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Distinct Neutralising and Complement-Fixing Antibody Responses Can Be Induced to the Same Antigen in Haemodialysis Patients After Immunisation with Different Vaccine Platforms.

Authors :
Wall, Nadezhda
Lamerton, Rachel
Ashford, Fiona
Perez-Toledo, Marisol
Jasiulewicz, Aleksandra
Banham, Gemma D.
Newby, Maddy L.
Faustini, Sian E.
Richter, Alex G.
Selvaskandan, Haresh
Billany, Roseanne E.
Adenwalla, Sherna F.
Henderson, Ian R.
Crispin, Max
Graham-Brown, Matthew
Harper, Lorraine
Cunningham, Adam F.
Source :
Vaccines; Jan2025, Vol. 13 Issue 1, p7, 17p
Publication Year :
2025

Abstract

Background/Objectives: Generalised immune dysfunction in chronic kidney disease, especially in patients requiring haemodialysis (HD), significantly enhances the risk of severe infections. Vaccine-induced immunity is typically reduced in HD populations. The SARS-CoV-2 pandemic provided an opportunity to examine the magnitude and functionality of antibody responses in HD patients to a previously unencountered antigen—Spike (S)-glycoprotein—after vaccination with different vaccine platforms (viral vector (VV); mRNA (mRV)). Methods: We compared the total and functional anti-S antibody responses (cross-variant neutralisation and complement binding) in 187 HD patients and 43 healthy controls 21–28 days after serial immunisation. Results: After 2 doses of the same vaccine, HD patients had anti-S antibody levels and a complement binding capacity comparable to controls. However, 2 doses of mRV induced greater polyfunctional antibody responses than VV (defined by the presence of both complement binding and cross-variant neutralisation activity). Interestingly, an mRV boost after 2 doses of VV significantly enhanced antibody functionality in HD patients without a prior history of SARS-CoV-2 infection. Conclusions: HD patients can generate near-normal, functional antigen-specific antibody responses following serial vaccination to a novel antigen. Encouragingly, exploiting immunological memory by using mRNA vaccines and boosting may improve the success of vaccination strategies in this vulnerable patient population. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2076393X
Volume :
13
Issue :
1
Database :
Complementary Index
Journal :
Vaccines
Publication Type :
Academic Journal
Accession number :
182474571
Full Text :
https://doi.org/10.3390/vaccines13010007