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      Novel G‐CSF conjugated anionic globular dendrimer: Preparation and biological activity assessment

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          Abstract

          The most crucial role of granulocyte colony‐stimulating factor (G‐CSF) in the body is to increase the strength of immune system. In recent years, research on the use of nanoparticles in pharmaceuticals has been considered, most of which have been for drug‐loading purposes. In this study, a novel G‐CSF conjugated dendrimer was synthesized and characterized using different techniques. In vitro cytotoxicity was assessed on A549 and L929 cells, while abnormal toxicity was studied in mice. In vitro and in vivo biological activities were assessed in NFS60 cells and rats, respectively. In addition, in vivo distribution, plasma half‐life, and histopathological effect were studied in rat. The characterization tests confirmed the successful conjugation. There was no difference between G‐CSF cytotoxicity before and after conjugation, and no difference with the control group. No mice showed abnormal toxicity. Although in vitro biological activity revealed both conjugated and free G‐CSF promote proliferation cells, biological activity decreased significantly after conjugation about one‐third of the unconjugated form. Nonetheless, in vivo biological activity of conjugated G‐CSF increased by more than 2.5‐fold relative to the unconjugated form, totally. Fortunately, no histopathologic adverse effect was observed in vital rat tissues. Also, in vivo distribution of the conjugate was similar to the native protein with an enhanced terminal half‐life. Our data revealed that G‐CSF conjugated dendrimer could be considered as a candidate to improve the in vivo biological activity of G‐CSF. Moreover, multivalent capability of the dendrimer may be used for other new potentials of G‐CSF in future perspectives.

          Abstract

          Novel G‐CSF conjugated anionic globular dendrimer

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          Development of therapeutic antibodies for the treatment of diseases

          It has been more than three decades since the first monoclonal antibody was approved by the United States Food and Drug Administration (US FDA) in 1986, and during this time, antibody engineering has dramatically evolved. Current antibody drugs have increasingly fewer adverse effects due to their high specificity. As a result, therapeutic antibodies have become the predominant class of new drugs developed in recent years. Over the past five years, antibodies have become the best-selling drugs in the pharmaceutical market, and in 2018, eight of the top ten bestselling drugs worldwide were biologics. The global therapeutic monoclonal antibody market was valued at approximately US$115.2 billion in 2018 and is expected to generate revenue of $150 billion by the end of 2019 and $300 billion by 2025. Thus, the market for therapeutic antibody drugs has experienced explosive growth as new drugs have been approved for treating various human diseases, including many cancers, autoimmune, metabolic and infectious diseases. As of December 2019, 79 therapeutic mAbs have been approved by the US FDA, but there is still significant growth potential. This review summarizes the latest market trends and outlines the preeminent antibody engineering technologies used in the development of therapeutic antibody drugs, such as humanization of monoclonal antibodies, phage display, the human antibody mouse, single B cell antibody technology, and affinity maturation. Finally, future applications and perspectives are also discussed.
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            The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY

            Abstract The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been ‘forked’ from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions.
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              Granulocyte colony-stimulating factor: molecular mechanisms of action during steady state and 'emergency' hematopoiesis.

              Neutrophils are phagocytes whose principal function is to maintain anti-bacterial immunity. Neutrophils ingest and kill invading bacteria, releasing cytotoxic, chemotactic and inflammatory mediators at sites of infection. This serves to control the immediate host immune response and attract other cells, such as macrophages and dendritic cells, which are important for establishing long-term adaptive immunity. Neutrophils thus contribute to both the initiation and the maintenance of inflammation at sites of infection. Aberrant neutrophil activity is deleterious; suppressed responses can cause extreme susceptibility to infection while overactivation can lead to excessive inflammation and tissue damage. This review will focus on neutrophil regulation by granulocyte colony-stimulating factor (G-CSF), the principal cytokine controlling neutrophil development and function. The review will emphasize the molecular aspects of G-CSF-driven granulopoiesis in steady state (healthy) conditions and during demand-driven or 'emergency' conditions elicited by infection or clinical administration of G-CSF. Understanding the molecular control of granulopoiesis will aid in the development of new approaches designed to treat disorders of neutrophil production and function.
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                Author and article information

                Contributors
                cohan_r@yahoo.com
                shafieeardestani@gmail.com
                Journal
                Pharmacol Res Perspect
                Pharmacol Res Perspect
                10.1002/(ISSN)2052-1707
                PRP2
                Pharmacology Research & Perspectives
                John Wiley and Sons Inc. (Hoboken )
                2052-1707
                16 July 2021
                August 2021
                : 9
                : 4 ( doiID: 10.1002/prp2.v9.4 )
                : e00826
                Affiliations
                [ 1 ] Department of Nanobiotechnology New Technologies Research Group Pasteur Institute of Iran Tehran Iran
                [ 2 ] Faculty of Pharmacy Tehran University of Medical Sciences Tehran Iran
                [ 3 ] Biotechnology Research Center Pasteur Institute of Iran Tehran Iran
                [ 4 ] Department of Molecular Virology Pasteur Institute of Iran Tehran Iran
                [ 5 ] Department of Biotechnology, Food and Drug Control Laboratories National Food and Drug Organization Tehran Iran
                Author notes
                [*] [* ] Correspondence

                Reza Ahangari Cohan, Department of Nanobiotechnology, New Technologies Research Group, Pasteur Institute of Iran, No. 69, Pasteur street, Tehran 1316943551, Iran.

                Email: cohan_r@ 123456yahoo.com

                Mehdi Shafiee Ardestani, Faculty of Pharmacy, Tehran University of Medical Sciences, 16 Azar street, Tehran 1417614411, Iran.

                Email: shafieeardestani@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-0490-4184
                Article
                PRP2826
                10.1002/prp2.826
                8283867
                34269522
                c0bb49a3-44e6-42cb-b142-01e2f4cb477a
                © 2021 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 May 2021
                : 01 June 2021
                Page count
                Figures: 17, Tables: 0, Pages: 16, Words: 6800
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                August 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.4 mode:remove_FC converted:16.07.2021

                biodistribution,biological activity,conjugate,dendrimer,granulocyte colony‐stimulating factor,toxicity

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