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SARS-CoV-2 Infection during the Omicron Surge among Patients Receiving Dialysis: The Role of Circulating Receptor-Binding Domain Antibodies and Vaccine Doses.
Montez-Rath, Maria E; Garcia, Pablo; Han, Jialin; Cadden, LinaCel; Hunsader, Patti; Morgan, Curt; Kerschmann, Russell; Beyer, Paul; Dittrich, Mary; Block, Geoffrey A; Parsonnet, Julie; Chertow, Glenn M; Anand, Shuchi.
  • Montez-Rath ME; Department of Medicine (Nephrology), Stanford University, Palo Alto, California.
  • Garcia P; Department of Medicine (Nephrology), Stanford University, Palo Alto, California.
  • Han J; Department of Medicine (Nephrology), Stanford University, Palo Alto, California.
  • Cadden L; Ascend Clinical Laboratory, Redwood City, California.
  • Hunsader P; Ascend Clinical Laboratory, Redwood City, California.
  • Morgan C; Ascend Clinical Laboratory, Redwood City, California.
  • Kerschmann R; Ascend Clinical Laboratory, Redwood City, California.
  • Beyer P; Ascend Clinical Laboratory, Redwood City, California.
  • Dittrich M; US Renal Care, Plano, Texas.
  • Block GA; US Renal Care, Plano, Texas.
  • Parsonnet J; Department of Medicine (Infectious Diseases and Geographic Medicine), Stanford University, Palo Alto, California.
  • Chertow GM; Department of Epidemiology and Population Health, Stanford University, Palo Alto, California.
  • Anand S; Department of Medicine (Nephrology), Stanford University, Palo Alto, California.
J Am Soc Nephrol ; 2022 Aug 16.
Article in English | MEDLINE | ID: covidwho-1993605
ABSTRACT

BACKGROUND:

It is unclear whether circulating antibody levels conferred protection against SARS-CoV-2 infection among patients receiving dialysis during the Omicron-dominant period.

METHODS:

We followed monthly semiquantitative SARS-CoV-2 RBD IgG index values in a randomly selected nationwide cohort of patients receiving dialysis and ascertained SARS-CoV-2 infection during the Omicron-dominant period of December 25, 2021 to January 31, 2022 using electronic health records. We estimated the relative risk for documented SARS-CoV-2 infection by vaccination status and by circulating RBD IgG using a log-binomial model accounting for age, sex, and prior COVID-19.

RESULTS:

Among 3576 patients receiving dialysis, 901 (25%) received a third mRNA vaccine dose as of December 24, 2021. Early antibody responses to third doses were robust (median peak index IgG value at assay limit of 150). During the Omicron-dominant period, SARS-CoV-2 infection was documented in 340 (7%) patients. Risk for infection was higher among patients without vaccination and with one to two doses (RR, 2.1; 95% CI, 1.6 to 2.8, and RR, 1.3; 95% CI, 1.0 to 1.8 versus three doses, respectively). Irrespective of the number of vaccine doses, risk for infection was higher among patients with circulating RBD IgG <23 (506 BAU/ml) (RR range, 2.1 to 3.2, 95% CI, 1.3 to 3.4 and 95% CI, 2.2 to 4.5, respectively) compared with RBD IgG ≥23.

CONCLUSIONS:

Among patients receiving dialysis, a third mRNA vaccine dose enhanced protection against SARS-CoV-2 infection during the Omicron-dominant period, but a low circulating RBD antibody response was associated with risk for infection independent of the number of vaccine doses. Measuring circulating antibody levels in this high-risk group could inform optimal timing of vaccination and other measures to reduce risk of SARS-CoV-2 infection.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Language: English Journal subject: Nephrology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Language: English Journal subject: Nephrology Year: 2022 Document Type: Article