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1.
Int J Hyg Environ Health ; 231: 113653, 2021 01.
Article in English | MEDLINE | ID: mdl-33137564

ABSTRACT

BACKGROUND: The ongoing global SARS-CoV-2 pandemic has caused over 4.7 million infections greatly challenging healthcare workers (HCW) and medical institutions worldwide. The SARS-CoV-2 pandemic has shown to significantly impact mental and physical health of HCW. Thus, implementation of testing facilities supporting HCW are urgently needed. METHODS: A low-threshold SARS-CoV-2 testing facility was introduced at the University Hospital Bonn, Germany, in March 2020. Irrespective of clinical symptoms employees were offered a voluntary and free SARS-CoV-2 test. Furthermore, employees returning from SARS-CoV-2 risk regions and employees after risk contact with SARS-CoV-2 infected patients or employees were tested for SARS-CoV-2 infection. Pharyngeal swabs were taken and reverse transcription polymerase chain reaction for detection of SARS-CoV-2 was performed, test results being available within 24 h. Profession, symptoms and reason for SARS-CoV-2 testing of employees were recorded. RESULTS: Between 9th March and April 30, 2020, a total of 1510 employees were tested for SARS-CoV-2 infection. 1185 employees took advantage of the low-threshold testing facility. One percent (n = 11) were tested positive for SARS-CoV-2 infection, 18% being asymptomatic, 36% showing mild and 36% moderate/severe symptoms (missing 10%). Furthermore, of 56 employees returning from SARS-CoV-2 risk regions, 18% (10/56) were tested SARS-CoV-2 positive. After risk contact tracking by the hospital hygiene 6 patient-to-employee transmissions were identified in 163 employees with contact to 55 SARS-CoV-2 positive patients. CONCLUSION: In the absence of easily accessible public SARS-CoV-2 testing facilities low-threshold SARS-CoV-2 testing facilities in hospitals with rapid testing resources help to identify SARS-CoV-2 infected employees with absent or mild symptoms, thus stopping the spread of infection in vulnerable hospital environments. High levels of professional infection prevention training and implementation of specialized wards as well as a perfectly working hospital hygiene network identifying and tracking risk contacts are of great importance in a pandemic setting.


Subject(s)
COVID-19 Testing , COVID-19/diagnosis , COVID-19/epidemiology , Disease Outbreaks/prevention & control , Hospitals, University , Personnel, Hospital , SARS-CoV-2 , Adult , Female , Germany , Humans , Male , Middle Aged
2.
Public Health ; 182: 170-172, 2020 May.
Article in English | MEDLINE | ID: mdl-32334183

ABSTRACT

OBJECTIVE: With the current SARS-CoV2 outbreak, countless tests need to be performed on potential symptomatic individuals, contacts and travellers. The gold standard is a quantitative polymerase chain reaction (qPCR)-based system taking several hours to confirm positivity. For effective public health containment measures, this time span is too long. We therefore evaluated a rapid test in a high-prevalence community setting. STUDY DESIGN: Thirty-nine randomly selected individuals at a COVID-19 screening centre were simultaneously tested via qPCR and a rapid test. Ten previously diagnosed individuals with known SARS-CoV-2 infection were also analysed. METHODS: The evaluated rapid test is an IgG/IgM-based test for SARS-CoV-2 with a time to result of 20 min. Two drops of blood are needed for the test performance. RESULTS: Of 49 individuals, 22 tested positive by repeated qPCR. In contrast, the rapid test detected only eight of those positive correctly (sensitivity: 36.4%). Of the 27 qPCR-negative individuals, 24 were detected correctly (specificity: 88.9%). CONCLUSION: Given the low sensitivity, we recommend not to rely on an antibody-based rapid test for public health measures such as community screenings.


Subject(s)
Betacoronavirus/isolation & purification , Clinical Laboratory Techniques/standards , Community Health Services , Coronavirus Infections/diagnosis , Disease Outbreaks , Mass Screening/standards , Pneumonia, Viral/diagnosis , Point-of-Care Testing , Adult , Aged , COVID-19 , COVID-19 Testing , Coronavirus Infections/epidemiology , Female , Humans , Male , Mass Screening/methods , Middle Aged , Pandemics , Pneumonia, Viral/epidemiology , Polymerase Chain Reaction , SARS-CoV-2 , Sensitivity and Specificity , Time Factors
3.
HLA ; 88(4): 155-63, 2016 10.
Article in English | MEDLINE | ID: mdl-27620852

ABSTRACT

Since the beginning of the epidemic, more than 70 million people have been infected with human immunodeficiency virus (HIV) and about 38 million have died from acquired immune deficiency syndrome (AIDS)-related illnesses. While the discovery of highly active antiretroviral therapy (HAART) in the mid 90's has saved millions of lives, a complete eradication of HIV is still not possible as HIV can persist for decades in a small reservoir of latently infected cells. Once reactivated, these latently infected cells can actively produce viral particles. Recent studies suggest that several sanctuaries exist within infected individuals where HIV can remain undetected by the immune system. These cellular, anatomical and microanatomical viral reservoirs represent a major obstacle for the eradication of HIV. Here we review recent findings on potential sanctuaries of HIV and address potential avenues to overcome these immunological barriers.


Subject(s)
Anti-HIV Agents/therapeutic use , CD4-Positive T-Lymphocytes/drug effects , HIV Infections/drug therapy , Hydroxyurea/therapeutic use , Virus Activation/drug effects , Virus Latency/drug effects , Antiretroviral Therapy, Highly Active , Blood-Brain Barrier/drug effects , Blood-Brain Barrier/immunology , Blood-Brain Barrier/virology , CD4-Positive T-Lymphocytes/immunology , CD4-Positive T-Lymphocytes/virology , Cell Compartmentation , Combined Modality Therapy , HIV Infections/immunology , HIV Infections/virology , HIV-1/drug effects , HIV-1/immunology , HIV-1/pathogenicity , Humans , Immunologic Memory , Lymph Nodes/drug effects , Lymph Nodes/immunology , Lymph Nodes/virology , Male , Sertoli Cells/drug effects , Sertoli Cells/immunology , Sertoli Cells/virology , Virus Activation/immunology , Virus Latency/immunology
4.
Mucosal Immunol ; 9(6): 1584-1595, 2016 11.
Article in English | MEDLINE | ID: mdl-26883728

ABSTRACT

Although the development of a fully protective HIV vaccine is the ultimate goal of HIV research, to date only one HIV vaccine trial, the RV144, has successfully induced a weakly protective response. The 31% protection from infection achieved in the RV144 trial was linked to the induction of nonneutralizing antibodies, able to mediate antibody-dependent cell-mediated cytotoxicity (ADCC), suggestive of an important role of Fc-mediated functions in protection. Similarly, Fc-mediated antiviral activity was recently shown to play a critical role in actively suppressing the viral reservoir, but the Fc effector mechanisms within tissues that provide protection from or after infection are largely unknown. Here we aimed to define the landscape of effector cells and Fc receptors present within vulnerable tissues. We found negligible Fc receptor-expressing natural killer cells in the female reproductive and gastrointestinal mucosa. Conversely, Fc receptor-expressing macrophages were highly enriched in most tissues, but neutrophils mediated superior antibody-mediated phagocytosis. Modifications in Fc domain of VRC01 antibody increased phagocytic responses in both phagocytes. These data suggest that non-ADCC-mediated mechanisms, such as phagocytosis and neutrophil activation, are more likely to play a role in preventative vaccine or reservoir-eliminating therapeutic approaches.


Subject(s)
AIDS Vaccines/immunology , HIV Infections/immunology , HIV Infections/metabolism , HIV-1/immunology , Phagocytosis/immunology , Receptors, Fc/metabolism , Adult , Antibodies, Monoclonal/immunology , Biomarkers , Broadly Neutralizing Antibodies , Cytokines/metabolism , Female , Gene Expression , HIV Antibodies/immunology , HIV Infections/prevention & control , HIV Infections/virology , Humans , Immunity, Innate , Inflammation Mediators/metabolism , Killer Cells, Natural/immunology , Killer Cells, Natural/metabolism , Macrophages/immunology , Macrophages/metabolism , Middle Aged , Mucous Membrane/immunology , Mucous Membrane/metabolism , Mucous Membrane/virology , Neutrophils/immunology , Neutrophils/metabolism , Receptors, Fc/genetics , Young Adult
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