Changes in Salivary Parameters of Oral Immunity after Biologic Therapy for Inflammatory Bowel Disease.

Crohn’s disease biologic therapy biomarkers immunoglobulin A inflammatory bowel disease myeloperoxidase oral health oral immunity saliva ulcerative colitis

Journal

Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444

Informations de publication

Date de publication:
16 Dec 2021
Historique:
received: 19 11 2021
revised: 14 12 2021
accepted: 15 12 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 25 12 2021
Statut: epublish

Résumé

We previously observed that inflammatory bowel disease (IBD) may compromise oral host defense, as assessed by decreased salivary levels of immunoglobulin A (IgA) and myeloperoxidase (MPO). Biologic therapy with inhibitors of cytokines or adhesion molecules is increasingly used for patients with IBD. Little is known, however, about how this treatment modality affects the release and properties of saliva. Here, we aimed to determine how biologic therapy in patients who had not responded to previous standard treatment with conventional drugs affected the salivary concentration of IgA and MPO. To this end, unstimulated whole mixed saliva was collected before treatment or after 10-12 weeks of therapy from 27 patients with Crohn's disease (CD) and 24 patients with ulcerative colitis (UC). After the induction phase of therapy with biologics, salivary levels of IgA and MPO increased significantly in UC, but not in CD patients. These increases were approximately 8-fold and 6-fold, for IgA and MPO, respectively. Moreover, these effects occurred in UC patients who responded successfully to therapy, but not in those who failed to improve. Furthermore, the relative increases in salivary IgA and MPO correlated with the relative decrease in UC severity, as assessed by the Mayo scale. These data indicate that the successful therapy with biologics in UC patients results also in improved oral host defense. However, it remains to be determined why such an effect does not occur during therapy for CD.

Identifiants

pubmed: 34947940
pii: life11121409
doi: 10.3390/life11121409
pmc: PMC8708388
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Arch Biochem Biophys. 2018 Feb 15;640:47-52
pubmed: 29336940
Int J Mol Sci. 2020 Oct 10;21(20):
pubmed: 33050496
Dtsch Zahnarztl Z. 1977 Jan;32(1):44-7
pubmed: 264444
Nat Med. 2005 Apr;11(4 Suppl):S45-53
pubmed: 15812489
Ir J Med Sci. 1999 Jan-Mar;168(1):33-5
pubmed: 10098341
Int J Mol Sci. 2020 Nov 13;21(22):
pubmed: 33202858
Acta Odontol Scand. 1964 Feb;22:121-35
pubmed: 14158464
Gastroenterology. 2007 Feb;132(2):763-86
pubmed: 17258735
Ger Med Sci. 2011 Feb 16;9:Doc03
pubmed: 21394194
Clin Gastroenterol Hepatol. 2016 Mar;14(3):348-354.e17
pubmed: 26071941
DNA Res. 2014 Feb;21(1):15-25
pubmed: 24013298
Arch Oral Biol. 2011 May;56(5):428-36
pubmed: 21145038
Oral Dis. 2021 Mar;27(2):280-289
pubmed: 32643850
Gastroenterology. 1976 Mar;70(3):439-44
pubmed: 1248701
J Oral Rehabil. 2018 Sep;45(9):730-746
pubmed: 29878444
Clin Exp Immunol. 2004 Mar;135(3):483-9
pubmed: 15008983
Microbiol Mol Biol Rev. 1998 Mar;62(1):71-109
pubmed: 9529888
Pol Arch Intern Med. 2018 Jun 30;128(6):362-370
pubmed: 29806822
Anal Biochem. 1976 May 7;72:248-54
pubmed: 942051
Acta Odontol Scand. 1963 Dec;21:533-51
pubmed: 14121956
J Crohns Colitis. 2017 Jan;11(1):3-25
pubmed: 27660341
Prz Gastroenterol. 2015;10(2):57-60
pubmed: 26557934
J Crohns Colitis. 2017 Feb;11(2):135-149
pubmed: 27660342
Inflamm Bowel Dis. 2020 Sep 18;26(10):1588-1596
pubmed: 32725166
Pol Arch Med Wewn. 2012;122(5):200-8
pubmed: 22538761
J Crohns Colitis. 2017 Jul 1;11(7):769-784
pubmed: 28513805
Life (Basel). 2021 Sep 09;11(9):
pubmed: 34575091
Scand J Gastroenterol. 2005 Dec;40(12):1444-8
pubmed: 16316893
Int J Mol Sci. 2020 Oct 29;21(21):
pubmed: 33137905
J Crohns Colitis. 2017 Jun 1;11(6):649-670
pubmed: 28158501
World J Gastroenterol. 2021 Apr 28;27(16):1828-1840
pubmed: 33967560
EBioMedicine. 2021 Apr;66:103329
pubmed: 33862588
Arch Oral Biol. 2019 Nov;107:104528
pubmed: 31442931
Helv Odontol Acta. 1971 Oct;15(2):107-13
pubmed: 5315729
Ann N Y Acad Sci. 1993 Sep 20;694:72-7
pubmed: 8215087
N Engl J Med. 1987 Dec 24;317(26):1625-9
pubmed: 3317057
Chest. 2004 Aug;126(2):389-93
pubmed: 15302722
Antioxid Redox Signal. 2009 Nov;11(11):2899-937
pubmed: 19622015

Auteurs

Kacper Nijakowski (K)

Department of Conservative Dentistry and Endodontics, Poznan University of Medical Sciences, 60-812 Poznan, Poland.

Rafał Rutkowski (R)

Department of Pathophysiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.

Piotr Eder (P)

Department of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, 60-355 Poznan, Poland.

Katarzyna Korybalska (K)

Department of Pathophysiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.

Janusz Witowski (J)

Department of Pathophysiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.

Anna Surdacka (A)

Department of Conservative Dentistry and Endodontics, Poznan University of Medical Sciences, 60-812 Poznan, Poland.

Classifications MeSH