Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Apr 4;11(4):799.
doi: 10.3390/vaccines11040799.

Immunogenicity of a Third Dose of BNT162b2 Vaccine among Lung Transplant Recipients-A Prospective Cohort Study

Affiliations

Immunogenicity of a Third Dose of BNT162b2 Vaccine among Lung Transplant Recipients-A Prospective Cohort Study

Yael Shostak et al. Vaccines (Basel). .

Abstract

Two doses of mRNA SARS-CoV-2 vaccines elicit an attenuated humoral immune response among immunocompromised patients. Our study aimed to assess the immunogenicity of a third dose of the BNT162b2 vaccine among lung transplant recipients (LTRs). We prospectively evaluated the humoral response by measuring anti-spike SARS-CoV-2 and neutralizing antibodies in 139 vaccinated LTRs ~4-6 weeks following the third vaccine dose. The t-cell response was evaluated by IFNγ assay. The primary outcome was the seropositivity rate following the third vaccine dose. Secondary outcomes included: positive neutralizing antibody and cellular immune response rate, adverse events, and COVID-19 infections. Results were compared to a control group of 41 healthcare workers. Among LTRs, 42.4% had a seropositive antibody titer, and 17.2% had a positive t-cell response. Seropositivity was associated with younger age (t = 3.736, p < 0.001), higher GFR (t = 2.355, p = 0.011), and longer duration from transplantation (t = -1.992, p = 0.024). Antibody titer positively correlated with neutralizing antibodies (r = 0.955, p < 0.001). The current study may suggest the enhancement of immunogenicity by using booster doses. Since monoclonal antibodies have limited effectiveness against prevalent sub-variants and LTRs are prone to severe COVID-19 morbidity, vaccination remains crucial for this vulnerable population.

Keywords: BNT162b2 COVID-19 vaccine; immunogenicity; lung transplantation; third dose.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Seropositivity among LTRs and control group before and after the third vaccine dose. A column scatter plot graph representing the BNT162b2 vaccine-induced S1-IgG antibody levels (AU/mL) in lung transplant recipients and control group before and after the third vaccine dose. The bars represent median values. Abbreviations: LTRs, lung transplant recipients; AU, antibody units; Neg, LTRs with seronegative antibody titer: Pos, LTRs with seropositive antibody titer; C, control group antibody titer.
Figure 2
Figure 2
Neutralizing antibodies and seropositive s-IgG titer Correlation. A Pearson correlation plot representing the correlation between S1-IgG antibody levels (AU/mL) and neutralizing antibody titer among vaccinated lung transplant recipients. The small upper Pearson correlation plot represents a magnified view with a scale of 5000 Total Abs (AU/mL). Abs, antibodies; AU, antibody units.

Similar articles

Cited by

References

    1. WHO Coronavirus (COVID-19) Dashboard|WHO Coronavirus (COVID-19) Dashboard with Vaccination Data. [(accessed on 9 January 2023)]. Available online: https://covid19.who.int/
    1. Jamison D.A., Anand Narayanan S., Trovão N.S., Guarnieri J.W., Topper M.J., Moraes-Vieira P.M., Zaksas V., Singh K.K., Wurtele E.S., Beheshti A. A comprehensive SARS-CoV-2 and COVID-19 review, Part 1: Intracellular overdrive for SARS-CoV-2 infection. Eur. J. Hum. Genet. 2022;30:889–898. doi: 10.1038/s41431-022-01108-8. - DOI - PMC - PubMed
    1. Levin M.J., Ustianowski A., De Wit S., Launay O., Avila M., Templeton A., Yuan Y., Seegobin S., Ellery A., Levinson D.J., et al. Intramuscular AZD7442 (Tixagevimab-Cilgavimab) for Prevention of COVID-19. N. Engl. J. Med. 2022;386:2188–2200. doi: 10.1056/NEJMoa2116620. - DOI - PMC - PubMed
    1. FDA Announces Evusheld Is Not Currently Authorized for Emergency Use in the U.S.|FDA. [(accessed on 30 January 2023)]; Available online: https://www.fda.gov/drugs/drug-safety-and-availability/fda-announces-evu....
    1. Polack F.P., Thomas S.J., Kitchin N., Absalon J., Gurtman A., Lockhart S., Perez J.L., Pérez Marc G., Moreira E.D., Zerbini C., et al. Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine. N. Engl. J. Med. 2020;383:2603–2615. doi: 10.1056/NEJMoa2034577. - DOI - PMC - PubMed

LinkOut - more resources