Search Results - "Raes, G."
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Antigen-presenting cell-targeted lentiviral vectors do not support the development of productive T-cell effector responses: implications for in vivo targeted vaccine delivery
Published in Gene therapy (01-06-2017)“…Targeting transgene expression specifically to antigen-presenting cells (APCs) has been put forward as a promising strategy to direct the immune system towards…”
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Evaluation of single domain antibodies as nuclear tracers for imaging of the immune checkpoint receptor human lymphocyte activation gene-3 in cancer
Published in EJNMMI research (02-11-2021)“…Recent advancements in the field of immune-oncology have led to a significant increase in life expectancy of patients with diverse forms of cancer, such as…”
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3
Development of the Nanobody display technology to target lentiviral vectors to antigen-presenting cells
Published in Gene therapy (01-12-2012)“…Lentiviral vectors (LVs) provide unique opportunities for the development of immunotherapeutic strategies, as they transduce a variety of cells in situ ,…”
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Claudin-1, Claudin-2 and Claudin-11 Genes Differentially Associate with Distinct Types of Anti-inflammatory Macrophages In vitro and with Parasite- and Tumour-elicited Macrophages In vivo
Published in Scandinavian journal of immunology (01-06-2012)“…Macrophages altered by various Th2‐associated and anti‐inflammatory mediators – including IL‐4 and IL‐13 [inducing alternatively activated macrophages (AAMs)],…”
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Development of LAG-3 nanobodies as potent cancer imaging tracers
Published in Annals of oncology (01-12-2019)Get full text
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6
Heterogeneity of macrophage activation in fish
Published in Developmental and comparative immunology (01-12-2011)“…In this review, we focus on four different activation states of fish macrophages. In vitro, stimulation with microbial ligands induces the development of…”
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Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a)
Published in Journal of medical genetics (1992)“…We aimed to estimate the size of the duplication using additional polymorphic DNA markers located in 17p11.2-p12. Two other 17p11.2 markers, pVAW412R3…”
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Arginase-1 and Ym1 are markers for murine, but not human, alternatively activated myeloid cells
Published in The Journal of immunology (1950) (01-06-2005)Get full text
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9
A locus-specific mutation database for the neural cell adhesion molecule L1CAM (Xq28)
Published in Human mutation (1996)Get full text
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10
Alternatively activated macrophages during parasite infections
Published in Trends in parasitology (01-03-2004)“…Depending on the cytokine environment, macrophages can differentiate into distinct subsets that perform specific immunological roles. In this regard, the…”
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Alternatively activated macrophages in protozoan infections
Published in Current Opinion in Immunology (01-08-2007)“…A type 1 cytokine-dependent pro-inflammatory response inducing classically activated macrophages is crucial for parasite control during protozoan infections…”
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Active antitumor immunotherapy, with or without B7-mediated costimulation, increases tumor progression in an immunogenic murine T cell lymphoma model
Published in Cancer Immunology, Immunotherapy (01-01-1998)“…BW-Sp3 is a BW-5147-derived T cell lymphoma with limited immunogenicity since, despite regression of the majority of subcutaneous tumors, an important fraction…”
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Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages
Published in Journal of leukocyte biology (01-04-2002)“…Alternatively activated macrophages (aaMφ) display molecular and biological characteristics that differ from those of classically activated macrophages (caMφ)…”
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14
Effects of altered antigen processing on T-cell responses toward murine T-lymphomas
Published in Advances in experimental medicine and biology (1998)Get more information
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15
Macrophage galactose-type C-type lectins as novel markers for alternatively activated macrophages elicited by parasitic infections and allergic airway inflammation
Published in Journal of leukocyte biology (01-03-2005)“…Molecular markers, especially surface markers associated with type II, cytokine‐dependent, alternatively activated macrophages (aaMF), remain scarce. Besides…”
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Reactive Oxygen Species and 12/15-Lipoxygenase Contribute to the Antiproliferative Capacity of Alternatively Activated Myeloid Cells Elicited during Helminth Infection
Published in The Journal of immunology (1950) (15-05-2005)“…Understanding the role of CD11b(+)GR-1(+) myeloid suppressor cells in the immune suppression and immunoregulation associated with a variety of diseases may…”
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17
The Man and Machine Robot Orchestra at Logos
Published in Computer music journal (01-12-2011)“…This article provides an overview of the various automata of the Man and Machine robot orchestra found at the Logos Foundation in Ghent, Belgium. The…”
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18
African trypanosomosis: From immune escape and immunopathology to immune intervention
Published in Veterinary parasitology (19-08-2007)“…African trypanosomes can cause prolonged chronic infections through a mechanism of antigen variation whereby they manipulate the humoral immune system of their…”
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Nitric Oxide-Independent CTL Suppression during Tumor Progression: Association with Arginase-Producing (M2) Myeloid Cells
Published in The Journal of immunology (1950) (15-05-2003)“…Most of the mice bearing a s.c. BW-Sp3 lymphoma tumor mount a CD8(+) T cell-mediated response resulting in tumor regression. Nonetheless, tumor progression…”
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The dermal microenvironment induces the expression of the alternative activation marker CD301/mMGL in mononuclear phagocytes, independent of IL-4/IL-13 signaling
Published in Journal of leukocyte biology (01-10-2006)“…Recently, we have shown that mononuclear phagocytes comprise the majority of interstitial cells in the mouse dermis, as indicated by their phenotypic and…”
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