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
. 2021 Jun 30;9(7):708.
doi: 10.3390/vaccines9070708.

Serological Response in Lung Transplant Recipients after Two Doses of SARS-CoV-2 mRNA Vaccines

Affiliations

Serological Response in Lung Transplant Recipients after Two Doses of SARS-CoV-2 mRNA Vaccines

Madhusudhanan Narasimhan et al. Vaccines (Basel). .

Abstract

Background: Lung-transplant (LT) recipients are at high risk for COVID-19 due to immunosuppression and respiratory tropism of SARS-CoV-2. The information on the effect of COVID-19 mRNA vaccines to elicit immunogenic responses after a two-dose (2D) regimen in LT recipients is sparse. Thus, we assessed the effect of Pfizer-BioNTech and Moderna mRNA vaccines' 2D regimen on anti-spike responses in immunocompromised LT recipients.

Methods: We utilized serum samples from LT recipients vaccinated for SARS-CoV-2 with 2D of either the Pfizer-BioNTech or Moderna vaccines and 2D-vaccinated naïve (non-transplanted and non-exposed to COVID-19) group. Antibody responses were assessed using the FDA-approved SARS-CoV-2 anti-nucleocapsid protein IgG assay (IgGNC), the SARS-CoV-2 anti-spike protein IgM assay (IgMSP), and the SARS-CoV-2 anti-spike protein IgG II assay (IgGSP). CD4+ T-cell activity was assessed as a marker of immune competence using the ImmuKnow® assay.

Results: About 25% (18/73) of SARS-CoV-2 uninfected-LT patients generated a positive spike-IgG response following 2D of vaccines, with 36% (9/25) in the Moderna cohort and only 19% (9/48) in the Pfizer cohort. 2D in LT patients elicited a significantly lesser median IgGSP response (1.7 AU/mL, 95% CI: 0.6-7.5 AU/mL) compared to non-transplanted, uninfected naïve subjects (14,209 AU/mL, 95% CI: 11,261-18,836 AU/mL; p < 0.0001). In LT patients, the Moderna-evoked seropositivity trend was higher than Pfizer.

Conclusion: 2D COVID-19 vaccination elicits a dampened serological response in LT patients. Whether assessing other arms of host immunity combined with a higher vaccine dose can better capture and elicit improved immunogenicity in this immunocompromised population warrants investigation.

Keywords: COVID-19 mRNA vaccines; IgG; IgM; SARS-CoV-2; Spike; lung transplantation; nucleocapsid; serological response; two doses.

PubMed Disclaimer

Conflict of interest statement

Abbott Diagnostics, while providing a part of the antibody testing reagents, did not have any role in the study’s design, collection, analyses, or interpretation of the data; drafting the manuscript; or in the decision to publish the results. The authors declare no other conflicts of interest.

Figures

Figure 1
Figure 1
Frequency distribution of IgGSP versus days after the second dose of COVID-19 vaccines in LT recipients (a) BNT162b2 (Pfizer-BioNTech); (b) mRNA-1273 (Moderna). DA2D, days after the second dose of COVID-19 vaccines; prior-infected, pink-filled circle (Figure 1a); broken red and blue lines, IgGSP serology assay’s manufacturer-recommended positive cut-off value.
Figure 2
Figure 2
IgGSP levels in naïve subjects and LT patients after 2 doses of COVID-19 vaccine. NA2D, naïve subjects (non-transplanted and not had previous SARS-CoV-2 infection) after 2 doses of vaccine; TA2D, LT patients after 2 doses of vaccine; thick red line, median value.
Figure 3
Figure 3
Evaluation of immunogenicity following the double-dose Pfizer and Moderna vaccine regimen in LT recipients. Thick red line, median value; median (95% CI) (Pfizer—0.9 (0.0–4.1); Moderna—20.6 (0.8–80.2)).

References

    1. Boyarsky B.J., Werbel W.A., Avery R.K., Tobian A.A., Massie A.B., Segev D.L., Garonzik-Wang J.M. Immunogenicity of a Single Dose of SARS-CoV-2 Messenger RNA Vaccine in Solid Organ Transplant Recipients. JAMA. 2021;325:1784–1786. doi: 10.1001/jama.2021.4385. - DOI - PMC - PubMed
    1. Boyarsky B.J., Werbel W.A., Avery R.K., Tobian A.A., Massie A.B., Segev D.L., Garonzik-Wang J.M. Antibody Response to 2-Dose SARS-CoV-2 mRNA Vaccine Series in Solid Organ Transplant Recipients. JAMA. 2021;325:2204–2206. doi: 10.1001/jama.2021.7489. - DOI - PMC - PubMed
    1. Havlin J., Svorcova M., Dvorackova E., Lastovicka J., Lischke R., Kalina T., Hubacek P. Immunogenicity of BNT162b2 mRNA COVID-19 vaccine and SARS-CoV-2 infection in lung transplant recipients. J. Heart Lung Transpl. 2021 doi: 10.1016/j.healun.2021.05.004. in press. - DOI - PMC - PubMed
    1. SARS-CoV-2 Vaccination in Heart and Lung Transplantation: Recommendations from the ISHLT COVID-19 Task Force. [(accessed on 7 June 2021)]; Available online: https://ishlt.org/ishlt/media/Documents/COVID19_Vaccine-Recommendations_....
    1. Narasimhan M., Mahimainathan L., Araj E., Clark A.E., Markantonis J., Green A., Xu J., SoRelle J.A., Alexis C., Fankhauser K., et al. Clinical evaluation of the Abbott Alinity SARS-CoV-2 spike-specific quantitative IgG and IgM assays in infected, recovered, and vaccinated groups. J. Clin. Microbiol. 2021;59:e0038821. doi: 10.1128/JCM.00388-21. - DOI - PMC - PubMed