Villitis of unknown etiology and chronic deciduitis are not associated with human papilloma virus and enterovirus infection.


Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 02 09 2019
accepted: 30 01 2020
revised: 17 01 2020
pubmed: 7 2 2020
medline: 10 7 2020
entrez: 7 2 2020
Statut: ppublish

Résumé

Villitis of unknown etiology (VUE) and chronic deciduitis with plasma cells (CD) are supposed to be non infectious placental lesions caused by a pathologic immune reaction similar to a host versus graft mechanism. In some investigations, infection of human trophoblastic cells with human papilloma virus (HPV) has been described, and a relationship with miscarriage, preeclampsia, and chronic inflammatory placental lesions has been suspected. Infection with enterovirus, especially Coxsackievirus, has been observed in cases with spontaneous abortion and adverse perinatal outcome, respectively. We investigated 20 cases with VUE and 30 cases with chronic deciduitis with plasma cells. The placenta specimens were analyzed for expression of HPV capsid protein by immunohistochemistry, for presence of HPV DNA via polymerase chain reaction (PCR), and for presence of enterovirus mRNA using RT-PCR, respectively. VUE was associated with maternal diseases: atopic lesions in 21%, other autoimmune diseases in 15.5%, and obesity in 31.5%, respectively. Birth weight below the 10th percentile was detected in 63% of the cases with VUE. Chronic deciduitis was associated with preterm labor and preterm premature rupture of membranes (26%). Intrauterine fetal demise occurred in 5 cases with CD (18.5%). HPV DNA, HPV capsid protein, and enterovirus mRNA were not detected in all investigated VUE or CD cases. Our investigations show that a causal role for enterovirus and human papilloma virus in the development of VUE and CD is unlikely. Therefore, HPV vaccination is unlikely to reduce the incidence of VUE and CD in the future.

Identifiants

pubmed: 32025822
doi: 10.1007/s00428-020-02765-0
pii: 10.1007/s00428-020-02765-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

73-81

Auteurs

Henning Feist (H)

Department of Pathology, Diakonissenkrankenhaus Flensburg, Knuthstraße 1, 24939, Flensburg, Germany. feisthe@diako.de.

Kais Hussein (K)

Department of Pathology, Medical School Hannover, Hannover, Germany.

Angelika Stucki-Koch (A)

Department of Pathology, Medical School Hannover, Hannover, Germany.

Jeremias Wohlschlaeger (J)

Department of Pathology, Diakonissenkrankenhaus Flensburg, Knuthstraße 1, 24939, Flensburg, Germany.

Thomas Hager (T)

Department of Pathology, University of Essen, Essen, Germany.

Thordis Blöcker (T)

Department of Obstetrics and Gynecology, Diakonissenkrankenhaus Flensburg, Flensburg, Germany.

Albert Heim (A)

Department of Virology, Medical School Hannover, Hannover, Germany.

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Classifications MeSH