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Predictors of humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in patients receiving maintenance dialysis

OBJECTIVE: Patients on dialysis are at high risk for severe COVID-19 and associated morbidity and mortality. We examined the humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in a maintenance dialysis population. DESIGN: Single-center cohort study. SETTING AND PARTICIPANTS: Adult maintenance dial...

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Detalles Bibliográficos
Autores principales: Li, Tingting, Gandra, Sumanth, Reske, Kimberly A., Olsen, Margaret A., Bommarito, Silvana, Miller, Candace, Hock, Karl G., Ballman, Claire A., Su, Christina, Le Dang, Na, Kwon, Jennie H., Warren, David K., Fraser, Victoria J., Farnsworth, Christopher W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615013/
https://www.ncbi.nlm.nih.gov/pubmed/36310813
http://dx.doi.org/10.1017/ash.2022.31
Descripción
Sumario:OBJECTIVE: Patients on dialysis are at high risk for severe COVID-19 and associated morbidity and mortality. We examined the humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in a maintenance dialysis population. DESIGN: Single-center cohort study. SETTING AND PARTICIPANTS: Adult maintenance dialysis patients at 3 outpatient dialysis units of a large academic center. METHODS: Participants were vaccinated with 2 doses of BNT162b2, 3 weeks apart. We assessed anti–SARS-CoV-2 spike antibodies (anti-S) ∼4–7 weeks after the second dose and evaluated risk factors associated with insufficient response. Definitions of antibody response are as follows: nonresponse (anti-S level, <50 AU/mL), low response (anti-S level, 50–839 AU/mL), and sufficient response (anti-S level, ≥840 AU/mL). RESULTS: Among the 173 participants who received 2 vaccine doses, the median age was 60 years (range, 28–88), 53.2% were men, 85% were of Black race, 86% were on in-center hemodialysis and 14% were on peritoneal dialysis. Also, 7 participants (4%) had no response, 27 (15.6%) had a low response, and 139 (80.3%) had a sufficient antibody response. In multivariable analysis, factors significantly associated with insufficient antibody response included end-stage renal disease comorbidity index score ≥5 and absence of prior hepatitis B vaccination response. CONCLUSIONS: Although most of our study participants seroconverted after 2 doses of BNT162b2, 20% of our cohort did not achieve sufficient humoral response. Our findings demonstrate the urgent need for a more effective vaccine strategy in this high-risk patient population and highlight the importance of ongoing preventative measures until protective immunity is achieved.