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Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells
Abstract
Lymph nodes prevent the systemic dissemination of pathogens such as viruses that infect peripheral tissues after penetrating the body's surface barriers. They are also the staging ground of adaptive immune responses to pathogen-derived antigens. It is unclear how virus particles are cleared from afferent lymph and presented to cognate B cells to induce antibody responses. Here we identify a population of CD11b+CD169+MHCII+ macrophages on the floor of the subcapsular sinus (SCS) and in the medulla of lymph nodes that capture viral particles within minutes after subcutaneous injection. Macrophages in the SCS translocated surface-bound viral particles across the SCS floor and presented them to migrating B cells in the underlying follicles. Selective depletion of these macrophages compromised local viral retention, exacerbated viraemia of the host, and impaired local B-cell activation. These findings indicate that CD169+ macrophages have a dual physiological function. They act as innate 'flypaper' by preventing the systemic spread of lymph-borne pathogens and as critical gatekeepers at the lymph-tissue interface that facilitate the recognition of particulate antigens by B cells and initiate humoral immune responses.
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“These macrophages can capture larger molecules, viruses, and bacteria (89, 90) and are capable of mounting a protective immune response even in the absence of antigen-presenting DCs (91).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [90]
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Cites
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
Self-citationMACROPHAGE RECEPTORS AND IMMUNE RECOGNITION
Taylor, P. R., Martínez‐Pomares, L., Stacey, M. A., Lin, H.-H., Brown, G. D., & Gordon, S. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115816 · Cited by 1,366
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
Self-citationCD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs
Shiow, L. R., Rosen, D. B., Brdičková, N., Xu, Y., An, J., Lanier, L. L., Cyster, J. G., & Matloubian, M. (2006) · Nature · doi:10.1038/nature04606 · Cited by 1,189
Control of Early Viral and Bacterial Distribution and Disease by Natural Antibodies
Ochsenbein, A. F., Fehr, T. H., Lutz, C., Suter, M., Brombacher, F., Hengartner, H., & Zinkernagel, R. M. (1999) · Science · doi:10.1126/science.286.5447.2156 · Cited by 911
Okada, T., Miller, M. J., Parker, I., Krummel, M. F., Neighbors, M., Hartley, S. B., O’Garra, A., Cahalan, M. D., & Cyster, J. G. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030150 · Cited by 586
Balanced responsiveness to chemoattractants from adjacent zones determines B-cell position
Reif, K., Ekland, E. H., Ohl, L., Nakano, H., Lipp, M., Förster, R., & Cyster, J. G. (2002) · Nature · doi:10.1038/416094a · Cited by 572
B cell receptor signal strength determines B cell fate
Casola, S. S., Otipoby, K. L., Alimzhanov, M. B., Humme, S., Uyttersprot, N., Kutok, J. L., Carroll, M. C., & Rajewsky, K. (2004) · Nature Immunology · doi:10.1038/ni1036 · Cited by 561
Extrafollicular Activation of Lymph Node B Cells by Antigen-Bearing Dendritic Cells
Qi, H., Egen, J. G., Huang, A. Y.-C., & Germain, R. N. (2006) · Science · doi:10.1126/science.1125703 · Cited by 521
Wessels, M. R., Butko, P., Ma, M., Warren, H. B., Lage, A. L., & Carroll, M. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11490 · Cited by 503
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Xu, C., Nedergaard, M., Fowell, D. J., Friedl, P., & Ji, N. (2024) · Cell · doi:10.1016/j.cell.2024.07.036 · Cited by 182
Lymphatic system: An active pathway for immune protection
Liao, S., & von der Weid, P. Y. (2015) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2014.11.012 · Cited by 174
A particulate saponin/TLR agonist vaccine adjuvant alters lymph flow and modulates adaptive immunity
Silva, M., Kato, Y., Melo, M. B., Phung, I., Freeman, B. L., Li, Z., Roh, K., van Wijnbergen, J. W., Watkins, H. C., Enemuo, C. A., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abf1152 · Cited by 174
Weber, M., Treanor, B., Depoil, D., Shinohara, H., Harwood, N. E., Hikida, M., Kurosaki, T., & Batista, F. D. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072619 · Cited by 170
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 178
Targeted modulation of immune cells and tissues using engineered biomaterials
Yousefpour, P., Ni, K., & Irvine, D. J. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-022-00016-2 · Cited by 170
Sette, A., Moutaftsi, M., Moyron-Quiroz, J., McCausland, M. M., Davies, D. H., Johnston, R. J., Peters, B., Rafii-El-Idrissi Benhnia, M., Hoffmann, J., Su, H.-P., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.04.018 · Cited by 168
Influenza virosomes as a vaccine adjuvant and carrier system
Moser, C., Amacker, M., & Zurbriggen, R. (2011) · Expert Review of Vaccines · doi:10.1586/erv.11.15 · Cited by 168
Wilson, E. H., Harris, T. H., Mrass, P., John, B., Wojno, E. D. T., Wu, G. F., Pepper, M., Wherry, E. J., Dzierzinski, F., Roos, D. S., et al. (2009) · Immunity · doi:10.1016/j.immuni.2008.12.013 · Cited by 167
Immunological functions of hyaluronan and its receptors in the lymphatics
Jackson, D. G. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00803.x · Cited by 169
Nanoparticle Vaccines Adopting Virus-like Features for Enhanced Immune Potentiation
Chattopadhyay, S., Chen, J.-Y., Chen, H., & Hu, C. J. (2017) · Nanotheranostics · doi:10.7150/ntno.19796 · Cited by 171
Stromal infrastructure of the lymph node and coordination of immunity
Chang, J. E., & Turley, S. J. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.11.003 · Cited by 170
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Link, A., Zabel, F., Schnetzler, Y., Titz, A., Brombacher, F., & Bachmann, M. F. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103312 · Cited by 162
Lin, L. C. W., Huang, C., Yao, B., Lin, J., Agrawal, A. S., Algaissi, A. A., Peng, B., Liu, Y., Huang, P., Juang, R., et al. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201807616 · Cited by 162
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Karsten, C. M., & Köhl, J. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.07.015 · Cited by 164
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Nassi, J. J., Cepko, C. L., Born, R. T., & Beier, K. T. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00080 · Cited by 161
Moseman, E. A., Iannacone, M., Bosurgi, L., Tonti, E., Chevrier, N., Tumanov, A. V., Fu, Y., Hacohen, N., & von Andrian, U. H. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.013 · Cited by 155
Self-citationType I interferons: diversity of sources, production pathways and effects on immune responses
Swiecki, M. K., & Colonna, M. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.10.026 · Cited by 162
Tamburini, B. A., Burchill, M. A., & Kedl, R. M. (2014) · Nature Communications · doi:10.1038/ncomms4989 · Cited by 153
Programmable multistage drug delivery to lymph nodes
Schudel, A., Chapman, A. P., Yau, M., Higginson, C. J., Francis, D. M., Manspeaker, M. P., Avecilla, A. R. C., Rohner, N. A., Finn, M. G., & Thomas, S. N. (2020) · Nature Nanotechnology · doi:10.1038/s41565-020-0679-4 · Cited by 153
The spatio-temporal control of effector T cell migration
Fowell, D. J., & Kim, M. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00507-0 · Cited by 154
Chtanova, T., Han, S., Schaeffer, M., van Dooren, G. G., Herzmark, P., Striepen, B., & Robey, E. A. (2009) · Immunity · doi:10.1016/j.immuni.2009.06.023 · Cited by 146
Lymphatic Endothelial Cells Control Initiation of Lymph Node Organogenesis
Onder, L., Mörbe, U., Pikor, N. B., Novković, M., Cheng, H., Hehlgans, T., Pfeffer, K., Becher, B., Waisman, A., Rülicke, T., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.05.008 · Cited by 146
N-Glycosylation and Inflammation; the Not-So-Sweet Relation
Radovani, B., & Gudelj, I. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.893365 · Cited by 150
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Thaunat, O., Granja, A. G., Barral, P., Filby, A. J., Montaner, B., Collinson, L., Martínez, N., Harwood, N. E., Bruckbauer, A., & Batista, F. D. (2012) · Science · doi:10.1126/science.1214100 · Cited by 143
Growth and Immune Evasion of Lymph Node Metastasis
Jones, D., Pereira, E. R., & Padera, T. P. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00036 · Cited by 146
Sialoadhesin – a macrophage‐restricted marker of immunoregulation and inflammation
O’Neill, A. S. G., van den Berg, T. K., & Mullen, G. E. D. (2012) · Immunology · doi:10.1111/imm.12042 · Cited by 142
The influence of innate and pre‐existing immunity on adenovirus therapy
Zaiss, A. K., Machado, H. B., & Herschman, H. R. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22328 · Cited by 144
B cell antigen extraction is regulated by physical properties of antigen-presenting cells
Spillane, K. M., & Tolar, P. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201607064 · Cited by 141
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Irvine, D. J., & Read, B. J. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.01.007 · Cited by 141
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González, S., Degn, S. E., Pitcher, L. A., Woodruff, M. C., Heesters, B. A., & Carroll, M. C. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101255 · Cited by 146
Lymph node subcapsular sinus macrophages as the frontline of lymphatic immune defense
Louie, D. A. P., & Liao, S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00347 · Cited by 137
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Dong, X., Chu, D., & Wang, Z. (2017) · Theranostics · doi:10.7150/thno.18069 · Cited by 137
Lymphotoxin signalling in immune homeostasis and the control of microorganisms
Upadhyay, V., & Fu, Y. (2013) · Nature reviews. Immunology · doi:10.1038/nri3406 · Cited by 136
Sagoo, P., Garcia, Z., Bréart, B., Lemaı̂tre, F., Michonneau, D., Albert, M. L., Lévy, Y., & Bousso, P. (2015) · Nature Medicine · doi:10.1038/nm.4016 · Cited by 141
van Dinther, D., Veninga, H., Iborra, S., Borg, E. G. F., Hoogterp, L., Olesek, K., Beijer, M. R., Schetters, S. T. T., Kalay, H., García-Vallejo, J. J., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.021 · Cited by 139
Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis
Zumerle, S., Calì, B., Munari, F., Angioni, R., Virgilio, F. D., Molon, B., & Viola, A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.011 · Cited by 133
B Cell Activation Is Regulated by the Stiffness Properties of the Substrate Presenting the Antigens
Wan, Z., Zhang, S., Fan, Y., Liu, K., Du, F., Davey, A. M., Zhang, H., Han, W., Xiong, C., & Liu, W. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202976 · Cited by 137
Antigen affinity discrimination is an intrinsic function of the B cell receptor
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T Cell Zone Resident Macrophages Silently Dispose of Apoptotic Cells in the Lymph Node
Baratin, M., Simon, L., Jorquera, A., Ghigo, C., Dembélé, D., Nowak, J., Gentek, R., Wienert, S., Klauschen, F., MALISSEN, B., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.07.019 · Cited by 136
The lymph node at a glance – how spatial organization optimizes the immune response
Grant, S. M., Lou, M., Li, Y., Germain, R. N., & Radtke, A. J. (2020) · Journal of Cell Science · doi:10.1242/jcs.241828 · Cited by 135
Inflammation-induced disruption of SCS macrophages impairs B cell responses to secondary infection
Gaya, M., Castello, A., Montaner, B., Rogers, N. C., Sousa, C. R. E., Bruckbauer, A., & Batista, F. D. (2015) · Science · doi:10.1126/science.aaa1300 · Cited by 135
Dynamic Imaging of CD8+ T Cells and Dendritic Cells during Infection with Toxoplasma gondii
John, B., Harris, T. H., Wojno, E. D. T., Wilson, E. H., Gregg, B., Ng, L. G., Mrass, P., Roos, D. S., Dzierszinski, F. S., Weninger, W., et al. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000505 · Cited by 139
Grabowska, J. A., Venegas, M. L., Affandi, A. J., & den Haan, J. M. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02472 · Cited by 136
Detienne, S., Welsby, I., Collignon, C., Wouters, S., Coccia, M., Delhaye, S., Maele, L. V., Thomas, S., Swertvaegher, M., Detavernier, A., et al. (2016) · Scientific Reports · doi:10.1038/srep39475 · Cited by 128
Hsu, K. M., Pratt, J. R., Akers, W. J., Achilefu, S. A., & Yokoyama, W. M. (2008) · Journal of General Virology · doi:10.1099/vir.0.006668-0 · Cited by 128
Kourtis, I. C., Hirosue, S., de Titta, A., Kontos, S., Stegmann, T., Hubbell, J. A., & Swartz, M. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061646 · Cited by 129
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Lämmermann, T., & Sixt, M. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00592.x · Cited by 126
Complement and humoral immunity
Carroll, M. C. (2008) · Vaccine · doi:10.1016/j.vaccine.2008.11.022 · Cited by 126
Modeling Lymph Flow and Fluid Exchange with Blood Vessels in Lymph Nodes
Jafarnejad, M., Woodruff, M. C., Zawieja, D. C., Carroll, M. C., & Moore, J. E. (2015) · Lymphatic Research and Biology · doi:10.1089/lrb.2015.0028 · Cited by 125
Chen, F., Li, T., Zhang, H., Saeed, M., Liu, X., Huang, L., Wang, X., Gao, J., Hou, B., Lai, Y., et al. (2022) · Advanced Materials · doi:10.1002/adma.202209910 · Cited by 125
Cervantes‐Barragán, L., Kalinke, U., Züst, R., König, M. F., Reizis, B., López-Macías, C. I. R., Thiel, V., & Ludewig, B. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.2.1099 · Cited by 128
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Izquierdo‐Useros, N., Lorizate, M., McLaren, P. J., Telenti, A., Kräusslich, H., & Martínez‐Picado, J. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004146 · Cited by 135
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 124
Lymph nodes—The neglected battlefield in tuberculosis
Ganchua, S. K. C., White, A. G., Klein, E. C., & Flynn, J. L. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008632 · Cited by 127
Probing cellular processes by long-term live imaging – historic problems and current solutions
Coutu, D. L., & Schroeder, T. (2013) · Journal of Cell Science · doi:10.1242/jcs.118349 · Cited by 119
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Lam, J. H., & Baumgarth, N. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801208 · Cited by 127
Lymphatic Endothelial Cells Are Essential Components of the Subcapsular Sinus Macrophage Niche
Mondor, I., Baratin, M., Lagueyrie, M., Saro, L., Henri, S., Gentek, R., Suerinck, D., Kastenmüller, W., Jiang, J. X., & Bajénoff, M. (2019) · Immunity · doi:10.1016/j.immuni.2019.04.002 · Cited by 125
Inflammatory monocytes hinder antiviral B cell responses
Sammicheli, S., Kuka, M., Lucia, P. D., de Oya, N. J., Giovanni, M. D., Fioravanti, J., Cristofani, C., Maganuco, C. G., Fallet, B., Ganzer, L., et al. (2016) · Science Immunology · doi:10.1126/sciimmunol.aah6789 · Cited by 116
Self-citationBajénoff, M., & Germain, R. N. (2009) · Blood · doi:10.1182/blood-2009-06-229567 · Cited by 116
Exploiting lymphatic vessels for immunomodulation: Rationale, opportunities, and challenges
Maisel, K., Sasso, M. S., Potin, L., & Swartz, M. A. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.07.005 · Cited by 115
Early BCR Events and Antigen Capture, Processing, and Loading on MHC Class II on B Cells
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Fibroblastic reticular cells at the nexus of innate and adaptive immune responses
Perez‐Shibayama, C., Gil‐Cruz, C., & Ludewig, B. (2019) · Immunological Reviews · doi:10.1111/imr.12748 · Cited by 111
Influence of ageing on the microarchitecture of the spleen and lymph nodes
Turner, V. M., & Mabbott, N. A. (2017) · Biogerontology · doi:10.1007/s10522-017-9707-7 · Cited by 111
The Role of BAFF System Molecules in Host Response to Pathogens
Sakai, J., & Akkoyunlu, M. (2017) · Clinical Microbiology Reviews · doi:10.1128/cmr.00046-17 · Cited by 109
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Moran, I., Nguyen, A., Khoo, W. H., Butt, D., Bourne, K., Young, C., Hermes, J. R., Biro, M., Gracie, G., Ma, C. S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05772-7 · Cited by 114
Antigen presentation by dendritic cells for B cell activation
Heath, W. R., Kato, Y., Steiner, T. M., & Caminschi, I. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.04.003 · Cited by 109
Germinal center reutilization by newly activated B cells
Schwickert, T. A., Alabyev, B., Manser, T. L., & Nussenzweig, M. C. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091225 · Cited by 109
Sokol, C. L., Camire, R. B., Jones, M. C., & Luster, A. D. (2018) · Immunity · doi:10.1016/j.immuni.2018.07.012 · Cited by 110
Camara, A., Cordeiro, O. G., Alloush, F., Sponsel, J., Chypre, M., Onder, L., Asano, K., Tanaka, M., Yagita∥, H., Ludewig, B., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.05.008 · Cited by 111
Dynamic imaging of host–pathogen interactions in vivo
Coombes, J. L., & Robey, E. A. (2010) · Nature reviews. Immunology · doi:10.1038/nri2746 · Cited by 107
Schnaar, R. L. (2015) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.10.057 · Cited by 105
Xu, Y., & Liu, L. (2017) · Influenza and Other Respiratory Viruses · doi:10.1111/irv.12459 · Cited by 104
Inhibition of the lymphotoxin pathway as a therapy for autoimmune disease
Browning, J. L. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00633.x · Cited by 104
Perez, O. A., Yeung, S. T., Vera‐Licona, P., Romagnoli, P. A., Samji, T., Ural, B. B., Maher, L. A., Tanaka, M., & Khanna, K. M. (2017) · Science Immunology · doi:10.1126/sciimmunol.aah5520 · Cited by 99
Inflammatory Cell Migration in Rheumatoid Arthritis: A Comprehensive Review
Nevius, E., Gomes, A. C., & Pereira, J. P. (2015) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-015-8520-9 · Cited by 100
Macrophages induce differentiation of plasma cells through CXCL10/IP-10
Xu, W. D., Joo, H., Clayton, S., Dullaers, M., Herve, M.-C., Blankenship, D., de la Morena, M. T., BALDERAS, R. S., Pïcard, C., Casanova, J., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20112142 · Cited by 102
Mosquito Biting Modulates Skin Response to Virus Infection
Pingen, M., Schmid, M., Harris, E., & McKimmie, C. S. (2017) · Trends in Parasitology · doi:10.1016/j.pt.2017.04.003 · Cited by 97
Synthetic mast-cell granules as adjuvants to promote and polarize immunity in lymph nodes
John, A. L. S., Chan, C. Y., Staats, H. F., Leong, K. W., & Abraham, S. N. (2012) · Nature Materials · doi:10.1038/nmat3222 · Cited by 96
Interferon-γ mediates chemokine-dependent recruitment of natural killer cells during viral infection
Pak-Wittel, M. A., Yang, L., Sojka, D. K., Rivenbark, J. G., & Yokoyama, W. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220456110 · Cited by 95
Imaging techniques for assaying lymphocyte activation in action
Balagopalan, L., Sherman, E., Barr, V. A., & Samelson, L. E. (2010) · Nature reviews. Immunology · doi:10.1038/nri2903 · Cited by 95
Pfeiffer, F., Kumar, V. V., Butz, S., Vestweber, D., Imhof, B. A., Stein, J. V., & Engelhardt, B. (2008) · European Journal of Immunology · doi:10.1002/eji.200838140 · Cited by 99
The Inhibitory Receptor BTLA Controls γδ T Cell Homeostasis and Inflammatory Responses
Bekiaris, V., Šedý, J. R., Macauley, M. G., Rhode-Kurnow, A., & Ware, C. F. (2013) · Immunity · doi:10.1016/j.immuni.2013.10.017 · Cited by 95
Metabolic features of macrophages in inflammatory diseases and cancer
Na, Y. R., Je, S., & Seok, S. H. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.10.044 · Cited by 96
Same yet different — how lymph node heterogeneity affects immune responses
de Casas, P. C., Knöpper, K., Sarkar, R. D., & Kastenmüller, W. (2023) · Nature reviews. Immunology · doi:10.1038/s41577-023-00965-8 · Cited by 99
Gray, E. E., Friend, S. L., Suzuki, K., Phan, T. G., & Cyster, J. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038258 · Cited by 99
Multiple roles of lymphatic vessels in peripheral lymph node development
Bovay, E., Sabine, A., Prat-Luri, B., Kim, S., Son, K., Willrodt, A., Olsson, C., Halin, C., Kiefer, F., Betsholtz, C., et al. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20180217 · Cited by 95
Continuous germinal center invasion contributes to the diversity of the immune response
Hägglöf, T., Cipolla, M., Loewe, M., Chen, S. T., Kara, E. E., Mesin, L., Hartweger, H., ElTanbouly, M. A., Cho, A., Gazumyan, A., et al. (2022) · Cell · doi:10.1016/j.cell.2022.11.032 · Cited by 102
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Hickman, H. D., Li, L. Y., Reynoso, G. V., Rubin, E. J., Skon-Hegg, C., Mays, J. W., Gibbs, J. S., Schwartz, O., Bennink, J. R., & Yewdell, J. W. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20102545 · Cited by 93
Acton, S. E., Onder, L., Novković, M., Martínez, V. G., & Ludewig, B. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.07.003 · Cited by 93
Lymph node conduits transport virions for rapid T cell activation
Reynoso, G. V., Weisberg, A. S., Shannon, J. P., McManus, D. T., Shores, L. S., Americo, J. L., Stan, R. V., Yewdell, J. W., & Hickman, H. D. (2019) · Nature Immunology · doi:10.1038/s41590-019-0342-0 · Cited by 90
Moseman, E. A., Wu, T., de la Torre, J. C., Schwartzberg, P. L., & McGavern, D. B. (2016) · Science Immunology · doi:10.1126/sciimmunol.aah3565 · Cited by 89
Self-citationPhenotypically distinct neutrophils patrol uninfected human and mouse lymph nodes
Lok, L. S. C., Dennison, T. W., Mahbubani, K., Saeb‐Parsy, K., Chilvers, E. R., & Clatworthy, M. R. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905054116 · Cited by 89
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Hughes, C. E., Benson, R. A., Bedaj, M., & Maffia, P. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00481 · Cited by 88
Antigen Presentation the Macrophage Way
Martínez‐Pomares, L., & Gordon, S. (2007) · Cell · doi:10.1016/j.cell.2007.10.046 · Cited by 88
Woodruff, M. C., Heesters, B. A., Herndon, C. N., Groom, J. R., Thomas, P. G., Luster, A. D., Turley, S. J., & Carroll, M. C. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20132327 · Cited by 90
T‐follicular helper cell differentiation and the co‐option of this pathway by non‐helper cells
Linterman, M. A., Liston, A., & Vinuesa, C. G. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01121.x · Cited by 87
Subcapsular Sinus Macrophages: The Seat of Innate and Adaptive Memory in Murine Lymph Nodes
Moran, I., Grootveld, A. K., Nguyen, A., & Phan, T. G. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.11.004 · Cited by 92
Metadata
- Authors
- Junt, T., Moseman, E. A., Iannacone, M., Massberg, S., Lang, P. A., Boes, M., Fink, K., Henrickson, S. E., Shayakhmetov, D. M., Di Paolo, N. C., van Rooijen, N., Mempel, T. R., Whelan, S. P., & von Andrian, U. H.
- Affiliations
- Harvard University (US)
- University Hospital Zurich (CH)
- Brigham and Women's Hospital (US)
- Novartis Institute For Tropical Diseases (SG)
- University of Washington (US)
- Vrije Universiteit Amsterdam (NL)
- Corresponding author
- von Andrian, Ulrich H.
- ORCID
- Venue
- Nature
- Published
- 2007-10-14
- Volume
- 450
- Issue
- 7166
- Pages
- 110-114
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2019206924
- Cited by
- 846
- References
- 29
- Citations by year
- 2026: 21 · 2025: 38 · 2024: 37 · 2023: 34 · 2022: 35 · 2021: 55 · 2020: 46 · 2019: 49 · 2018: 53 · 2017: 53 · 2016: 46 · 2015: 53 · 2014: 46 · 2013: 38 · 2012: 66
- FWCI
- 17.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- mediaTUM (Technical University of Munich) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM007753)
- National Institute of Allergy and Infectious Diseases (R01AI059371)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- subcapsular sinus macrophages, lymph node macrophages, CD169+ macrophages, viral clearance, B cell activation, antigen presentation, afferent lymph, humoral immune response, viremia, macrophage depletion
- MeSH terms
- Animals, Antibody Formation, B-Lymphocytes, Cell Line, Lymph, Lymph Nodes, Macrophages, Membrane Glycoproteins, Mice, Inbred C57BL, Receptors, Immunologic, Vesiculovirus, CD11b Antigen, Mice, Sialic Acid Binding Ig-like Lectin 1
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