Shaping of Peripheral T Cell Responses by Lymphatic Endothelial Cells
Open accessAbstract
Lymph node stromal cells (LNSCs) have newly been promoted to the rank of new modulators of T cell responses. The different non-hematopoietic cell subsets in LN were considered for years as a simple scaffold, forming routes and proper environment for antigen-lymphocyte encountering. Though, deeper characterization of those cells has recently clearly shown their impact on both DC and T cell functions. In particular, lymphatic endothelial cells (LECs) control lymphocyte trafficking and homeostasis in lymph nodes (LNs), and limit adaptive immune responses. Therefore, the new role of LECs in shaping immune responses has drawn the attention of immunologists. Striking is the discovery that LECs, among other LNSCs, ectopically express a large range of peripheral tissue antigens (PTAs), and further present PTA-derived peptides through MHC class I (MHC-I) molecules to induce self-reactive CD8+ T cell deletional tolerance. In addition, both steady-state and tumor-associated LECs were described to be capable of exogenous antigen cross-presentation. Whether LECs can similarly impact CD4+ T cell responses through MHC class II (MHC-II) restricted Ag presentation is still a matter of debate. Here we review and discuss our current knowledge on the contribution of Ag-presenting LECs as regulators of peripheral T cell responses in different immunological contexts, including autoimmunity and cancer.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Structural cells (epithelium, endothelium, and fibroblasts) have been shown to contribute in important ways to mammalian immunity.
“These three cell types, which we refer to as “structural cells”, have been shown to contribute in important ways to mammalian immunity7–11.”
From Structural cells are key regulators of organ-specific immune responses (2020) · cites this paper as [7]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Type, Density, and Location of Immune Cells Within Human Colorectal Tumors Predict Clinical Outcome
Galon, J., Costes, A., Sanchez-Cabo, F., Kirilovsky, A., Mlecnik, B., Lagorce-Pagès, C., Tosolini, M., Camus, M., Berger, A., Wind, P., et al. (2006) · Science · doi:10.1126/science.1129139 · Cited by 6,516 · see citing works
The immune contexture in human tumours: impact on clinical outcome
Fridman, W. H., Pagès, F., Sautès-Fridman, C., & Galon, J. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3245 · Cited by 4,981 · see citing works
Structural and functional features of central nervous system lymphatic vessels
Louveau, A., Smirnov, I., Keyes, T. J., Eccles, J. D., Rouhani, S. J., Peske, J. D., Derecki, N. C., Castle, D., Mandell, J. W., Lee, K. S., et al. (2015) · Nature · doi:10.1038/nature14432 · Cited by 4,413 · see citing works
Steinman, R. M., Hawiger, D., & Nussenzweig, M. C. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141040 · Cited by 3,124 · see citing works
Projection of an Immunological Self Shadow Within the Thymus by the Aire Protein
Anderson, M. S., Venanzi, E. S., Klein, L., Chen, Z., Berzins, S. P., Turley, S. J., von Boehmer, H., Bronson, R. T., Dierich, A., Benoist, C. O., et al. (2002) · Science · doi:10.1126/science.1075958 · Cited by 2,474 · see citing works
Interleukin-7 mediates the homeostasis of naïve and memory CD8 T cells in vivo
Schluns, K. S., Kieper, W. C., Jameson, S. C., & Lefrançois, L. (2000) · Nature Immunology · doi:10.1038/80868 · Cited by 1,619 · see citing works
Prox1 Function Is Required for the Development of the Murine Lymphatic System
Wigle, J. T., & Oliver, G. C. (1999) · Cell · doi:10.1016/s0092-8674(00)81511-1 · Cited by 1,581 · see citing works
Kaipainen, A., Korhonen, J., Mustonen, T., van Hinsbergh, V. W. M., Fang, G. H., Dumont, D., Breitman, M. L., & Alitalo, K. K. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.8.3566 · Cited by 1,420 · see citing works
Rapid leukocyte migration by integrin-independent flowing and squeezing
Lämmermann, T., Bader, B. L., Monkley, S. J., Worbs, T., Wedlich-Söldner, R., Hirsch, K., Keller, M., Förster, R., Critchley, D. R., Fässler, R., et al. (2008) · Nature · doi:10.1038/nature06887 · Cited by 1,397 · see citing works
Positive and negative selection of the T cell repertoire: what thymocytes see (and don't see)
Klein, L., Kyewski, B., Allen, P. M., & Hogquist, K. A. (2014) · Nature reviews. Immunology · doi:10.1038/nri3667 · Cited by 1,387 · 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
Hyperplasia of Lymphatic Vessels in VEGF-C Transgenic Mice
Jeltsch, M., Kaipainen, A., Joukov, V., Meng, X., Lakso, M., Rauvala, H., Swartz, M. A., Fukumura, D., Jain, R. K., & Alitalo, K. K. (1997) · Science · doi:10.1126/science.276.5317.1423 · Cited by 1,279 · see citing works
The ins and outs of MHC class II-mediated antigen processing and presentation
Roche, P. A., & Furuta, K. (2015) · Nature reviews. Immunology · doi:10.1038/nri3818 · Cited by 1,207 · see citing works
The Induction of Tolerance by Dendritic Cells That Have Captured Apoptotic Cells
Steinman, R. M., Turley, S. J., Mellman, I., & Inaba, K. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.3.411 · Cited by 1,172 · see citing works
Promiscuous gene expression in medullary thymic epithelial cells mirrors the peripheral self
Derbinski, J., Schulte, A., Kyewski, B., & Klein, L. (2001) · Nature Immunology · doi:10.1038/ni723 · Cited by 1,068 · see citing works
Roberts, E. W., Broz, M. L., Binnewies, M., Headley, M. B., Nelson, A. E., Wolf, D. M., Kaisho, T., Bogunovic, D., Bhardwaj, N., & Krummel, M. F. (2016) · Cancer Cell · doi:10.1016/j.ccell.2016.06.003 · Cited by 1,030 · see citing works
Functionally specialized junctions between endothelial cells of lymphatic vessels
Baluk, P., Fuxe, J., Hashizume, H., Romano, T., Lashnits, E., Butz, S., Vestweber, D., Corada, M., Molendini, C., Dejana, E., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062596 · Cited by 1,006 · see citing works
Moon, J. J., Chu, H., Pepper, M., McSorley, S. J., Jameson, S. C., Kedl, R. M., & Jenkins, M. K. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.007 · Cited by 977 · see citing works
An essential role for Prox1 in the induction of the lymphatic endothelial cell phenotype
Wigle, J. T., Harvey, N., Detmar, M., Lagutina, I., Grosveld, G., Gunn, M. D., Jackson, D. G., & Oliver, G. (2002) · The EMBO Journal · doi:10.1093/emboj/21.7.1505 · Cited by 943 · see citing works
Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells
Link, A., Vogt, T. K., Favre, S., Britschgi, M. R., Acha‐Orbea, H., Hinz, B., Cyster, J. G., & Luther, S. A. (2007) · Nature Immunology · doi:10.1038/ni1513 · Cited by 934 · see citing works
Cytokine control of memory T-cell development and survival
Schluns, K. S., & Lefrançois, L. (2003) · Nature reviews. Immunology · doi:10.1038/nri1052 · Cited by 879 · see citing works
Cardiovascular Failure in Mouse Embryos Deficient in VEGF Receptor-3
Dumont, D., Jussila, L., Taipale, J., Lymboussaki, A., Mustonen, T., Pajusola, K., Breitman, M. L., & Alitalo, K. K. (1998) · Science · doi:10.1126/science.282.5390.946 · Cited by 873 · see citing works
Toll-dependent selection of microbial antigens for presentation by dendritic cells
Blander, J. M., & Medzhitov, R. M. (2006) · Nature · doi:10.1038/nature04596 · Cited by 841 · see citing works
Lymphangiogenesis and lymphatic vessel remodelling in cancer
Stacker, S. A., Williams, S. P., Karnezis, T., Shayan, R., Fox, S. B., & Achen, M. G. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3677 · Cited by 812 · see citing works
Limmer, A., Ohl, J., Kurts, C., Ljunggren, H.-G., Reiss, Y., Groettrup, M., Momburg, F., Arnold, B., & Knolle, P. A. (2000) · Nature Medicine · doi:10.1038/82161 · Cited by 758 · cited 1× · see citing works
“First described in 1970 (27), LSECs possess a high ability to filter fluids, solutes, and particles from hepatic circulation, occupy a large surface area exposed to blood that carries external food and commensal bacterial Ag, and are known to cross-present exogenous Ag to T cells (28).”
BackgroundSixt, M., Kanazawa, N., Selg, M., Samson, T., Roos, G., Reinhardt, D. P., Pabst, R., Lutz, M. B., & Sorokin, L. M. (2005) · Immunity · doi:10.1016/j.immuni.2004.11.013 · Cited by 749 · see citing works
Allan, R. S., Waithman, J. C., Bedoui, S., Jones, C. M., Villadangos, J. A., Zhan, Y., Lew, A. M., Shortman, K., Heath, W. R., & Carbone, F. (2006) · Immunity · doi:10.1016/j.immuni.2006.04.017 · Cited by 748 · see citing works
Kukk, E., Lymboussaki, A., Taira, S., Kaipainen, A., Jeltsch, M., Joukov, V., & Alitalo, K. K. (1996) · Development · doi:10.1242/dev.122.12.3829 · Cited by 689 · see citing works
An electron microscopic study of the fenestrated endothelial lining of rat liver sinusoids
Wisse, E. (1970) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(70)90150-4 · Cited by 655 · see citing works
Petrova, T. V., Mäkinen, T., Mäkelä, T. P., Saarela, J., Virtanen, I., Ferrell, R. E., Finegold, D. N., Kerjaschki, D., Ylä‐Herttuala, S., & Alitalo, K. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf470 · Cited by 632 · see citing works
Regulatory T cells: recommendations to simplify the nomenclature
Abbas, A. K., Benoist, C., Bluestone, J. A., Campbell, D. J., Ghosh, S., Hori, S., Jiang, S., Kuchroo, V. K., Mathis, D., Roncarolo, M. G., et al. (2013) · Nature Immunology · doi:10.1038/ni.2554 · Cited by 623 · see citing works
The enemy within: keeping self-reactive T cells at bay in the periphery
Walker, L. S. K., & Abbas, A. K. (2002) · Nature reviews. Immunology · doi:10.1038/nri701 · Cited by 595 · see citing works
Luther, S. A., Bidgol, A., Hargreaves, D. C., Schmidt, A., Xu, Y., Paniyadi, J., Matloubian, M., & Cyster, J. G. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.1.424 · Cited by 583 · see citing works
T-Cell Tolerance: Central and PeripheralPreprint
Xing, Y., & Hogquist, K. A. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a006957 · Cited by 580 · see citing works
Epidermal Viral Immunity Induced by CD8α + Dendritic Cells But Not by Langerhans Cells
Allan, R. S., Smith, C. M., Belz, G. T., van Lint, A. L., Wakim, L. M., Heath, W. R., & Carbone, F. (2003) · Science · doi:10.1126/science.1087576 · Cited by 567 · see citing works
Sabin, F. R. (1902) · American Journal of Anatomy · doi:10.1002/aja.1000010310 · Cited by 557 · see citing works
Promiscuous gene expression in thymic epithelial cells is regulated at multiple levels
Derbinski, J., Gäbler, J., Brors, B., Tierling, S., Jonnakuty, S., Hergenhahn, M., Peltonen, L., Walter, J., & Kyewski, B. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050471 · Cited by 550 · 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
Induction of Lymphoidlike Stroma and Immune Escape by Tumors That Express the Chemokine CCL21
Shields, J. D., Kourtis, I. C., Tomei, A. A., Roberts, J., & Swartz, M. A. (2010) · Science · doi:10.1126/science.1185837 · Cited by 506 · see citing works
Cardiac lymphatics are heterogeneous in origin and respond to injury
Klotz, L., Norman, S., Vieira, J. M., Masters, M., Rohling, M., Dubé, K. N., Bollini, S., Matsuzaki, F., Carr, C. A., & Riley, P. R. (2015) · Nature · doi:10.1038/nature14483 · Cited by 505 · see citing works
Atypical MHC class II-expressing antigen-presenting cells: can anything replace a dendritic cell?
Kambayashi, T., & Laufer, T. M. (2014) · Nature reviews. Immunology · doi:10.1038/nri3754 · Cited by 498 · see citing works
Deletional Tolerance Mediated by Extrathymic Aire-Expressing Cells
Gardner, J. M., DeVoss, J., Friedman, R. S., Wong, D. J., Tan, Y. X., Zhou, X., Johannes, K., Su, M. A., Chang, H. Y., Krummel, M. F., et al. (2008) · Science · doi:10.1126/science.1159407 · Cited by 492 · see citing works
Central Tolerance to Tissue-specific Antigens Mediated by Direct and Indirect Antigen Presentation
Gallegos, A. M., & Bevan, M. J. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20041457 · Cited by 490 · see citing works
Live imaging of lymphatic development in the zebrafish
Yaniv, K., Isogai, S., Castranova, D., Dye, L., Hitomi, J., & Weinstein, B. M. (2006) · Nature Medicine · doi:10.1038/nm1427 · Cited by 486 · see citing works
Molecular characterization of lymphatic endothelial cells
Podgrabinska, S., Falter‐Braun, P., Velasco, P., Kloos, B., Pepper, M. S., Jackson, D. G., & Skobe, M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242401399 · Cited by 486 · see citing works
Regulation of MHC class II gene expression by the class II transactivator
Reith, W., LeibundGut‐Landmann, S., & Waldburger, J. (2005) · Nature reviews. Immunology · doi:10.1038/nri1708 · Cited by 463 · see citing works
Lymphatic vasculature development
Oliver, G. C. (2004) · Nature reviews. Immunology · doi:10.1038/nri1258 · Cited by 460 · see citing works
Malhotra, D., Fletcher, A. L., Astarita, J. L., Lukacs‐Kornek, V., Tayalia, P., González, S., Elpek, K. G., Chang, S. K., Knoblich, K., Hemler, M. E., et al. (2012) · Nature Immunology · doi:10.1038/ni.2262 · Cited by 454 · see citing works
Endogenous naive CD8+ T cell precursor frequency regulates primary and memory responses to infection
Obar, J. J., Khanna, K. M., & Lefrançois, L. (2008) · Immunity · doi:10.1016/j.immuni.2008.04.010 · Cited by 449 · 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
Pham, T. H. M., Baluk, P., Xu, Y., Grigorova, I., Bankovich, A. J., Pappu, R., Coughlin, S. R., McDonald, D. M., Schwab, S. R., & Cyster, J. G. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20091619 · Cited by 444 · see citing works
Hirakawa, S., Hong, Y., Harvey, N. L., Schacht, V., Matsuda, K. M., Libermann, T. A., & Detmar, M. J. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63851-5 · Cited by 439 · see citing works
Pham, T. H. M., Okada, T., Matloubian, M., Lo, C. G., & Cyster, J. G. (2008) · Immunity · doi:10.1016/j.immuni.2007.11.017 · Cited by 427 · see citing works
Clonal deletion of thymocytes by circulating dendritic cells homing to the thymus
Bonasio, R., Scimone, M. L., Schaerli, P., Grabie, N., Lichtman, A. H., & von Andrian, U. H. (2006) · Nature Immunology · doi:10.1038/ni1385 · Cited by 424 · 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
Cosmi, L., Liotta, F., Lazzeri, E., Francalanci, M., Angeli, R., Mazzinghi, B., Santarlasci, V., Manetti, R., Vanini, V., Romagnani, P., et al. (2003) · Blood · doi:10.1182/blood-2003-04-1320 · Cited by 382 · see citing works
Tammela, T., Saaristo, A. M., Holopainen, T., Lyytikkä, J., Kotronen, A., Pitkonen, M., Abo‐Ramadan, U., Ylä‐Herttuala, S., Petrova, T. V., & Alitalo, K. K. (2007) · Nature Medicine · doi:10.1038/nm1689 · Cited by 362 · 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
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
An inflammation-induced mechanism for leukocyte transmigration across lymphatic vessel endothelium
Johnson, L. A., Clasper, S., Holt, A. P., Lalor, P. F., Baban, D., & Jackson, D. G. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20051759 · Cited by 346 · see citing works
Lund, A. W., Durães, F. V., Hirosue, S., Raghavan, V. R., Nembrini, C., Thomas, S. N., Issa, A., Hugues, S., & Swartz, M. A. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.01.005 · Cited by 341 · see citing works
Self-citationFletcher, 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
Lymphatic endothelial cell identity is reversible and its maintenance requires Prox1 activityPreprint
Johnson, N. C., Dillard, M. E., Bałuk, P., McDonald, D. M., Harvey, N. L., Frase, S., & Oliver, G. C. (2008) · Genes & Development · doi:10.1101/gad.1727208 · Cited by 335 · see citing works
Acton, S. E., Astarita, J. L., Malhotra, D., Lukacs‐Kornek, V., Franz, B., Hess, P. R., Jakus, Z., Kuligowski, M., Fletcher, A. L., Elpek, K. G., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.05.022 · Cited by 318 · see citing works
Cross-dressed dendritic cells drive memory CD8+ T-cell activation after viral infection
Wakim, L. M., & Bevan, M. J. (2011) · Nature · doi:10.1038/nature09863 · Cited by 307 · 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
Gerner, M. Y., Torabi‐Parizi, P., & Germain, R. N. (2014) · Immunity · doi:10.1016/j.immuni.2014.12.024 · Cited by 297 · see citing works
Adler, A. J., Marsh, D. W., Yochum, G. S., Guzzo, J. L., Nigam, A., Nelson, W. G., & Pardoll, D. M. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.10.1555 · Cited by 294 · see citing works
Hadeiba, H., Lahl, K., Edalati, A., Oderup, C., Habtezion, A., Pachynski, R. K., Nguyen, L. P., Ghodsi, A., Adler, S., & Butcher, E. C. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.017 · Cited by 292 · see citing works
Diehl, L., Schurich, A., Grochtmann, R., Hegenbarth, S., Chen, L., & Knolle, P. A. (2008) · Hepatology · doi:10.1002/hep.21965 · Cited by 291 · see citing works
Liston, A., Gray, D. H. D., Lesage, S., Fletcher, A. L., Wilson, J., Webster, K. E., Scott, H. S., Boyd, R. L., Peltonen, L., & Goodnow, C. C. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20040581 · Cited by 290 · see citing works
Davis, D. M. (2007) · Nature reviews. Immunology · doi:10.1038/nri2020 · Cited by 288 · see citing works
Tewalt, E. F., Cohen, J. N., Rouhani, S. J., Guidi, C. J., Qiao, H., Fahl, S. P., Conaway, M. R., Bender, T. P., Tung, K. S., Vella, A. T., et al. (2012) · Blood · doi:10.1182/blood-2012-04-427013 · Cited by 270 · see citing works
Anderson, A. C., Nicholson, L. B., Legge, K. L., Turchin, V., Zaghouani, H., & Kuchroo, V. K. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.5.761 · Cited by 269 · see citing works
Tumor masses support naive T cell infiltration, activation, and differentiation into effectors
Thompson, E. D., Enriquez, H. L., Fu, Y., & Engelhard, V. H. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20092454 · Cited by 250 · see citing works
The thymic medulla: a unique microenvironment for intercellular self-antigen transfer
Koble, C., & Kyewski, B. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20082449 · Cited by 240 · see citing works
Lymphangiogenesis and lymphangiodysplasia: From molecular to clinical lymphology
Witte, M. H., Bernas, M. J., Martin, C. P., & Witte, C. L. (2001) · Microscopy Research and Technique · doi:10.1002/jemt.1163 · Cited by 238 · see citing works
Dubrot, J., Durães, F. V., Potin, L., Capotosti, F., Brighouse, D., Suter, T. B., LeibundGut‐Landmann, S., Garbi, N., Reith, W., Swartz, M. A., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20132000 · Cited by 227 · see citing works
Self-citationThe anatomy and development of the jugular lymph sacs in the domestic cat (Felis domestica)
Huntington, G. S., & McClure, C. F. W. (1910) · American Journal of Anatomy · doi:10.1002/aja.1000100108 · Cited by 222 · see citing works
Lymphatic vessels arise from specialized angioblasts within a venous niche
Nicenboim, J., Malkinson, G., Lupo, T., Asaf, L., Sela, Y., Mayseless, O., Gibbs-Bar, L., Senderovich, N., Hashimshony, T., Shin, M., et al. (2015) · Nature · doi:10.1038/nature14425 · Cited by 215 · see citing works
Cross-tolerance: A Pathway for Inducing Tolerance to Peripheral Tissue Antigens
Heath, W. R., Kurts, C., Miller, J. F. A. P., & Carbone, F. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.10.1549 · Cited by 209 · see citing works
Tumor-induced stromal reprogramming drives lymph node transformation
Riedel, A., Shorthouse, D., Haas, L., Hall, B. A., & Shields, J. D. (2016) · Nature Immunology · doi:10.1038/ni.3492 · Cited by 206 · see citing works
Podgrabinska, S., Kamalu, O., Mayer, L. F., Shimaoka, M., Snoeck, H. W., Randolph, G. J., & Skobe, M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802167 · Cited by 205 · see citing works
Hirosue, S., Vokali, E., Raghavan, V. R., Rincón-Restrepo, M., Lund, A. W., Corthésy-Henrioud, P., Capotosti, F., Halin, C., Hugues, S., & Swartz, M. A. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302492 · Cited by 200 · see citing works
Self-citationCortical sinus probing, S1P1-dependent entry and flow-based capture of egressing T cells
Grigorova, I., Schwab, S. R., Phan, T. G., Pham, T. H. M., Okada, T., & Cyster, J. G. (2008) · Nature Immunology · doi:10.1038/ni.1682 · Cited by 187 · see citing works
Lymphangiogenic Gene Therapy With Minimal Blood Vascular Side Effects
Saaristo, A. M., Veikkola, T., Tammela, T., Enholm, B., Karkkainen, M. J., Pajusola, K., Büeler, H., Ylä‐Herttuala, S., & Alitalo, K. K. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020587 · Cited by 171 · see citing works
IL-7–producing stromal cells are critical for lymph node remodeling
Onder, L., Narang, P., Scandella, E., Chai, Q., Iolyeva, M. E., Hoorweg, K., Halin, C., Richie, E. R., Kaye, P. M., Westermann, J., et al. (2012) · Blood · doi:10.1182/blood-2012-03-416859 · Cited by 169 · see citing works
Control of central and peripheral tolerance by Aire
Metzger, T. C., & Anderson, M. S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01008.x · Cited by 163 · see citing works
Gibson, T. J., Ramu, C., Gemünd, C., & Aasland, R. (1998) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(98)01231-6 · Cited by 158 · see citing works
Gardner, J. M., Metzger, T. C., McMahon, E., Au‐Yeung, B. B., Krawisz, A. K., Lu, W., Price, J. D., Johannes, K., Satpathy, A. T., MURPHY, K. M. M., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.005 · Cited by 156 · see citing works
Tamburini, B. A., Burchill, M. A., & Kedl, R. M. (2014) · Nature Communications · doi:10.1038/ncomms4989 · Cited by 153 · see citing works
The New Era of the Lymphatic System: No Longer Secondary to the Blood Vascular SystemPreprint
Choi, I., Lee, S., & Hong, Y. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006445 · Cited by 146 · see citing works
Tumor lymphangiogenesis and new drug development
Dieterich, L. C., & Detmar, M. J. (2015) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2015.12.011 · Cited by 145 · see citing works
Rouhani, S. J., Eccles, J. D., Riccardi, P., Peske, J. D., Tewalt, E. F., Cohen, J. N., Liblau, R., Mäkinen, T., & Engelhard, V. H. (2015) · Nature Communications · doi:10.1038/ncomms7771 · Cited by 144 · see citing works
Hara, T., Shitara, S., Imai, K., Miyachi, H., Kitano, S., Yao, H., Tani‐ichi, S., & Ikuta, K. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200586 · Cited by 143 · see citing works
Enouz, S., Carrié, L., Merkler, D., Bevan, M. J., & Zehn, D. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20120905 · Cited by 142 · see citing works
Nichols, L. A., Chen, Y., Colella, T. A., Bennett, C. L., Clausen, B. E., & Engelhard, V. H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.2.993 · Cited by 140 · see citing works
Yip, L., Su, L., Sheng, D., Chang, P. P., Atkinson, M. A., Czesak, M., Albert, P. R., Collier, A.-R. Y., Turley, S. J., Fathman, C. G., et al. (2009) · Nature Immunology · doi:10.1038/ni.1773 · Cited by 140 · see citing works
Immune cell trafficking from the brain maintains CNS immune tolerance
Mohammad, M. G., Tsai, V. W.-W., Ruitenberg, M. J., Hassanpour, M., Li, H., Hart, P. H., Breit, S. N., Sawchenko, P. E., & Brown, D. A. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71544 · Cited by 131 · see citing works
Intestinal Tolerance Is Converted to Autoimmune Enteritis upon PD-1 Ligand Blockade
Reynoso, E. D., Elpek, K. G., Francisco, L. M., Bronson, R. T., Bellemare‐Pelletier, A., Sharpe, A. H., Freeman, G. J., & Turley, S. J. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802769 · Cited by 125 · see citing works
On the development of the superficial lymphatics in the skin of the pig
Sabin, F. R. (1904) · American Journal of Anatomy · doi:10.1002/aja.1000030205 · Cited by 123 · see citing works
Griffin, J. P., Chu, R., & Harding, C. V. (1997) · The Journal of Immunology · doi:10.4049/jimmunol.158.4.1523 · Cited by 120 · see citing works
Impaired Humoral Immunity and Tolerance in K14-VEGFR-3-Ig Mice That Lack Dermal Lymphatic Drainage
Thomas, S. N., Rutkowski, J. M., Pasquier, M. C., Kuan, E. L., Alitalo, K. K., Randolph, G. J., & Swartz, M. A. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103545 · Cited by 120 · see citing works
CD8+CD28− Regulatory T Lymphocytes Prevent Experimental Inflammatory Bowel Disease in Mice
Marcq, I., Pomié, C., Romagnoli, P., & van Meerwijk, J. P. M. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.09.008 · Cited by 119 · see citing works
Lymph node stromal cells constrain immunity via MHC class II self-antigen presentation
Baptista, A. P., Roozendaal, R., Reijmers, R. M., Koning, J. J., Unger, W. W. J., Greuter, M., Keuning, E. D., Molenaar, R., Goverse, G., Sneeboer, M. M. S., et al. (2014) · eLife · doi:10.7554/elife.04433 · Cited by 110 · see citing works
Cupovic, J., Onder, L., Gil-Cruz, C., Weiler, E., Caviezel-Firner, S., Perez-Shibayama, C., Rülicke, T., Bechmann, I., & Ludewig, B. (2016) · Immunity · doi:10.1016/j.immuni.2015.12.022 · Cited by 98 · see citing works
Cohen, J. N., Tewalt, E. F., Rouhani, S. J., Buonomo, E. L., Bruce, A. N., Xu, X., Bekiranov, S., Fu, Y., & Engelhard, V. H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087740 · Cited by 93 · see citing works
Magnusson, F. C., Liblau, R., von Boehmer, H., Pittet, M. J., Lee, J., Turley, S. J., & Khazaie, K. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.01.070 · Cited by 88 · see citing works
Böttcher, J. P., Schanz, O., Wohlleber, D., Abdullah, Z., Debey-Pascher, S., Staratschek-Jox, A., Höchst, B., Hegenbarth, S., Grell, J., Limmer, A., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.02.008 · Cited by 82 · see citing works
Lukacs-Kornek, V., Burgdorf, S., Diehl, L., Specht, S., Kornek, M., & Kurts, C. (2008) · Journal of Immunology · doi:10.4049/jimmunol.180.2.706 · Cited by 81 · see citing works
Miller, C. N., Hartigan-O’Connor, D. J., Lee, M. S., Laidlaw, G., Cornelissen, I., Matloubian, M., Coughlin, S. R., McDonald, D. M., & McCune, J. M. (2013) · International Immunology · doi:10.1093/intimm/dxt012 · Cited by 71 · see citing works
Interleukin-7 is produced by afferent lymphatic vessels and supports lymphatic drainage
Iolyeva, M. E., Aebischer, D., Proulx, S. T., Willrodt, A., Ecoiffier, T., Häner, S., Bouchaud, G., Krieg, C., Onder, L., Ludewig, B., et al. (2013) · Blood · doi:10.1182/blood-2013-01-478073 · Cited by 67 · see citing works
Modes of Antigen Presentation by Lymph Node Stromal Cells and Their Immunological Implications
Hirosue, S., & Dubrot, J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00446 · Cited by 65 · see citing works
Self-citationNörder, M., Gutierrez, M. G., Zicari, S., Cervi, E., Caruso, A., & Guzmán, C. A. (2012) · The FASEB Journal · doi:10.1096/fj.12-205278 · Cited by 65 · see citing works
Tolerogenic and Activatory Plasmacytoid Dendritic Cells in Autoimmunity
Guéry, L., & Hugues, S. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00059 · Cited by 62 · see citing works
Self-citationMurine CD8+ regulatory T lymphocytes: The new era
Pomié, C., Marcq, I., & van Meerwijk, J. P. M. (2008) · Human Immunology · doi:10.1016/j.humimm.2008.08.288 · Cited by 55 · see citing works
Zhang, Q.-J., Li, X., Wang, D., Huang, X., Mathis, J. M., Duan, W., Knight, D., Shi, R., Glass, J., Zhang, D., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003097 · Cited by 51 · see citing works
Cross-presentation: inducing CD8 T cell immunity and tolerance
Kurts, C. (2000) · Journal of Molecular Medicine · doi:10.1007/s001090000108 · Cited by 49 · see citing works
The Lymph Self-Antigen Repertoire
Clement, C. C., & Santambrogio, L. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00424 · Cited by 47 · see citing works
Lymph Node Stromal Cells Negatively Regulate Antigen-Specific CD4+ T Cell Responses
Abe, J., Shichino, S., Ueha, S., Hashimoto, S., Tomura, M., Inagaki, Y., Stein, J. V., & Matsushima, K. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302946 · Cited by 44 · see citing works
Unique patterns of metastases in common and rare types of malignancy
Leong, S. P. L., Nakakura, E. K., Pollock, R. E., Choti, M. A., Morton, D. L., Henner, W. D., Lal, A., Pillai, R., Clark, O. H., & Cady, B. (2011) · Journal of Surgical Oncology · doi:10.1002/jso.21841 · Cited by 33 · see citing works
Mouse and human CD8+ CD28low regulatory T lymphocytes differentiate in the thymus
Vuddamalay, Y., Attia, M., Vicente, R., Pomié, C., Enault, G., Léobon, B., Joffre, O. P., Romagnoli, P., & van Meerwijk, J. P. M. (2016) · Immunology · doi:10.1111/imm.12600 · Cited by 30 · see citing works
Lohse, A. W., Dinkelmann, M., Kimmig, M., Herkel, J., & Büschenfelde, K.-H. M. Z. (1996) · Journal of Autoimmunity · doi:10.1006/jaut.1996.0087 · Cited by 28 · see citing works
High-density lipoprotein endocytosis in endothelial cells
Fruhwürth, S., Pavelka, M., Bittman, R., Kovacs, W. J., Walter, K., Röhrl, C., & Stangl, H. (2013) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v4.i4.131 · Cited by 26 · see citing works
Lymphangiogenesis and lymphangiodysplasia: From molecular to clinical lymphology
Witte, M. H., Bernas, M. J., Martin, C. P., et al. (2001) · Microscopy Research and Technique · doi:10.1002/jemt.1163.abs · Cited by 25 · see citing works
Bidirectional MHC molecule exchange between migratory and resident dendritic cells
de Heusch, M., Blocklet, D., Egrise, D., Hauquier, B., Vermeersch, M., Goldman, S., & Moser, M. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0307167 · Cited by 23 · see citing works
Durães, F. V., Thelemann, C., Sarter, K., Acha‐Orbea, H., Hugues, S., & Reith, W. (2013) · Tissue Antigens · doi:10.1111/tan.12136 · Cited by 17 · see citing works
Self-citationFriedlaender, M. H., Chisari, F. V., & Baer, H. (1973) · The Journal of Immunology · doi:10.4049/jimmunol.111.1.164 · Cited by 15 · see citing works
Making Central T-Cell Tolerance Efficient: Thymic Stromal Cells Sample Distinct Self-Antigen Pools
Kyewski, B., Röttinger, B., & Klein, L. (2000) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-57276-0_18 · Cited by 14 · see citing works
Ciré, S., Rocha, S. D., Ferrand, M., Collins, M. K., & Galy, A. H. M. (2016) · Molecular Therapy · doi:10.1038/mt.2016.168 · Cited by 10 · see citing works
Collier, A. Y., Lee, J., & Turley, S. J. (2008) · Mucosal Immunology · doi:10.1038/mi.2008.19 · Cited by 9 · see citing works
Bonasio, R., Scimone, M. L., Schaerli, P., Grabie, N., Lichtman, A. H., & von Andrian, U. H. (2006) · Nature Immunology · doi:10.1038/ni1106-1234b · Cited by 5 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Structural cells are key regulators of organ-specific immune responses
Krausgruber, T., Fortelny, N., Fife-Gernedl, V., Senekowitsch, M., Schuster, L. C., Lercher, A., Nemc, A., Schmidl, C., Rendeiro, A. F., Bergthaler, A., et al. (2020) · Nature · doi:10.1038/s41586-020-2424-4 · Cited by 434 · see citing works
T Cell Dysfunction in Cancer Immunity and Immunotherapy
Xia, A., Zhang, Y., Jiang, X., Yin, T., & Lu, X. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01719 · Cited by 338 · see citing works
Vascular Endothelial Cells and Innate Immunity
Shao, Y., Saredy, J., Yang, W. Y., Sun, Y., Lu, Y., Saaoud, F., Drummer, C., Johnson, C., Xu, K., Jiang, X., et al. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.314330 · Cited by 302 · see citing works
Borges, V. F., Lyons, T. R., Germain, D., & Schedin, P. S. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-3448 · Cited by 99 · see citing works
Certo, M., Elkafrawy, H., Pucino, V., Cucchi, D., Cheung, K. C.-P., & Mauro, C. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15002 · Cited by 52 · see citing works
Viperin controls chikungunya virus–specific pathogenic T cell IFNγ Th1 stimulation in mice
Carissimo, G., Teo, T., Chan, Y., Lee, C. Y., Lee, B. T. K., Torres‐Ruesta, A., Tan, J. J. L., Chua, T., Fong, S., Lum, F., et al. (2019) · Life Science Alliance · doi:10.26508/lsa.201900298 · Cited by 40 · see citing works
The Development and Treatment of Lymphatic Dysfunction in Cancer Patients and Survivors
Aldrich, M. B., Rasmussen, J. C., Fife, C. E., Shaitelman, S. F., & Sevick-Muraca, E. M. (2020) · Cancers · doi:10.3390/cancers12082280 · Cited by 36 · see citing works
Dendritic Cells and T Cells Interact Within Murine Afferent Lymphatic Capillaries
Hunter, M. C., Teijeira, Á., Montecchi, R., Russo, E., Runge, P., Kiefer, F., & Halin, C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00520 · Cited by 28 · see citing works
Wang, J., Gan, L., Li, F., Li, Q., Wu, T., Wu, Z., Chen, P., Scicluna, B. P., Feng, X., Gu, J., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122340 · Cited by 22 · see citing works
Cx47 fine-tunes the handling of serum lipids but is dispensable for lymphatic vascular function
Meens, M. J. P. M. T., Kutkut, I., Rochemont, V., Dubrot, J., Kaladji, F. R., Sabine, A., Lyons, O., Hendrikx, S., Bernier‐Latmani, J., Kiefer, F., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181476 · Cited by 22 · see citing works
Self-citationTamburini, B. A. J., Elder, A. M., Finlon, J. M., Winter, A. B., Wessells, V. M., Borges, V. F., & Lyons, T. R. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01313 · Cited by 21 · see citing works
Neuroinflammation-Driven Lymphangiogenesis in CNS Diseases
Hsu, M., Laaker, C. J., Sándor, M., & Fábry, Z. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.683676 · Cited by 20 · see citing works
Zhang, Q., Mu, X., Dong, H., Hu, G., Zhang, T., He, C., & Siddique, N. (2020) · Virology Journal · doi:10.1186/s12985-020-01341-x · Cited by 17 · see citing works
Cell-targeted vaccines: implications for adaptive immunity
Ung, T. W.-M., Rutledge, N. S., Weiss, A. M., Esser-Kahn, A. P., & Deak, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1221008 · Cited by 18 · see citing works
Hsu, M., Sándor, M., & Fábry, Z. (2021) · Biologia Futura · doi:10.1007/s42977-021-00066-4 · Cited by 16 · see citing works
Jung, Y. J., Park, Y., Kim, H. S., Lee, H. J., Kim, Y., Lee, J. H., Kim, Y. H., Maeng, Y., & Kwon, J. (2018) · American Journal of Reproductive Immunology · doi:10.1111/aji.12970 · Cited by 16 · see citing works
The Lymphatic System in Kidney Disease
Baker, M., & Cantley, L. (2023) · Kidney360 · doi:10.34067/kid.0000000000000120 · Cited by 14 · see citing works
Kwon, H., Kwon, J., Parksong, J., & Maeng, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084237 · Cited by 12 · see citing works
Rojas, C. M., Velasquez, F. C., Morton, J. E., Clemente, L. C., Parra, E. R., Torres-Cabala, C. A., & Sevick-Muraca, E. M. (2022) · Cancers · doi:10.3390/cancers14071823 · Cited by 11 · see citing works
Lymphatic Connexins and Pannexins in Health and Disease
Ehrlich, A., Molica, F., Hautefort, A., & Kwak, B. R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115734 · Cited by 11 · see citing works
Shi, Q., Carman, C. V., Chen, Y., Sage, P. T., Xue, F., Liang, X. M., & Gilbert, G. E. (2020) · Blood Advances · doi:10.1182/bloodadvances.2020001468 · Cited by 7 · see citing works
Lane, J. I., Nieves-Ortiz, E., Ndatabaye, O., Fatkhullina, A. R., Lopez, S., Dermody, T. S., & Esterházy, D. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20241181 · Cited by 3 · see citing works
Jin, P., Liu, X., Li, C., Gao, M., & Wang, H. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10535 · Cited by 3 · see citing works
Zhang, L., Li, H., Liu, J., Sun, G., Tang, X., Xu, S., Zhang, L., Zhang, W., & Ai, B. (2023) · Cancer Medicine · doi:10.1002/cam4.5744 · Cited by 2 · see citing works
Peng, J., Liu, X., Li, C., Gao, M., & Wang, H. (2020) · Research Square · doi:10.21203/rs.3.rs-52892/v2
Wang, H., Peng, J., Liu, X., Li, C., & Gao, M. (2020) · Research Square · doi:10.21203/rs.3.rs-52892/v1
Hirschi, K. K. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727824417.793562749
1 Lymphatic System Lymphatic system
(2024) · Haug Verlag in Georg Thieme Verlag KG eBooks · doi:10.1055/b-0044-201933
Fry, L., de Jesus, F. N., Carneiro, M. B. H., Roys, H., Bowlin, A. K., Peters, N. C., von der Weid, P., & Weinkopff, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.01.651666
Chen, W., Wang, Y., Zhang, D., Zhang, Y., Qin, X., & Wang, X. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06228-8
Yang, M., Zhang, L., Luo, C.-H., Zhang, B.-B., & Zhao, J. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48101034
- Authors
- Humbert, M., Hugues, S., & Dubrot, J.
- Affiliations
- University of Geneva (CH)
- Corresponding author
- Hugues, Stéphanie
- Dubrot, Juan
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2017-01-12
- Volume
- 7
- Pages
- 684-684
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC5226940
- OpenAlex
- W2576305170
- Cited by
- 32
- References
- 131
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 4 · 2022: 2 · 2021: 5 · 2020: 9 · 2019: 5 · 2018: 1 · 2017: 1
- FWCI
- 0.45
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion, other-oa)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (310030_166541)
- European Research Council (281365)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
- Keywords
- lymphatic endothelial cells, lymph node stromal cells, lymphocyte migration, MHC class I antigen presentation, MHC class II antigen presentation, autoimmunity, CD4+ T cell responses
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review