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

Programming of CTL with heat-killed Brucella abortus and antigen allows soluble antigen alone to generate effective secondary CTL

Inoue, S., Golding, B., & Scott, D. E. (2004) · Vaccine · doi:10.1016/j.vaccine.2004.09.034 · Cited by 4

Recent progress in peptide vaccination in cancer with a focus on non-small-cell lung cancer

Yazdi, M. T., Keene, K., Hiemstra, P., & van der Burg, S. (2014) · Expert Review of Vaccines · doi:10.1586/14760584.2014.862499 · Cited by 5

Development of a novel immunoproteasome digestion assay for synthetic long peptide vaccine design

Wada, H., Shimizu, A., Osada, T., Tanaka, Y., Fukaya, S., & Sasaki, E. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199249 · Cited by 4

Utility of Mouse Models in Vaccine Design and Development

Bosio, C. M., MacLeod, M. K. L., Marrack, P., & Kedl, R. M. (2012) · doi:10.1002/9781118345313.ch7 · Cited by 4

Oxidative stress and type 1 diabetes

Liu, C., Mathews, C. E., & Chen, J. (2016) · Wiley eBooks · doi:10.1002/9781118832431.ch19 · Cited by 5

Immunemodulation and Cancer

Liu, J., & Huang, J. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-50977-3_3 · Cited by 3

Accurate enumeration of pathogen-specific and virtual memory CD8 T cells after infection

Berton, R. R., Heidarian, M., Kannan, S. K., Shah, M., Butler, N. S., Harty, J. T., & Badovinac, V. P. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf007 · Cited by 3

The wonderous chaperones: A highlight on therapeutics of cancer and potentially malignant disorders

Tyagi, N., & Tyagi, R. (2015) · Journal of Oral and Maxillofacial Pathology · doi:10.4103/0973-029x.164535 · Cited by 3

The Immunotherapeutic Effect of SIRP α ‐Silenced DCs against Cervical Cancer

Li, X., Zhou, W., Liang, Y., Xu, C., Xie, Z., Liang, J., & Hu, B. (2020) · Journal of Immunology Research · doi:10.1155/2020/1705187 · Cited by 3

Sarcostemma viminale activates macrophages to a pro-inflammatory phenotype

Brestovac, B., Coghlan, O., Jackaman, C., Nelson, D. J., & Townsend, D. (2014) · Comparative Clinical Pathology · doi:10.1007/s00580-014-1988-5 · Cited by 3

Adjuvants and the Initiation of T-Cell Responses

Mescher, M. F., Curtsinger, J., & Jenkins, M. K. (2006) · Humana Press eBooks · doi:10.1007/978-1-59259-970-7_4 · Cited by 3

Prevention of Type I Diabetes Mellitus: The Role of Immune Interventions

Ngugi, M. P. (2011) · Journal of Clinical & Cellular Immunology · doi:10.4172/2155-9899.s2-005 · Cited by 3

Crosspresentation: a matter of pH

Nencioni, A., & Brossart, P. (2008) · Blood · doi:10.1182/blood-2008-08-175703 · Cited by 3

Immunotherapy of brain tumors

Marshall, D., Mitchell, D. A., Graner, M. W., & Bigner, D. D. (2012) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52138-5.00020-7 · Cited by 3

Nanoparticulate carrier(s): an emerging paradigm in new generation vaccine development

Sharma, R. K., Mody, N., Dubey, S., & Vyas, S. P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-46143-6.00017-8 · Cited by 4

Osteomyelitis and Septicemia Secondary to Listeria Monocytogenes in a Young Dog

Doolittle, J. (2017) · Journal of Dairy Veterinary & Animal Research · doi:10.15406/jdvar.2017.06.00170 · Cited by 3

Antigen Presentation to Lymphocytes

Udono, H., Wang, J. O., & Watanabe, T. (2007) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0001227.pub2 · Cited by 3

APCs size up antigens

Bahjat, K. S., & Schoenberger, S. P. (2004) · Nature Medicine · doi:10.1038/nm0704-679 · Cited by 3

“One size fits it all”: translocation of foreign antigens by Yersinia type III secretion system (TTSS) leads to concomitant CD4 and CD8 T-cell priming

Rüssmann, H., & Panthel, K. (2004) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2004.03.002 · Cited by 3

Host–Pathogen Interactions

Smits, M. A., & Schokker, D. (2011) · Wiley eBooks · doi:10.1002/9780470963012.ch10 · Cited by 3

Etiology of acute myeloid leukemia following intensive therapy for AML – relapse, secondary disease or bad luck?

Braess, J., Schoch, C., Fiegl, M., Schmid, C. D., Hiddemann, W., & Kolb, H.-J. (2002) · Leukemia · doi:10.1038/sj.leu.2402772 · Cited by 3

Functional Specialization of Dendritic Cell Subsets

Heger, L., Amon, L., Lehmann, C. H. K., Barańska, A., Heidkamp, G. F., & Dudziak, D. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00257-1 · Cited by 3

Synergistic anti-tumor effects of oncolytic virus and anti-programmed cell death protein 1 antibody combination therapy: For suppression of lymph node and distant metastasis in a murine melanoma model

Sasaki, Y., Maeda, T., Hojo, M., Miura, T., Ishikawa, K., Funayama, E., Okada, K., & Yamamoto, Y. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.151011 · Cited by 2

HyperAcute Vaccines

Rossi, G. R., Vahanian, N. N., Ramsey, W. J., & Link, C. J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-394296-8.00029-4 · Cited by 2

Lewis-antigen-containing ICAM-2/3 on Jurkat leukemia cells interact with DC-SIGN to regulate DC functions

Jin, X., Bu, Q., Zou, Y., Feng, Y., & Wei, M. (2018) · Glycoconjugate Journal · doi:10.1007/s10719-018-9822-y · Cited by 2

Odour preferred males led to a higher offspring number in the common vole

Bílková, P., Vlček, J., Cvetković, T., Štefka, J., & Sedláček, F. (2024) · Mammalian Biology · doi:10.1007/s42991-024-00406-6 · Cited by 2

BDCM: a novel B‐cell line with genetic and functional similarity to dendritic cells

Kharbanda, S., Salter, R. D., Dong, X. Z., Tuma‐Warrino, R. J., & Steinman, R. A. (2002) · British Journal of Haematology · doi:10.1046/j.1365-2141.2002.03908.x · Cited by 2

Optimal conditions required for influenza A infection‐enhanced cross‐priming of CD8+ T cells specific to cell‐associated antigens

Wei, J., Waithman, J. C., Xiao, K., Oveissi, S., & Chen, W. (2013) · Immunology and Cell Biology · doi:10.1038/icb.2013.46 · Cited by 2

Ex Vivo Loading of Autologous Dendritic Cells with Tumor Antigens

Rizzo, M., Alaniz, L. D., & Mazzolini, G. D. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0345-0_5 · Cited by 2

A computational docking study on the pH dependence of peptide binding to HLA-B27 sub-types differentially associated with ankylosing spondylitis

Serçinoğlu, O., Özcan, G., Kabaş, Z. K., & Özbek, P. (2016) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-016-9934-z · Cited by 2

The Skin Immune System and Tumor Immunosurveillance

Muller, H., Halliday, G., & Woods, G. M. (2004) · CRC Press eBooks · doi:10.1201/b14248-27 · Cited by 2

Life after death: Controlling autoreactive CD8+ T-cell responses

Braciale, T. J. (2001) · Nature Medicine · doi:10.1038/89886 · Cited by 2

Adaptive Immunity to Listeria monocytogenes

Messingham, K. N., & Harty, J. T. (2007) · Springer eBooks · doi:10.1007/978-0-387-49376-3_11 · Cited by 2

Antigen Expression During Murine g-Herpesvirus Infection

Woodland, D. L., Flaño, E., Usherwood, E. J., Liu, L., Kim, I.-J., Husain, S. M., Sample, J. T., & Blackman, M. A. (2001) · Immunobiology · doi:10.1078/0171-2985-00104 · Cited by 2

Les cellules dendritiques

Voisine, C., Trinité, B., & Josien, R. (2002) · Revue Française des Laboratoires · doi:10.1016/s0338-9898(02)80179-2 · Cited by 2

Non-digestible polysaccharides to support the intestinal immune barrier: in vitro models to unravel molecular mechanisms

Tang, Y. (2017) · doi:10.18174/425674 · Cited by 2

Antigen Processing and Presentation

Eisenlohr, L. C., & Rothstein, J. L. (2007) · Springer eBooks · doi:10.1007/0-387-27545-2_1 · Cited by 2

The potential allergens in Moringa oleifera leaf proteins functionally activate murine bone marrow-derived dendritic cells and induce their differentiation toward a Th2-polarizing phenotypePreprint

Xi, C., Li, W., Liu, X., Xie, J., Li, S., Tian, Y., & Song, S. (2023) · doi:10.22541/au.168800428.85383878/v1 · Cited by 2

Fc Receptor Targeting With Recombinant Immunoglobulins and Immunoglobulin Formulations

Bot, A. I., & Smith, D. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-745-1_16 · Cited by 2

CD8+ T Cells in Multiple Sclerosis

Friese, M. A., & Fugger, L. H. (2007) · Springer eBooks · doi:10.1007/978-0-387-36003-4_13 · Cited by 2

Exploratory characterization of IgG1/IgG4 glycosylation and monocyte-derived dendritic cell responses in esophageal squamous cell carcinoma

Wang, H., Li, J., Wang, Y., Shi, Y., Tang, P., Li, Y., Gu, J., & Wang, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1832782 · Cited by 1

Dendritic Cells: From Inducers of Specific T-Cell Responses to Promoters of Angiogenesis

Coukos, G., & Benencia, F. (2009) · Springer eBooks · doi:10.1007/978-0-387-88611-4_16 · Cited by 1

CHARACTERIZATION OF DENDRITIC CELL HANDLING OF CELL-ASSOCIATED MEMBRANE AND CYTOPLASMIC PROTEINS FROM LIVE AND APOPTOTIC CELLS

Gleason, S. M. (2008) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

Efficacy of Hepatitis B Virus Surface Antigen Vaccine as a Therapeutic Tool, in Inactive Hepatitis B Virus Carriers

Montazeri, G., Farzadi, Z., Fazllolahi, A., Abedian, S., Montazeri, F., Estakhri, A., Noori, N., & Malekzadeh, R. (2005) · Cited by 1

Dendritic skin cells

Carneiro, S. C. D. S., Medeiros, R., Brollo, M. A., Ramos‐e‐Silva, M., & Sotto, M. N. (2008) · Expert Review of Dermatology · doi:10.1586/17469872.3.4.509 · Cited by 1

Cell Fusion and Dendritic Cell-Based Vaccines

Gong, J., & Koido, S. (2010) · Springer eBooks · doi:10.1007/978-90-481-9772-9_15 · Cited by 1

Transcriptional Targeting of Mature Dendritic Cells with Adenoviral Vectors via a Modular Promoter System for Antigen Expression and Functional Manipulation

Knippertz, I., Deinzer, A., Dörrie, J., Schaft, N., Nettelbeck, D. M., & Steinkasserer, A. (2016) · Journal of Immunology Research · doi:10.1155/2016/6078473 · Cited by 1

Discovery of a new dendritic cell subset derived from immature granulocytes

Geng, S. (2011) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1

Autoimmunity

Kilpatrick, T. J., Ransohoff, R. M., & Wesselingh, S. L. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195805.006 · Cited by 1

Dendritic Cell-Based Cancer Therapies: Current Status and Future Directions

Miah, S. M. S., Erick, T. K., & Emerich, D. F. (2017) · Molecular and translational medicine · doi:10.1007/978-3-319-57153-9_6 · Cited by 1

Future Directions in Dendritic Cell Research in Cancer

Dhodapkar, M. V. (2009) · Springer eBooks · doi:10.1007/978-0-387-88611-4_25 · Cited by 1

Dendritic Cells (DCs) in Innate Immunity

Kim, C.-H. (2022) · Springer eBooks · doi:10.1007/978-981-16-9081-5_2 · Cited by 1

Phagocyte-targeted Effects of Yersinia pseudotuberculosis Proteins and Their Role in Bacterial Colonization of the Liver

Dolmatova, L. S. (2024) · Gene Expression · doi:10.14218/ge.2023.00167 · Cited by 1

Divergence in CD8+ T cell epitopes of HIV -1 as an immune escape mechanism

Colleton, B. A. (2007) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

The Role of Heat Shock Protein 70 in Infection and Immunity

Rey-Ladino, J., Senok, A. C., Sarkar, A. E. H., & Al-Shedoukhy, A. A. (2015) · Heat shock proteins · doi:10.1007/978-3-319-17211-8_6 · Cited by 1

Metal Oxides and Related Nanostructures

Zhou, R. (2015) · Springer eBooks · doi:10.1007/978-3-319-15382-7_7 · Cited by 1

Principles of innate immunity

Kaisho, T., & Akira, S. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-06551-1.00016-6 · Cited by 1

Crosspresentation and Loading of Tumor Antigens for Dendritic Cell Vaccination against Cancer

Dhodapkar, M. V. (2006) · Wiley eBooks · doi:10.1002/9783527619696.ch54 · Cited by 1

Dendritic Cells in Autoimmune Diseases

Mathian, A., Koutouzov, S., Pascual, V., Palucka, A. K., & Banchereau, J. (2006) · Wiley eBooks · doi:10.1002/9783527619696.ch45 · Cited by 1

Immune cell communication in liver disease and liver regeneration

Boghal, R. H., Stephenson, B. F., & Afford, S. C. (2015) · Wiley eBooks · doi:10.1002/9781118663387.ch8 · Cited by 1

On CD4+ T Lymphocytes in Solid Tumours

Marits, P. (2007) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

In vivo splenic CD11c cells downregulate CD4 T-cell response thereby decreasing systemic immunity to gene-modified tumour cell vaccine

Cayeux, S., Bukarica, B., Buschow, C., Charo, J., Bunse, M., Dörken, B., & Blankenstein, T. J. F. (2007) · Gene Therapy · doi:10.1038/sj.gt.3303003 · Cited by 1

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

Acuto, O. (2003) · Science s STKE · doi:10.1126/stke.2003.192.pe28 · Cited by 1

Type 1 diabetes (T1D) in NOD mouse models : the role of toll-like receptor 7 and an enteric bacterial pathogen in accelerating the development of T1D

Lee, A. S.-T. (2009) · cIRcle (University of British Columbia) · doi:10.14288/1.0067201 · Cited by 1

Kupffer Cells in Immunity

Alabraba, E., & Oo, Y. H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.03003-4 · Cited by 1

Dendritic Cells in SLE

Obermoser, G., Palucka, K., Ueno, H., Banchereau, J., & Pascual, V. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-374994-9.10006-3 · Cited by 1

Sunscreens, Photoimmunosuppression, and Photoaging

Halliday, G. M., & Hönigsmann, H. (2008) · Basic and clinical dermatology · doi:10.3109/9781420080858.008 · Cited by 1

Distinct Precursors of the Dendritic Cell Subtypes

Naik, S. H. (2009) · Minerva Access (University of Melbourne) · Cited by 1

Antigen Processing and Cross‐Presentation

Pawlak, J. B., & van Kasteren, S. I. (2017) · Wiley eBooks · doi:10.1002/9780470015902.a0027590 · Cited by 1

Modelling T cell activation

Chan, C. C. W. (2002) · Cited by 1

Overview of Hematopoietic Cell Transplantation Immunology

Martin, P. J. (2003) · doi:10.1002/9780470987070.ch3 · Cited by 1

Co-stimulation Regulation of Immune Tolerance and Autoimmunity

Dong, C., Nurieva, R., & Martín‐Orozco, N. (2007) · Springer eBooks · doi:10.1007/978-0-387-36003-4_7 · Cited by 1

Identifizierung und Charakterisierung des differentiell in dendritischen Zellen exprimierten Genes PTPRO (GLEPP 1)

Samal, J. (2011)

Mécanisme d'action et fonction d'une sous-population de cellules dendritiques cytotoxiques chez le rat

Chauvin, C. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)

Pattern recognition receptors are subset specific in dendritic cells

Luber, C. A. (2009) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.12001

Qualitative und quantitative Analyse krankheitsassoziierter MHC-Klasse-I-Liganden durch massenspektrometrische Verfahren

Lemmel, C. (2004)

Regulation of immune responses by apoptotic cells

Gurung, P. (2011) · doi:10.17077/etd.hn2nz4q9

Polymorphisms in heat shock protein receptors

Muppala, V. (2009) · eDiss (Georg-August-Universität Göttingen)

Immunological and Clinical Long-Term Effects of Idiotype Vaccination in Multiple Myeloma Patients

Abdalla, A. O. (2007) · Figshare

Regulatory properties of dendritic cells and B cells in adaptive immunity

Johansson‐Lindbom, B. (2002) · Lund University Publications (Lund University)

Mechanisms of virally vectored immunocontraception

Lloyd, M. L. (2007) · UWA Profiles and Research Repository (UWA)

Antigen‐Presenting Dendritic Cells and Macrophages

Lambrecht, B. N., & Hammad, H. (2008) · Wiley eBooks · doi:10.1002/9781444300918.ch8

DENDRITIC CELLS, RAPAMYCIN AND TRANSPLANT TOLERANCE

Taner, T. (2005) · D-Scholarship@Pitt (University of Pittsburgh)

Active specific immunotherapy for solid tumors

Baars, A. (2007) · Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam)

INDUCTION OF TYPE I INTERFERONS AND VIRAL IMMUNITY

Hidmark, A. S. (2007) · Figshare

Anti-tumor and pro-tumor interactions of human NK cells in cancer

Wong, J. L. (2013) · D-Scholarship@Pitt (University of Pittsburgh)

Immune Cell Communication and Signaling Systems in Liver Disease

Bhogal, R. H., & Afford, S. C. (2009) · Springer eBooks · doi:10.1007/978-3-642-00150-5_8

The Fates of Dendritic Cells and Antigen Regulate CD4+ T Cell Responses

Ma, J. Z.-I. (2010) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.16973662.v1

A Novel Therapeutic Vaccine for Metastatic Mammary Carcinoma: Focusing MHC/Peptide Complexes to Lipid Rafts

Dolan, B. P. (2005) · doi:10.21236/ada437901

Lentivector based gene transfer for immunotherapy – application of integration deficient vectors and PDL1knockdown as tools to manipulate immune responses

Karwacz, K. (2012) · UCL Discovery (University College London)

Artificial Antigen‐Presenting Cells: Large Multivalent Immunogens

Mescher, M. F., & Curtsinger, J. (2012) · doi:10.1002/9781118345313.ch19

Analyse des Bewegungsmusters von T-Zellsubtypen im zentralen Nervensystem

Radbruch, H. (2010) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-12733

Modulación del sistema inmune por el ácido docosahexanoico: Efecto sobre la célula dendrítica.

Zapata-Gonzalez, F. (2005) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)

Vaccination in gastrointestinal cancer

Staff, C. (2014) · Figshare

Generierung und Charakterisierung von spezifischen T-Zell-Antworten gegen Pilz- und Tumorantigene

Maurer, D. (2008)

Immunobiology and Immunotherapy of Multiple Myeloma

Dhodapkar, M. V. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-564-0_11

Modulação fenotípica e funcional de células dendríticas derivadas in vitro de monócitos por contato com linfócitos preé-aquecidos e/ou irradiados.

do Carmo, J. P. M. (2008) · doi:10.11606/t.42.2008.tde-18112008-164720

The use of tetramers in the quantitative analysis of T-cell responses

Gillespie, G. M. A., Appay, V., Rowland‐Jones, S., & McMichael, A. J. (2002) · Methods in microbiology · doi:10.1016/s0580-9517(02)32090-7

Dendritic cell responses to apoptotic cells : Is there life after death?

Johansson, U. (2010) · Figshare

Human dendritic cells and hepatitis C Virus

Landi, A. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)

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