Evaluation of the SARS-CoV-2 Antibody Response to the BNT162b2 Vaccine in Patients Undergoing Hemodialysis.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 09 2021
Historique:
entrez: 2 9 2021
pubmed: 3 9 2021
medline: 18 9 2021
Statut: epublish

Résumé

Patients undergoing hemodialysis have a high mortality rate associated with COVID-19, and this patient population often has a poor response to vaccinations. Randomized clinical trials for COVID-19 vaccines included few patients with kidney disease; therefore, vaccine immunogenicity is uncertain in this population. To evaluate the SARS-CoV-2 antibody response in patients undergoing chronic hemodialysis following 1 vs 2 doses of BNT162b2 COVID-19 vaccination compared with health care workers serving as controls and convalescent serum. A prospective, single-center cohort study was conducted between February 2 and April 17, 2021, in Toronto, Ontario, Canada. Participants included 142 patients receiving in-center hemodialysis and 35 health care worker controls. BNT162b2 (Pfizer-BioNTech) COVID-19 vaccine. SARS-CoV-2 IgG antibodies to the spike protein (anti-spike), receptor binding domain (anti-RBD), and nucleocapsid protein (anti-NP). Among the 142 participants undergoing maintenance hemodialysis, 94 (66%) were men; median age was 72 (interquartile range, 62-79) years. SARS-CoV-2 IgG antibodies were measured in 66 patients receiving 1 vaccine dose following a public health policy change, 76 patients receiving 2 vaccine doses, and 35 health care workers receiving 2 vaccine doses. Detectable anti-NP suggestive of natural SARS-CoV-2 infection was detected in 15 of 142 (11%) patients at baseline, and only 3 patients had prior COVID-19 confirmed by reverse transcriptase polymerase chain reaction testing. Two additional patients contracted COVID-19 after receiving 2 doses of vaccine. In 66 patients receiving a single BNT162b2 dose, seroconversion occurred in 53 (80%) for anti-spike and 36 (55%) for anti-RBD by 28 days postdose, but a robust response, defined by reaching the median levels of antibodies in convalescent serum from COVID-19 survivors, was noted in only 15 patients (23%) for anti-spike and 4 (6%) for anti-RBD in convalescent serum from COVID-19 survivors. In patients receiving 2 doses of BNT162b2 vaccine, seroconversion occurred in 69 of 72 (96%) for anti-spike and 63 of 72 (88%) for anti-RBD by 2 weeks following the second dose and median convalescent serum levels were reached in 52 of 72 patients (72%) for anti-spike and 43 of 72 (60%) for anti-RBD. In contrast, all 35 health care workers exceeded the median level of anti-spike and anti-RBD found in convalescent serum 2 to 4 weeks after the second dose. This study suggests poor immunogenicity 28 days following a single dose of BNT162b2 vaccine in the hemodialysis population, supporting adherence to recommended vaccination schedules and avoiding delay of the second dose in these at-risk individuals.

Identifiants

pubmed: 34473256
pii: 2783679
doi: 10.1001/jamanetworkopen.2021.23622
pmc: PMC8414193
doi:

Substances chimiques

COVID-19 Vaccines 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2123622

Commentaires et corrections

Type : ErratumIn

Références

Nat Med. 2020 Jul;26(7):1033-1036
pubmed: 32398876
JCI Insight. 2020 Oct 2;5(19):
pubmed: 32870820
Clin J Am Soc Nephrol. 2021 Apr 7;16(4):613-614
pubmed: 33208402
Nat Commun. 2021 Feb 15;12(1):1018
pubmed: 33589636
CMAJ. 2021 Feb 22;193(8):E278-E284
pubmed: 33542093
Am J Kidney Dis. 2021 Apr;77(4 Suppl 1):A7-A8
pubmed: 33752804
JAMA. 2021 May 4;325(17):1784-1786
pubmed: 33720292
BMJ. 2021 Mar 18;372:n710
pubmed: 33737404
Nat Med. 2021 Jul;27(7):1205-1211
pubmed: 34002089
Lancet Oncol. 2021 Jun;22(6):765-778
pubmed: 33930323
Clin J Am Soc Nephrol. 2021 Apr 6;:
pubmed: 33824157
Am J Kidney Dis. 2020 Mar;75(3):417-425
pubmed: 31585683
Sci Immunol. 2020 Oct 8;5(52):
pubmed: 33033173
N Engl J Med. 2020 Dec 31;383(27):2603-2615
pubmed: 33301246
Am J Kidney Dis. 2020 Nov;76(5):690-695.e1
pubmed: 32681983

Auteurs

Kevin Yau (K)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Division of Nephrology, Department of Medicine, Unity Health Toronto, Toronto, Ontario, Canada.

Kento T Abe (KT)

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health System, Toronto, Ontario, Canada.

David Naimark (D)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Matthew J Oliver (MJ)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Jeffrey Perl (J)

Division of Nephrology, Department of Medicine, Unity Health Toronto, Toronto, Ontario, Canada.
Li Ka Shing Knowledge Institute, St Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.

Jerome A Leis (JA)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Division of Infectious Diseases, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Shelly Bolotin (S)

Public Health Ontario, Toronto, Ontario, Canada.
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Vanessa Tran (V)

Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Sarah I Mullin (SI)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Ellen Shadowitz (E)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Anny Gonzalez (A)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Tatjana Sukovic (T)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Julie Garnham-Takaoka (J)

Li Ka Shing Knowledge Institute, St Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.

Keelia Quinn de Launay (KQ)

Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health System, Toronto, Ontario, Canada.

Alyson Takaoka (A)

Li Ka Shing Knowledge Institute, St Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.

Sharon E Straus (SE)

Li Ka Shing Knowledge Institute, St Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.

Allison J McGeer (AJ)

Sinai Health System, Toronto, Ontario, Canada.

Christopher T Chan (CT)

Division of Nephrology, University Health Network, Toronto, Ontario, Canada.

Karen Colwill (K)

Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health System, Toronto, Ontario, Canada.

Anne-Claude Gingras (AC)

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health System, Toronto, Ontario, Canada.

Michelle A Hladunewich (MA)

Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

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