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suck abstract from ncbi


10.1016/j.ebiom.2021.103524

http://scihub22266oqcxt.onion/10.1016/j.ebiom.2021.103524
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34391096!8357427!34391096
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suck abstract from ncbi

pmid34391096      EBioMedicine 2021 ; 70 (?): 103524
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  • Cellular and humoral immunogenicity of a SARS-CoV-2 mRNA vaccine in patients on haemodialysis #MMPMID34391096
  • Strengert M; Becker M; Ramos GM; Dulovic A; Gruber J; Juengling J; Lurken K; Beigel A; Wrenger E; Lonnemann G; Cossmann A; Stankov MV; Dopfer-Jablonka A; Kaiser PD; Traenkle B; Rothbauer U; Krause G; Schneiderhan-Marra N; Behrens GMN
  • EBioMedicine 2021[Aug]; 70 (?): 103524 PMID34391096show ga
  • BACKGROUND: Patients with chronic renal insufficiency on maintenance haemodialysis face an increased risk of COVID-19 induced mortality and impaired vaccine responses. To date, only a few studies have addressed SARS-CoV-2 vaccine elicited immunity in this immunocompromised population. METHODS: We assessed immunogenicity of the mRNA vaccine BNT162b2 in at-risk dialysis patients and characterised systemic cellular and humoral immune responses in serum and saliva using interferon gamma release assay and multiplex-based cytokine and immunoglobulin measurements. We further compared binding capacity and neutralization efficacy of vaccination-induced immunoglobulins against emerging SARS-CoV-2 variants Alpha, Beta, Epsilon and Cluster 5 by ACE2-RBD competition assay. FINDINGS: Patients on maintenance haemodialysis exhibit detectable but variable cellular and humoral immune responses against SARS-CoV-2 and variants of concern after a two-dose regimen of BNT162b2. Although vaccination-induced immunoglobulins were detectable in saliva and plasma, both anti-SARS-CoV-2 IgG and neutralization efficacy was reduced compared to a vaccinated non-dialysed control population. Similarly, T-cell mediated interferon gamma release after stimulation with SARS-CoV-2 spike peptides was significantly diminished. INTERPRETATION: Quantifiable humoral and cellular immune responses after BNT162b2 vaccination in individuals on maintenance haemodialysis are encouraging, but urge for longitudinal follow-up to assess longevity of immunity. Diminished virus neutralization and interferon gamma responses in the face of emerging variants of concern may favour this at-risk population for re-vaccination using modified vaccines at the earliest opportunity. FUNDING: Initiative and Networking Fund of the Helmholtz Association of German Research Centres, EU Horizon 2020 research and innovation program, State Ministry of Baden-Wurttemberg for Economic Affairs, Labour and Tourism.
  • |Aged[MESH]
  • |Antibodies, Neutralizing/immunology[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |BNT162 Vaccine[MESH]
  • |COVID-19 Vaccines/*immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunity, Cellular/*immunology[MESH]
  • |Immunity, Humoral/*immunology[MESH]
  • |Immunogenicity, Vaccine/*immunology[MESH]
  • |Immunoglobulin G/immunology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Renal Dialysis/methods[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/immunology[MESH]
  • |T-Lymphocytes/immunology[MESH]
  • |Vaccination/methods[MESH]
  • |Vaccines, Synthetic/*immunology[MESH]


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