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The Era of Infectious & Respiratory Disease

Durability of antibodies post vaccination with two doses of inactivated BBIBP-CorV vaccine

ORCID Icon, ORCID Icon, ORCID Icon, , ORCID Icon, , ORCID Icon, & show all
Pages 2069-2075 | Received 15 Sep 2022, Accepted 21 Oct 2022, Published online: 07 Nov 2022
 

Abstract

Background

Breakthrough infections post-COVID-19 vaccination occur with the emerging variants of the SARS-CoV virus which might be either due to the newer variants escaping immune response or the waning of antibodies over time. However, there is lack of long-term follow-up evidence on the waning of immune response following inactivated COVID-19 vaccine.

Methods

A retrospective, observational study was conducted on serum samples of individuals who had received two doses of BBIBP-CorV vaccine. Individual’s antibody responses were evaluated based on IgG anti-S and neutralizing antibodies measurements. Antibody samples were categorized into four groups, defined by the time interval from the individual’s receipt of the BBIBP-CorV vaccine: <30 days, 30–90 days, 91–180 days and >180 days.

Results

A total of 6668 serum samples from inactivated BBIBP-CorV vaccine recipients were analyzed for IgG anti-S and neutralizing antibodies. 571 (8.6%) samples were tested during the first 29 days interval post vaccination, 3642 (54.6%) were tested during 30–90 days interval, 2173 (32.6%) samples were tested during 91 to 180 days interval and 282(4.2%) were tested at >180 days interval post vaccination. We found that more than 50% of the individuals had antibody titers below the average cut-off range at the 91–180 days interval post vaccination. Older age (>60 years), male gender, chronic kidney disease, hypertension, immunodeficiencies and increased interval post vaccination emerged as independent risk factors associated with lower immune response.

Conclusion

Inactivated BBIBP-CorV vaccine recipients, based on age, gender and associated comorbid conditions might need booster doses at an earlier interval than the currently followed six months interval.

Transparency

Declaration of funding

The authors did not receive any funding for this study.

Declaration of financial/other relationships

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Author contributions

SM, SG, NA, WZ – contributed to the study concept and design; SM, SG, FC, NA – assisted with data collection; SG, NS – conducted the data analysis; SG- drafted the manuscript; SG, SM, NS, HW, PO, RH, WZ – revised the manuscript, SG, SM, NS, FC, HW, PO, RH, NA, WZ critically reviewed the final draft of the manuscript. All authors approved the final version of the manuscript.

Acknowledgements

Authors thank all lab personnel, skilled technicians at the Biogenix lab, who contributed to this study.

Data availability statement

All supporting data are availability with the corresponding author and will be shared upon approval of request.

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