothelial cells of lymphatic vessels

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Lymphatic Metastasis in the Absence of Functional Intratumor Lymphatics

Padera, T. P., Kadambi, A., di Tomaso, E., Carreira, C. M., Brown, E. B., Boucher, Y., Choi, N. C., Mathisen, D. J., Wain, J. R., Mark, E. J., et al. (2002) · Science · doi:10.1126/science.1071420 · Cited by 964 · see citing works

A Discrete Subpopulation of Dendritic Cells Transports Apoptotic Intestinal Epithelial Cells to T Cell Areas of Mesenteric Lymph Nodes

Huang, F., Platt, N., Wykes, M., Major, J. R., Powell, T. J., Jenkins, C. D., & MacPherson, G. G. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.3.435 · Cited by 902 · see citing works

Cancer cells compress intratumour vessels

Padera, T. P., Stoll, B. R., Tooredman, J. B., Capen, D., Tomaso, E. D., & Jain, R. K. (2004) · Nature · doi:10.1038/427695a · Cited by 857 · see citing works

Chemokines, sphingosine-1-phosphate, and cell migration in secondary lymphoid organs

Cyster, J. G. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115628 · Cited by 856 · see citing works

Lymphoid organ development: from ontogeny to neogenesis

Drayton, D. L., Liao, S., Mounzer, R. H., & Ruddle, N. H. (2006) · Nature Immunology · doi:10.1038/ni1330 · Cited by 777 · see citing works

Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages

Maruyama, K., Ii, M., Cursiefen, C., Jackson, D. G., Keino, H., Tomita, M., van Rooijen, N., Takenaka, H., D'Amore, P. A., Stein‐Streilein, J., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23874 · Cited by 712 · see citing works

Microlymphatics and lymph flow

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Effect of Vascular Normalization by Antiangiogenic Therapy on Interstitial Hypertension, Peritumor Edema, and Lymphatic Metastasis: Insights from a Mathematical Model

Jain, R. K., Tong, R. T., & Munn, L. L. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4102 · Cited by 612 · see citing works

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

Gretz, J. E., Norbury, C. C., Anderson, A. O., Proudfoot, A. E. I., & Shaw, S. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.10.1425 · Cited by 587 · see citing works

Interstitial dendritic cell guidance by haptotactic chemokine gradients

Weber, M., Hauschild, R., Schwarz, J., Moussion, C., de Vries, I., Legler, D. F., Luther, S. A., Bollenbach, T., & Sixt, M. (2013) · Science · doi:10.1126/science.1228456 · Cited by 555 · see citing works

Lymphatic and interstitial flow in the tumour microenvironment: linking mechanobiology with immunity

Swartz, M. A., & Lund, A. W. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3186 · Cited by 544 · see citing works

CD169-Positive Macrophages Dominate Antitumor Immunity by Crosspresenting Dead Cell-Associated Antigens

Asano, K., Nabeyama, A., Miyake, Y., Qiu, C., Kurita, A., Tomura, M., Kanagawa, O., Fujii, S., & Tanaka, M. (2010) · Immunity · doi:10.1016/j.immuni.2010.12.011 · Cited by 454 · see citing works

Conduits Mediate Transport of Low-Molecular-Weight Antigen to Lymph Node Follicles

Roozendaal, R., Mempel, T. R., Pitcher, L. A., González, S., Verschoor, A., Mebius, R. E., von Andrian, U. H., & Carroll, M. C. (2009) · Immunity · doi:10.1016/j.immuni.2008.12.014 · Cited by 446 · see citing works

Impact of negative selection on the T cell repertoire reactive to a self-peptide: a large fraction of T cell clones escapes clonal deletion.

Bouneaud, C., Kourilsky, P., & Bousso, P. (2000) · Immunity · doi:10.1016/s1074-7613(00)00080-7 · Cited by 431 · see citing works

Dendritic Cell Function in Vivo during the Steady State: A Role in Peripheral Tolerance

Steinman, R. M., Hawiger, D., Liu, K., Bonifaz, L. C., Bonnyay, D., Mahnke, K., Iyoda, T., Ravetch, J. V., Dhodapkar, M. V., Inaba, K., et al. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb06029.x · Cited by 427 · see citing works

B Cell-Driven Lymphangiogenesis in Inflamed Lymph Nodes Enhances Dendritic Cell Mobilization

Angeli, V., Ginhoux, F., Llodrá, J., Quéméneur, L., Frenette, P. S., Skobe, M., Jessberger, R., Mérad, M., & Randolph, G. J. (2006) · Immunity · doi:10.1016/j.immuni.2006.01.003 · Cited by 425 · see citing works

Immune complex relay by subcapsular sinus macrophages and noncognate B cells drives antibody affinity maturation

Phan, T. G., Green, J. A., Gray, E. E., Xu, Y., & Cyster, J. G. (2009) · Nature Immunology · doi:10.1038/ni.1745 · Cited by 423 · see citing works

Cords, channels, corridors and conduits: critical architectural elements facilitating cell interactions in the lymph node cortex

Gretz, J. E., Anderson, A. O., & Shaw, S. (1997) · Immunological Reviews · doi:10.1111/j.1600-065x.1997.tb00955.x · Cited by 409 · see citing works

Critical role of CD11b+ macrophages and VEGF in inflammatory lymphangiogenesis, antigen clearance, and inflammation resolution

Kataru, R. P., Jung, K., Jang, C., Yang, H., Schwendener, R. A., Baik, J. E., Han, S. H., Alitalo, K. K., & Koh, G. Y. (2009) · Blood · doi:10.1182/blood-2008-09-176776 · Cited by 403 · see citing works

Peripheral antigen display by lymph node stroma promotes T cell tolerance to intestinal self

Lee, J.-W., Epardaud, M., Sun, J., Becker, J. E., Cheng, A. C., Yonekura, A., Heath, J., & Turley, S. (2007) · Nature Immunology · doi:10.1038/ni1427 · Cited by 391 · see citing works

Constitutive Presentation of a Natural Tissue Autoantigen Exclusively by Dendritic Cells in the Draining Lymph Node

Scheinecker, C., McHugh, R. S., Shevach, E. M., & Germain, R. N. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020991 · Cited by 382 · see citing works

Imaging Steps of Lymphatic Metastasis Reveals That Vascular Endothelial Growth Factor-C Increases Metastasis by Increasing Delivery of Cancer Cells to Lymph Nodes: Therapeutic Implications

Hoshida, T., Isaka, N., Hagendoorn, J., di Tomaso, E., Chen, Y.-L., Pytowski, B., Fukumura, D., Padera, T. P., & Jain, R. K. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-1392 · Cited by 361 · see citing works

Lymphatic endothelial progenitor cells contribute to de novo lymphangiogenesis in human renal transplants

Kerjaschki, D., Huttary, N., Raab, I., Regele, H. M., Bojarski-Nagy, K., Bond, G., Kröber, S. M., Greinix, H. T., Rosenmaier, A., Karlhofer, F. M., et al. (2006) · Nature Medicine · doi:10.1038/nm1340 · Cited by 358 · see citing works

Most lymphoid organ dendritic cell types are phenotypically and functionally immature

Wilson, N. S., El-Sukkari, D., Belz, G. T., Smith, C. M., Steptoe, R. J., Heath, W. R., Shortman, K., & Villadangos, J. A. (2003) · Blood · doi:10.1182/blood-2003-02-0513 · Cited by 357 · see citing works

Lymph node–resident lymphatic endothelial cells mediate peripheral tolerance via Aire-independent direct antigen presentation

Cohen, J. N., Guidi, C. J., Tewalt, E. F., Qiao, H., Rouhani, S. J., Ruddell, A., Farr, A. G., Tung, K. S. K., & Engelhard, V. H. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20092465 · Cited by 347 · see citing works

Lymph node fibroblastic reticular cells directly present peripheral tissue antigen under steady-state and inflammatory conditions

Fletcher, A. L., Lukacs‐Kornek, V., Reynoso, E. D., Pinner, S. E., Bellemare‐Pelletier, A., Curry, M. S., Collier, A.-R. Y., Boyd, R. L., & Turley, S. J. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20092642 · Cited by 341 · see citing works

Afferent lymph-derived T cells and DCs use different chemokine receptor CCR7-dependent routes for entry into the lymph node and intranodal migration

Braun, A., Worbs, T., Moschovakis, G. L., Halle, S., Hoffmann, K., Bölter, J., Münk, A., & Förster, R. (2011) · Nature Immunology · doi:10.1038/ni.2085 · Cited by 337 · see citing works

Subcapsular sinus macrophages prevent CNS invasion on peripheral infection with a neurotropic virus

Iannacone, M., Moseman, E. A., Tonti, E., Bosurgi, L., Junt, T., Henrickson, S. E., Whelan, S. P. J., Guidotti, L. G., & von Andrian, U. H. (2010) · Nature · doi:10.1038/nature09118 · Cited by 329 · see citing works

Immobilized Chemokine Fields and Soluble Chemokine Gradients Cooperatively Shape Migration Patterns of Dendritic Cells

Schumann, K., Lämmermann, T., Bruckner, M., Legler, D. F., Polleux, J., Spatz, J. P., Schuler, G., Förster, R., Lutz, M. B., Sorokin, L. M., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.04.017 · Cited by 324 · see citing works

Cyclical modulation of sphingosine-1-phosphate receptor 1 surface expression during lymphocyte recirculation and relationship to lymphoid organ transit

Lo, C. G., Xu, Y., Proia, R. L., & Cyster, J. G. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041509 · Cited by 319 · see citing works

The α(1,3)fucosyltransferases FucT-IV and FucT-VII Exert Collaborative Control over Selectin-Dependent Leukocyte Recruitment and Lymphocyte Homing

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Preparing the “Soil”: The Primary Tumor Induces Vasculature Reorganization in the Sentinel Lymph Node before the Arrival of Metastatic Cancer Cells

Qian, C.-N., Berghuis, B. D., Tsarfaty, G., Bruch, M., Kort, E. J., Ditlev, J., Tsarfaty, I., Hudson, E., Jackson, D. G., Petillo, D., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-2977 · Cited by 313 · see citing works

Dendritic cells control lymphocyte entry to lymph nodes through high endothelial venules

Moussion, C., & Girard, J. (2011) · Nature · doi:10.1038/nature10540 · Cited by 312 · see citing works

Preformed portals facilitate dendritic cell entry into afferent lymphatic vessels

Pflicke, H., & Sixt, M. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091739 · Cited by 301 · see citing works

Impaired lymphatic contraction associated with immunosuppression

Liao, S., Cheng, G., Conner, D. A., Huang, Y., Kucherlapati, R. S., Munn, L. L., Ruddle, N. H., Jain, R. K., Fukumura, D., & Padera, T. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116152108 · Cited by 296 · see citing works

Cutting Edge: Lymphatic Vessels, Not Blood Vessels, Primarily Mediate Immune Rejections After Transplantation

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Sulfation-dependent recognition of high endothelial venules (HEV)-ligands by L-selectin and MECA 79, and adhesion-blocking monoclonal antibody.

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DC mobilization from the skin requires docking to immobilized CCL21 on lymphatic endothelium and intralymphatic crawling

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Regulation of Homeostatic Chemokine Expression and Cell Trafficking During Immune Responses

Mueller, S. N., Hosiawa-Meagher, K. A., Konieczny, B. T., Sullivan, B. M., Bachmann, M. F., Locksley, R. M., Ahmed, R., & Matloubian, M. (2007) · Science · doi:10.1126/science.1144830 · Cited by 259 · see citing works

Transmural Flow Modulates Cell and Fluid Transport Functions of Lymphatic Endothelium

Miteva, D., Rutkowski, J. M., Dixon, J. B., Kilarski, W. W., Shields, J. D., & Swartz, M. A. (2010) · Circulation Research · doi:10.1161/circresaha.109.207274 · Cited by 254 · see citing works

Lymphangiogenesis and lymphangiodysplasia: From molecular to clinical lymphology

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THE LYMPHATIC VASCULATURE: Recent Progress and Paradigms

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T Lymphocytes Negatively Regulate Lymph Node Lymphatic Vessel Formation

Kataru, R. P., Kim, H., Jang, C., Choi, D. K., Koh, B. I., Kim, M., Gollamudi, S., Kim, Y.-K., Lee, S., & Koh, G. Y. (2011) · Immunity · doi:10.1016/j.immuni.2010.12.016 · Cited by 225 · see citing works

A Novel, High Endothelial Venule–Specific Sulfotransferase Expresses 6-Sulfo Sialyl Lewisx, an L-Selectin Ligand Displayed by CD34

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Lymphedema: Anatomy, Physiology and Pathogenesis

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The Strategy of T Cell Antigen-presenting Cell Encounter in Antigen-draining Lymph Nodes Revealed by Imaging of Initial T Cell Activation

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Dendritic cells constitutively present self antigens in their immature state in vivo and regulate antigen presentation by controlling the rates of MHC class II synthesis and endocytosis

Wilson, N. S., El-Sukkari, D., & Villadangos, J. A. (2003) · Blood · doi:10.1182/blood-2003-08-2729 · Cited by 212 · see citing works

Sophisticated strategies for information encounter in the lymph node: the reticular network as a conduit of soluble information and a highway for cell traffic

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Migratory and Lymphoid-Resident Dendritic Cells Cooperate to Efficiently Prime Naive CD4 T cells

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Perivascular nitric oxide gradients normalize tumor vasculature

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Lymphocyte emigration from high endothelial venules in rat lymph nodes.

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Contraction-initiated NO-dependent lymphatic relaxation: a self-regulatory mechanism in rat thoracic duct

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Synchrony of High Endothelial Venules and Lymphatic Vessels Revealed by Immunization

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Skin antigens in the steady state are trafficked to regional lymph nodes by transforming growth factor-β1-dependent cells

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VEGF-A produced by chronically inflamed tissue induces lymphangiogenesis in draining lymph nodes

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Lymphangiogenesis and cancer metastasis

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Sulfation of L-Selectin Ligands by an HEV-Restricted Sulfotransferase Regulates Lymphocyte Homing to Lymph Nodes

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Studies on the structure and permeability of the microvasculature in normal rat lymph nodes.

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The influence of afferent lymphatic vessel interruption on vascular addressin expression.

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Travellers in many guises: The origins and destinations of dendritic cells

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Quantification of lymph node transit times reveals differences in antigen surveillance strategies of naïve CD4 + and CD8 + T cells

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Immunopathogenesis of lymphatic filarial disease

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Endothelial Nitric Oxide Synthase Mediates Lymphangiogenesis and Lymphatic Metastasis

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Differential roles of migratory and resident DCs in T cell priming after mucosal or skin HSV-1 infection

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Deletional Self-Tolerance to a Melanocyte/Melanoma Antigen Derived from Tyrosinase Is Mediated by a Radio-Resistant Cell in Peripheral and Mesenteric Lymph Nodes

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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

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Breast Cancer-Related Lymphedema

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Vascular endothelial growth factor-C stimulates the lymphatic pump by a VEGF receptor-3-dependent mechanism

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Role of CD11b+ Macrophages in Intraperitoneal Lipopolysaccharide-Induced Aberrant Lymphangiogenesis and Lymphatic Function in the Diaphragm

Kim, K.-E., Koh, Y.-J., Jeon, B.-H., Jang, C., Han, J., Kataru, R. P., Schwendener, R. A., Kim, J., & Koh, G. Y. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.090133 · Cited by 130 · see citing works

Profound but Dysfunctional Lymphangiogenesis via Vascular Endothelial Growth Factor Ligands from CD11b+ Macrophages in Advanced Ovarian Cancer

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Aparnaa, R., Immanuel, C., Rao, D. N., & Kaliraj, P. (2015) · Lymphatic Research and Biology · doi:10.1089/lrb.2014.0034 · Cited by 7 · see citing works

The amazing brain drain

Blanchette, M., & Daneman, R. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20172031 · Cited by 7 · see citing works

Laboratory diagnosis of a new outbreak of acute African swine fever in smallholder pig farms in Jos, Nigeria

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Focus on the Lymphatic Route to Optimize Drug Delivery in Cardiovascular Medicine

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On-chip engineered human lymphatic microvasculature for physio-/pathological transport phenomena studiesPreprint

Serrano, J. C., Gillrie, M. R., Li, R., Ishamuddin, S. H., & Kamm, R. D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.06.483122 · Cited by 7 · see citing works

In vivo spatiotemporal characterizing diverse body transportation of optical labeled high immunity aluminium adjuvants with photoacoustic tomography

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Microphysiological Systems of Lymphatics and Immune Organs

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Recent advances in interstitial fluid dynamics for diagnostic, targeted drug delivery and precision medicine applications

Somandi, K., Kulati, H., Holman, D. E., Abrahams, A.-I., Ngoepe, M. P., Keyster, M., & Choonara, Y. E. (2026) · Drug Delivery and Translational Research · doi:10.1007/s13346-026-02106-9 · Cited by 6 · see citing works

Sleep Medicine - Asleep or Awake?

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Pharmacological Properties of Platycarpha glomerata Extracts—A Plant Used to Treat and Manage Elephantiasis

Lamula, S. Q. N., Taliwe, A., & Buwa-Komoreng, L. V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020646 · Cited by 5 · see citing works

Sodium-Directed Crosstalk Between Immune Cells and Lymphatic Vessels

Ahmad, T., Crescenzi, R. L., Kon, V., Kirabo, A., & Shelton, E. L. (2025) · Current Hypertension Reports · doi:10.1007/s11906-024-01322-3 · Cited by 5 · see citing works

Defective lymphatic vasculature in obesity

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Murine gut microbiota dysbiosis via enteric infection modulates the foreign body response to a distal biomaterial implant

Yang, B., Rutkowski, N., Ruta, A., Gray-Gaillard, E. F., Maestas, D. R., Kelly, S. H., Krishnan, K., Wu, X., Wu, S., Chen, A. R., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2422169122 · Cited by 4 · see citing works

Bilateral hyperplasia of choroid plexus with severe CSF production: a case report and review of the glymphatic system

Páez-Nova, M., Andaur, K., Campos, G., García-Ballestas, E., Moscote‐Salazar, L. R., Osvaldo Koller, C., & Valenzuela, S. (2021) · Child s Nervous System · doi:10.1007/s00381-021-05325-2 · Cited by 6 · see citing works

Vascular regulation of disseminated tumor cells during metastatic spread

Sturgess, V. E., Azubuike, U. F., & Tanner, K. (2023) · Biophysics Reviews · doi:10.1063/5.0106675 · Cited by 8 · see citing works

Opportunities for Studying the Hydrodynamic Context for Breast Cancer Cell Spread Through Lymph Flow

Morley, S. T., Walsh, M. T., & Newport, D. T. (2017) · Lymphatic Research and Biology · doi:10.1089/lrb.2017.0005 · Cited by 5 · see citing works

Mechanistic understanding of crosstalk between blood vessels and immunity and inflammation in diseases

Cao, Y. (2026) · Immunity & Inflammation · doi:10.1007/s44466-025-00021-1 · Cited by 4 · see citing works

Proteomic profiling of lymphedema development in mouse model

Lee, J., Song, H., Roh, K., Cho, S., Lee, S., Yeom, C., & Park, S. (2016) · Cell Biochemistry and Function · doi:10.1002/cbf.3192 · Cited by 4 · see citing works

Computational Fluid Dynamic Model Prediction of Enhanced Glymphatic Clearance in Response to Focused Ultrasound‐Mediated Blood‐Brain Barrier Opening

Gladwell, R. A., Fisher, D. G., Wythe, J. D., Highley, C. B., Lukens, J. R., & Price, R. J. (2025) · Advanced Science · doi:10.1002/advs.202510684 · Cited by 3 · see citing works

Decellularized lymph node sections with preserved extracellular matrix for stromal cell culture

Esparza, E., Teles, L. N., Fedotova, A., deHaseth, N. H., Sayegh, M. H., Hernandez, A. V., Ho, L., Ziebarth, N., & Tomei, A. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-28782-0 · Cited by 3 · see citing works

Dendritic cell activation by iron oxide nanoparticles depends on the extracellular environment

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Extended human lymph node explants for evaluation of adaptive immunity

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Lymphangiogenesis after nonvascularized lymph node transplantation: Lymphangiographic findings in mice and minipigs

Kim, K. M., & Kim, K. Y. (2023) · PLoS ONE · doi:10.1371/journal.pone.0295836 · Cited by 3 · see citing works

Metabolomics and the Gut–Brain Axis

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Structure and Function of the Immune System

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Innate Immunity and Parkinson's DiseasePreprint

Oludipe, D. B., Du, X., Akter, S., Zhang, C., Mosley, R. L., Gendelman, H. E., & Sil, S. (2025) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041640 · Cited by 3 · see citing works

Lymphocytes and immunoglobulins in peripheral blood and lymphatic fluid of neonates with chylothorax

Rose, D. U. D., Landolfo, F., Pugnaloni, F., Gassabi, F. Z., Martini, L., Santisi, A., Columbo, C., Giliberti, P., Gazzotti, F., Porzio, O., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1666366 · Cited by 2 · see citing works

Proteomic Analysis of Small Extracellular Vesicles From Lymphatic Affluents in Developing Premetastatic Niche in Melanoma

Suman, S., Geng, L., Nevala, W. K., Moore, R. M., Atherton, C. L., Zhao, X., Sung, J., Guo, R., Jakub, J. W., Kandasamy, R. K., et al. (2025) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2025.101472 · Cited by 2 · see citing works

Effects of prenatal cannabis exposure on offspring mental health: A focus on the role of the immune system

Vecchiarelli, H. A., Baglot, S. L., Black, T., Choi, E. Y., Cupo, L., Sandberg, C., Siron, L., Chakravarty, M. M., Hill, M. N., Howland, J. G., et al. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106488 · Cited by 3 · see citing works

Unveiling the Uncommon: A Rare Case of Group A Streptococcus Axillary Lymphadenitis With Ambiguous Presentation Leading to Multiple Misdiagnoses

Badaro, G., Passeggiata, M., Casio, N., Thomas, D. M., & Shattahi, E. (2024) · Cureus · doi:10.7759/cureus.60806 · Cited by 2 · see citing works

Lymphatic complication in open venous harvesting versus endoscopic venous harvesting: a systematic review and meta-analysis

Razavi, A., Mahalleh, M., Vanaki, A., Fallah, A., Bahanesteh, A., Ahmadi, A., Yarmohammadi, H., Kooshkqazi, M. S., & Soltanipur, M. (2025) · General Thoracic and Cardiovascular Surgery · doi:10.1007/s11748-025-02126-1 · Cited by 2 · see citing works

Extracellular RNA Profile in Mesenteric Lymph from Exemplar Rat Models of Acute and Critical Illness

Hong, J., Blenkiron, C., Tsai, P., Premkumar, R., Nachkebia, S., Tun, S. M., Petzer, A., Windsor, J. A., Hickey, A. J., & Phillips, A. R. J. (2019) · Lymphatic Research and Biology · doi:10.1089/lrb.2018.0044 · Cited by 2 · see citing works

The development and physiological and pathophysiological functions of resident macrophages and glial cells

Blank-Stein, N., Mayer, M., & Mass, E. (2021) · Advances in immunology · doi:10.1016/bs.ai.2021.08.001 · Cited by 2 · see citing works

ELM: A New, Simple, and Economic Assay to Measure Motility of Lymphatic Endothelial Cells

Torri, F., Dell’Era, P., & Garrafa, E. (2017) · Lymphatic Research and Biology · doi:10.1089/lrb.2016.0032 · Cited by 1 · see citing works

An Update on the Role of Lymphatic Function in Skin Inflammatory Disorders: A Scoping Review

Ter-Ovanesyan, I., Tashjian, M., Escruceria, S., Fernandez, R., Estadella, B., & MAYROVITZ, H. N. (2025) · Cureus · doi:10.7759/cureus.77981 · Cited by 1 · see citing works

Isolation and Characterization of Equine Lymph Node Endothelial Cells

Lugo, T., Myers, S., & Nguyen, T. A. (2025) · Veterinary Sciences · doi:10.3390/vetsci12090905 · Cited by 1 · see citing works

AP ‐1 Is an Initial Convergent Transcriptional Response in Lymphatic Endothelium to VEGF ‐C or TNFα

Kreft, E. A., Juśkiewicz, Z. J., & Isakson, B. E. (2025) · Microcirculation · doi:10.1111/micc.70035 · Cited by 1 · see citing works

Cellular landscape of reactive and neoplastic human lymph nodes in 3D

Diederich, V. J., Scharf, S., Schäfer, H., Hartmann, S., Hansmann, M., & Wurzel, P. (2025) · Acta Histochemica · doi:10.1016/j.acthis.2025.152308 · Cited by 1 · see citing works

Lymphatic dysfunction and ZFP36 deficiency contribute to myxomatous valve degeneration in Marfan syndrome mice

Tan, C., Ren, Z., Kurup, S., Xianpeng, L., Ge, Z., Suzuki, S., Jakka, P., Tang, C., Iruela‐Arispe, M. L., & Kume, T. (2026) · Journal of Clinical Investigation · doi:10.1172/jci195507 · Cited by 1 · see citing works

Continuous blood pressure recordings simultaneously with functional brain imaging: studies of the glymphatic system

Zienkiewicz, A., Huotari, N., Raitamaa, L., Raatikainen, V., Ferdinando, H., Vihriälä, E., Korhonen, V. O., Myllylä, T., & Kiviniemi, V. J. (2017) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2252032 · Cited by 1 · see citing works

Effect of the Nucleotide and Turmeric Extract Supplementation and different Cage Floors on the Blood Profile and Physiological Status of Broiler Chicken

Tugiyanti, E., Ismoyowati, I., Rosidi, Saleh, D. M., Heriyanto, S., & Wigati, T. L. (2023) · Journal of Experimental Biology and Agricultural Sciences · doi:10.18006/2023.11(4).696.706 · Cited by 1 · see citing works

NeuroHIV and the glymphatic system

Tice, C. M., & Langford, D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99744-7.00023-7 · Cited by 1 · see citing works

The lymphatic vasculature in disease

Alitalo, K. K. (2011) · Nature Medicine · doi:10.1038/nm.2545 · Cited by 964 · see citing works

Lymphatic vessels in health and disease

Padera, T. P. (2020) · Proceedings for Annual Meeting of The Japanese Pharmacological Society · doi:10.1254/jpssuppl.93.0_1-s05-1

Exploring the Role of the Lymphatic System in Immune Regulation: Implications for Autoimmunity, Cancer, and Infection

Norouzian, M., & Abdi, S. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1002802 · Cited by 1 · see citing works

The Functional Unit of the Lymphatic System: Towards Understanding the Importance of a Well-Rehearsed Interaction of Lymphatic Capillaries, Collecting Vessels, and Lymph Nodes

Roth, K., & Pabst, R. (2025) · Journal of Vascular Research · doi:10.1159/000545084 · Cited by 2 · see citing works

Immune Function оf the Lymphatic System

Lobov, G. I. (2023) · Успехи физиологических наук · doi:10.31857/s0301179823030049 · Cited by 4 · see citing works