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  1. Article: Role of therapeutic plasma exchange in the management of COVID-19-induced cytokine storm syndrome.

    Beraud, Mickael / Hashami, Sabria Al / Lozano, Miquel / Bah, Aicha / Keith, Philip

    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

    2022  Volume 61, Issue 4, Page(s) 103433

    Abstract: The risk of mortality in patients with coronavirus disease 2019 (COVID-19) is largely related to an excessive immune response, resulting in a hyperinflammatory and hypercoagulable condition collectively referred to as cytokine storm syndrome (CSS). ... ...

    Abstract The risk of mortality in patients with coronavirus disease 2019 (COVID-19) is largely related to an excessive immune response, resulting in a hyperinflammatory and hypercoagulable condition collectively referred to as cytokine storm syndrome (CSS). Management of critically ill patients with COVID-19 has included attempts to abate this process, prevent disease progression, and reduce mortality. In this context, therapeutic plasma exchange (TPE) offers an approach to eliminate inflammatory factors and cytokines, offset the pathologic coagulopathy, and reduce the CSS effects. The aim of this review is to analyze available data on the use of TPE for the treatment of CSS in patients with COVID-19. Systematic searches of PubMed, Scopus and COVID-19 Research were conducted to identify articles published between March 1, 2020 and May 26, 2021 reporting the use of TPE for the treatment of COVID-19-induced CSS. A total of 34 peer-reviewed articles (1 randomized controlled trial, 4 matched case-control series, 15 single-group case series, and 14 case reports), including 267 patients, were selected. Despite the low evidence level of the available data, TPE appeared to be a safe intervention for critically ill patients with COVID-19-induced CSS. Although inconsistencies exist between studies, they showed a general trend for decreased interleukin-6, C-reactive protein, ferritin, D-dimer, and fibrinogen levels and increased lymphocyte counts following TPE, supporting the immunomodulatory effect of this treatment. Moreover, TPE was associated with improvements in clinical outcomes in critically ill patients with COVID-19. While TPE may offer a valuable option to treat patients with COVID-19-induced CSS, high-quality randomized controlled clinical trials are needed to confirm its potential clinical benefits, feasibility, and safety. Moreover, clear criteria should be established to identify patients with CSS who might benefit from TPE.
    MeSH term(s) COVID-19/complications ; COVID-19/therapy ; Critical Illness/therapy ; Cytokine Release Syndrome/etiology ; Cytokine Release Syndrome/therapy ; Humans ; Plasma Exchange ; Randomized Controlled Trials as Topic ; SARS-CoV-2
    Language English
    Publishing date 2022-03-23
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2046795-3
    ISSN 1878-1683 ; 1473-0502
    ISSN (online) 1878-1683
    ISSN 1473-0502
    DOI 10.1016/j.transci.2022.103433
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Lessons learned from the use of convalescent plasma for the treatment of COVID-19 and specific considerations for immunocompromised patients.

    Beraud, Mickael / Goodhue Meyer, Erin / Lozano, Miquel / Bah, Aicha / Vassallo, Ralph / Brown, Bethany L

    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

    2022  Volume 61, Issue 3, Page(s) 103355

    Abstract: Coronavirus disease 2019 (COVID-19) convalescent plasma (CovCP) infusions have been widely used for the treatment of hospitalized patients with COVID-19. The aims of this narrative review were to analyze the safety and efficacy of CovCP infusions in the ... ...

    Abstract Coronavirus disease 2019 (COVID-19) convalescent plasma (CovCP) infusions have been widely used for the treatment of hospitalized patients with COVID-19. The aims of this narrative review were to analyze the safety and efficacy of CovCP infusions in the overall population and in immunocompromised patients with COVID-19 and to identify the lessons learned concerning the use of convalescent plasma (CP) to fill treatment gaps for emerging viruses. Systematic searches (PubMed, Scopus, and COVID-19 Research) were conducted to identify peer-reviewed articles and pre-prints published between March 1, 2020 and May 1, 2021 on the use of CovCP for the treatment of patients with COVID-19. From 261 retrieved articles, 37 articles reporting robust controlled studies in the overall population of patients with COVID-19 and 9 articles in immunocompromised patients with COVID-19 were selected. While CovCP infusions are well tolerated in both populations, they do not seem to improve clinical outcomes in critically-ill patients with COVID-19 and no conclusion could be drawn concerning their potential benefits in immunocompromised patients with COVID-19. To be better prepared for future epidemics/pandemics and to evaluate potential benefits of CP treatment, only CP units with high neutralizing antibodies (NAbs) titers should be infused in patients with low NAb titers, patient eligibility criteria should be based on the disease pathophysiology, and measured clinical outcomes and methods should be comparable across studies. Even if CovCP infusions did not improve clinical outcomes in patients with COVID-19, NAb-containing CP infusions remain a safe, widely available and potentially beneficial treatment option for future epidemics/pandemics.
    MeSH term(s) COVID-19/therapy ; Humans ; Immunization, Passive/methods ; Immunocompromised Host ; Pandemics ; SARS-CoV-2
    Language English
    Publishing date 2022-01-13
    Publishing country England
    Document type Journal Article ; Review ; Systematic Review
    ZDB-ID 2046795-3
    ISSN 1878-1683 ; 1473-0502
    ISSN (online) 1878-1683
    ISSN 1473-0502
    DOI 10.1016/j.transci.2022.103355
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Macrophage Autophagy and Bacterial Infections.

    Bah, Aïcha / Vergne, Isabelle

    Frontiers in immunology

    2017  Volume 8, Page(s) 1483

    Abstract: Autophagy is a well-conserved lysosomal degradation pathway that plays key roles in bacterial infections. One of the most studied is probably xenophagy, the selective capture and degradation of intracellular bacteria by lysosomes. However, the impact of ... ...

    Abstract Autophagy is a well-conserved lysosomal degradation pathway that plays key roles in bacterial infections. One of the most studied is probably xenophagy, the selective capture and degradation of intracellular bacteria by lysosomes. However, the impact of autophagy goes beyond xenophagy and involves intensive cross-talks with other host defense mechanisms. In addition, autophagy machinery can have non-canonical functions such as LC3-associated phagocytosis. In this review, we intend to summarize the current knowledge on the many functions of autophagy proteins in cell defenses with a focus on bacteria-macrophage interaction. We also present the strategies developed by pathogens to evade or to exploit this machinery in order to establish a successful infection. Finally, we discuss the opportunities and challenges of autophagy manipulation in improving therapeutics and vaccines against bacterial pathogens.
    Language English
    Publishing date 2017
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2606827-8
    ISSN 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2017.01483
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Remodelling whole blood processing through automation and pathogen reduction technology at the Luxembourg Red Cross.

    Malvaux, Nicolas / Schuhmacher, Anne / Defraigne, Fanette / Jacob, Remy / Bah, Aicha / Cardoso, Marcia

    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

    2021  Volume 60, Issue 5, Page(s) 103195

    Abstract: In 2014-2015, the Luxembourg Red Cross (LRC) implemented a fully automated system (FAS) able to process 4 whole blood units simultaneously, and a pathogen reduction technology (PRT) based on riboflavin and ultraviolet light to improve safety of platelet ... ...

    Abstract In 2014-2015, the Luxembourg Red Cross (LRC) implemented a fully automated system (FAS) able to process 4 whole blood units simultaneously, and a pathogen reduction technology (PRT) based on riboflavin and ultraviolet light to improve safety of platelet concentrates (PCs). In this observational study, the impact of both technologies to enable this centralised blood transfusion centre to provide safe and timely blood components supply for the whole country was analysed. Standard quality control parameters for blood components, productivity and safety were compared from data collected with the conventional semi- automated buffy coat method and with FAS/PRT. The FAS decreased processing time when compared with the buffy coat method and facilitated the daily routine at the LRC. Red blood cell concentrates, plasma units and PCs prepared with both methods were conform to the European Directorate for the Quality of Medicines & HealthCare specifications. PCs prepared by FAS showed high yields, with decreased variability when the device-related software (T-Pool Select) was used. PRT had minimal impact on platelet yields and product quality and induced no increase in transfusion reaction notifications. The FAS and PRT transformed the daily routine of blood component manufacture by allowing increased productivity and efficiency, notwithstanding resource containment and without impacting quality, yet promoting safety.
    MeSH term(s) Automation ; Blood Component Transfusion/instrumentation ; Blood Component Transfusion/methods ; Blood Platelets/drug effects ; Blood Preservation/instrumentation ; Blood Preservation/methods ; Blood Safety ; Erythrocytes/cytology ; Humans ; Luxembourg ; Plasma ; Platelet Count ; Platelet Transfusion/instrumentation ; Platelet Transfusion/methods ; Quality Control ; Red Cross ; Retrospective Studies ; Riboflavin/pharmacology ; Software
    Chemical Substances Riboflavin (TLM2976OFR)
    Language English
    Publishing date 2021-06-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 2046795-3
    ISSN 1878-1683 ; 1473-0502
    ISSN (online) 1878-1683
    ISSN 1473-0502
    DOI 10.1016/j.transci.2021.103195
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: The Lipid Virulence Factors of

    Bah, Aïcha / Sanicas, Merlin / Nigou, Jérôme / Guilhot, Christophe / Astarie-Dequeker, Catherine / Vergne, Isabelle

    Cells

    2020  Volume 9, Issue 3

    Abstract: Autophagy is an important innate immune defense mechanism that ... ...

    Abstract Autophagy is an important innate immune defense mechanism that controls
    MeSH term(s) Autophagy/immunology ; Bacterial Proteins/drug effects ; Bacterial Proteins/metabolism ; Humans ; Lipids/pharmacology ; Macrophages/drug effects ; Macrophages/metabolism ; Macrophages/microbiology ; Mycobacterium tuberculosis/drug effects ; Mycobacterium tuberculosis/metabolism ; Mycobacterium tuberculosis/pathogenicity ; Phagocytosis/drug effects ; Phagocytosis/immunology ; Phagosomes/metabolism ; Phagosomes/microbiology ; Virulence Factors/metabolism
    Chemical Substances Bacterial Proteins ; Lipids ; Virulence Factors ; phthiocerol dimycocerosate (63642-22-8)
    Language English
    Publishing date 2020-03-09
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells9030666
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Reflections on the dynamics of bacterial and viral contamination of blood components and the levels of efficacy for pathogen inactivation processes.

    Bah, Aicha / Cardoso, Marcia / Seghatchian, Jerard / Goodrich, Raymond P

    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

    2018  Volume 57, Issue 5, Page(s) 683–688

    Abstract: Blood transfusion safety has been increasingly improving during the past two decades. However, threats from both known and emerging pathogens require continual improvement and re-assessment of blood safety measures. In this respect, we are currently ... ...

    Abstract Blood transfusion safety has been increasingly improving during the past two decades. However, threats from both known and emerging pathogens require continual improvement and re-assessment of blood safety measures. In this respect, we are currently witnessing the broader implementation of Pathogen reduction technology (PRT) for blood complements. These methods, combined with existing safety measures, have helped to reduce the pathogen risks of transfusion-transmitted infections. Currently multiple reviews have compared levels of inactivation between different commercialized PRTs. However, to analyze levels of pathogen inactivation, it is necessary to understand the dynamics of infectivity as well as the modes of disease transmission by blood transfusion for various pathogens. It is well known that contributing variables include donor characteristics through the processing of blood components to ultimately the recipient characteristics, which create enormous variability in overall outcomes relative to disease transmission. The aim of this paper is to discuss bacterial and viral contamination of blood components in order to determine adequate levels of efficacy and subsequent disease transmission safety of current pathogen inactivation protocols that are designed to reduce the risk of transfusion-transmitted infections. In such a conceptual analysis, however, it is important to understand several contributing factors including the measurement of pathogen load in blood products and the dynamics, infectivity and disease transmission of various pathogens via transfusion of blood components and products. In many cases, the log reduction values observed do not truly reflect the extent of reduction in the levels of infectivity that are observed clinically. Results from clinical trials and hemovigilance programs upon routine implementation of PRT methods provide a more direct insight into effectiveness with regard to clinical relevance of in vitro spiking studies. These issues are briefly addressed in this manuscript.
    MeSH term(s) Blood/microbiology ; Blood/virology ; Blood Component Transfusion/methods ; Disease Transmission, Infectious/prevention & control ; Humans
    Language English
    Publishing date 2018-09-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2046795-3
    ISSN 1878-1683 ; 1473-0502
    ISSN (online) 1878-1683
    ISSN 1473-0502
    DOI 10.1016/j.transci.2018.09.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Autophagy-Related Proteins Target Ubiquitin-Free Mycobacterial Compartment to Promote Killing in Macrophages.

    Bah, Aïcha / Lacarrière, Camille / Vergne, Isabelle

    Frontiers in cellular and infection microbiology

    2016  Volume 6, Page(s) 53

    Abstract: Autophagy is a lysosomal degradative process that plays essential functions in innate immunity, particularly, in the clearance of intracellular bacteria such as Mycobacterium tuberculosis. The molecular mechanisms involved in autophagy activation and ... ...

    Abstract Autophagy is a lysosomal degradative process that plays essential functions in innate immunity, particularly, in the clearance of intracellular bacteria such as Mycobacterium tuberculosis. The molecular mechanisms involved in autophagy activation and targeting of mycobacteria, in innate immune responses of macrophages, are only partially characterized. Autophagy targets pathogenic M. tuberculosis via a cytosolic DNA recognition- and an ubiquitin-dependent pathway. In this report, we show that non-pathogenic M. smegmatis induces a robust autophagic response in THP-1 macrophages with an up regulation of several autophagy-related genes. Autophagy activation relies in part on recognition of mycobacteria by Toll-like receptor 2 (TLR2). Notably, LC3 targeting of M. smegmatis does not rely on membrane damage, ubiquitination, or autophagy receptor recruitment. Lastly, M. smegmatis promotes recruitment of several autophagy proteins, which are required for mycobacterial killing. In conclusion, our study uncovered an alternative autophagic pathway triggered by mycobacteria which involves cell surface recognition but not bacterial ubiquitination.
    MeSH term(s) Autophagy-Related Proteins/metabolism ; Cell Line ; Humans ; Macrophages/immunology ; Macrophages/microbiology ; Mycobacterium smegmatis/immunology ; Toll-Like Receptor 2/metabolism ; Ubiquitin/metabolism
    Chemical Substances Autophagy-Related Proteins ; TLR2 protein, human ; Toll-Like Receptor 2 ; Ubiquitin
    Language English
    Publishing date 2016
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2619676-1
    ISSN 2235-2988 ; 2235-2988
    ISSN (online) 2235-2988
    ISSN 2235-2988
    DOI 10.3389/fcimb.2016.00053
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Pilot study of repeated blood-brain barrier disruption in patients with mild Alzheimer's disease with an implantable ultrasound device.

    Epelbaum, Stéphane / Burgos, Ninon / Canney, Michael / Matthews, Dawn / Houot, Marion / Santin, Mathieu D / Desseaux, Carole / Bouchoux, Guillaume / Stroer, Sebastian / Martin, Cyril / Habert, Marie-Odile / Levy, Marcel / Bah, Aicha / Martin, Karine / Delatour, Benoît / Riche, Maximilien / Dubois, Bruno / Belin, Lisa / Carpentier, Alexandre

    Alzheimer's research & therapy

    2022  Volume 14, Issue 1, Page(s) 40

    Abstract: Background: Temporary disruption of the blood-brain barrier (BBB) using pulsed ultrasound leads to the clearance of both amyloid and tau from the brain, increased neurogenesis, and mitigation of cognitive decline in pre-clinical models of Alzheimer's ... ...

    Abstract Background: Temporary disruption of the blood-brain barrier (BBB) using pulsed ultrasound leads to the clearance of both amyloid and tau from the brain, increased neurogenesis, and mitigation of cognitive decline in pre-clinical models of Alzheimer's disease (AD) while also increasing BBB penetration of therapeutic antibodies. The goal of this pilot clinical trial was to investigate the safety and efficacy of this approach in patients with mild AD using an implantable ultrasound device.
    Methods: An implantable, 1-MHz ultrasound device (SonoCloud-1) was implanted under local anesthesia in the skull (extradural) of 10 mild AD patients to target the left supra-marginal gyrus. Over 3.5 months, seven ultrasound sessions in combination with intravenous infusion of microbubbles were performed twice per month to temporarily disrupt the BBB.
    Results: A total of 63 BBB opening procedures were performed in nine subjects. The procedure was well-tolerated. A non-significant decrease in amyloid accumulation at 4 months of - 6.6% (SD = 7.2%) on
    Conclusions: These results demonstrate the safety of ultrasound-based BBB disruption and the potential of this technology to be used as a therapy for AD patients. Research of this technique in a larger clinical trial with a device designed to sonicate larger volumes of tissue and in combination with disease-modifying drugs may further enhance the effects observed.
    Trial registration: ClinicalTrials.gov, NCT03119961.
    MeSH term(s) Alzheimer Disease/diagnostic imaging ; Alzheimer Disease/metabolism ; Alzheimer Disease/therapy ; Blood-Brain Barrier/diagnostic imaging ; Blood-Brain Barrier/metabolism ; Brain/diagnostic imaging ; Brain/metabolism ; Cognitive Dysfunction/metabolism ; Humans ; Neuroimaging/methods ; Pilot Projects ; Positron-Emission Tomography/methods
    Language English
    Publishing date 2022-03-08
    Publishing country England
    Document type Clinical Trial ; Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2506521-X
    ISSN 1758-9193 ; 1758-9193
    ISSN (online) 1758-9193
    ISSN 1758-9193
    DOI 10.1186/s13195-022-00981-1
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  9. Article ; Online: The distinct fate of smooth and rough Mycobacterium abscessus variants inside macrophages.

    Roux, Anne-Laure / Viljoen, Albertus / Bah, Aïcha / Simeone, Roxane / Bernut, Audrey / Laencina, Laura / Deramaudt, Therese / Rottman, Martin / Gaillard, Jean-Louis / Majlessi, Laleh / Brosch, Roland / Girard-Misguich, Fabienne / Vergne, Isabelle / de Chastellier, Chantal / Kremer, Laurent / Herrmann, Jean-Louis

    Open biology

    2016  Volume 6, Issue 11

    Abstract: Mycobacterium abscessus is a pathogenic, rapidly growing mycobacterium responsible for pulmonary and cutaneous infections in immunocompetent patients and in patients with Mendelian disorders, such as cystic fibrosis (CF). Mycobacterium abscessus is known ...

    Abstract Mycobacterium abscessus is a pathogenic, rapidly growing mycobacterium responsible for pulmonary and cutaneous infections in immunocompetent patients and in patients with Mendelian disorders, such as cystic fibrosis (CF). Mycobacterium abscessus is known to transition from a smooth (S) morphotype with cell surface-associated glycopeptidolipids (GPL) to a rough (R) morphotype lacking GPL. Herein, we show that M. abscessus S and R variants are able to grow inside macrophages and are present in morphologically distinct phagosomes. The S forms are found mostly as single bacteria within phagosomes characterized by a tightly apposed phagosomal membrane and the presence of an electron translucent zone (ETZ) surrounding the bacilli. By contrast, infection with the R form leads to phagosomes often containing more than two bacilli, surrounded by a loose phagosomal membrane and lacking the ETZ. In contrast to the R variant, the S variant is capable of restricting intraphagosomal acidification and induces less apoptosis and autophagy. Importantly, the membrane of phagosomes enclosing the S forms showed signs of alteration, such as breaks or partial degradation. Although not frequently encountered, these events suggest that the S form is capable of provoking phagosome-cytosol communication. In conclusion, M. abscessus S exhibits traits inside macrophages that are reminiscent of slow-growing mycobacterial species.
    Language English
    Publishing date 2016-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2630944-0
    ISSN 2046-2441 ; 2046-2441
    ISSN (online) 2046-2441
    ISSN 2046-2441
    DOI 10.1098/rsob.160185
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  10. Article ; Online: Tuberculosis Exacerbates HIV-1 Infection through IL-10/STAT3-Dependent Tunneling Nanotube Formation in Macrophages.

    Souriant, Shanti / Balboa, Luciana / Dupont, Maeva / Pingris, Karine / Kviatcovsky, Denise / Cougoule, Céline / Lastrucci, Claire / Bah, Aicha / Gasser, Romain / Poincloux, Renaud / Raynaud-Messina, Brigitte / Al Saati, Talal / Inwentarz, Sandra / Poggi, Susana / Moraña, Eduardo Jose / González-Montaner, Pablo / Corti, Marcelo / Lagane, Bernard / Vergne, Isabelle /
    Allers, Carolina / Kaushal, Deepak / Kuroda, Marcelo J / Sasiain, Maria Del Carmen / Neyrolles, Olivier / Maridonneau-Parini, Isabelle / Lugo-Villarino, Geanncarlo / Vérollet, Christel

    Cell reports

    2019  Volume 26, Issue 13, Page(s) 3586–3599.e7

    Abstract: The tuberculosis (TB) bacillus, Mycobacterium tuberculosis (Mtb), and HIV-1 act synergistically; however, the mechanisms by which Mtb exacerbates HIV-1 pathogenesis are not well known. Using in vitro and ex vivo cell culture systems, we show that human M( ...

    Abstract The tuberculosis (TB) bacillus, Mycobacterium tuberculosis (Mtb), and HIV-1 act synergistically; however, the mechanisms by which Mtb exacerbates HIV-1 pathogenesis are not well known. Using in vitro and ex vivo cell culture systems, we show that human M(IL-10) anti-inflammatory macrophages, present in TB-associated microenvironment, produce high levels of HIV-1. In vivo, M(IL-10) macrophages are expanded in lungs of co-infected non-human primates, which correlates with disease severity. Furthermore, HIV-1/Mtb co-infected patients display an accumulation of M(IL-10) macrophage markers (soluble CD163 and MerTK). These M(IL-10) macrophages form direct cell-to-cell bridges, which we identified as tunneling nanotubes (TNTs) involved in viral transfer. TNT formation requires the IL-10/STAT3 signaling pathway, and targeted inhibition of TNTs substantially reduces the enhancement of HIV-1 cell-to-cell transfer and overproduction in M(IL-10) macrophages. Our study reveals that TNTs facilitate viral transfer and amplification, thereby promoting TNT formation as a mechanism to be explored in TB/AIDS potential therapeutics.
    MeSH term(s) Adult ; Aged ; Animals ; Cells, Cultured ; Coinfection/pathology ; Coinfection/virology ; Female ; HIV Infections/complications ; HIV Infections/immunology ; HIV Infections/pathology ; HIV Infections/virology ; Humans ; Interleukin-10/metabolism ; Macaca mulatta ; Macrophage Activation ; Macrophages/pathology ; Macrophages/virology ; Male ; Middle Aged ; Mycobacterium tuberculosis ; Nanotubes ; STAT3 Transcription Factor/metabolism ; Signal Transduction ; Tuberculosis, Pulmonary/complications ; Tuberculosis, Pulmonary/immunology ; Tuberculosis, Pulmonary/pathology ; Virus Replication ; Young Adult
    Chemical Substances IL10 protein, human ; STAT3 Transcription Factor ; STAT3 protein, human ; Interleukin-10 (130068-27-8)
    Language English
    Publishing date 2019-03-27
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2019.02.091
    Database MEDical Literature Analysis and Retrieval System OnLINE

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