Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort

Abstract Introduction Vaccination plays a fundamental role in mastering the COVID‐19 pandemic and protecting vulnerable groups. Persons with autoimmune inflammatory rheumatic diseases (AIIRD) requiring immunosuppressive therapies are prioritized for vaccination. However, data concerning immunogenici...

Full description

Bibliographic Details
Main Authors: Batool Zamani, Amin Moradi Hasan‐Abad, Ahmad Piroozmand, Mahsa Dehghani, Maryam Arfaatabar, Hossein Motedayyen
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:Immunity, Inflammation and Disease
Subjects:
Online Access:https://doi.org/10.1002/iid3.858
_version_ 1797816622608547840
author Batool Zamani
Amin Moradi Hasan‐Abad
Ahmad Piroozmand
Mahsa Dehghani
Maryam Arfaatabar
Hossein Motedayyen
author_facet Batool Zamani
Amin Moradi Hasan‐Abad
Ahmad Piroozmand
Mahsa Dehghani
Maryam Arfaatabar
Hossein Motedayyen
author_sort Batool Zamani
collection DOAJ
description Abstract Introduction Vaccination plays a fundamental role in mastering the COVID‐19 pandemic and protecting vulnerable groups. Persons with autoimmune inflammatory rheumatic diseases (AIIRD) requiring immunosuppressive therapies are prioritized for vaccination. However, data concerning immunogenicity and safety of the BBIBP‐CorV vaccine in immunosuppressed patients are not found. This study presents data on the efficacy and safety of the BBIBP‐CorV vaccine in immunosuppressed patients compared to healthy controls. Methods Study population consisted of 100 healthy controls and 100 patients with AIIRD. Vaccination was performed according to national guidelines with the BBIBP‐CorV vaccine. SARS‐CoV‐2 neutralizing antibody titers were quantified by enzyme‐linked immunosorbent assay before initial vaccination and 1–3 months after secondary vaccination. Adverse events were assessed before study initiation and 7 days after the second dose. Disease activity was studied before entering the study and 3–8 weeks after the second dose. Results Vaccination‐induced positive immunogenic response rates and SARS‐CoV‐2 neutralizing antibody titers were significantly lower in the AIIRD patients than healthy subjects (p < .05). There are significant differences in neutralizing antibody titers among patients suffering from rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), systemic sclerosis, and ankylosing spondylitis (p < .01–.05). The rates of seropositive vaccine responses were similarly distributed across all diseases. Healthy and AIIRD individuals had a similar profile in adverse events. No significant difference was observed in SARS‐CoV‐2 antibody titers between subjects suffering from side effects and those who did not have. SARS‐CoV‐2 neutralizing antibody levels were significantly higher in subjects with a history of COVID‐19 infection than seronegative individuals (p < .01–0.05). Seropositive subjects had a significant increase in the percentage of vaccine‐related adverse events compared to seronegative persons (p < .05). Despite a minor change in the disease activity of patients with RA and SLE, disease activity indices were overall stable in the AIIRD patients. Conclusion These findings revealed that the BBIBP‐CorV vaccine is effective in the development of neutralizing antibodies in immunosuppressed patients without considerable reactogenicity or induction of disease flares.
first_indexed 2024-03-13T08:40:22Z
format Article
id doaj.art-b968e546511648288eb6e48ea8fa6277
institution Directory Open Access Journal
issn 2050-4527
language English
last_indexed 2024-03-13T08:40:22Z
publishDate 2023-05-01
publisher Wiley
record_format Article
series Immunity, Inflammation and Disease
spelling doaj.art-b968e546511648288eb6e48ea8fa62772023-05-30T12:34:31ZengWileyImmunity, Inflammation and Disease2050-45272023-05-01115n/an/a10.1002/iid3.858Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohortBatool Zamani0Amin Moradi Hasan‐Abad1Ahmad Piroozmand2Mahsa Dehghani3Maryam Arfaatabar4Hossein Motedayyen5Autoimmune Diseases Research Center Kashan University of Medical Sciences Kashan IranAutoimmune Diseases Research Center Kashan University of Medical Sciences Kashan IranAutoimmune Diseases Research Center Kashan University of Medical Sciences Kashan IranAutoimmune Diseases Research Center Kashan University of Medical Sciences Kashan IranDepartment of Medical Laboratory Sciences, Kashan Branch Islamic Azad University Kashan IranAutoimmune Diseases Research Center Kashan University of Medical Sciences Kashan IranAbstract Introduction Vaccination plays a fundamental role in mastering the COVID‐19 pandemic and protecting vulnerable groups. Persons with autoimmune inflammatory rheumatic diseases (AIIRD) requiring immunosuppressive therapies are prioritized for vaccination. However, data concerning immunogenicity and safety of the BBIBP‐CorV vaccine in immunosuppressed patients are not found. This study presents data on the efficacy and safety of the BBIBP‐CorV vaccine in immunosuppressed patients compared to healthy controls. Methods Study population consisted of 100 healthy controls and 100 patients with AIIRD. Vaccination was performed according to national guidelines with the BBIBP‐CorV vaccine. SARS‐CoV‐2 neutralizing antibody titers were quantified by enzyme‐linked immunosorbent assay before initial vaccination and 1–3 months after secondary vaccination. Adverse events were assessed before study initiation and 7 days after the second dose. Disease activity was studied before entering the study and 3–8 weeks after the second dose. Results Vaccination‐induced positive immunogenic response rates and SARS‐CoV‐2 neutralizing antibody titers were significantly lower in the AIIRD patients than healthy subjects (p < .05). There are significant differences in neutralizing antibody titers among patients suffering from rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), systemic sclerosis, and ankylosing spondylitis (p < .01–.05). The rates of seropositive vaccine responses were similarly distributed across all diseases. Healthy and AIIRD individuals had a similar profile in adverse events. No significant difference was observed in SARS‐CoV‐2 antibody titers between subjects suffering from side effects and those who did not have. SARS‐CoV‐2 neutralizing antibody levels were significantly higher in subjects with a history of COVID‐19 infection than seronegative individuals (p < .01–0.05). Seropositive subjects had a significant increase in the percentage of vaccine‐related adverse events compared to seronegative persons (p < .05). Despite a minor change in the disease activity of patients with RA and SLE, disease activity indices were overall stable in the AIIRD patients. Conclusion These findings revealed that the BBIBP‐CorV vaccine is effective in the development of neutralizing antibodies in immunosuppressed patients without considerable reactogenicity or induction of disease flares.https://doi.org/10.1002/iid3.858adverse eventsBBIBP‐CorV vaccinedisease activityimmunogenicitypatients with AIIRD
spellingShingle Batool Zamani
Amin Moradi Hasan‐Abad
Ahmad Piroozmand
Mahsa Dehghani
Maryam Arfaatabar
Hossein Motedayyen
Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
Immunity, Inflammation and Disease
adverse events
BBIBP‐CorV vaccine
disease activity
immunogenicity
patients with AIIRD
title Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
title_full Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
title_fullStr Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
title_full_unstemmed Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
title_short Immunogenicity and safety of the BBIBP‐CorV vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
title_sort immunogenicity and safety of the bbibp corv vaccine in patients with autoimmune inflammatory rheumatic diseases undergoing immunosuppressive therapy in a monocentric cohort
topic adverse events
BBIBP‐CorV vaccine
disease activity
immunogenicity
patients with AIIRD
url https://doi.org/10.1002/iid3.858
work_keys_str_mv AT batoolzamani immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort
AT aminmoradihasanabad immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort
AT ahmadpiroozmand immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort
AT mahsadehghani immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort
AT maryamarfaatabar immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort
AT hosseinmotedayyen immunogenicityandsafetyofthebbibpcorvvaccineinpatientswithautoimmuneinflammatoryrheumaticdiseasesundergoingimmunosuppressivetherapyinamonocentriccohort