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Cross-protective immunity following coronavirus vaccination and coronavirus infection
Tanushree Dangi, … , Justin M. Richner, Pablo Penaloza-MacMaster
Tanushree Dangi, … , Justin M. Richner, Pablo Penaloza-MacMaster
Published October 8, 2021
Citation Information: J Clin Invest. 2021;131(24):e151969. https://doi.org/10.1172/JCI151969.
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Research Article COVID-19 Vaccines

Cross-protective immunity following coronavirus vaccination and coronavirus infection

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Abstract

Although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines have shown efficacy against SARS-CoV-2, it is unknown if coronavirus vaccines can also protect against other coronaviruses that may infect humans in the future. Here, we show that coronavirus vaccines elicited cross-protective immune responses against heterologous coronaviruses. In particular, we show that a severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1) vaccine developed in 2004 and known to protect against SARS-CoV-1 conferred robust heterologous protection against SARS-CoV-2 in mice. Similarly, prior coronavirus infections conferred heterologous protection against distinct coronaviruses. Cross-reactive immunity was also reported in patients with coronavirus disease 2019 (COVID-19) and in individuals who received SARS-CoV-2 vaccines, and transfer of plasma from these individuals into mice improved protection against coronavirus challenges. These findings provide the first demonstration to our knowledge that coronavirus vaccines (and prior coronavirus infections) can confer broad protection against heterologous coronaviruses and establish a rationale for universal coronavirus vaccines.

Authors

Tanushree Dangi, Nicole Palacio, Sarah Sanchez, Mincheol Park, Jacob Class, Lavanya Visvabharathy, Thomas Ciucci, Igor J. Koralnik, Justin M. Richner, Pablo Penaloza-MacMaster

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Figure 2

Cross-reactive antibody responses following SARS-CoV-2 infection in humans.

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Cross-reactive antibody responses following SARS-CoV-2 infection in huma...
Antibody responses following SARS-CoV-2 infection. (A) Participants in the COVID-19 group had a positive RT-PCR test accompanied by mild to severe symptoms. Serum samples (35 COVID-19 and 17 healthy controls) were collected once from week 3 to week 45 following symptom onset for the COVID-19 cohort. The healthy control cohort refers to human plasma collected prior to 2019. (B) SARS-CoV-2 spike–specific antibody responses. (C) SARS-CoV-1 spike–specific antibody responses. (D) OC43-specific antibody responses. OC43-infected cell lysate was used as a coating antigen. (E) SARS-CoV-2 nucleocapsid–specific antibody responses. (F) Influenza virus H1N1 HA–specific antibodies. Antibody responses were evaluated by ELISA. Dashed lines represent the LOD. ****P < 0.0001, by nonparametric Mann-Whitney U test. Error bars indicate the SEM.

Copyright © 2023 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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