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  1. Article ; Online: Development of SARS-CoV2 humoral response including neutralizing antibodies is not sufficient to protect patients against fatal infection.

    Choteau, Mathilde / Scohy, Anaïs / Messe, Stéphane / Luyckx, Mathieu / Dechamps, Mélanie / Montiel, Virginie / Yombi, Jean Cyr / Gruson, Damien / Limaye, Nisha / Michiels, Thomas / Dumoutier, Laure

    Scientific reports

    2022  Volume 12, Issue 1, Page(s) 2077

    Abstract: More than a year after the start of the pandemic, COVID-19 remains a global health emergency. Although the immune response against SARS-CoV-2 has been extensively studied, some points remain controversial. One is the role of antibodies in viral clearance ...

    Abstract More than a year after the start of the pandemic, COVID-19 remains a global health emergency. Although the immune response against SARS-CoV-2 has been extensively studied, some points remain controversial. One is the role of antibodies in viral clearance and modulation of disease severity. While passive transfer of neutralizing antibodies protects against SARS-CoV-2 infection in animal models, titers of anti-SARS-CoV-2 antibodies have been reported to be higher in patients suffering from more severe forms of the disease. A second key question for pandemic management and vaccine design is the persistence of the humoral response. Here, we characterized the antibody response in 187 COVID-19 patients, ranging from asymptomatic individuals to patients who died from COVID-19, and including patients who recovered. We developed in-house ELISAs to measure titers of IgG, IgM and IgA directed against the RBD or N regions in patient serum or plasma, and a spike-pseudotyped neutralization assay to analyse seroneutralization. Higher titers of virus-specific antibodies were detected in patients with severe COVID-19, including deceased patients, compared to asymptomatic patients. This demonstrates that fatal infection is not associated with defective humoral response. Finally, most of recovered patients still had anti-SARS-CoV-2 IgG more than 3 months after infection.
    MeSH term(s) Adult ; Aged ; Antibodies, Neutralizing/immunology ; Antibodies, Viral/immunology ; COVID-19/immunology ; COVID-19/mortality ; Female ; Humans ; Immunity, Humoral ; Male ; Middle Aged ; SARS-CoV-2/immunology
    Chemical Substances Antibodies, Neutralizing ; Antibodies, Viral
    Language English
    Publishing date 2022-02-08
    Publishing country England
    Document type Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-022-06038-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A case of convergent evolution: Several viral and bacterial pathogens hijack RSK kinases through a common linear motif.

    Sorgeloos, Frédéric / Peeters, Michael / Hayashi, Yohei / Borghese, Fabian / Capelli, Nicolas / Drappier, Melissa / Cesaro, Teresa / Colau, Didier / Stroobant, Vincent / Vertommen, Didier / de Bodt, Grégory / Messe, Stéphane / Forné, Ignasi / Mueller-Planitz, Felix / Collet, Jean-François / Michiels, Thomas

    Proceedings of the National Academy of Sciences of the United States of America

    2022  Volume 119, Issue 5

    Abstract: Microbes have been coevolving with their host for millions of years, exploiting host resources to their own benefit. We show that viral and bacterial pathogens convergently evolved to hijack cellular mitogen-activated protein kinase (MAPK) p90-ribosomal ... ...

    Abstract Microbes have been coevolving with their host for millions of years, exploiting host resources to their own benefit. We show that viral and bacterial pathogens convergently evolved to hijack cellular mitogen-activated protein kinase (MAPK) p90-ribosomal S6-kinases (RSKs). Theiler's virus leader (L) protein binds RSKs and prevents their dephosphorylation, thus maintaining the kinases active. Recruitment of RSKs enables L-protein-mediated inhibition of eukaryotic translation initiation factor 2 alpha kinase 2 (EIF2AK2 or PKR) and stress granule formation. Strikingly, ORF45 protein of Kaposi's sarcoma-associated herpesvirus (KSHV) and YopM protein of
    MeSH term(s) Bacteria/pathogenicity ; Bacterial Infections/genetics ; Bacterial Infections/metabolism ; Biological Evolution ; Cell Line ; Gene Expression Regulation, Viral/genetics ; Host Microbial Interactions/genetics ; Host Microbial Interactions/physiology ; Humans ; Immediate-Early Proteins/genetics ; MAP Kinase Signaling System/physiology ; Mitogen-Activated Protein Kinase Kinases/metabolism ; Ribosomal Protein S6 Kinases, 90-kDa/genetics ; Ribosomal Protein S6 Kinases, 90-kDa/metabolism ; Virus Diseases/genetics ; Virus Diseases/metabolism ; Virus Replication/physiology ; Viruses/pathogenicity
    Chemical Substances Immediate-Early Proteins ; Ribosomal Protein S6 Kinases, 90-kDa (EC 2.7.11.1) ; Mitogen-Activated Protein Kinase Kinases (EC 2.7.12.2)
    Language English
    Publishing date 2022-01-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2114647119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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