MO906: Antibody Response to COVID-19 Vaccination in Patients Under Dialysis

Abstract BACKGROUND AND AIMS Patients (pts) with end-stage kidney disease (ESRD) may be more vulnerable to infections and may have a suboptimal response to vaccination. Dialysis patient (pt) began to be vaccinated against COVID-19 in February 2021. However, there were many doubts about whether immun...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)
Hauptverfasser: Choulitoudi, Vasiliki, Oikonomaki, Theodora, Bletsa, Anastasia, Ampelakiotou, Kleio, Panagakou, Stella, Koutroumpas, Georgios, Palla, Vasiliki, Panagopoulou, Panagiota, Adamidis, Konstantinos, Kogkaki, Eleni, Dardioti, Vasiliki, Kousouls, Varvara, Kolovos, Vasileios, Pomoni, Stella, Kontou, Elisavet, Tsirogianni, Alexandra, Christodoulidou, Christallenia
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Sprache:eng
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Zusammenfassung:Abstract BACKGROUND AND AIMS Patients (pts) with end-stage kidney disease (ESRD) may be more vulnerable to infections and may have a suboptimal response to vaccination. Dialysis patient (pt) began to be vaccinated against COVID-19 in February 2021. However, there were many doubts about whether immunization would be effective for them, as these pts have an impaired immune system, and it seems that this population responds poorly to vaccinations. Serum neutralizing antibodies (AbN) rapidly appear after the SARS-CoV-2 infection and the vaccination and are maintained for several months. The emergence of SARS-CoV-2 variants has raised concerns about the breadth of the neutralizing antibody responses. METHOD Serum samples were obtained from 181 patients receiving dialysis. Levels of circulating SARS-CoV-2 anti-spike IgG(S) and anti-nucleocapsid IgG (N) antibodies were quantified using the Abbott Diagnostics SARS-CoV-2 IgG chemiluminescent microparticle immunoassay (Abbott Diagnostics, Abbott Park, IL, USA) on an Abbott Diagnostics Architect i2000 SR and an Alinity analyzer, according to the manufacturer's instructions. Serum neutralizing antibodies (AbN) by commercially available assays (cPass SARS-CoV-2 Neutralization Antibody Detection Kit), at the first and the third months after the vaccination, were identified. Table 1. Paired samples statistics Mean N Std. deviation Std. error mean Pair 1 AbN1 77.7373 153 24.17986 1.95483 AbN3 57.0906 153 31.29075 2.52971 Pair 2 AbIgGspike1 5360.8569 144 6252.38034 521.03169 AbIgGspike3 1670.8667 144 3814.62641 317.88553 Comparison of neutralizers and antiSpikes between measurements 1 month and 3 months after vaccination (method: paired t-test). RESULTS The IgG-spike Abs had a statistically significant decrease at 3 months after the vaccination in relation to the measurements 1 month after that. AbN had a statistically significant decline at 3 months after the vaccination in relation to the measurements 1 month after. Pts with cardiovascular disease (CD) had significantly lower levels of antibodies than those who did not have CD. Additionally, CD was an aggravating factor in combination with the other comorbidities for the development of antibodies. Pts with a history of malignancy had significantly lower levels of antibodies in relation to those who did not. Those under therapy with antihistamines in the 1st month after the vaccination presented a statistically lower level of the AbNs, but this difference did not exist in
ISSN:0931-0509
1460-2385
DOI:10.1093/ndt/gfac084.001