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Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
Tanushree Dangi, … , Justin M. Richner, Pablo Penaloza-MacMaster
Tanushree Dangi, … , Justin M. Richner, Pablo Penaloza-MacMaster
Published October 11, 2022
Citation Information: J Clin Invest. 2022;132(23):e162282. https://doi.org/10.1172/JCI162282.
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Research Article Immunology

Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody

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Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contribution to the antiviral response remains unclear. Here, we interrogated whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine and then transferred sera from these mice into naive mice, followed by challenge with SARS-CoV-2. We show that mice that received nucleocapsid-specific sera or a nucleocapsid-specific mAb exhibited enhanced control of SARS-CoV-2. Nucleocapsid-specific antibodies elicited NK-mediated, antibody-dependent cellular cytotoxicity (ADCC) against infected cells. To our knowledge, these findings provide the first demonstration in the coronavirus literature that antibody responses specific to the nucleocapsid protein can improve viral clearance, providing a rationale for the clinical evaluation of nucleocapsid-based mAb therapies to treat COVID-19.

Authors

Tanushree Dangi, Sarah Sanchez, Jacob Class, Michelle Richner, Lavanya Visvabharathy, Young Rock Chung, Kirsten Bentley, Richard J. Stanton, Igor J. Koralnik, Justin M. Richner, Pablo Penaloza-MacMaster

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Figure 1

SARS-CoV-2 nucleocapsid–specific antibody after SARS-CoV-2 infection in a cohort of patients admitted to Northwestern University Hospital.

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SARS-CoV-2 nucleocapsid–specific antibody after SARS-CoV-2 infection in ...
(A) Human pre-2019 plasma samples from healthy individuals were used as a control. Data shown are from an ongoing study, in which participants were infected on different dates, hence the heterogeneity in the nucleocapsid-specific antibody responses. SARS-CoV-2 infection was confirmed by RT-PCR. Antibody responses were evaluated by ELISA. (B) Summary of SARS-CoV-2 nucleocapsid–specific antibodies in sera. (C) Summary of influenza HA–specific antibodies in sera (used as an irrelevant antigen control). Dashed lines represent the LOD. Significance in B and C was determine by Mann-Whitney U test. Error bars represent the SEM.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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