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      No interactions between heparin and atacicept, an antagonist of B cell survival cytokines

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          Abstract

          Background and Purpose

          The TNF family ligands, B cell activating factor of the TNF family (BAFF, also known as B lymphocyte stimulator, BLyS) and a proliferation‐inducing ligand (APRIL), share the transmembrane activator and calcium‐modulator and cyclophilin ligand (CAML)‐interactor (TACI) as one of their common receptors. Atacicept, a chimeric recombinant TACI/IgG1‐Fc fusion protein, inhibits both ligands. TACI and APRIL also bind to proteoglycans and to heparin that is structurally related to proteoglycans. It is unknown whether the portion of TACI contained in atacicept can bind directly to proteoglycans, or indirectly via APRIL, and whether this could interfere with the anti‐coagulant properties of heparin.

          Experimental Approach

          Binding of atacicept and APRIL to proteoglycan‐positive cells was measured by FACS. Activities of heparin and atacicept were measured with activated factor Xa inhibition and cell‐based assays. Effects of heparin on circulating atacicept was monitored in mice.

          Key Results

          Atacicept did not bind to proteoglycan‐positive cells, but when complexed to APRIL could do so indirectly via APRIL. Multimers of atacicept obtained after exposure to cysteine or BAFF 60‐mer bound directly to proteoglycans. Atacicept alone, or in complex with APRIL, or in a multimeric form did not interfere with heparin activity in vitro. Conversely, heparin did not influence inhibition of BAFF and APRIL by atacicept and did not change circulating levels of atacicept.

          Conclusions and Implications

          Lack of detectable interference of APRIL‐bound or free atacicept on heparin activity makes it unlikely that atacicept at therapeutic doses will interfere with the function of heparin in vivo.

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          Most cited references25

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          Experimental design and analysis and their reporting II: updated and simplified guidance for authors and peer reviewers.

          This article updates the guidance published in 2015 for authors submitting papers to British Journal of Pharmacology (Curtis et al., 2015) and is intended to provide the rubric for peer review. Thus, it is directed towards authors, reviewers and editors. Explanations for many of the requirements were outlined previously and are not restated here. The new guidelines are intended to replace those published previously. The guidelines have been simplified for ease of understanding by authors, to make it more straightforward for peer reviewers to check compliance and to facilitate the curation of the journal's efforts to improve standards.
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            BAFF, a Novel Ligand of the Tumor Necrosis Factor Family, Stimulates B Cell Growth

            Members of the tumor necrosis factor (TNF) family induce pleiotropic biological responses, including cell growth, differentiation, and even death. Here we describe a novel member of the TNF family, designated BAFF (for B cell activating factor belonging to the TNF family), which is expressed by T cells and dendritic cells. Human BAFF was mapped to chromosome 13q32-34. Membrane-bound BAFF was processed and secreted through the action of a protease whose specificity matches that of the furin family of proprotein convertases. The expression of BAFF receptor appeared to be restricted to B cells. Both membrane-bound and soluble BAFF induced proliferation of anti-immunoglobulin M–stimulated peripheral blood B lymphocytes. Moreover, increased amounts of immunoglobulins were found in supernatants of germinal center–like B cells costimulated with BAFF. These results suggest that BAFF plays an important role as costimulator of B cell proliferation and function.
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              Demystifying heparan sulfate-protein interactions.

              Numerous proteins, including cytokines and chemokines, enzymes and enzyme inhibitors, extracellular matrix proteins, and membrane receptors, bind heparin. Although they are traditionally classified as heparin-binding proteins, under normal physiological conditions these proteins actually interact with the heparan sulfate chains of one or more membrane or extracellular proteoglycans. Thus, they are more appropriately classified as heparan sulfate-binding proteins (HSBPs). This review provides an overview of the various modes of interaction between heparan sulfate and HSBPs, emphasizing biochemical and structural insights that improve our understanding of the many biological functions of heparan sulfate.
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                Author and article information

                Contributors
                pascal.schneider@unil.ch
                Journal
                Br J Pharmacol
                Br. J. Pharmacol
                10.1111/(ISSN)1476-5381
                BPH
                British Journal of Pharmacology
                John Wiley and Sons Inc. (Hoboken )
                0007-1188
                1476-5381
                15 October 2019
                October 2019
                15 October 2019
                : 176
                : 20 ( doiID: 10.1111/bph.v176.20 )
                : 4019-4033
                Affiliations
                [ 1 ] Department of Biochemistry University of Lausanne Epalinges Switzerland
                [ 2 ] Clinical Pharmacology, Quantitative Pharmacology, Global Early Development Merck KGaA Darmstadt Germany
                [ 3 ] EMD Serono Research & Development Institute, Inc. Billerica MA USA
                [ 4 ] Biotech Process Sciences Merck KGaA Corsier‐sur‐Vevey Switzerland
                Author notes
                [*] [* ] Correspondence

                Pascal Schneider, Department of Biochemistry, University of Lausanne, Boveresses 155, CH‐1066, Epalinges, Switzerland

                Email: pascal.schneider@ 123456unil.ch

                Author information
                https://orcid.org/0000-0003-0677-9409
                Article
                BPH14811 2018-BJP-1430-RP.R1
                10.1111/bph.14811
                6811742
                31355456
                2ad84549-9935-4477-93c6-f8e40109607c
                © 2019 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

                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
                : 09 November 2018
                : 29 May 2019
                : 05 July 2019
                Page count
                Figures: 6, Tables: 1, Pages: 15, Words: 8638
                Funding
                Funded by: Merck KGaA , open-funder-registry 10.13039/100009945;
                Funded by: Swiss National Science Foundation , open-funder-registry 10.13039/501100001711;
                Award ID: 310030A_176256
                Categories
                Research Paper
                Research Papers
                Custom metadata
                2.0
                October 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.0 mode:remove_FC converted:24.10.2019

                Pharmacology & Pharmaceutical medicine
                Pharmacology & Pharmaceutical medicine

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