dc.contributor.author
Friebel, Julian
dc.contributor.author
Schinnerling, Katina
dc.contributor.author
Geelhaar‐Karsch, Anika
dc.contributor.author
Allers, Kristina
dc.contributor.author
Schneider, Thomas
dc.contributor.author
Moos, Verena
dc.date.accessioned
2024-12-19T14:13:35Z
dc.date.available
2024-12-19T14:13:35Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/46040
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-45750
dc.description.abstract
Background & Aims: Classical Whipple's disease (CWD) affects the gastrointestinal tract and causes chronic diarrhea, malabsorption, and barrier dysfunction with microbial translocation (MT). Immune reconstitution inflammatory syndrome (IRIS) is a serious complication during antimicrobial treatment of CWD. The pathomechanisms of IRIS have not been identified and mucosal barrier integrity has not been studied in patients with IRIS CWD.
Methods: In 96 CWD patients (n = 23 IRIS, n = 73 non-IRIS) and 30 control subjects, we analysed duodenal morphology by histology, measured serum markers of MT, and proinflammatory cytokines in biopsy supernatants, and correlated microbial translocation with T cell reconstitution and activation.
Results: Before treatment, duodenal specimens from patients who later developed IRIS exhibited a more pronounced morphological transformation that suggested a disturbed barrier integrity when compared with the non-IRIS group. Villous atrophy was mediated by increased apoptosis of epithelial cells, which was insufficiently counterbalanced by regenerative proliferation of crypt cells. Pretreatment deficiencies in the mucosal secretion of proinflammatory cytokines and chemokines (e.g., IL-6, CCL2) in these patients markedly resolved after therapy induction. High serum levels of lipopoly-saccharides (LPS), soluble CD14 (sCD14), and LPS-binding protein (LBP) combined with low endotoxin core antibody (EndoCAb) titres suggested systemic MT in CWD patients developing IRIS. CD4(+) T cell count and activation in IRIS CWD patients correlated positively with sCD14 levels and negatively with EndoCAb titres. Furthermore, the degree of intestinal barrier dysfunction and MT was predictive for the onset of IRIS.
Conclusion: Prolonged MT across a dysfunctional intestinal mucosal barrier due to severe tissue damage favors dysbalanced immune reconstitution and systemic immune activation in IRIS CWD. Therefore, the monitoring of inflammatory and MT markers in CWD patients might be helpful in identifying patients who are at risk of developing IRIS. Therapeutic strategies to reconstitute the mucosal barrier and control inflammation could assist in the prevention of IRIS.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
barrier dysfunction
en
dc.subject
immune reconstitution inflammatory syndrome
en
dc.subject
inflammation
en
dc.subject
microbial translocation
en
dc.subject
Whipple's disease
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Intestinal barrier dysfunction mediates Whipple's disease immune reconstitution inflammatory syndrome (IRIS)
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e622
dcterms.bibliographicCitation.doi
10.1002/iid3.622
dcterms.bibliographicCitation.journaltitle
Immunity, Inflammation and Disease
dcterms.bibliographicCitation.number
5
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.volume
10
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
35478447
dcterms.isPartOf.eissn
2050-4527