Cross-Presentation, Dendritic Cells, Tolerance and Immunity

Dendritic cells and the control of immunity

Banchereau, J., & Steinman, R. M. (1998) · Nature · doi:10.1038/32588 · Cited by 14,486

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631

A human homologue of the Drosophila Toll protein signals activation of adaptive immunity

Medzhitov, R., Preston-Hurlburt, P., & Janeway, C. A. J. (1997) · Nature · doi:10.1038/41131 · Cited by 6,137

Tolerance, Danger, and the Extended Family

Matzinger, P. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.005015 · Cited by 4,848

T-cell help for cytotoxic T lymphocytes is mediated by CD40–CD40L interactions

Schoenberger, S. P., Toes, R. E. M., van der Voort, E. I. H., Offringa, R., & Melief, C. J. M. (1998) · Nature · doi:10.1038/31002 · Cited by 2,615

Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products.

Sallusto, F., Cella, M., Danieli, C., & Lanzavecchia, A. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.2.389 · Cited by 2,501

IDENTIFICATION OF A NOVEL CELL TYPE IN PERIPHERAL LYMPHOID ORGANS OF MICE

Steinman, R. M., & Cohn, Z. A. (1973) · The Journal of Experimental Medicine · doi:10.1084/jem.137.5.1142 · Cited by 2,443

Innate Immunity: The Virtues of a Nonclonal System of Recognition

Medzhitov, R., & Janeway, C. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80412-2 · Cited by 2,434

A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell

Ridge, J. P., Rosa, F. D., & Matzinger, P. (1998) · Nature · doi:10.1038/30989 · Cited by 2,360

Dendritic cells acquire antigen from apoptotic cells and induce class I-restricted CTLs

Albert, M. L., Sauter, B., & Bhardwaj, N. (1998) · Nature · doi:10.1038/32183 · Cited by 2,350

Listeria monocytogenes: Pathogenesis and Host Response

Goldfine, H., & Shen, H. (2007) · Springer eBooks · doi:10.1007/978-0-387-49376-3 · Cited by 61

Upregulation of the CLIP self peptide on mature dendritic cells antagonizes T helper type 1 polarization

Röhn, T. A., Boes, M. L., Wolters, D. A., Spindeldreher, S., Müller, B., Langen, H., Ploegh, H. L., Vogt, A. B., & Kropshofer, H. (2004) · Nature Immunology · doi:10.1038/ni1108 · Cited by 60

Immunotherapy Via Dendritic Cells

Palucka, A. K., Laupèze, B., Aspord, C., Saito, H., Jégo, G., Fay, J. W., Paczesny, S., Pascual, V., & Banchereau, J. (2005) · Advances in experimental medicine and biology · doi:10.1007/0-387-24180-9_14 · Cited by 59

Intestinal cDC1 drive cross-tolerance to epithelial-derived antigen via induction of FoxP3 + CD8 + T regs

Joeris, T., Gómez‐Casado, C., Holmkvist, P., Tavernier, S. J., Silva-Sánchez, A., Klotz, L., Randall, T. D., Mowat, A. M., Kotarsky, K., MALISSEN, B., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abd3774 · Cited by 58

DNA vaccines: are they still just a powerful tool for the future?

Běláková, J., Horynová, M., Křupka, M., Weigl, E., & Raška, M. (2007) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-007-0044-4 · Cited by 58

Enrichment of low-molecular-weight proteins from biofluids for biomarker discovery

Chertov, O., Simpson, J. T., Biragyn, A., Conrads, T. P., Veenstra, T. D., & Fisher, R. J. (2005) · Expert Review of Proteomics · doi:10.1586/14789450.2.1.139 · Cited by 58

Mobilizing the low-avidity T cell repertoire to kill tumors

McMahan, R. H., & Slansky, J. E. (2007) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2007.06.006 · Cited by 58

Erythropoietin enhances immune responses in mice

Katz, O., Gil, L., Lifshitz, L., Prutchi‐Sagiv, S., Gassmann, M., Mittelman, M., & Neumann, D. (2007) · European Journal of Immunology · doi:10.1002/eji.200637025 · Cited by 58

Antitumor Efficacy of Radiation plus Immunotherapy Depends upon Dendritic Cell Activation of Effector CD8+ T Cells

Dovedi, S. J., Lipowska‐Bhalla, G., Beers, S. A., Cheadle, E. J., Mu, L., Glennie, M. J., Illidge, T., & Honeychurch, J. (2016) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-15-0253 · Cited by 58

The chemokine receptor CCR7 controls lymph node‐dependent cytotoxic T cell priming in alloimmune responses

Höpken, U. E., Droese, J., Li, J., Joergensen, J., Breitfeld, D., Zerwes, H., & Lipp, M. (2004) · European Journal of Immunology · doi:10.1002/eji.200324690 · Cited by 58

Regulation of cytotoxic T lymphocyte triggering by PIR-B on dendritic cells

Endo, S., Sakamoto, Y., Kobayashi, E., Nakamura, A., & Takai, T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804571105 · Cited by 57

CCL21 Cancer Immunotherapy

Lin, Y., Sharma, S. P., & John, M. A. S. (2014) · Cancers · doi:10.3390/cancers6021098 · Cited by 56

Apoptosis, tolerance, and regulatory T cells – old wine, new wineskins

Ferguson, T. A., Stuart, P. M., Herndon, J., & Griffith, T. S. (2003) · Immunological Reviews · doi:10.1034/j.1600-065x.2003.00042.x · Cited by 72

Induction of Anti-Human Immunodeficiency Virus Type 1 (HIV-1) CD8+and CD4+T-Cell Reactivity by Dendritic Cells Loaded with HIV-1 X4-Infected Apoptotic Cells

Zhao, X., Huang, X., Gupta, P., Borowski, L., Fan, Z., Watkins, S. C., Thomas, E. K., & Rinaldo, C. R. (2002) · Journal of Virology · doi:10.1128/jvi.76.6.3007-3014.2002 · Cited by 57

DC-virus interplay: a double edged sword

Larsson, M., Beignon, A., & Bhardwaj, N. (2004) · Seminars in Immunology · doi:10.1016/j.smim.2004.02.002 · Cited by 56

Nonhematopoietic antigen blocks memory programming of alloreactive CD8+ T cells and drives their eventual exhaustion in mouse models of bone marrow transplantation

Flutter, B. R., Edwards, N., Fallah‐Arani, F., Henderson, S. R., Chai, J., Sivakumaran, S., Ghorashian, S., Bennett, C. L., Freeman, G. J., Sykes, M., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41446 · Cited by 56

Activation-induced non-responsiveness (anergy) limits CD8 T cell responses to tumors

Mescher, M. F., Popescu, F. E., Gerner, M. Y., Hammerbeck, C. D., & Curtsinger, J. (2007) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2007.06.008 · Cited by 55

Cell fusion: from hybridoma to dendritic cell-based vaccine

Gong, J., Koido, S., & Calderwood, S. K. (2008) · Expert Review of Vaccines · doi:10.1586/14760584.7.7.1055 · Cited by 56

Immune Evasion Proteins of Murine Cytomegalovirus Preferentially Affect Cell Surface Display of Recently Generated Peptide Presentation Complexes

Lemmermann, N. A. W., Gergely, K. M., Böhm, V., Deegen, P., Däubner, T., & Reddehase, M. J. (2009) · Journal of Virology · doi:10.1128/jvi.02087-09 · Cited by 54

Roadmap to a Better Therapeutic Tumor Vaccine

Emens, L. A. (2006) · International Reviews of Immunology · doi:10.1080/08830180600992423 · Cited by 53

1st Class Ticket to Class I: Protein Toxins as Pathfinders for Antigen Presentation

Smith, D. C., Lord, J. M., Roberts, L. M., Tartour, É., & Johannes, L. (2002) · Traffic · doi:10.1034/j.1600-0854.2002.31001.x · Cited by 53

Dendritic Cells Transfected with Cytopathic Self-Replicating RNA Induce Crosspriming of CD8+ T Cells and Antiviral Immunity

Racanelli, V., Behrens, S., Aliberti, J., & Rehermann, B. (2004) · Immunity · doi:10.1016/s1074-7613(03)00353-4 · Cited by 53

Disruption of the C5a receptor gene fails to protect against experimental allergic encephalomyelitis

Reiman, R. M., Gerard, C. J., Campbell, I. L., & Barnum, S. R. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200204)32:4 · Cited by 53

Cross priming or direct priming: is that really the question?

Norbury, C. C., & Sigal, L. J. (2003) · Current Opinion in Immunology · doi:10.1016/s0952791502000031 · Cited by 53

Dendritic cells, DRiPs, and DALIS in the control of antigen processing

Pierre, P. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00300.x · Cited by 41

CD8α–11b+ dendritic cells but not CD8α+ dendritic cells mediate cross-tolerance toward intestinal antigens

Chung, Y., Chang, J.-H., Kweon, M., Rennert, P., & Kang, C.-Y. (2005) · Blood · doi:10.1182/blood-2004-11-4240 · Cited by 58

Ligation of the OX40 co‐stimulatory receptor reverses self‐Ag and tumor‐induced CD8 T‐cell anergy in vivo

Redmond, W. L., Gough, M. J., & Weinberg, A. D. (2009) · European Journal of Immunology · doi:10.1002/eji.200939348 · Cited by 52

Understanding Dendritic Cells and Their Role in Cutaneous Carcinoma and Cancer Immunotherapy

Yanofsky, V. R., Mitsui, H., Felsen, D., & Carucci, J. A. (2013) · Clinical and Developmental Immunology · doi:10.1155/2013/624123 · Cited by 51

Dendritic cells and isolevuglandins in immunity, inflammation, and hypertension

Dixon, K. B., Davies, S. S., & Kirabo, A. (2016) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00603.2016 · Cited by 52

Cross-Priming of Diabetogenic T Cells Dissociated from CTL-Induced Shedding of β Cell Autoantigens

Yamanouchi, J., Verdaguer, J., Han, B., Amrani, A., Serra, P., & Santamaría, P. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.12.6900 · Cited by 52

Basophils Can Directly Present or Cross-Present Antigen to CD8 Lymphocytes and Alter CD8 T Cell Differentiation into IL-10-Producing Phenotypes

Kim, S., Shen, T., & Min, B. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900332 · Cited by 52

In vivo depletion of DC impairs the anti‐tumor effect of agonistic anti‐CD137 mAb

Murillo, O., Dubrot, J., Palazón, A., Arina, A., Azpilikueta, A., Alfaro, C., Solano, S., Ochoa, M. C., Berasain, C., Gabari, I., et al. (2009) · European Journal of Immunology · doi:10.1002/eji.200838958 · Cited by 51

Trogocytosis of MHC-I/Peptide Complexes Derived from Tumors and Infected Cells Enhances Dendritic Cell Cross-Priming and Promotes Adaptive T Cell Responses

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

Biomedical Nanotechnology Using Virus-Based Nanoparticles

Destito, G., Schneemann, A., & Manchester, M. (2009) · Current topics in microbiology and immunology · doi:10.1007/978-3-540-69379-6_5 · Cited by 51

Capsid-Incorporation of Antigens into Adenovirus Capsid Proteins for a Vaccine Approach

Matthews, Q. L. (2010) · Molecular Pharmaceutics · doi:10.1021/mp100214b · Cited by 50

Gene Expression Changes in the Injured Spinal Cord Following Transplantation of Mesenchymal Stem Cells or Olfactory Ensheathing Cells

Espin, A. T., Hernández, J., & Navarro, X. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076141 · Cited by 50

Efficient scavenger receptor‐mediated uptake and cross‐presentation of negatively charged soluble antigens by dendritic cells

Shakushiro, K., Yamasaki, Y., Nishikawa, M., & Takakura, Y. (2004) · Immunology · doi:10.1111/j.1365-2567.2004.01871.x · Cited by 50

Glucosylated Nanovaccines for Dendritic Cell-Targeted Antigen Delivery and Amplified Cancer Immunotherapy

Liu, J., Cui, Y., Cabral, H., Tong, A., Yue, Q., Zhao, L., Sun, X., & Mi, P. (2024) · ACS Nano · doi:10.1021/acsnano.4c09053 · Cited by 51

Immune Tolerance Regulation Is Critical to Immune Homeostasis

Han, L., Wu, T., Zhang, Q., Qi, A., & Zhou, X. (2025) · Journal of Immunology Research · doi:10.1155/jimr/5006201 · Cited by 49

Cell death programs in Yersinia immunity and pathogenesis

Philip, N. H., & Brodsky, I. E. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00149 · Cited by 45

HIV/AIDS Vaccines: 2007

Robinson, H. L. (2007) · Clinical Pharmacology & Therapeutics · doi:10.1038/sj.clpt.6100408 · Cited by 49

Chemotactic activity of extracellular nucleotideson human immune cells.

Myrtek, D., & Idzko, M. (2007) · Purinergic Signalling · doi:10.1007/s11302-006-9032-0 · Cited by 49

New Targets and Possible New Therapeutic Approaches in the Chemotherapy of Chronic Hepatitis B

Feld, J. J., Jy, L., & Locarnini, S. (2003) · Hepatology · doi:10.1053/jhep.2003.50389 · Cited by 49

Listeria monocytogenes Infection Overcomes the Requirement for CD40 Ligand in Exogenous Antigen Presentation to CD8+ T Cells

Hamilton, S. E., Tvinnereim, A., & Harty, J. T. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.10.5603 · Cited by 49

The ratio between dendritic cells and T cells determines the outcome of their encounter: Proliferation versus deletion

Höpken, U. E., Lehmann, I., Droese, J., Lipp, M., Schüler, T., & Rehm, A. (2005) · European Journal of Immunology · doi:10.1002/eji.200526298 · Cited by 48

Differential Pattern Recognition Receptor Expression but Stereotyped Responsiveness in Rat Spleen Dendritic Cell Subsets

Hubert, F., Voisine, C., Louvet, C., Heslan, J., Ouabed, A., Heslan, M., & Josien, R. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1007 · Cited by 48

Characterization and functional analysis of skin-derived dendritic cells from swine without a requirement for in vitro propagation

Bautista, E. M., Gregg, D. A., & Golde, W. T. (2002) · Veterinary Immunology and Immunopathology · doi:10.1016/s0165-2427(02)00152-6 · Cited by 48

Development of a Murine Model of Autoimmune Thyroiditis Induced with Homologous Mouse Thyroid Peroxidase

Ng, H., Banga, J. P., & Kung, A. W. C. (2003) · Endocrinology · doi:10.1210/en.2003-0656 · Cited by 48

Selective Rac1 inhibition in dendritic cells diminishes apoptotic cell uptake and cross-presentation in vivo

Kerksiek, K. M., Niedergang, F., Chavrier, P., Busch, D. H., & Brocker, T. (2004) · Blood · doi:10.1182/blood-2004-05-1891 · Cited by 48

Multiple proteases process viral antigens for presentation by MHC class I molecules to CD8+ T lymphocytes

Val, M. D., & López, D. (2002) · Molecular Immunology · doi:10.1016/s0161-5890(02)00104-9 · Cited by 48

Tails of wonder: endocytic-sorting motifs key for exogenous antigen presentation

Lizee, G. A., Basha, G., & Jefferies, W. A. (2005) · Trends in Immunology · doi:10.1016/j.it.2005.01.005 · Cited by 47

The delivery of an antigen from the endocytic compartment into the cytosol for cross‐presentation is restricted to early immature dendritic cells

Hotta, C., Fujimaki, H., Yoshinari, M., Nakazawa, M., & Minami, M. (2005) · Immunology · doi:10.1111/j.1365-2567.2005.02270.x · Cited by 47

Dendritic Cell Aggresome-Like-Induced Structure Formation and Delayed Antigen Presentation Coincide in Influenza Virus-Infected Dendritic Cells

Herter, S., Osterloh, P., Hilf, N., Rechtsteiner, G., Höhfeld, J., Rammensee, H., & Schild, H. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.2.891 · Cited by 47

Clinical implications of antigen transfer mechanisms from malignant to dendritic cells

Arina, A., Tirapu, I., Alfaro, C., Rodrı́guez-Calvillo, M., Mazzolini, G. D., Inogés, S., López, A., Feijoó, E., Bendandi, M., & Melero, I. (2002) · Experimental Hematology · doi:10.1016/s0301-472x(02)00956-6 · Cited by 48

In vivo impact of cytomegalovirus evasion of CD8 T-cell immunity: Facts and thoughts based on murine models

Lemmermann, N. A. W., Böhm, V., Holtappels, R., & Reddehase, M. J. (2010) · Virus Research · doi:10.1016/j.virusres.2010.09.022 · Cited by 46

Detection of CD4 + - and CD8 + -T-Cell Responses to Human Papillomavirus Type 1 Antigens Expressed at Various Stages of the Virus Life Cycle by Using an Enzyme-Linked Immunospot Assay of Gamma Interferon Release

Steele, J. C., Roberts, S., Rookes, S. M., & Gallimore, P. H. (2002) · Journal of Virology · doi:10.1128/jvi.76.12.6027-6036.2002 · Cited by 46

Polyomavirus EGFP‐pseudocapsids: Analysis of model particles for introduction of proteins and peptides into mammalian cells

Bouřa, E., Liebl, D., Špíšek, R., Frič, J., Marek, M., Štokrová, J., Holáň, V., & Forstová, J. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.10.062 · Cited by 46

Nanoparticle Platforms for Antigen-Specific Immune Tolerance

Thorp, E. B., Boada, C., Jarbath, C., & Luo, X. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00945 · Cited by 45

Targeting lymph node delivery with nanovaccines for cancer immunotherapy: recent advances and future directions

Li, Y., Shen, L., Jiang, Z., Tan, K., Meng, Y., Zhang, D., & Ma, X. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-01977-1 · Cited by 48

Immunization with wild-type p53 gene sequences coadministered with Flt3 ligand induces an antigen-specific type 1 T-cell response.

Parajuli, P., Писарев, В. М., Sublet, J., Steffel, A., Varney, M. L., Singh, R. K., LaFace, D., & Talmadge, J. E. (2001) · PubMed · Cited by 45

Histone deacetylase regulation of immune gene expression in tumor cells

Khan, A. N. H., & Tomasi, T. B. (2007) · Immunologic Research · doi:10.1007/s12026-007-0085-0 · Cited by 45

Long term disease-free survival and T cell and antibody responses in women with high-risk Her2+ breast cancer following vaccination against Her2

Morse, M. A., Hobeika, A. C., Osada, T., Niedzwiecki, D., Marcom, P. K., Blackwell, K., Anders, C. K., Devi, G. R., Lyerly, H. K., & Clay, T. M. (2007) · Journal of Translational Medicine · doi:10.1186/1479-5876-5-42 · Cited by 45

An epigenetic vaccine model active in the prevention and treatment of melanoma

Khan, A. N. H., Magner, W. J., & Tomasi, T. B. (2007) · Journal of Translational Medicine · doi:10.1186/1479-5876-5-64 · Cited by 45

Perspectives: towards a peptide-based vaccine against hepatitis C virus

Hunziker, I. P., Zurbriggen, R., Glueck, R., Engler, O. B., Reichen, J., Dai, W. J., Pichler, W. J., & Cerny, A. (2001) · Molecular Immunology · doi:10.1016/s0161-5890(01)00083-9 · Cited by 45

Distinct Roles of Adenovirus Vector-Transduced Dendritic Cells, Myoblasts, and Endothelial Cells in Mediating an Immune Response against a Transgene Product

Mercier, S., Gahéry‐Ségard, H., Monteil, M., Lengagne, R., Guillet, J., Éloit, M., & Denesvre, C. (2002) · Journal of Virology · doi:10.1128/jvi.76.6.2899-2911.2002 · Cited by 44

Factors determining the spontaneous activation of splenic dendritic cells in culture

Vremec, D., O’Keeffe, M. A., Wilson, A., Ferrero, I., Koch, U., Radtke, F., Scott, B., Hertzog, P. J., Villadangos, J. A., & Shortman, K. (2010) · Innate Immunity · doi:10.1177/1753425910371396 · Cited by 44

Relationship of Enhanced Butyrate Production by Colonic Butyrate-Producing Bacteria to Immunomodulatory Effects in Normal Mice Fed an Insoluble Fraction of Brassica rapa L

Tanaka, S., Yamamoto, K., Yamada, K., Furuya, K., & Uyeno, Y. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.03343-15 · Cited by 44

Myeloid Differentiation Factor 88 Is Required for Cross-Priming In Vivo

Palliser, D., Ploegh, H. L., & Boes, M. L. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.6.3415 · Cited by 44

Update on immunopathogenesis in inflammatory myopathies

Nagaraju, K. (2001) · Current Opinion in Rheumatology · doi:10.1097/00002281-200111000-00002 · Cited by 44

Dendritic cells and autoimmunity

Bayry, J., Thirion, M., Delignat, S., Misra, N., Lacroix‐Desmazes, S., Kazatchkine, M. D., & Kaveri, S. V. (2003) · Autoimmunity Reviews · doi:10.1016/s1568-9972(03)00104-6 · Cited by 44

New approaches in vaccine development

Leclerc, C. (2003) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/s0147-9571(03)00018-3 · Cited by 44

Utilising T cell receptor transgenic mice to define mechanisms of maternal T cell tolerance in pregnancy

Moldenhauer, L. M., Hayball, J. D., & Robertson, S. A. (2010) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2010.05.007 · Cited by 43

Emerging Mechanisms of Innate Immunity and Their Translational Potential in Inflammatory Bowel Disease

Corridoni, D., Chapman, T., Ambrose, T., & Simmons, A. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00032 · Cited by 45

Reflections on the “intrathymic pathogenesis” of myasthenia gravis

Hohlfeld, R., & Wekerle, H. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.05.020 · Cited by 43

Combining the Antigen Processing Components TAP and Tapasin Elicits Enhanced Tumor-Free Survival

Lou, Y., Basha, G., Seipp, R. P., Cai, B., Chen, S. S., Moise, A. R., Jeffries, A. P., Gopaul, R., Vitalis, T. Z., & Jefferies, W. A. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-1066 · Cited by 43

Inefficient Cross-Presentation Limits the CD8+ T Cell Response to a Subdominant Tumor Antigen Epitope

Otáhal, P., Hutchinson, S. C., Mylin, L. M., Tevethia, M. J., Tevethia, S. S., & Schell, T. D. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.2.700 · Cited by 43

Immunology of β-Cell Destruction

Torre, D. L., & Lernmark, Å. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-3271-3_24 · Cited by 43

The role of endosomes in innate and adaptive immunity

Gleeson, P. A. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.03.002 · Cited by 47

The ins and outs of cross-presentation

Rock, K. L. (2003) · Nature Immunology · doi:10.1038/ni1003-941 · Cited by 42

Dendritic cells in the initiation of immune responses against central nervous system-derived antigens

Kármán, J. (2004) · Immunology Letters · doi:10.1016/j.imlet.2003.10.017 · Cited by 42

Overcoming immune tolerance to cancer by heat shock protein vaccines.

Liu, B., DeFilippo, A. M., & Li, Z. (2002) · PubMed · Cited by 42

Differential Ability of Surface and Endosomal TLRs To Induce CD8 T Cell Responses In Vivo

Mandraju, R., Murray, S. E., Forman, J., & Pasare, C. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302244 · Cited by 41

Dissecting the Multiplicity of Immune Effects of Immunosuppressive Drugs to Better Predict the Risk of de novo Malignancies in Solid Organ Transplant Patients

Cangemi, M., Montico, B., Faè, D. A., Steffan, A., & Dolcetti, R. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00160 · Cited by 44

High-level expression of B7-H1 molecules by dendritic cells suppresses the function of activated T cells and desensitizes allergen-primed animals

Kim, H. K., Guan, H., Zu, G., Li, H. J., Wu, L., Xu, F., Elmets, C. A., Fu, Y., & Xu, H. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0805436 · Cited by 41

MyD88 Expression Is Required for Efficient Cross-Presentation of Viral Antigens from Infected Cells

Chen, M., Barnfield, C., Näslund, T. I., Fleeton, M. N., & Liljeström, P. (2005) · Journal of Virology · doi:10.1128/jvi.79.5.2964-2972.2005 · Cited by 41

Spontaneous or Mycobacterium tuberculosis‐induced apoptotic neutrophils exert opposite effects on the dendritic cell‐mediated immune response

Alemán, M., de la Barrera, S., Schierloh, P., Yokobori, N. K., Baldini, M., Musella, R. M., Abbate, E. H., & Sasiain, M. D. C. (2007) · European Journal of Immunology · doi:10.1002/eji.200636771 · Cited by 40

Myosin II Synergizes with F-Actin to Promote DNGR-1-Dependent Cross-Presentation of Dead Cell-Associated Antigens

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