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 14,496

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 5,107

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

Toll-like Receptors - Link between Innate and Adaptive Immunity

Braedel-Ruoff, S. (2007)

Engineering Adult Stem Cells for Cancer Immunotherapy

Burnside, W. M., & Cui, Y. R. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0170-5_11

Phagocytes Part 1: Macrophages

Brown, G. D., & Gordon, S. (2010) · doi:10.1002/9780470688618.taw0084

Development of CTL-based liposomal vaccines

Uchida, T. (2010) · Drug Delivery System · doi:10.2745/dds.25.29

Mechanistic studies on long peptide based vaccins for the use in cancer therapy.

Bijker, M. S. (2007) · Leiden Repository (Leiden University)

NK cell and dendritic cell interactions in innate immune responses

Persson, C. M. (2009) · Figshare

Dendritic Cells in Transplantation: Origin, Immune Activation, and Allograft Tolerance

Swanson, K. A., & Wilkes, D. S. (2004) · Springer eBooks · doi:10.1007/978-1-4419-8999-4_12

HER2/neu-specific Breast Cancer Vaccine

Chen, Y. (2013) · University Library - University of Saskatchewan (University of Saskatchewan)

Dendritic Cells Loaded with Tumor B Cells Elicit Broad Immunity against Murine Gammaherpesvirus 68 but Fail To Prevent Long-Term Latency

Weslow-Schmidt, J. L., Ye, F., Cush, S. S., Stuller, K. A., Blackman, M. A., & Flaño, E. (2010) · Journal of Virology · doi:10.1128/jvi.00571-10

Dendritic Cell Vaccines

Dhodapkar, M. V. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-680-5_21

Monocyte-Derived Dendritic Cells: A Promising Armament for Immunotherapy in Human Malignancies

Yi, Q., & Kwak, L. W. (2005) · Clinical Cancer Research · doi:10.1158/1078-0432.966.11.3

Dissertation zur Erlangung des Doktorgrades der Fakultät für Chemie und Pharmazie der Ludwig-Maximilians-Universität München Pattern recognition receptors are subset specific in dendritic cells In vivo quantitative proteomic investigations using label-free analysis and the SILAC mouse

Luber, C. A. (2009)

FVIII Immunity: Early Events and Tolerance Mechanisms to FVIII

Qadura, M. (2008) · QSpace (Queen's University Library)

Vaccination in gastrointestinal cancer

Liljefors, M. G., Sundqvist, K., Mellstedt, H., Ullén, D. H., & Mattsson, D. J. (2014)

Immunothérapie : espoirs et réalités

Chouaı̈b, S., Hage, F. E., Benlalam, H., & Mami‐Chouaib, F. (2006)

Hematopoiesis, including lymphocyte development and maturation

Quesniaux, V. F. J., Down, J. D., & Schuurman, H. (2006) · Birkhäuser-Verlag eBooks · doi:10.1007/3-7643-7408-x_1

Aus der Universitätsklinik für Kinder- und Jugendmedizin Tübingen Abteilung Kinderheilkunde I mit Poliklinik (Schwerpunkt: Allgemeine Pädiatrie, Hämatologie und Onkologie)

Direktor, Ä., & Handgretinger, R. (2010)

Listeria monocytogenesInfection of Mice: an Elegant Probe To Dissect Innate and T-Cell Immune Responses

Haring, J. S., & Harty, J. T. (2014) · ASM Press eBooks · doi:10.1128/9781555816513.ch50

A new TLR2 agonist is able to promote cross-presentation

Santone, M. (2013) · Padua@research (University of Padova)

Tumor-Induced Immune Suppression and Immune Escape

Campoli, M. R., & Ferrone, S. (2006) · Humana Press eBooks · doi:10.1385/1-59745-011-1:263

Two novel mechanisms of MHC class I down-regulation in human cancer: accelerated degradation of TAP-1 mRNA and disruption of TAP-1 protein function

Yang, T. (2004) · OhioLink ETD Center (Ohio Library and Information Network)

Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70

Chan, T. H. M. (2006) · University Library - University of Saskatchewan (University of Saskatchewan)

Comparison with Sarcoidosis

Bezuidenhout, J. (2005)

Generierung und Charakterisierung einer kontinuierlich proliferierenden dendritischen Zelllinie der NOD-Maus

Scherbaum, W. A. (2003)

JOÃO PAULO MARTINS DO CARMO MODULAÇÃO FENOTÍPICA E FUNCIONAL DE CÉLULAS DENDRÍTICAS DERIVADAS DE MONÓCITOS HUMANOS IN VITRO POR CONTATO COM LINFÓCITOS PRÉ-AQUECIDOS E/OU IRRADIADOS

Paulo, S. (2008)

The killing project : increasing the efficiency of cytotoxic T lymphocyte in killing cytomegalovirus-infected cells in an in vitro setting

Ferguson, H. A. (2011)

Nanomedicine: Implications from Nanotoxicity

Zhou, R. (2015) · Springer eBooks · doi:10.1007/978-3-319-15382-7_9

CD8+T cell-mediated autoimmune diseases of the CNS

Walter, L. M., & Albert, M. L. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195805.008

Principles of innate immunity

Kaisho, T., & Akira, S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-09138-1.00016-4

Immunotherapy of Neuroendocrine Tumors

Seißler, J., Schott, M., & Scherbaum, W. A. (2004) · Informa Healthcare eBooks · doi:10.1201/9780203021941.ch35

IMMUNOGENIC PROPERTIES OF CALICIVIRUS-LIKE PARTICLES AS VACCINE VECTORS

Crisci, E. (2011) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Effekte von Prostaglandin E2 und EP-Rezeptoragonisten auf die Ausreifung, Antigenaufnahme und Antigenpräsentation von humanen Monozyten-abgeleiteten dendritischen Zellen

München, K. D. L.-M.-U. (2010)

Dendritic cell-based tumor vaccination for high-grade gliomas

Ardon, H. (2011)

Increased endogenous antigen presentation in the periphery enhances susceptibility to inflammation‐induced gastric autoimmunity in mice

Overall, S. A., Bourges, D., van Driel, I. R., & Gleeson, P. A. (2016) · European Journal of Immunology · doi:10.1002/eji.201646572

An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo

Dunbar, E. M. (2007)

Investigating Antigen Presentation by Inactivated Lymphocytic Choriomeningitis Virus and by Baculovirus Encoding the LCMV-Nucleoprotein

Spence, T. F. (2009) · QSpace (Queen's University Library)

The impact of lifelong viral infection on development and maintenance of memory CD8+ T cells

Lang, A. M. (2007) · doi:10.6083/m4v9863j

Pathways of paternal antigen presentation to initiate antigen-specific immune responses in pregnancy.

Moldenhauer, L. M. (2008) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

33D1+ Dendritic Cells in Tolerance and Immunity

Stolley, J. M. (2016) · ResearchWorks at the University of Washington (University of Washington)

Caractérisation des cellules microgliales adultes et de leur potentiel en immunothérapie des tumeurs cérébrales

Donnou, S., & Couez, D. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)

Functional Dissection of Lupus Susceptibility Loci on the New Zealand Black Mouse Chromosome 1

Cheung, Y. H. (2010) · TSpace (University of Toronto)

Mesenchymal stem cells in inflammatory bowel disease and cancer

Miller, S. (2017) · Victoria University Research Repository (Victoria University)

Double Face of eHsp70 in Front of Different Situations

Barreca, M. M., & Geraci, F. (2018) · Heat shock proteins · doi:10.1007/978-3-319-89551-2_7

Principles of the Immune System Central to Transfusion Medicine

Geiger, T. L. (2007) · Elsevier eBooks · doi:10.1016/b978-0-443-06981-9.50007-7

Principles of Tumor Immunology

Bonavida, B. (2006) · Elsevier eBooks · doi:10.1016/b978-012088393-6/50072-5

New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes

Selck, C. (2018) · Minerva Access (University of Melbourne)

The Role of Tumour Necrosis Factor Receptor Family Members CD137 (4-1BB) and CD30 in Antiviral T Cell Responses

Zhou, A. (2018) · TSpace (University of Toronto)

Dendritic Cells

Pulendran, B., Agrawal, A., Dillon, S. M., & Agrawal, S. (2006) · Humana Press eBooks · doi:10.1007/978-1-59259-970-7_2

The Role of Human Dendritic Cell Subsets in Antitumor Immunity

马, 莉. (2020) · Advances in Clinical Medicine · doi:10.12677/acm.2020.103037

HIV vaccines

Peters, B. S. (2010) · Elsevier eBooks · doi:10.1016/b978-0-323-04579-7.00087-3

The Role of Lymphatic Endothelial Cells in T Cell Tolerance

Rouhani, S. J. (2014) · doi:10.18130/v3q83q

High-Grade Gliomas: Dendritic Cell Therapy

Ardon, H., Vleeschouwer, S. D., Calenbergh, F. V., & Gool, S. W. V. (2011) · Springer eBooks · doi:10.1007/978-94-007-0618-7_32

Faculty Opinions recommendation of In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens.

Jensen, P. E. (2002) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1006428.122658

Generierung dendritischer Zellen zur Tumorimmuntherapie: Differenzierung, Antigenbeladung und Reifung innerhalb von 48 Stunden

Obermaier, B. (2005) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.4523

Faculty Opinions recommendation of Chloroquine enhances human CD8+ T cell responses against soluble antigens in vivo.

Adorini, L. (2005) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1028072.336029

Synergistic Anti-Tumor Efficacy of Hollow Mesoporous Silica-Based Cancer Vaccine and Immune Checkpoint Inhibitor at Local SitePreprint

Wang, X., Li, X., Ito, A., Sogo, Y., & Ohno, T. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3979935

Intradermal Vaccination

Zaric, M., & Kissenpfennig, A. (2015) · Wiley eBooks · doi:10.1002/9781118734506.ch4

Faculty Opinions recommendation of Dendritic cells induce peripheral T cell unresponsiveness under steady state conditions in vivo.

Gleeson, P. A. (2001) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1000913.16210

Faculty Opinions recommendation of Marginating dendritic cells of the tumor microenvironment cross-present tumor antigens and stably engage tumor-specific T cells.

Hurwitz, A. A. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.714797904.793453800

Cross‐Presentation

(2004) · Encyclopedic Dictionary of Genetics, Genomics and Proteomics · doi:10.1002/0471684228.egp02899

Faculty Opinions recommendation of Marginating dendritic cells of the tumor microenvironment cross-present tumor antigens and stably engage tumor-specific T cells.

Kaech, S. M., & Ho, P. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.714797904.793462775

Loss of Transgene following ex vivo Gene Transfer is Associated with a Dominant Th2 Response: Implications for Cutaneous Gene Therapy

Lu, Z., & Ghazizadeh, S. (2007) · Molecular Therapy · doi:10.1038/sj.mt.6300086

The Immune Interaction between HIV-1 Infection andMycobacterium tuberculosis

Bruyn, E. D., & Wilkinson, R. J. (2017) · ASM Press eBooks · doi:10.1128/9781555819569.ch12

T Cell-Dendritic Cell Interaction in Vivo: Random Encounters Favor Development of Long-Lasting Ties

Acuto, O. (2003) · Science Signaling · doi:10.1126/scisignal.1922003pe28

Faculty Opinions recommendation of Induction of tumor-specific T cell immunity by anti-DR5 antibody therapy.

Engwerda, C. R. (2004) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1019328.218485

Cell-Mediated Immunity

Kamperschroer, C., Collinge, M., Heyen, J. R., Ji, C., O’Donnell, L. M., & Zhu, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00104-2

PI3Kδ Bridges Microbial Surveillance with Antigen Presentation to Reinforce Intestinal ImmunityPreprint

Gonzalez-Nuñez, M., Vasconcellos, L. R. C., Garrido‐Mesa, J., Silva, R. C. M. C., Hachani, A., Agudo, A. B., Simeoli, R., Gonzalez, L. M., Filloux, A., Welch, H. C. E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.13.653657

Recent Advances in Host Immune Mechanisms Against Listeria monocytogenes Infection

Shang, L., Xiang, W., Lun, M., Qu, S., Yin, Y., Ya, X., Zhou, Y.-Q., Zhu, P., & Song, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s535302

Kupffer Cells in Immunity

Alabraba, E., & Oo, Y. H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00526-3

Dendritic cell vaccination and optimal antigen presentation

Noorbergen, T. P. (2014) · Utrecht University Repository (Utrecht University)

To cleave or not to cleave - Das Schnittverhalten des 20S-Proteasoms : von der in vitro Analyse zur in silico Modellierung

Tenzer, S. (2004)

Evaluation and characterization of the capability of dendritic cells generated by exposure of human peripheral blood monocytes to GM-CSF and IFN-alpha of inducing CD8 T cell priming and TH1 polarization

Accademico, A., & Ferrantini, M. (2008)

Dendritic Cell and Pathogen Interactions in the Subversion of Protective Immunity

Connolly, J. E., Chaussabe, D., & Banchereau, J. (2007) · Springer eBooks · doi:10.1007/978-0-387-33785-2_3

Activation of CD8+ and CD4+ T cells in response to self-antigen : from the lymphoid tissue to the target organ

Espinosa-Carrasco, G. (2016) · theses.fr (ABES) · doi:10.70675/f4c31cbcz110ez48dbza3eaz9a7512ef00fe

Il-26 : une cytokine pro-inflammatoire stimulant les cellules immunitaires innées myéloïdes

Poli, C. (2017) · theses.fr (ABES) · doi:10.70675/154b0002zc293z47a9z8bfbz9909e15c15e6

Infections virales par l’Hépatite E et Zika : pathogenèse à l’interface mère-fœtus et rôle de la réponse immune

Gouilly, J. (2018) · theses.fr (ABES) · doi:10.70675/e8f87c4fz838ez4254zafdazcc06fa9ee7ea

Cancer immunotherapy: Pros, cons, and beyond

Natarajan, K., Natarajan, K., Rajaram, G., Arulsamy, S., & Babu, D. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-41551-7.00007-2

Development and validation of an in vitro model of dendritic cell identification and activation

Clark, A. (2008) · SUNScholar (Stellenbosch University)

Modulation of phosphoinositide metabolism by intracellular pathogenic bacteria Listeria monocytogenes

Wang, J. (2012) · Research Explorer (The University of Manchester)

Cytokines and tuberculosis : an investigation of tuberculous lung tissue and a comparison with sarcoidosis

Bezuidenhout, J. (2005) · SUNScholar (Stellenbosch University)

Untitled work

Kalina (2002) · doi:10.1002/1521-4141(200209)32:9

Cross-presentation by dendritic cells

Joffre, O. P., Segura, É., Savina, A., & Amigorena, S. (2012) · Nature reviews. Immunology · doi:10.1038/nri3254 · Cited by 1,764

Regulation of Antigen Presentation and Cross-Presentation in the Dendritic Cell Network: Facts, Hypothesis, and Immunological Implications

Wilson, N. S., & Villadangos, J. A. (2005) · Advances in immunology · doi:10.1016/s0065-2776(04)86007-3 · Cited by 181

Cross‐presentation: underlying mechanisms and role in immune surveillance

Rock, K. L., & Shen, L. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00301.x · Cited by 469

The evolving biology of cross-presentation

Ohara, R. A., & MURPHY, K. M. M. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101711 · Cited by 37

Cross-Presentation of Antigens by Dendritic Cells

Heath, W. R., Carbone, F., & Belz, G. T. (2002) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.v22.i5-6.50 · Cited by 70