COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment

Immune-modifying treatment in inflammatory bowel disease (IBD) impairs the humoral response. The role of T lymphocytes in this setting is still unclear. This study aims to assess if a booster shot (third dose) of BNT162b2 mRNA COVID-19 vaccine enhanced the humoral response and elicited cellular immu...

Full description

Bibliographic Details
Main Authors: Grazia Pavia, Rocco Spagnuolo, Angela Quirino, Nadia Marascio, Aida Giancotti, Silvio Simeone, Cristina Cosco, Elena Tino, Federico Carrabetta, Gianfranco Di Gennaro, Carmelo Nobile, Aida Bianco, Giovanni Matera, Patrizia Doldo
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/11/3/591
_version_ 1797608688962240512
author Grazia Pavia
Rocco Spagnuolo
Angela Quirino
Nadia Marascio
Aida Giancotti
Silvio Simeone
Cristina Cosco
Elena Tino
Federico Carrabetta
Gianfranco Di Gennaro
Carmelo Nobile
Aida Bianco
Giovanni Matera
Patrizia Doldo
author_facet Grazia Pavia
Rocco Spagnuolo
Angela Quirino
Nadia Marascio
Aida Giancotti
Silvio Simeone
Cristina Cosco
Elena Tino
Federico Carrabetta
Gianfranco Di Gennaro
Carmelo Nobile
Aida Bianco
Giovanni Matera
Patrizia Doldo
author_sort Grazia Pavia
collection DOAJ
description Immune-modifying treatment in inflammatory bowel disease (IBD) impairs the humoral response. The role of T lymphocytes in this setting is still unclear. This study aims to assess if a booster shot (third dose) of BNT162b2 mRNA COVID-19 vaccine enhanced the humoral response and elicited cellular immunity in IBD patients on different immuno-therapy regimens compared to healthy controls (HCs). Five months after a booster dose, serological and T-cell responses were assessed. The measurements were described using geometric means with 95% confidence intervals. The differences between study groups were assessed by Mann–Whitney tests. Seventy-seven subjects (<i>n</i> = 53 IBD patients and <i>n</i> = 24 HCs), who were fully vaccinated and not previously SARS-CoV-2 infected, were recruited. Regarding the IBD patients, 19 were affected by Crohn’s disease and 34 by ulcerative colitis. During the vaccination cycle, half of the patients (53%) were on stable treatment with aminosalicylates, and 32% were on biological therapy. No differences in antibody concentrations between IBD patients and HCs, nor T-cell responses, were found. Stratifying IBD patients based on the type of treatment (anti-TNFα agents vs. other treatment regimens), a decrease only in antibody titer (<i>p</i> = 0.008), but not in cellular response, was observed. Even after the COVID-19 vaccine booster dose, the TNFα inhibitors selectively decreased the humoral immune response compared to patients on other treatment regimens. The T-cell response was preserved in all study groups. These findings highlight the importance of evaluating T-cell immune responses following COVID-19 vaccination in a routine diagnostic setting, particularly for immunocompromised cohorts.
first_indexed 2024-03-11T05:48:09Z
format Article
id doaj.art-6073daf441de4f63bf25dc8d7a1699a8
institution Directory Open Access Journal
issn 2076-393X
language English
last_indexed 2024-03-11T05:48:09Z
publishDate 2023-03-01
publisher MDPI AG
record_format Article
series Vaccines
spelling doaj.art-6073daf441de4f63bf25dc8d7a1699a82023-11-17T14:18:13ZengMDPI AGVaccines2076-393X2023-03-0111359110.3390/vaccines11030591COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα TreatmentGrazia Pavia0Rocco Spagnuolo1Angela Quirino2Nadia Marascio3Aida Giancotti4Silvio Simeone5Cristina Cosco6Elena Tino7Federico Carrabetta8Gianfranco Di Gennaro9Carmelo Nobile10Aida Bianco11Giovanni Matera12Patrizia Doldo13Unit of Clinical Microbiology, Department of Health Sciences, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Clinical Microbiology, Department of Health Sciences, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Clinical Microbiology, Department of Health Sciences, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Clinical Microbiology, Department of Health Sciences, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyDepartment of Health Sciences, School of Medicine, “Magna Græcia” University of Catanzaro, 88100 Catanzaro, ItalyDepartment of Health Sciences, School of Medicine, “Magna Græcia” University of Catanzaro, 88100 Catanzaro, ItalyDepartment of Health Sciences, School of Medicine, “Magna Græcia” University of Catanzaro, 88100 Catanzaro, ItalyUnit of Clinical Microbiology, Department of Health Sciences, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyUnit of Gastroenterology, Department of Clinical and Experimental Medicine, “Magna Græcia” University of Catanzaro—“Mater Domini” Teaching Hospital, 88100 Catanzaro, ItalyImmune-modifying treatment in inflammatory bowel disease (IBD) impairs the humoral response. The role of T lymphocytes in this setting is still unclear. This study aims to assess if a booster shot (third dose) of BNT162b2 mRNA COVID-19 vaccine enhanced the humoral response and elicited cellular immunity in IBD patients on different immuno-therapy regimens compared to healthy controls (HCs). Five months after a booster dose, serological and T-cell responses were assessed. The measurements were described using geometric means with 95% confidence intervals. The differences between study groups were assessed by Mann–Whitney tests. Seventy-seven subjects (<i>n</i> = 53 IBD patients and <i>n</i> = 24 HCs), who were fully vaccinated and not previously SARS-CoV-2 infected, were recruited. Regarding the IBD patients, 19 were affected by Crohn’s disease and 34 by ulcerative colitis. During the vaccination cycle, half of the patients (53%) were on stable treatment with aminosalicylates, and 32% were on biological therapy. No differences in antibody concentrations between IBD patients and HCs, nor T-cell responses, were found. Stratifying IBD patients based on the type of treatment (anti-TNFα agents vs. other treatment regimens), a decrease only in antibody titer (<i>p</i> = 0.008), but not in cellular response, was observed. Even after the COVID-19 vaccine booster dose, the TNFα inhibitors selectively decreased the humoral immune response compared to patients on other treatment regimens. The T-cell response was preserved in all study groups. These findings highlight the importance of evaluating T-cell immune responses following COVID-19 vaccination in a routine diagnostic setting, particularly for immunocompromised cohorts.https://www.mdpi.com/2076-393X/11/3/591cellular immune responsehumoral immune responseanti-SARS-CoV-2 immunogenicityinflammatory bowel diseaseanti-TNFα agents
spellingShingle Grazia Pavia
Rocco Spagnuolo
Angela Quirino
Nadia Marascio
Aida Giancotti
Silvio Simeone
Cristina Cosco
Elena Tino
Federico Carrabetta
Gianfranco Di Gennaro
Carmelo Nobile
Aida Bianco
Giovanni Matera
Patrizia Doldo
COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
Vaccines
cellular immune response
humoral immune response
anti-SARS-CoV-2 immunogenicity
inflammatory bowel disease
anti-TNFα agents
title COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
title_full COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
title_fullStr COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
title_full_unstemmed COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
title_short COVID-19 Vaccine Booster Shot Preserves T Cells Immune Response Based on Interferon-Gamma Release Assay in Inflammatory Bowel Disease (IBD) Patients on Anti-TNFα Treatment
title_sort covid 19 vaccine booster shot preserves t cells immune response based on interferon gamma release assay in inflammatory bowel disease ibd patients on anti tnfα treatment
topic cellular immune response
humoral immune response
anti-SARS-CoV-2 immunogenicity
inflammatory bowel disease
anti-TNFα agents
url https://www.mdpi.com/2076-393X/11/3/591
work_keys_str_mv AT graziapavia covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT roccospagnuolo covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT angelaquirino covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT nadiamarascio covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT aidagiancotti covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT silviosimeone covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT cristinacosco covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT elenatino covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT federicocarrabetta covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT gianfrancodigennaro covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT carmelonobile covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT aidabianco covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT giovannimatera covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment
AT patriziadoldo covid19vaccineboostershotpreservestcellsimmuneresponsebasedoninterferongammareleaseassayininflammatoryboweldiseaseibdpatientsonantitnfatreatment