Publication:
Alveolar echinococcosis in immunocompromised hosts.

cris.virtual.author-orcid0000-0003-0782-3723
cris.virtualsource.author-orcidb5003064-5858-4751-a6c6-c434f9af49ee
datacite.rightsopen.access
dc.contributor.authorAutier, Brice
dc.contributor.authorGottstein, Bruno
dc.contributor.authorMillon, Laurence
dc.contributor.authorRamharter, Michael
dc.contributor.authorGruener, Beate
dc.contributor.authorBresson-Hadni, Solange
dc.contributor.authorDion, Sarah
dc.contributor.authorRobert-Gangneux, Florence
dc.date.accessioned2024-10-14T22:49:12Z
dc.date.available2024-10-14T22:49:12Z
dc.date.issued2023-05
dc.description.abstractBACKGROUND Alveolar echinococcosis (AE) results of an infection with the larval stage of Echinococcus multilocularis. It has been increasingly described in individuals with impaired immune responsiveness. OBJECTIVES This narrative review aims at describing the presentation of AE according to the type of immune impairment, based on retrospective cohorts and case reports. Implications for patient management and future research are proposed accordingly. SOURCES Targeted search was conducted in PubMed using ((alveolar echinococcosis) OR (multilocularis)) AND ((immunosuppressive) OR (immunodeficiency) OR (AIDS) OR (solid organ transplant) OR (autoimmunity) OR (immune deficiency)). Only publications in English were considered. CONTENT Seventeen publications were found, including 13 reports of 55 AE in immunocompromised patients (AE/IS) and 4 retrospective studies of 755 AE immunocompetent patients (AE/IC) and 115 AE/IS (13%). The cohorts included 9 (1%) solid organ transplantation (SOT) recipients, 2 (0.2%) HIV patients, 41 (4.7%) with chronic inflammatory/autoimmune diseases (I/AID) and 72 (8.3%) with malignancies. SOT, I/AID and malignancies, but not HIV infection, were significantly associated with AE (odds ratios of 10.8, 1.6, 5.9 and 1.3, respectively). Compared to AE/IC, AE/IS was associated with earlier diagnosis (PNM stages I-II: 49/85 (58%) vs 137/348 (39%), p<0.001), higher rate of atypical imaging (24/50 (48%) vs 106/375 (28%), p<0.01) and lower sensitivity of serology (19/77 (25%) vs 265/329 (81%), p<0.001). Unusually extensive or disseminated infections were described in SOT and I/AID patients. IMPLICATIONS Patients who live in endemic areas should benefit from serology before onset of a long-term immunosuppressive therapy, even if the cost-benefit ratio has to be evaluated. Physicians should explain AE to immunocompromised patients and think about AE when finding a liver lesion. Further research should address gaps in knowledge of AE/IS. Especially, extensive and accurate records of AE cases have to be collected by multinational registries.
dc.description.numberOfPages7
dc.description.sponsorshipInstitut für Infektionskrankheiten (IFIK)
dc.identifier.doi10.48350/176044
dc.identifier.pmid36528295
dc.identifier.publisherDOI10.1016/j.cmi.2022.12.010
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/116284
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofClinical microbiology and infection
dc.relation.issn1469-0691
dc.relation.organizationDCD5A442BA19E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BA1AE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BD12E17DE0405C82790C4DE2
dc.subjectAlveolar echinococcosis Cancer Echinococcus multilocularis HIV Immunosuppressive therapy Malignant haemopathy Primary immune deficiency Transplantation
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleAlveolar echinococcosis in immunocompromised hosts.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage599
oaire.citation.issue5
oaire.citation.startPage593
oaire.citation.volume29
oairecerif.author.affiliationInstitut für Infektionskrankheiten (IFIK)
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unibe.date.embargoChanged2023-12-14 23:25:06
unibe.date.licenseChanged2023-12-14 23:25:06
unibe.description.ispublishedpub
unibe.eprints.legacyId176044
unibe.refereedtrue
unibe.subtype.articlereview

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