Evidence map›Paper›PMID 31355456›Full record

ArticleBritish journal of pharmacology2019

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

Christine Kowalczyk-Quintas, Daniela Willen, Laure Willen, Michaela Golob, Sonia Schuepbach-Mallepell, Benjamin Peter, Mahya Eslami, Michele Vigolo, Hervé Broly, Eileen Samy and 2 more

Open access · hybridAbstract read
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Article in British journal of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 4 countries.

Christine Kowalczyk-QuintasDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Daniela WillenClinical Pharmacology, Quantitative Pharmacology, Global Early Development, Merck KGaA, Darmstadt, Germany.
Laure WillenDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Michaela GolobClinical Pharmacology, Quantitative Pharmacology, Global Early Development, Merck KGaA, Darmstadt, Germany.
Sonia Schuepbach-MallepellDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Benjamin PeterDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Mahya EslamiDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Michele VigoloDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Hervé BrolyBiotech Process Sciences, Merck KGaA, Corsier-sur-Vevey, Switzerland.
Eileen SamyEMD Serono Research & Development Institute, Inc., Billerica, MA, USA.
Özkan YalkinogluClinical Pharmacology, Quantitative Pharmacology, Global Early Development, Merck KGaA, Darmstadt, Germany.
Pascal SchneiderDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.ORCID 0000-0003-0677-9409
University of Lausanne · CHMerck (Germany) · DEMerck Serono (Switzerland) · CHOno Pharmaceutical (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe 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

resultsAtacicept 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.

Indexed as

AnimalsB-LymphocytesCell ProliferationCells, CulturedCell SurvivalCytokinesDose-Response Relationship, DrugFactor XaFemaleHEK293 CellsHeparinHumansInjections, SubcutaneousMiceMice, Inbred C57BLRecombinant Fusion ProteinsCytokinesFactor XaHeparinRecombinant Fusion ProteinsTACI receptor-IgG Fc fragment fusion protein

Identifiers

PMID31355456
PMCPMC6811742
OpenAlexW2964502948

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.