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  1. Article: Acute HIV-1 and SARS-CoV-2 Infections Share Slan+ Monocyte Depletion—Evidence from an Hyperacute HIV-1 Case Report

    Farias, Guilherme B. / Badura, Robert / Conceição, Carolina M. / Gomes, André M. C. / Godinho-Santos, Ana / Laia, Joel / Rosmaninho, Pedro / Santos, Diana F. / Mota, Catarina / Almeida, Afonso R. M. / Fernandes, Susana M. / Trombetta, Amelia C. / Sousa, Ana E.

    Viruses. 2021 Sept. 10, v. 13, no. 9

    2021  

    Abstract: Monocytes are key modulators in acute viral infections, determining both inflammation and development of specific B- and T-cell responses. Recently, these cells were shown to be associated to different SARS-CoV-2 infection outcome. However, their role in ...

    Abstract Monocytes are key modulators in acute viral infections, determining both inflammation and development of specific B- and T-cell responses. Recently, these cells were shown to be associated to different SARS-CoV-2 infection outcome. However, their role in acute HIV-1 infection remains unclear. We had the opportunity to evaluate the mononuclear cell compartment in an early hyper-acute HIV-1 patient in comparison with an untreated chronic HIV-1 and a cohort of SARS-CoV-2 infected patients, by high dimensional flow cytometry using an unsupervised approach. A distinct polarization of the monocyte phenotype was observed in the two viral infections, with maintenance of pro-inflammatory M1-like profile in HIV-1, in contrast to the M2-like immunosuppressive shift in SARS-CoV-2. Noticeably, both acute infections had reduced CD14ˡᵒʷ/⁻CD16⁺ non-classical monocytes, with depletion of the population expressing Slan (6-sulfo LacNac), which is thought to contribute to immune surveillance through pro-inflammatory properties. This depletion indicates a potential role of these cells in acute viral infection, which has not previously been explored. The inflammatory state accompanied by the depletion of Slan+ monocytes may provide new insights on the critical events that determine the rate of viral set-point in acute HIV-1 infection and subsequent impact on transmission and reservoir establishment.
    Keywords HIV infections ; Severe acute respiratory syndrome coronavirus 2 ; T-lymphocytes ; case studies ; flow cytometry ; immunosuppression ; inflammation ; monitoring ; monocytes ; patients ; phenotype
    Language English
    Dates of publication 2021-0910
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2516098-9
    ISSN 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v13091805
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Acute HIV-1 and SARS-CoV-2 Infections Share Slan+ Monocyte Depletion-Evidence from an Hyperacute HIV-1 Case Report.

    Farias, Guilherme B / Badura, Robert / Conceição, Carolina M / Gomes, André M C / Godinho-Santos, Ana / Laia, Joel / Rosmaninho, Pedro / Santos, Diana F / Mota, Catarina / Almeida, Afonso R M / Fernandes, Susana M / Trombetta, Amelia C / Sousa, Ana E

    Viruses

    2021  Volume 13, Issue 9

    Abstract: Monocytes are key modulators in acute viral infections, determining both inflammation and development of specific B- and T-cell responses. Recently, these cells were shown to be associated to different SARS-CoV-2 infection outcome. However, their role in ...

    Abstract Monocytes are key modulators in acute viral infections, determining both inflammation and development of specific B- and T-cell responses. Recently, these cells were shown to be associated to different SARS-CoV-2 infection outcome. However, their role in acute HIV-1 infection remains unclear. We had the opportunity to evaluate the mononuclear cell compartment in an early hyper-acute HIV-1 patient in comparison with an untreated chronic HIV-1 and a cohort of SARS-CoV-2 infected patients, by high dimensional flow cytometry using an unsupervised approach. A distinct polarization of the monocyte phenotype was observed in the two viral infections, with maintenance of pro-inflammatory M1-like profile in HIV-1, in contrast to the M2-like immunosuppressive shift in SARS-CoV-2. Noticeably, both acute infections had reduced CD14
    MeSH term(s) Adult ; Aged ; Amino Sugars/immunology ; COVID-19/immunology ; Cohort Studies ; Female ; HIV Infections/immunology ; HIV-1/immunology ; Humans ; Leukocyte Count ; Male ; Middle Aged ; Monocytes/immunology ; Young Adult
    Chemical Substances 6-sulfo-LacNac ; Amino Sugars
    Language English
    Publishing date 2021-09-10
    Publishing country Switzerland
    Document type Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v13091805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Severe COVID-19 Recovery Is Associated with Timely Acquisition of a Myeloid Cell Immune-Regulatory Phenotype.

    Trombetta, Amelia C / Farias, Guilherme B / Gomes, André M C / Godinho-Santos, Ana / Rosmaninho, Pedro / Conceição, Carolina M / Laia, Joel / Santos, Diana F / Almeida, Afonso R M / Mota, Catarina / Gomes, Andreia / Serrano, Marta / Veldhoen, Marc / Sousa, Ana E / Fernandes, Susana M

    Frontiers in immunology

    2021  Volume 12, Page(s) 691725

    Abstract: After more than one year since the COVID-19 outbreak, patients with severe disease still constitute the bottleneck of the pandemic management. Aberrant inflammatory responses, ranging from cytokine storm to immune-suppression, were described in COVID-19 ... ...

    Abstract After more than one year since the COVID-19 outbreak, patients with severe disease still constitute the bottleneck of the pandemic management. Aberrant inflammatory responses, ranging from cytokine storm to immune-suppression, were described in COVID-19 and no treatment was demonstrated to change the prognosis significantly. Therefore, there is an urgent need for understanding the underlying pathogenic mechanisms to guide therapeutic interventions. This study was designed to assess myeloid cell activation and phenotype leading to recovery in patients surviving severe COVID-19. We evaluated longitudinally patients with COVID-19 related respiratory insufficiency, stratified according to the need of intensive care unit admission (ICU, n = 11, and No-ICU, n = 9), and age and sex matched healthy controls (HCs, n = 11), by flow cytometry and a wide array of serum inflammatory/immune-regulatory mediators. All patients featured systemic immune-regulatory myeloid cell phenotype as assessed by both unsupervised and supervised analysis of circulating monocyte and dendritic cell subsets. Specifically, we observed a reduction of CD14lowCD16+ monocytes, and reduced expression of CD80, CD86, and Slan. Moreover, mDCs, pDCs, and basophils were significantly reduced, in comparison to healthy subjects. Contemporaneously, both monocytes and DCs showed increased expression of CD163, CD204, CD206, and PD-L1 immune-regulatory markers. The expansion of M2-like monocytes was significantly higher at admission in patients featuring detectable SARS-CoV-2 plasma viral load and it was positively correlated with the levels of specific antibodies. In No-ICU patients, we observed a peak of the alterations at admission and a progressive regression to a phenotype similar to HCs at discharge. Interestingly, in ICU patients, the expression of immuno-suppressive markers progressively increased until discharge. Notably, an increase of M2-like HLA-DRhighPD-L1+ cells in CD14++CD16- monocytes and in dendritic cell subsets was observed at ICU discharge. Furthermore, IFN-γ and IL-12p40 showed a decline over time in ICU patients, while high values of IL1RA and IL-10 were maintained. In conclusion, these results support that timely acquisition of a myeloid cell immune-regulatory phenotype might contribute to recovery in severe systemic SARS-CoV-2 infection and suggest that therapeutic agents favoring an innate immune system regulatory shift may represent the best strategy to be implemented at this stage.
    MeSH term(s) Adult ; Aged ; COVID-19/immunology ; Cell Differentiation ; Critical Care ; Cytokines/metabolism ; Female ; Humans ; Immunomodulation ; Male ; Middle Aged ; Monocytes/immunology ; Myeloid-Derived Suppressor Cells/immunology ; Phenotype ; Respiratory Insufficiency ; SARS-CoV-2/physiology ; Severity of Illness Index ; Th2 Cells/immunology
    Chemical Substances Cytokines
    Language English
    Publishing date 2021-06-23
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2021.691725
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: SARS-CoV2 pneumonia recovery is linked to expansion of innate lymphoid cells type 2 expressing CCR10.

    Gomes, André M C / Farias, Guilherme B / Dias-Silva, Manuel / Laia, Joel / Trombetta, Amelia C / Godinho-Santos, Ana / Rosmaninho, Pedro / Santos, Diana F / Conceição, Carolina M / Costa-Reis, Renato / Adão-Serrano, Maria / Mota, Catarina / Almeida, Afonso R M / Sousa, Ana E / Fernandes, Susana M

    European journal of immunology

    2021  Volume 51, Issue 12, Page(s) 3194–3201

    Abstract: Accelerate lung repair in SARS-CoV-2 pneumonia is essential for pandemic handling. Innate lymphoid cells (ILCs) are likely players, given their role in mucosal protection and tissue homeostasis. We studied ILC subpopulations at two time points in a ... ...

    Abstract Accelerate lung repair in SARS-CoV-2 pneumonia is essential for pandemic handling. Innate lymphoid cells (ILCs) are likely players, given their role in mucosal protection and tissue homeostasis. We studied ILC subpopulations at two time points in a cohort of patients admitted in the hospital due to SARS-CoV-2 infection. COVID-19 patients with moderate/severe respiratory failure featured profound depletion of circulating ILCs at hospital admission, in agreement with overall lymphocyte depletion. However, ILCs recovered in direct correlation with lung function improvement as measured by oxygenation index and in negative association with inflammatory and lung/endothelial damage markers like RAGE. While both ILC1 and ILC2 expanded, ILC2 showed the most striking phenotype changes, with CCR10 upregulation in strong correlation with these parameters. Overall, CCR10
    MeSH term(s) Adult ; Aged ; Antigens, Neoplasm/metabolism ; Biomarkers/metabolism ; COVID-19/immunology ; Cell Proliferation ; Cytokines/metabolism ; Female ; Humans ; Immunity, Innate ; Lung/pathology ; Lymphocytes/immunology ; Male ; Middle Aged ; Mitogen-Activated Protein Kinases/metabolism ; Pneumonia, Viral/immunology ; Receptors, CCR10/metabolism ; Recovery of Function ; SARS-CoV-2/physiology ; Th2 Cells/immunology ; Up-Regulation
    Chemical Substances Antigens, Neoplasm ; Biomarkers ; CCR10 protein, human ; Cytokines ; Receptors, CCR10 ; MOK protein, human (EC 2.7.11.22) ; Mitogen-Activated Protein Kinases (EC 2.7.11.24)
    Language English
    Publishing date 2021-10-20
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120108-6
    ISSN 1521-4141 ; 0014-2980
    ISSN (online) 1521-4141
    ISSN 0014-2980
    DOI 10.1002/eji.202149311
    Database MEDical Literature Analysis and Retrieval System OnLINE

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