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Chemokine Receptor Expressions and Responsiveness of Cord Blood T Cells

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Dendritic Cell-based Immunotherapy Pulsed With Wilms Tumor 1 Peptide and Mucin 1 as an Adjuvant Therapy for Pancreatic Ductal Adenocarcinoma After Curative Resection: A Phase I/IIa Clinical Trial

Nagai, K., Adachi, T., Harada, H., Eguchi, S., Sugiyama, H., & Miyazaki, Y. (2020) · Anticancer Research · doi:10.21873/anticanres.14593 · Cited by 38

The specialized roles of immature and mature dendritic cells in antigen cross-presentation

Hopkins, R. A., & Connolly, J. E. (2012) · Immunologic Research · doi:10.1007/s12026-012-8300-z · Cited by 37

STAT3 and NF-κB are Simultaneously Suppressed in Dendritic Cells in Lung Cancer

Li, R., Fang, F., Jiang, M., Wang, C., Ma, J., Kang, W., Zhang, Q., Miao, Y., Wang, D., Guo, Y., et al. (2017) · Scientific Reports · doi:10.1038/srep45395 · Cited by 37

TGF‐β1 dampens the susceptibility of dendritic cells to environmental stimulation, leading to the requirement for danger signals for activation

Ohtani, T., Mizuashi, M., Nakagawa, S., Sasaki, Y., Fujimura, T., Okuyama, R., & Aiba, S. (2009) · Immunology · doi:10.1111/j.1365-2567.2008.02919.x · Cited by 37

Immunobiology of Genital Tract Trauma: Endocrine Regulation of HIV Acquisition in Women Following Sexual Assault or Genital Tract Mutilation

Ghosh, M., Rodríguez‐García, M., & Wira, C. R. (2012) · American Journal of Reproductive Immunology · doi:10.1111/aji.12027 · Cited by 37

CCL20 Is Negatively Regulated by TGF-β1 in Intestinal Epithelial Cells and Reduced in Crohn’s Disease Patients With a Successful Response to Mongersen, a Smad7 Antisense Oligonucleotide

Marafini, I., Monteleone, I., Dinallo, V., Fusco, D. D., Simone, V. D., Laudisi, F., Fantini, M. C., Sabatino, A. D., Pallone, F., & Monteleone, G. (2016) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjw191 · Cited by 35

Expression of CXC Chemokines and Their Receptors Is Modulated during Chondrogenic Differentiation of Human Mesenchymal Stem Cells Grown in Three-Dimensional Scaffold: Evidence in Native Cartilage

Cristino, S., Piacentini, A., Manferdini, C., Codeluppi, K., Grassi, F., Facchini, A., & Lisignoli, G. (2008) · Tissue Engineering Part A · doi:10.1089/ten.a.2007.0121 · Cited by 35

CCL20/Macrophage Inflammatory Protein 3α and Tumor Necrosis Factor Alpha Production by Primary Uterine Epithelial Cells in Response to Treatment with Lipopolysaccharide or Pam3Cys

Crane‐Godreau, M. A., & Wira, C. R. (2004) · Infection and Immunity · doi:10.1128/iai.73.1.476-484.2005 · Cited by 35

Herpes Simplex Virus Type 2–Infected Dendritic Cells Produce TNF-α, Which Enhances CCR5 Expression and Stimulates HIV Production from Adjacent Infected Cells

Marsden, V., Donaghy, H., Bertram, K. M., Harman, A. N., Nasr, N., Keoshkerian, E., Merten, S. L., Lloyd, A. R., & Cunningham, A. L. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401706 · Cited by 34

Induction of Human T Cell Leukemia Virus Type I Receptors on Quiescent Naive T Lymphocytes by TGF-β,

Jones, K. S., Akel, S. M., Petrow‐Sadowski, C., Huang, Y., Bertolette, D. C., & Ruscetti, F. W. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.7.4262 · Cited by 34

Up-regulation of CC chemokine receptor 6 on tonsillar T cells and its induction by in vitro stimulation with α-streptococci in patients with pustulosis palmaris et plantaris

Yoshizaki, T., Bandoh, N., Ueda, S., Nozawa, H., Goto, T., Kishibe, K., Takahara, M., & Harabuchi, Y. (2009) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2009.03945.x · Cited by 33

Dendritic cell-based cancer immunotherapy in the era of immune checkpoint inhibitors: From bench to bedside

Ghorbaninezhad, F., Asadzadeh, Z., Masoumi, J., Mokhtarzadeh, A., Kazemi, T., Maleki, L. A., Shotorbani, S. S., Shadbad, M. A., Baghbanzadeh, A., Hemmat, N., et al. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120466 · Cited by 34

Dendritic Cells in Cancer

Salter, R. D., & Shurin, M. R. (2009) · Springer eBooks · doi:10.1007/978-0-387-88611-4 · Cited by 32

Synergistic Induction of Apoptosis in Primary CD4+ T Cells by Macrophage-Tropic HIV-1 and TGF-β1

Wang, J., Guan, E., Roderiquez, G., & Norcross, M. A. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.6.3360 · Cited by 31

Liver-Targeting Nanoplatforms for the Induction of Immune Tolerance

Kusumoputro, S., Au, C., Lam, K. H., Park, N., Hyun, A., Kusumoputro, E., Wang, X., & Xia, T. (2023) · Nanomaterials · doi:10.3390/nano14010067 · Cited by 31

Allelic Combinations of Immune-Response Genes Associated with Glatiramer Acetate Treatment Response in Russian Multiple Sclerosis Patients

Tsareva, E., Кулакова, О. Г., Boyко, A., Shchur, S. G., Lvovs, D., Favorov, A. V., Gusev, E. I., Vandenbroeck, K., & Favorova, O. O. (2011) · Pharmacogenomics · doi:10.2217/pgs.11.136 · Cited by 26

Signaling events following chemokine receptor ligation in human dendritic cells at different developmental stages

Sato, K., Kawasaki, H., Nagayama, H., Enomoto, M., Morimoto, C., Tadokoro, K., Juji, T., & Takahashi, T. A. (2001) · International Immunology · doi:10.1093/intimm/13.2.167 · Cited by 26

TGF-β Suppresses β-Catenin-Dependent Tolerogenic Activation Program in Dendritic Cells

Lugt, B. V., Beck, Z. T., Fuhlbrigge, R. C., Hacohen, N., Campbell, J. J., & Boes, M. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020099 · Cited by 24

Effect ofEscherichia coliandLactobacillus rhamnosuson Macrophage Inflammatory Protein 3α, Tumor Necrosis Factor Alpha, and Transforming Growth Factor β Release by Polarized Rat Uterine Epithelial Cells in Culture

Crane‐Godreau, M. A., & Wira, C. R. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.1866-1873.2004 · Cited by 23

Comparative Pharmacogenetics of Multiple Sclerosis: IFN-β Versus Glatiramer Acetate

Кулакова, О. Г., Tsareva, E., Lvovs, D., Favorov, A. V., Boyко, A., & Favorova, O. O. (2014) · Pharmacogenomics · doi:10.2217/pgs.14.26 · Cited by 22

TGF-β insensitive dendritic cells: an efficient vaccine for murine prostate cancer

Wang, F.-L., Qin, W.-J., Wen, W.-H., Tian, F., Song, B., Zhang, Q., Lee, C., Zhong, W., Guo, Y.-L., & Wang, H. (2007) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-007-0322-3 · Cited by 22

Langerhans cells

Maurer, D., & Stingl, G. (2001) · Elsevier eBooks · doi:10.1016/b978-012455851-9/50044-4 · Cited by 21

Production of large numbers of Langerhans' cells with intraepithelial migration ability in vitro

Hubert, P., Bousarghin, L., Greimers, R., Franzen‐Detrooz, E., Boniver, J., & Delvenne, P. (2005) · Experimental Dermatology · doi:10.1111/j.0906-6705.2005.00299.x · Cited by 21

Chemotactic Response Toward Chemokines and Its Regulation by Transforming Growth Factor-β1 of Murine Bone Marrow Hematopoietic Progenitor Cell-Derived Different Subset of Dendritic Cells

Ogata, M., Zhang, Y., Wang, Y., Itakura, M., Zhang, Y.-Y., Harada, A., Hashimoto, S.-I., & Matsushima, K. (1999) · Blood · doi:10.1182/blood.v93.10.3225.410k25_3225_3232 · Cited by 76

The effect of TGF-β_1 to human monocyte-derived dendritic cells

Xue-guan, Z. (2005) · Chinese Clinical Oncology

Influence of maternal antibodies on vaccine responses: inhibition of antibody but not T cell responses allows successful early prime-boost strategies in mice

Siegrist, C., Barrios, C. S., Martínez, X., Brandt, C., Berney, M., Córdova, M., Kovařík, J., & Lambert, P. (1998) · European Journal of Immunology · doi:10.1002/(sici)1521-4141(199812)28:12 · Cited by 184

Receptor expression and responsiveness of human dendritic cells to a defined set of CC and CXC chemokines

Sozzani, S., Luini, W., Borsatti, A., Polentarutti, N., D, Z., D'Amico, G., Power, C. A., Wells, T. N. C., GOBBI, M. D., Allavena, P., et al. (1997) · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele

Transforming growth factor-β1 down-regulates expression of chemokine stromal cell–derived factor-1: functional consequences in cell migration and adhesion

Wright, N., de Lera, T. L., García-Moruja, C., Lillo, R., García‐Sánchez, F., Carúz, A., & Teixidó, J. (2003) · Blood · doi:10.1182/blood-2002-10-3190 · Cited by 96