Morning administration enhances humoral response to SARS-CoV-2 vaccination in kidney transplant recipients
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38460787
DOI
10.1016/j.ajt.2024.03.004
PII: S1600-6135(24)00199-0
Knihovny.cz E-zdroje
- Klíčová slova
- Bayesian modeling, SARS-CoV-2 mRNA vaccines, chronovaccination, circadian rhythms, immunosuppression, kidney transplantation, seroconversion, vaccination response, vaccination timing,
- MeSH
- chronické selhání ledvin chirurgie imunologie MeSH
- cirkadiánní rytmus imunologie MeSH
- COVID-19 * prevence a kontrola imunologie MeSH
- dospělí MeSH
- humorální imunita * MeSH
- imunoglobulin G krev imunologie MeSH
- imunosupresiva aplikace a dávkování terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- příjemce transplantátu MeSH
- protilátky virové * krev imunologie MeSH
- rejekce štěpu imunologie prevence a kontrola MeSH
- SARS-CoV-2 * imunologie MeSH
- senioři MeSH
- transplantace ledvin * MeSH
- vakcinace MeSH
- vakcíny proti COVID-19 * imunologie aplikace a dávkování MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- imunoglobulin G MeSH
- imunosupresiva MeSH
- protilátky virové * MeSH
- vakcíny proti COVID-19 * 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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