Evidence map›Paper›PMID 41137641›Full record

ArticleAmerican journal of hematology2026

Protein S Enhances the Phagocytosis of Phosphatidylserine-Exposing Erythrocytes: Implications in Sickle Cell Disease.

Claire Auditeau, Aurélie Fricot, Raphaël Gauthier, Abdoulaye Sissoko, Zeynep Cacan, Céline Gounou, Laure Joseph, Sandra Manceau, Slimane Allali, Michael Dussiot and 17 more

Abstract read
In one paragraph

Article in American journal of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

27 authors.

Claire AuditeauHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.ORCID 0000-0002-8499-1862
Aurélie FricotUniversité Paris Cité, INSERM, BIGR, Paris, France.
Raphaël GauthierUniversité Paris Cité, INSERM, BIGR, Paris, France.
Abdoulaye SissokoUniversité Paris Cité, INSERM, BIGR, Paris, France.
Zeynep CacanUniversité Paris Cité, INSERM, BIGR, Paris, France.
Céline GounouUMR-CBMN, CNRS-Université de Bordeaux-IPB, Pessac, France.
Laure JosephDepartment of Biotherapy, French National Sickle Cell Disease Referral Center, Hôpital Necker, Assistance-Publique Hôpitaux de Paris, Gr Ex, Paris, France.
Sandra ManceauDepartment of Biotherapy, French National Sickle Cell Disease Referral Center, Hôpital Necker, Assistance-Publique Hôpitaux de Paris, Gr Ex, Paris, France.
Slimane AllaliReference Centre for Sickle Cell Disease, Necker-Enfants Malades University Hospital, AP-HP Centre, Paris, France.ORCID 0000-0001-7068-4530
Michael DussiotLaboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, INSERM, Institut Imagine, Université Paris Cité, Paris, France.
Mickael MarinUniversité Paris Cité, INSERM, BIGR, Paris, France.ORCID 0000-0002-4094-022X
Alexis LavergneUniversité Paris Cité, INSERM, BIGR, Paris, France.ORCID 0000-0003-3471-6093
Mariem KhamariHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Sophie MoogHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Elsa BianchiniHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Laetitia ClaerUniversité Paris Cité, INSERM, BIGR, Paris, France.
Sandrine LauranceUniversité Paris Cité, INSERM, BIGR, Paris, France.
Valentine BrousseUniversité Paris Cité, INSERM, BIGR, Paris, France.
Sébastien EymieuxIBiSA Electron Microscopy Facility, University Hospital Center of Tours, Tours, France.ORCID 0000-0002-4738-510X
Philippe RoingeardIBiSA Electron Microscopy Facility, University Hospital Center of Tours, Tours, France.
Pascal AmireaultUniversité Paris Cité, INSERM, BIGR, Paris, France.
Thiago Trovati MacielLaboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, INSERM, Institut Imagine, Université Paris Cité, Paris, France.
Alain BrissonUMR-CBMN, CNRS-Université de Bordeaux-IPB, Pessac, France.
Pierre BuffetUniversité Paris Cité, INSERM, BIGR, Paris, France.
François SallerHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Delphine BorgelHémostase, Inflammation, Thrombose (HITh), UMR-S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Camille RousselService D'hématologie Biologique, Hôpital Necker Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

Funding

Agence Nationale de la Recherche ANR-22-CE140058CSL Behring
6 · The paper itself

Abstract

The major anticoagulant Protein S (PROS1) also contributes to the phagocytosis of apoptotic cells by bridging exposed phosphatidylserine (PtdSer) to the MerTK receptor on macrophages (efferocytosis). Whether PROS1 is involved in the splenic clearance of PtdSer-positive senescent and altered erythrocytes such as erythrocyte ghosts (eryghosts) is unknown. Here, we investigate the contribution of PROS1 and MerTK to the phagocytosis of intact RBC and eryghosts in healthy subjects and patients with sickle cell disease (SCD). We show that PROS1 enhances the phagocytosis of ionomycin-treated PtdSer-positive erythrocytes and of eryghosts generated in vitro. We confirm that eryghosts circulate in patients with SCD at higher levels than in healthy subjects and observe increased hemolysis and decreased levels of plasmatic PROS1 in patients with the highest concentration of eryghosts. The proportion of circulating eryghosts is correlated with the intensity of hyposplenism, and eryghosts are less frequently observed in sections of SCD compared to control spleens. We demonstrate that circulating eryghosts are procoagulant and adhere to endothelial cells. In SCD, PROS1 enhances their phagocytosis in a MerTK-dependent manner but has no such effect on intact erythrocytes. PROS1 is therefore involved in erythrophagocytosis, a physiological process insufficient in patients with SCD due to intense intravascular hemolysis and hyposplenism, leading to PROS1 consumption and the abnormal persistence of eryghosts in circulation. PROS1 deficiency may in turn initiate a pathogenic loop, enhancing unregulated activation of coagulation and defective clearance of procoagulant and adherent eryghosts. This deeper understanding of physiological and pathological erythrophagocytosis opens new therapeutic approaches targeting PROS1 in SCD.

Indexed as

Anemia, Sickle CellErythrocytesPhagocytosisPhosphatidylserinesProtein SAdolescentAdultc-Mer Tyrosine KinaseFemaleHemolysisHumansMacrophagesMaleMiddle AgedSpleenYoung Adultc-Mer Tyrosine KinaseMERTK protein, humanPhosphatidylserinesPROS1 protein, humanProtein Serythrocyte ghostsphagocytosisPROS1protein Ssickle cell disease

Identifiers

PMID41137641
PMCPMC12669952

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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.