Immune Response after mRNA COVID-19 Vaccination in Lung Transplant Recipients: A 6-Month Follow-Up.

COVID-19 T cell response humoral response immunosuppressive drugs lung transplant recipients

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
15 Jul 2022
Historique:
received: 08 06 2022
revised: 11 07 2022
accepted: 12 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

This prospective cohort study analyzed the immune response to COVID-19 mRNA vaccines in lung transplant recipients (LuTRs) compared to healthy controls (HCs) at a 6-month follow-up. After the first two doses of either BNT162b2 or mRNA-1273, SARS-CoV-2 antibodies were measured in LuTRs ( Seroconversion rates were 94% and 100% after the first and second vaccine dose, respectively, in HCs, while only 19% and 56% of LuTRs developed antibodies. Furthermore, 22 of 24 LuTRs who received the third vaccine dose showed seroconversion (five of seven primary non-responders and 17 of 17 primary responders). A T cell response against SARS-CoV-2-spike S1 and/or S2 was detected in 100% (16/16) of HCs and 50% (8/16) of LuTRs. The data suggest that LuTRs have reduced humoral and cellular immune responses after two doses of COVID-19 mRNA vaccination when compared to HCs. A third dose may be of substantial benefit.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
This prospective cohort study analyzed the immune response to COVID-19 mRNA vaccines in lung transplant recipients (LuTRs) compared to healthy controls (HCs) at a 6-month follow-up.
METHODS METHODS
After the first two doses of either BNT162b2 or mRNA-1273, SARS-CoV-2 antibodies were measured in LuTRs (
RESULTS RESULTS
Seroconversion rates were 94% and 100% after the first and second vaccine dose, respectively, in HCs, while only 19% and 56% of LuTRs developed antibodies. Furthermore, 22 of 24 LuTRs who received the third vaccine dose showed seroconversion (five of seven primary non-responders and 17 of 17 primary responders). A T cell response against SARS-CoV-2-spike S1 and/or S2 was detected in 100% (16/16) of HCs and 50% (8/16) of LuTRs.
CONCLUSIONS CONCLUSIONS
The data suggest that LuTRs have reduced humoral and cellular immune responses after two doses of COVID-19 mRNA vaccination when compared to HCs. A third dose may be of substantial benefit.

Identifiants

pubmed: 35891294
pii: vaccines10071130
doi: 10.3390/vaccines10071130
pmc: PMC9318026
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Selma Tobudic (S)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Alberto Benazzo (A)

Clinical Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria.

Maximilian Koblischke (M)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Lisa Schneider (L)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Stephan Blüml (S)

Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, 1090 Vienna, Austria.

Florian Winkler (F)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.
Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, 1090 Vienna, Austria.

Hannah Schmidt (H)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Stefan Vorlen (S)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Helmuth Haslacher (H)

Department of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Thomas Perkmann (T)

Department of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Heinz Burgmann (H)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Peter Jaksch (P)

Clinical Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria.

Judith H Aberle (JH)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Stefan Winkler (S)

Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria.

Classifications MeSH