Increased COVID-19 Mortality and Deficient SARS-CoV-2 Immune Response Are Not Associated with Higher Levels of Endemic Coronavirus Antibodies

Author:

Adhikari Bindu12,Oltz Eugene M.3,Bednash Joseph S.4,Horowitz Jeffrey C.4ORCID,Amimo Joshua O.2ORCID,Raev Sergei A.2ORCID,Fernández Soledad5,Anghelina Mirela5,Liu Shan-Lu3678ORCID,Rubinstein Mark P.910,Jones Daniel M.11,Saif Linda J.12ORCID,Vlasova Anastasia N.12ORCID

Affiliation:

1. Department of Veterinary Preventive Medicine, College of Veterinary Medicine, The Ohio State University, Wooster, OH 44691, USA

2. Center for Food Animal Health, Department of Animal Sciences, OARDC, College of Food, Agricultural and Environmental Sciences, The Ohio State University, Wooster, OH 44691, USA

3. Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH 43210, USA

4. Department of Internal Medicine, Division of Pulmonary, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, OH 43210, USA

5. Department of Biomedical Informatics, College of Medicine and Center for Biostatistics, The Ohio State University, Columbus, OH 43210, USA

6. Center for Retrovirus Research, The Ohio State University, Columbus, OH 43210, USA

7. Department of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210, USA

8. Viruses and Emerging Pathogens Program, Infectious Diseases Institute, The Ohio State University, Columbus, OH 43210, USA

9. Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA

10. The Pelotonia Institute of Immuno-Oncology, The Ohio State University James Comprehensive Cancer Center, Columbus, OH 43210, USA

11. Department of Pathology, The Ohio State University, Columbus, OH 43210, USA

Abstract

The impact of pre-existing common cold coronavirus (CCCoV) antibodies (Abs) on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) immune responses and pathogenesis remains poorly defined. We evaluated these associations in a cohort of hospitalized patients with COVID-19 and respiratory failure of varying severity. Patients with respiratory failure from other causes (non-COVID-19) were evaluated as controls. We demonstrated a positive correlation between levels of CCCoV and SARS-CoV-2 Abs using CCCoV and SARS-CoV-2 N and S protein peptide-specific ELISA. Consistent with the above, moderately increased levels of CCCoV-specific Abs in non-COVID-19 vs. COVID-19 patients suggest potential protective effects. Further, higher SARS-CoV-2 N protein-specific and CCCoV Ab levels were observed among surviving vs. non-surviving COVID-19 positive patients. However, the highest SARS-CoV-2 N and S protein-specific IgG and IgA Ab levels were noted in the patients with the most severe clinical disease. Finally, advanced age, cancer and immunosuppression were associated with significantly higher mortality and reduced SARS-CoV-2 and CCCoV Ab levels. Thus, our data highlight that sufficient SARS-CoV-2 N protein-specific Ab responses improve clinical outcomes in severely ill COVID-19 patients. We also confirmed that pre-existing CCCoV-specific Abs do not inhibit the SARS-CoV-2 Ab response and may further reduce the prevalence and/or severity of COVID-19.

Funder

National Cancer Institute of the NIH

Publisher

MDPI AG

Subject

General Medicine

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