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Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis

BACKGROUND: SARS-CoV-2 vaccine responses that could harbor potential risks to chronic liver diseased patients. AIMS: To assess immune response following Pfizer's SARS-CoV-2 vaccine in patients with different liver fibrosis severities of nonalcoholic fatty liver disease (NAFLD). METHODS: Clinica...

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Autores principales: Hakimian, David, Amer, Johnny, Jammal, Alaa, Shafrir, Asher, Milgrom, Yael, Masarowah, Mohammad, Hazou, Wadi, Ishay, Yuval, Imam, Ashraf, Francis, Adi, Khalaileh, Abed, Safadi, Rifaat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598407/
https://www.ncbi.nlm.nih.gov/pubmed/37885772
http://dx.doi.org/10.1016/j.jvacx.2023.100359
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author Hakimian, David
Amer, Johnny
Jammal, Alaa
Shafrir, Asher
Milgrom, Yael
Masarowah, Mohammad
Hazou, Wadi
Ishay, Yuval
Imam, Ashraf
Francis, Adi
Khalaileh, Abed
Safadi, Rifaat
author_facet Hakimian, David
Amer, Johnny
Jammal, Alaa
Shafrir, Asher
Milgrom, Yael
Masarowah, Mohammad
Hazou, Wadi
Ishay, Yuval
Imam, Ashraf
Francis, Adi
Khalaileh, Abed
Safadi, Rifaat
author_sort Hakimian, David
collection PubMed
description BACKGROUND: SARS-CoV-2 vaccine responses that could harbor potential risks to chronic liver diseased patients. AIMS: To assess immune response following Pfizer's SARS-CoV-2 vaccine in patients with different liver fibrosis severities of nonalcoholic fatty liver disease (NAFLD). METHODS: Clinical and histological (NAS-score and fibrosis stage) characteristics of NAFLD patients before vaccine were correlated with serologic vaccine responses of two doses of the BNT162b2. Serum SARS-CoV-2 spike immunoglobulins (anti-S) were assessed on day seven following immunization (Liaison assay). RESULTS: The mean-age of patients (n = 157) was 56.9 ± 13.2 years (46.5 % males). 94.8 % had a positive response (anti-S levels ≥ 19 AU/ml). The anti-S cutoff of 200 AU/ml used to separate strong vs. weak responses. A strong response (anti-S titers ≥ 200 AU/ml) was observed in 93/157 (59.2 %) patients with a mean-age of 53.1 ± 13.8 years (45.2 % males). A weak response (anti-S titers < 200 AU/ml) was observed in 64/157 (40.8 %) cases with a mean-age of 62.3 ± 10.2 years (p < 0.0001). The strong response subgroup had lower metabolic comorbidities, including glucose hemostasis, hypertension, and dyslipidemia (p < 0.04). Moreover, the strong response subgroup had fibrosis stages F0-F2 (75.3 % vs. 56.3 %) and lower rates of advanced stages F3-F4 (24.7 % vs. 43.8 %). The F0-F2 subgroups had significantly higher rates of strong responses than the F3-F4 stages. The anti-S ≥ 200 and anti-S ≥ 400 AU/ml response achieved in 66 % and 36.8 % of the F0-F2 population was significantly higher than the 45.1 % (p = 0.006) and 23.5 % (p = 0.05) in the F3-F4 population, respectively. The Fib-4 calculations and Fibroscan evaluations were consistent with histologic fibrosis assessment. CONCLUSION: Advanced liver fibrosis (assessed by histology, Fib-4, or Fibroscan) is a risk factor for lower response to Pfizer's BNT162b2 vaccine, and patients should be prioritized for the vaccine booster against SARS-CoV-2.
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spelling pubmed-105984072023-10-26 Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis Hakimian, David Amer, Johnny Jammal, Alaa Shafrir, Asher Milgrom, Yael Masarowah, Mohammad Hazou, Wadi Ishay, Yuval Imam, Ashraf Francis, Adi Khalaileh, Abed Safadi, Rifaat Vaccine X Regular paper BACKGROUND: SARS-CoV-2 vaccine responses that could harbor potential risks to chronic liver diseased patients. AIMS: To assess immune response following Pfizer's SARS-CoV-2 vaccine in patients with different liver fibrosis severities of nonalcoholic fatty liver disease (NAFLD). METHODS: Clinical and histological (NAS-score and fibrosis stage) characteristics of NAFLD patients before vaccine were correlated with serologic vaccine responses of two doses of the BNT162b2. Serum SARS-CoV-2 spike immunoglobulins (anti-S) were assessed on day seven following immunization (Liaison assay). RESULTS: The mean-age of patients (n = 157) was 56.9 ± 13.2 years (46.5 % males). 94.8 % had a positive response (anti-S levels ≥ 19 AU/ml). The anti-S cutoff of 200 AU/ml used to separate strong vs. weak responses. A strong response (anti-S titers ≥ 200 AU/ml) was observed in 93/157 (59.2 %) patients with a mean-age of 53.1 ± 13.8 years (45.2 % males). A weak response (anti-S titers < 200 AU/ml) was observed in 64/157 (40.8 %) cases with a mean-age of 62.3 ± 10.2 years (p < 0.0001). The strong response subgroup had lower metabolic comorbidities, including glucose hemostasis, hypertension, and dyslipidemia (p < 0.04). Moreover, the strong response subgroup had fibrosis stages F0-F2 (75.3 % vs. 56.3 %) and lower rates of advanced stages F3-F4 (24.7 % vs. 43.8 %). The F0-F2 subgroups had significantly higher rates of strong responses than the F3-F4 stages. The anti-S ≥ 200 and anti-S ≥ 400 AU/ml response achieved in 66 % and 36.8 % of the F0-F2 population was significantly higher than the 45.1 % (p = 0.006) and 23.5 % (p = 0.05) in the F3-F4 population, respectively. The Fib-4 calculations and Fibroscan evaluations were consistent with histologic fibrosis assessment. CONCLUSION: Advanced liver fibrosis (assessed by histology, Fib-4, or Fibroscan) is a risk factor for lower response to Pfizer's BNT162b2 vaccine, and patients should be prioritized for the vaccine booster against SARS-CoV-2. Elsevier 2023-10-12 /pmc/articles/PMC10598407/ /pubmed/37885772 http://dx.doi.org/10.1016/j.jvacx.2023.100359 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular paper
Hakimian, David
Amer, Johnny
Jammal, Alaa
Shafrir, Asher
Milgrom, Yael
Masarowah, Mohammad
Hazou, Wadi
Ishay, Yuval
Imam, Ashraf
Francis, Adi
Khalaileh, Abed
Safadi, Rifaat
Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title_full Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title_fullStr Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title_full_unstemmed Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title_short Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
title_sort weaker sars-cov-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis
topic Regular paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598407/
https://www.ncbi.nlm.nih.gov/pubmed/37885772
http://dx.doi.org/10.1016/j.jvacx.2023.100359
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