Morning administration enhances humoral response to SARS-CoV-2 vaccination in kidney transplant recipients
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
38460787
DOI
10.1016/j.ajt.2024.03.004
PII: S1600-6135(24)00199-0
Knihovny.cz E-resources
- Keywords
- Bayesian modeling, SARS-CoV-2 mRNA vaccines, chronovaccination, circadian rhythms, immunosuppression, kidney transplantation, seroconversion, vaccination response, vaccination timing,
- MeSH
- Kidney Failure, Chronic surgery immunology MeSH
- Circadian Rhythm immunology MeSH
- COVID-19 * prevention & control immunology MeSH
- Adult MeSH
- Immunity, Humoral * MeSH
- Immunoglobulin G blood immunology MeSH
- Immunosuppressive Agents administration & dosage therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Transplant Recipients MeSH
- Antibodies, Viral * blood immunology MeSH
- Graft Rejection immunology prevention & control MeSH
- SARS-CoV-2 * immunology MeSH
- Aged MeSH
- Kidney Transplantation * MeSH
- Vaccination MeSH
- COVID-19 Vaccines * immunology administration & dosage MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Immunoglobulin G MeSH
- Immunosuppressive Agents MeSH
- Antibodies, Viral * MeSH
- COVID-19 Vaccines * MeSH
Although severe acute respiratory syndrome coronavirus 2 messenger ribonucleic acid (SARS-CoV-2 mRNA) vaccines are effective in kidney transplant recipients (KTRs), their immune response to vaccination is blunted by immunosuppression. Other tools enhancing vaccination response are therefore needed. Interestingly, aligning vaccine administration with circadian rhythms (chronovaccination) has been shown to boost immune response. However, its applicability in KTRs, whose circadian rhythms are likely disrupted by immunosuppressants, remains unclear. To assess the impact of vaccination timing on seroconversion in the KTRs population, we analyzed data from 553 virus-naïve KTRs who received 2 doses of messenger ribonucleic acid (mRNA) vaccine. Bayesian logistic regression was employed, adjusting for previously identified predictors of seroconversion, including allograft function, maintenance immunosuppressants, or time since transplantation. SARS-CoV-2 immunoglobulin G (IgG) levels were measured with a median of 47 days after the second dose. The results did not reveal a reliable effect of timing of the first dose but did indicate that earlier timing for the second dose brings a notable benefit-every 1-hour delay in the application was associated with a 16% reduction in the odds of seroconversion (OR 0.84, 95% CI 0.71, 0.998). Similar results were obtained from quantile regression modeling IgG levels. In conclusion, morning vaccination is emerging as a promising and easily implementable strategy to enhance vaccine response in KTRs.
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