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      Early post-infection treatment of SARS-CoV-2 infected macaques with human convalescent plasma with high neutralizing activity had no antiviral effects but moderately reduced lung inflammation

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      1 , 2 , * , , 1 , 2 , 1 , 3 , 1 , 1 , 1 , 4 , 5 , 4 , 4 , 4 , 6 , 6 , 2 , 1 , 6 , 6 , 7 , 1 , 1 , 8 , 9 , 1 , 1 , 1 , 3 , 9 , 9 , 2 , 1 , 2 , 4 , 1 , 3 , 6 , 10 , * , , 1 , 2 , * ,
      PLoS Pathogens
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          Abstract

          Early in the SARS-CoV-2 pandemic, there was a high level of optimism based on observational studies and small controlled trials that treating hospitalized patients with convalescent plasma from COVID-19 survivors (CCP) would be an important immunotherapy. However, as more data from controlled trials became available, the results became disappointing, with at best moderate evidence of efficacy when CCP with high titers of neutralizing antibodies was used early in infection. To better understand the potential therapeutic efficacy of CCP, and to further validate SARS-CoV-2 infection of macaques as a reliable animal model for testing such strategies, we inoculated 12 adult rhesus macaques with SARS-CoV-2 by intratracheal and intranasal routes. One day later, 8 animals were infused with pooled human CCP with a high titer of neutralizing antibodies (RVPN NT 50 value of 3,003), while 4 control animals received normal human plasma. Animals were monitored for 7 days. Animals treated with CCP had detectable but low levels of antiviral antibodies after infusion. In comparison to the control animals, CCP-treated animals had similar levels of viral RNA in upper and lower respiratory tract secretions, similar detection of viral RNA in lung tissues by in situ hybridization, but lower amounts of infectious virus in the lungs. CCP-treated animals had a moderate, but statistically significant reduction in interstitial pneumonia, as measured by comprehensive lung histology. Thus overall, therapeutic benefits of CCP were marginal and inferior to results obtained earlier with monoclonal antibodies in this animal model. By highlighting strengths and weaknesses, data of this study can help to further optimize nonhuman primate models to provide proof-of-concept of intervention strategies, and guide the future use of convalescent plasma against SARS-CoV-2 and potentially other newly emerging respiratory viruses.

          Author summary

          The results of treating SARS-CoV-2 infected hospitalized patients with COVID-19 convalescent plasma (CCP), collected from survivors of natural infection, have been disappointing. The available data from various studies indicate at best moderate clinical benefits only when CCP with high titer of neutralizing antibodies was infused early in infection. The macaque model of SARS-CoV-2 infection can be useful to gain further insights in the value of CCP therapy. In this study, animals were infected with SARS-CoV-2 and the next day were infused with pooled human convalescent plasma, selected to have a very high titer of neutralizing antibodies. While administration of CCP had minimal effects on reducing virus replication in the respiratory tract, it significantly reduced lung inflammation. These data, combined with the results of monoclonal antibody studies, emphasize the need to use products with high titers of neutralizing antibodies, and guide the future development of antibody-based therapies.

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          Convergent Antibody Responses to SARS-CoV-2 in Convalescent Individuals

          During the COVID-19 pandemic, SARS-CoV-2 infected millions of people and claimed hundreds of thousands of lives. Virus entry into cells depends on the receptor binding domain (RBD) of the SARS-CoV-2 spike protein (S). Although there is no vaccine, it is likely that antibodies will be essential for protection. However, little is known about the human antibody response to SARS-CoV-2 1–5 . Here we report on 149 COVID-19 convalescent individuals. Plasmas collected an average of 39 days after the onset of symptoms had variable half-maximal pseudovirus neutralizing titers: less than 1:50 in 33% and below 1:1000 in 79%, while only 1% showed titers >1:5000. Antibody sequencing revealed expanded clones of RBD-specific memory B cells expressing closely related antibodies in different individuals. Despite low plasma titers, antibodies to three distinct epitopes on RBD neutralized at half-maximal inhibitory concentrations (IC50s) as low as single digit ng/mL. Thus, most convalescent plasmas obtained from individuals who recover from COVID-19 do not contain high levels of neutralizing activity. Nevertheless, rare but recurring RBD-specific antibodies with potent antiviral activity were found in all individuals tested, suggesting that a vaccine designed to elicit such antibodies could be broadly effective.
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            Effectiveness of convalescent plasma therapy in severe COVID-19 patients

            Significance COVID-19 is currently a big threat to global health. However, no specific antiviral agents are available for its treatment. In this work, we explore the feasibility of convalescent plasma (CP) transfusion to rescue severe patients. The results from 10 severe adult cases showed that one dose (200 mL) of CP was well tolerated and could significantly increase or maintain the neutralizing antibodies at a high level, leading to disappearance of viremia in 7 d. Meanwhile, clinical symptoms and paraclinical criteria rapidly improved within 3 d. Radiological examination showed varying degrees of absorption of lung lesions within 7 d. These results indicate that CP can serve as a promising rescue option for severe COVID-19, while the randomized trial is warranted.
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              A human neutralizing antibody targets the receptor binding site of SARS-CoV-2

              An outbreak of coronavirus disease 2019 (COVID-19)1-3, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)4, has spread globally. Countermeasures are needed to treat and prevent further dissemination of the virus. Here we report the isolation of two specific human monoclonal antibodies (termed CA1 and CB6) from a patient convalescing from COVID-19. CA1 and CB6 demonstrated potent SARS-CoV-2-specific neutralization activity in vitro. In addition, CB6 inhibited infection with SARS-CoV-2 in rhesus monkeys in both prophylactic and treatment settings. We also performed structural studies, which revealed that CB6 recognizes an epitope that overlaps with angiotensin-converting enzyme 2 (ACE2)-binding sites in the SARS-CoV-2 receptor-binding domain, and thereby interferes with virus-receptor interactions by both steric hindrance and direct competition for interface residues. Our results suggest that CB6 deserves further study as a candidate for translation to the clinic.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: Writing – original draftRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: MethodologyRole: ValidationRole: VisualizationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: MethodologyRole: Writing – review & editing
                Role: InvestigationRole: MethodologyRole: Validation
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: Formal analysisRole: InvestigationRole: Visualization
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: InvestigationRole: MethodologyRole: Writing – review & editing
                Role: InvestigationRole: Visualization
                Role: Investigation
                Role: Investigation
                Role: ConceptualizationRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: Investigation
                Role: Investigation
                Role: Formal analysisRole: Investigation
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Investigation
                Role: Investigation
                Role: Formal analysisRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: InvestigationRole: SupervisionRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: MethodologyRole: ValidationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: MethodologyRole: Validation
                Role: ConceptualizationRole: MethodologyRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: InvestigationRole: MethodologyRole: ValidationRole: VisualizationRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS Pathog
                PLoS Pathog
                plos
                PLoS Pathogens
                Public Library of Science (San Francisco, CA USA )
                1553-7366
                1553-7374
                20 April 2022
                April 2022
                : 18
                : 4
                : e1009925
                Affiliations
                [1 ] California National Primate Research Center, University of California, Davis, California, United States of America
                [2 ] Department of Pathology, Microbiology and Immunology, University of California, Davis, California, United States of America
                [3 ] Department of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, California, United States of America
                [4 ] Center for Immunology and Infectious Diseases, University of California, Davis, California, United States of America
                [5 ] Graduate Group in Immunology, University of California, Davis, California, United States of America
                [6 ] Vitalant Research Institute, San Francisco, California, United States of America
                [7 ] Vitalant Research Institute, Denver, Colorado; University of Colorado School of Medicine, Aurora, Colorado, United States of America
                [8 ] School of Veterinary Medicine, University of California, Davis, California, United States of America
                [9 ] Vaccine Research and Development Center, Department of Physiology and Biophysics, School of Medicine, University of California, Irvine, California, United States of America
                [10 ] Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, United States of America
                National Institute of Allergy and Infectious Diseases Division of Intramural Research, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                Author information
                https://orcid.org/0000-0002-7375-1337
                https://orcid.org/0000-0003-3271-0413
                https://orcid.org/0000-0002-0024-7826
                https://orcid.org/0000-0002-3405-4862
                https://orcid.org/0000-0002-6047-211X
                https://orcid.org/0000-0002-1715-0748
                https://orcid.org/0000-0003-2986-1827
                https://orcid.org/0000-0002-5514-9836
                https://orcid.org/0000-0002-4330-4659
                https://orcid.org/0000-0002-1446-125X
                https://orcid.org/0000-0003-3864-6731
                Article
                PPATHOGENS-D-21-01783
                10.1371/journal.ppat.1009925
                9060337
                35443018
                32eb51b1-302e-4cff-a3d5-538957e4655a
                © 2022 Van Rompay et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 31 August 2021
                : 24 March 2022
                Page count
                Figures: 8, Tables: 0, Pages: 25
                Product
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100000052, NIH Office of the Director;
                Award ID: P51OD011107
                Funded by: funder-id http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: 1R21AI143454-02S1
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: 3RF1AG061001
                Award Recipient :
                This study was funded by California National Primate Research Center: Office of Research Infrastructure Program, Office of The Director, National Institutes of Health under Award Number P51OD011107. SI received funding from the National Institute of Allergy and Infectious Diseases, grants 1R21AI143454-02S1 and 3RF1AG061001. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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