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Cytokines. --- Gene amplification. --- Genetic Techniques. --- Genetic Techniques --- Chemokines --- Cytokines

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The understanding of chemokines, the proteins that control the migration of cells, and their receptors, is critical to the study of causes and therapies for a wide range of human diseases and infections, including certain types of cancer, inflammatory diseases, HIV, and malaria. This volume, focusing on chemokine structure and function, as well as signaling, and its companion volume (Methods in Enzymology volume 461, focusing on chemokines as potential targets for disease intervention) provide a comprehensive overview and time-tested protocols in this field, making it an essential refer

Chemokines. --- Immune system. --- Immunological system --- Chemotactic cytokines --- Inflammatory peptides --- Intercrines --- Anatomy --- Immunology --- Cytokines --- Inflammation --- Peptides --- Mediators

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It is commonly acknowledged that the nervous system and the immune system, those most complex of networks, share attributes beyond their intricacy. Elements common to the two systems include memory, connectivity, flexibility and developmental selection of cellular composition by a rigorous process involving widespread programmed cell death. There is one salient difference: the cells of the immune system are predominantly in constant motion, while post-mitotic neurons and glia are largely fixed in place. Therefore, chemokines, initially characterized as leukocyte chemoattractants, have for t

Neuropathology --- Neuroimmunology. --- Chemokines. --- Chemotactic cytokines --- Inflammatory peptides --- Intercrines --- Cytokines --- Inflammation --- Peptides --- Neuroimmunomodulation --- Immunology --- Neurosciences --- Mediators

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Workshops on the mechanisms of B cell neoplasia have been organized alternatively in Bethesda and Basel since 1983. Prog­ ress in our understanding of the development and responses of B lymphocytes is presented and discussed with the aim and hope to understand what might go wrong when B lymphocytes are transformed into malignant cells. Such knowledge might lead to better diagnosis, prevention and even cure of these terri­ ble diseases. The presentations at the Bethesda workshops are published as papers in volumes of Current Topics in Microbiol­ ogy and Immunology, while the presentations and discussions in Basel were transcribed and published in Editions Roche. For the first time, a Basel workshop (held 4th-6th October 1998) that has been recorded and, in part, transcribed is being published as papers and discussions within Current Topics. This volume is the latest of a long series which documents the excitements of ground-breaking discoveries as well as the frustrations of our inability to fully understand the mechanisms leading to B cell neoplasia. The papers at the workshop are presented when possible in the sequence in which they were given. However, to facilitate the organization and reading of the book and to highlight gen­ eral topics and themes, the papers are organized into five sec­ tions: I B Cell and Plasma Cell Development II Chemokines and Chemokine Receptors III Chromosomal Translocations, DNA Rearrangements and Somatic Hypermutations IV Biology of Lymphomagenesis, B-CLL, Autoimmunity V Myeloma, Plasmacytomas and Related Subjects.

B-Lymphocytes --- Cell Transformation, Neoplastic --- Chemokines --- congresses --- Congresses --- congresses. --- Congresses. --- B cells --- Tumors --- Cancer cells --- Cell transformation --- Immunology. --- Cancer research. --- Internal medicine. --- Cancer Research. --- Internal Medicine. --- Medicine, Internal --- Medicine --- Cancer research --- Immunobiology --- Life sciences --- Serology --- B lymphocytes --- Bone marrow derived cells --- Bursa equivalent cells --- Antigen presenting cells --- Lymphocytes

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Nanoparticles (NPs) offer unique properties for biomedical applications, leading to new nanomedicines. Recent examples of advanced nanoparticle-based nanomedicines are COVID-19 RNA vaccines. Regardless of the delivery route of the NPs into the body (intravenous or subcutaneous injection, oral, intranasal, etc.), NPs inevitably come into contact with immune cells, such as macrophages. Macrophages are phagocytizing cells that determine the fate and the lifetime of NPs in relevant biological fluids or tissues, which has consequences for both nanosafety and nanomedicine. The aim of this Special Issue is to cover recent advancements in our understanding of NP–macrophage interactions, with a focus on in vitro models for nanosafety and novel nanomedicine approaches that allow the modulation of the immunological profile of macrophages. The current Special Issue compiles nine papers: seven research articles and two review articles. The original articles include studies on the interaction of different nanomaterials, such as multi-walled carbon nanotubes (MWCNTs), amorphous silica, gold nanoparticles, lipid carriers, and microspheres, with macrophages in different scenarios.

Medicine --- chronic wound --- device --- foot ulcer --- inflammation --- wound healing --- macrophage --- nanomaterial --- nanoparticle --- drug delivery --- immune system --- anti-inflammatory --- innate immunity --- osteoarthritis --- rifabutin --- nanostructured lipid carriers --- cell uptake --- Caco-2 cells --- oral administration --- Crohn’s disease --- nanomaterials --- macrophages --- class A type 1 scavenger receptors --- cytotoxicity --- macrophage–nanoparticle interaction --- monocytes --- gold nanoparticles --- in vitro models --- innate memory --- 2D cultures --- 3D cultures --- carbon nanotube --- scavenger receptor --- phagocytosis --- protein corona --- bovine serum albumin --- synthetic amorphous silica --- in vitro testing --- NR8383 alveolar macrophage --- ICP-MS analysis of cell bound SiO2 --- multi-walled carbon nanotubes --- nanoparticles --- chemokines --- transcriptomics --- zebrafish --- n/a --- Crohn's disease --- macrophage-nanoparticle interaction