Long-term antibody response after the third dose of inactivated SARS-CoV-2 vaccine in MASLD patients.

Long-term antibody response after the third dose of inactivated SARS-CoV-2 vaccine in MASLD patients.

Publication date: Sep 30, 2024

Metabolic dysfunction-associated steatotic liver disease (MASLD) patients are at an elevated risk of developing severe coronavirus disease 2019 (COVID-19). The objective of this study was to assess antibody responses and safety profiles six months after the third dose of the inactivated acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in MASLD patients. This study included MASLD patients and healthy volunteers without a history of SARS-CoV-2 infection. Blood samples were collected six months after receiving the third dose of the inactivated vaccine to measure the levels of neutralizing antibodies (NAbs) and anti-spike IgG antibodies against SARS-CoV-2. A total of 335 participants (214 MASLD patients and 121 healthy volunteers) were enrolled. The seroprevalence of NAb was 61. 7% (132 of 214) in MASLD patients and 74. 4% (90 of 121) in healthy volunteers, which was a significant difference (p = 0. 018). Statistically significant differences in IgG seroprevalence were also observed between MASLD patients and healthy volunteers (p = 0. 004). Multivariate analysis demonstrated that the severity of MASLD (OR, 2. 97; 95% CI, 1. 32-6. 68; p = 0. 009) and age (OR, 1. 03; 95% CI, 1. 01-1. 06; p = 0. 004) were independent risk factors for NAb negativity in MASLD patients. Moderate/severe MASLD patients had a lower NAb seroprevalence than mild MASLD patients (45. 0% vs. 65. 5%, p = 0. 016). Lower antibody responses were observed in MASLD patients six months after their third dose of the inactivated vaccine than in healthy volunteers, providing further assistance in monitoring patients who are more vulnerable to hypo-responsiveness to SARS-CoV-2 vaccines.

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Concepts Keywords
Antibodies Adult
Coronavirus Aged
Liver Antibodies, Neutralizing
Mild Antibodies, Neutralizing
Volunteers Antibodies, Viral
Antibodies, Viral
Antibody Formation
Antibody response
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
Immunoglobulin G
Immunoglobulin G
Male
Middle Aged
SARS-CoV-2
SARS-CoV-2
SARS-CoV-2 inactivated vaccines
Seroepidemiologic Studies
Vaccine
Vaccines, Inactivated
Vaccines, Inactivated

Semantics

Type Source Name
disease MESH liver disease
disease MESH coronavirus disease 2019
disease MESH syndrome
disease IDO history
pathway REACTOME SARS-CoV-2 Infection
disease IDO blood
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
drug DRUGBANK Dextrose unspecified form
pathway REACTOME Metabolism
disease MESH infections
disease IDO pathogen
drug DRUGBANK Trestolone
disease MESH inflammation
disease MESH oxidative stress
disease MESH breakthrough infection
disease MESH renal failure
disease MESH liver cirrhosis
disease MESH HIV infection
pathway REACTOME HIV Infection
disease MESH tumors
disease IDO infection
disease MESH cirrhosis
disease MESH liver steatosis
disease MESH alcohol abuse
drug DRUGBANK Sulodexide
disease MESH overweight
disease MESH abnormalities
disease MESH obesity
drug DRUGBANK Alkaline Phosphatase
drug DRUGBANK Urea
drug DRUGBANK Nitrogen
disease MESH coronary artery disease
drug DRUGBANK Creatinine
disease MESH diabetes mellitus
drug DRUGBANK Glutamic Acid
disease MESH hypertension
drug DRUGBANK Cholesterol
drug DRUGBANK Uric Acid
drug DRUGBANK Saquinavir
disease MESH Dyspnea
disease MESH Hypersensitivity
disease MESH Joint pain
disease MESH Syncope
disease MESH myocarditis
drug DRUGBANK Tretamine
disease IDO cell
disease IDO replication
disease MESH etiology
disease MESH hepatitis
disease MESH virus infection
disease MESH seroconversion
disease MESH NAFLD
disease MESH alcoholic fatty liver
drug DRUGBANK Lactulose
drug DRUGBANK Polyethylene glycol
disease MESH hepatic encephalopathy
disease MESH metabolic syndrome
drug DRUGBANK Guanosine

Original Article

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