In:
Liver International, Wiley, Vol. 43, No. 2 ( 2023-02), p. 452-461
Abstract:
A strategy to improve the low rate of anti‐SARS‐CoV‐2 mRNA vaccine‐induced immunogenicity in liver transplant recipients (LTs) is urgently needed. Methods We analysed the rate of positive (≥0.8 U/ml) anti‐SARS‐CoV‐2 receptor domain‐binding protein (RBD) antibody response 2 months after a third dose of the BNT16b2 vaccine in 107 LTs who completed the second vaccine dose 7 months earlier. Results A positive anti‐SARS‐CoV‐2‐s‐RBD antibody response after the third vaccine dose was detected in 98 (91.6%) LTs compared to 82 (76.6%) after the second vaccine dose ( p = .003). The median of anti‐SARS‐CoV‐2 RBD antibody titres increased from 22.9 U/ml 6 months after the second to 3500 U/ml 2 months after the third vaccine dose ( p 〈 .001). Fourteen (14.3%) responder patients presented antibody titres 〈 100 U/ml, 57 (58.2%) between 100 and 9999 U/ml and 27 (27.6%) ≥10 000 U/ml. Seropositivity after the second dose was maintained after the third dose. Independent predictors of antibody response failure after the third vaccine dose were taking a higher daily dose of mycophenolate mofetil (MMF, p 〈 .001) and had a lower ( 〈 60 ml/min/1.73 m 2 ) estimated glomerular filtration rate ( p = .007). Nine (9.1%) LTs experienced symptomatic SARS‐CoV‐2 infection after the third vaccine dose. Median antibody titres were not statistically different between infected and not infected LTs (1325 vs 3515 U/ml, p = .678). Conclusions The third dose of the BNT16b2 vaccine increased the number of LTs who developed a positive anti‐SARS‐CoV‐2 s‐RBD antibody response. A proportion of patients remained unresponsive, mainly for modifiable factors, such as the use of MMF or multiple immunosuppressants.
Type of Medium:
Online Resource
ISSN:
1478-3223
,
1478-3231
Language:
English
Publisher:
Wiley
Publication Date:
2023
detail.hit.zdb_id:
2124684-1
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