Long-term immune response after SARS-CoV2 vaccination in solid organ transplant recipients
- PMID: 40281454
- PMCID: PMC12032695
- DOI: 10.1186/s12879-024-10377-1
Long-term immune response after SARS-CoV2 vaccination in solid organ transplant recipients
Abstract
Background: Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) vaccination in solid organ transplant (SOT) recipients is associated with suboptimal antibody response (AbR) favouring breakthrough infection (BI). The role of cell-mediated immunity (CMI) remains uncertain.
Methods: Single-center prospective longitudinal cohort study of adult SOT recipients monitored for both AbR and CMI at 6 ± 2 months after booster dosage of SARS-CoV-2 vaccine. Primary end-point was BI diagnosis and CMI was the main risk factor. Relationship between CMI and BI was investigated by bivariate tests and multivariable logistic regression.
Results: CMI was performed in 139 patients. In 66 patients BI was documented before CMI, thus 73 (33 kidney, 24 liver, 14 lung, 2 heart) were analysed. The first 2 vaccine doses consisted of BNT162b2 and mRNA-1273 in 69.1% and 30.9% of cases, respectively. Whereas mRNA-1273 was used as for third dose in 91.2% of patients. At a median of 215 (IQR 181-252) days after booster dose, 40 (54.8%) patients displayed both AbR and CMI, 21 (28.8%) only AbR and 12 (16.4%) neither AbR or CMI; there were no patients showing negative AbR and positive CMI. Overall, 22 (30.1%) patients reported BI with no significant differences between those with positive vs. negative CMI (59.1% vs. 40.9%, p = 0.798), confirmed by multiple logistic regression after adjusting for age, type of vaccine and organs, high AbR and time from transplant.
Conclusion: Our data suggest that in the solid organ transplant population of our cohort, cell-mediated immunity does not appear to be a strong predictor of BI.
Keywords: Solid organ transplant; Antibody response; Cellular mediated immunity; Sars-CoV2 vaccine.
© 2024. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: The study was approved by the local institutional review board ethics committee “Comitato Etico Area Vasta Emilia Centro (AVEC)”, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy. Informed consent was obtained before enrollment. This study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
References
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- Manothummetha K, Chuleerarux N, Sanguankeo A, Kates OS, Hirankarn N, Thongkam A, et al. Immunogenicity and risk factors Associated with Poor Humoral Immune response of SARS-CoV-2 vaccines in recipients of solid organ transplant: a systematic review and Meta-analysis. JAMA Netw Open. 2022;5(4):e226822. - PMC - PubMed
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