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Immune responses and safety of COVID-19 vaccination in atypical hemolytic uremic syndrome patients in Taiwan.

Authors :
Chen, I.-Ru
Wang, Guei-Jane
Hsueh, Po-Ren
Chou, Chia-Hui
Jeng, Long-Bin
Lin, Hui-Ju
Liao, Huang-Jiun
Lai, Ping-Chin
Chang, Jan-Gowth
Huang, Chiu-Ching
Source :
Vaccine. Sep2023, Vol. 41 Issue 41, p5940-5945. 6p.
Publication Year :
2023

Abstract

• aHUS patients had poor T-cell responses compared to healthy controls. • COVID 19 vaccines effectively shield aHUS patients from severe COVID-19. • A double booster dose for the third vaccine is essential for optimal efficacy. • Anti-complement therapy did not influence vaccination effectiveness. Atypical hemolytic uremic syndrome is a rare, life-threatening disorder which can be triggered by COVID 19 infection and COVID 19 vaccination then induce multiple organ failure. Our study is the first to evaluate immune responses to COVID-19 vaccination and safety in a cohort of patients in a local single-center study in Taiwan.. Results indicate that vaccines effectively shield aHUS patients from severe COVID-19 complications without significant safety concerns. A double booster dose for the third vaccine is essential for optimal efficacy. Anti-complement therapy did not influence vaccination effectiveness. Transplant aHUS patients had the lowest immune response titers, indicating a need for additional vaccine doses. Compared to healthcare workers, aHUS patients had poor T-cell responses. We noted a superior trend with mixed-type COVID-19 vaccinations in aHUS patients, while fixed-type mRNA demonstrated better results in healthcare workers. Our findings endorse COVID-19 vaccination as a potent strategy to safeguard aHUS patients from severe complications, emphasizing the importance of vigilant monitoring pre- and post-vaccination. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0264410X
Volume :
41
Issue :
41
Database :
Academic Search Index
Journal :
Vaccine
Publication Type :
Academic Journal
Accession number :
172023842
Full Text :
https://doi.org/10.1016/j.vaccine.2023.08.020