Effect of natalizumab treatment on circulating plasmacytoid dendritic cells: A cross-sectional observational study in patients with multiple sclerosis
| dc.contributor.author | Kivisäkk, Pia | |
| dc.contributor.author | Francois, Katiana | |
| dc.contributor.author | Mbianda, Julvet | |
| dc.contributor.author | Gandhi, Roopali | |
| dc.contributor.author | Weiner, Howard L. | |
| dc.contributor.author | Khoury, Samia J. | |
| dc.contributor.department | Specialized Clinical Programs and Services | |
| dc.contributor.department | Abu-Haidar Neuroscience Institute (AHNI) | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T12:20:14Z | |
| dc.date.available | 2025-01-24T12:20:14Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | Objectives: Dendritic cells (DCs) serve a critical role both in promoting and inhibiting adaptive immunity. The goal of this study was to investigate the effect of natalizumab (NTZ) treatment on DC numbers, phenotype, and function in patients with multiple sclerosis (MS). Methods: Frequency and phenotype of myeloid and plasmacytoid DCs (MDCs and PDCs, respectively) were analyzed in blood from two separate cohorts of untreated, interferon-treated, or NTZ-treated MS patients. In addition, PDCs were stimulated with CpG-containing oligonucleotides or co-cultured with homologous T cells in the presence or absence of NTZ in vitro to determine functional effects of NTZ treatment. Results: We observed that NTZ treatment was associated with a 25-50% reduction in PDC frequency in peripheral blood as compared to untreated MS patients, while the frequency of MDCs was unchanged. PDCs in NTZ-treated patients displayed a mature, activated phenotype with increased expression of HLA-DR, TLR9, CCR7, IL-6 and IL-12. In contrast, in vitro treatment with NTZ did not increase markers of PDC activation or their ability to induce T cell differentiation. Conclusion: Our study shows that NTZ treatment is associated with a reduced frequency of PDCs in the peripheral circulation, but that PDCs in NTZ-treated individuals display an activated phenotype. Taken together the data suggests that transmigration of activated PDCs is preferentially affected by blockade of integrin α4 leading to an increased frequency of activated PDCs in blood. © 2014 Kivisäkk et al. | |
| dc.identifier.doi | https://doi.org/10.1371/journal.pone.0103716 | |
| dc.identifier.eid | 2-s2.0-84904981406 | |
| dc.identifier.pmid | 25075741 | |
| dc.identifier.uri | http://hdl.handle.net/10938/34208 | |
| dc.language.iso | en | |
| dc.publisher | Public Library of Science | |
| dc.relation.ispartof | PLoS ONE | |
| dc.source | Scopus | |
| dc.subject | Adult | |
| dc.subject | Aged | |
| dc.subject | Antibodies, monoclonal, humanized | |
| dc.subject | Cd4-positive t-lymphocytes | |
| dc.subject | Cell differentiation | |
| dc.subject | Cells, cultured | |
| dc.subject | Cross-sectional studies | |
| dc.subject | Dendritic cells | |
| dc.subject | Female | |
| dc.subject | Gene expression | |
| dc.subject | Humans | |
| dc.subject | Immunologic factors | |
| dc.subject | Male | |
| dc.subject | Middle aged | |
| dc.subject | Multiple sclerosis | |
| dc.subject | Young adult | |
| dc.subject | Beta interferon | |
| dc.subject | Beta1a interferon | |
| dc.subject | Cd40 antigen | |
| dc.subject | Cd83 antigen | |
| dc.subject | Chemokine receptor ccr7 | |
| dc.subject | Gamma interferon | |
| dc.subject | Hla dr antigen | |
| dc.subject | Interferon beta serine | |
| dc.subject | Interleukin 10 | |
| dc.subject | Interleukin 12 | |
| dc.subject | Interleukin 13 | |
| dc.subject | Interleukin 17 | |
| dc.subject | Interleukin 1beta | |
| dc.subject | Interleukin 23 | |
| dc.subject | Interleukin 27 | |
| dc.subject | Interleukin 4 | |
| dc.subject | Interleukin 6 | |
| dc.subject | Interleukin 9 | |
| dc.subject | Messenger rna | |
| dc.subject | Natalizumab | |
| dc.subject | Oligonucleotide | |
| dc.subject | Stat6 protein | |
| dc.subject | Toll like receptor 9 | |
| dc.subject | Transcription factor foxp3 | |
| dc.subject | Transcription factor gata 3 | |
| dc.subject | Transcription factor t bet | |
| dc.subject | Transforming growth factor beta | |
| dc.subject | Immunologic factor | |
| dc.subject | Monoclonal antibody | |
| dc.subject | Article | |
| dc.subject | Cd4+ t lymphocyte | |
| dc.subject | Cell activation | |
| dc.subject | Cell count | |
| dc.subject | Clinical article | |
| dc.subject | Coculture | |
| dc.subject | Cohort analysis | |
| dc.subject | Controlled study | |
| dc.subject | Cross-sectional study | |
| dc.subject | Drug effect | |
| dc.subject | Human | |
| dc.subject | Human cell | |
| dc.subject | In vitro study | |
| dc.subject | Lymphocyte differentiation | |
| dc.subject | Myeloid dendritic cell | |
| dc.subject | Observational study | |
| dc.subject | Phenotype | |
| dc.subject | Plasmacytoid dendritic cell | |
| dc.subject | Polarization | |
| dc.subject | Protein expression | |
| dc.subject | Regulatory t lymphocyte | |
| dc.subject | Th1 cell | |
| dc.subject | Th17 cell | |
| dc.subject | Th2 cell | |
| dc.subject | Blood | |
| dc.subject | Cell culture | |
| dc.subject | Dendritic cell | |
| dc.subject | Drug effects | |
| dc.subject | Immunology | |
| dc.subject | Physiology | |
| dc.title | Effect of natalizumab treatment on circulating plasmacytoid dendritic cells: A cross-sectional observational study in patients with multiple sclerosis | |
| dc.type | Article |
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