TY - JOUR
T1 - Predictors of humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in patients receiving maintenance dialysis
AU - Li, Tingting
AU - Gandra, Sumanth
AU - Reske, Kimberly A.
AU - Olsen, Margaret A.
AU - Bommarito, Silvana
AU - Miller, Candace
AU - Hock, Karl G.
AU - Ballman, Claire A.
AU - Su, Christina
AU - Dang, Na Le
AU - Kwon, Jennie H.
AU - Warren, David K.
AU - Fraser, Victoria J.
AU - Farnsworth, Christopher W.
N1 - Funding Information:
T.L. receives research support from Aurinia Pharmaceuticals, Genentech, and Omeros Corporation, and reports consultancy agreements with ChemoCentryx, Travere Therapeutics, GlaxoSmithKline, and Reata Pharmaceuticals. C.W.F. receives research funding from Abbott Laboratories, Roche Diagnostics, and Siemens Healthineers. D.K.W. has served as a consultant for Mölnlycke Health Care AB. M.A.O. has served as a consultant for Pfizer for work unrelated to this study. All other authors have no relevant disclosures.
Funding Information:
This work was supported by the CDC Epicenters Program (grant no. 6 U54CK000482-04), the Clinical and Translational Science Award (CTSA grant no. UL1 TR000448), and Siteman Comprehensive Cancer Center and NCI Cancer Center (grant no. P30 CA091842).
Publisher Copyright:
© The Author(s), 2022.
PY - 2022/3/23
Y1 - 2022/3/23
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85129848911&partnerID=8YFLogxK
U2 - 10.1017/ash.2022.31
DO - 10.1017/ash.2022.31
M3 - Article
C2 - 36310813
AN - SCOPUS:85129848911
SN - 2732-494X
VL - 2
JO - Antimicrobial Stewardship and Healthcare Epidemiology
JF - Antimicrobial Stewardship and Healthcare Epidemiology
IS - 1
M1 - e48
ER -