Evidence map›Paper›PMID 41633691›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

[Establishment of an Epstein-Barr virus infection model using human nasal organoids].

Jinyan Wei, Hairui Zheng, Yunteng Zhao, Yan Yu, Yingying Xu, Gang Li

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In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jinyan WeiDepartment of Otolaryngology, Southern Medical University, Guangzhou 510515, China.
Hairui ZhengDepartment of Otolaryngology, Southern Medical University, Guangzhou 510515, China.
Yunteng ZhaoDepartment of Otolaryngology, Southern Medical University, Guangzhou 510515, China.
Yan YuDepartment of Otolaryngology, Southern Medical University, Guangzhou 510515, China.
Yingying XuGuangdong Provincial Key Laboratory of Medical Image Processing, Southern Medical University, Guangzhou 510515, China.
Gang LiDepartment of Otolaryngology, Southern Medical University, Guangzhou 510515, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo develop an cost-effective and convenient method for culturing human nasal organoids to establish an

methodsNasal polyp tissue obtained from surgery was routinely washed, cut, digested and filtered to obtain cell clusters. The cell clusters were then expanded into undifferentiated nasal organoids through dynamic suspension culture under matrix-free conditions, followed by a 14-day differentiation induction treatment to obtain differentiated nasal organoids. The major cellular components of the organoids were identified by immunofluorescence staining and immunohistochemistry. The nasal organoids were infected by EBV

resultsNasal organoids consisting of basal cells, mucous cells, and ciliated cells in a martigel-free system were obtained successfully by dynamic suspension culture. The differentiated nasal organoids expressed high levels of EBV-associated receptors EphA2, NRP1, and NMHCII-A. Both the undifferentiated and differentiated nasal organoids could be infected by EBV. Viral replication in the organoids increased with the viral exposure load, and the differentiated organoids appeared more permissive to viral replication.

conclusionsThe matrigel-free dynamic suspension culture method is economical and simple for constructing nasal organoids, which can be used as a model of EBV infection for studies of epithelial EBV infection.

Indexed as

Epstein-Barr Virus InfectionsHerpesvirus 4, HumanNasal MucosaOrganoidsCell Culture TechniquesCell DifferentiationCells, CulturedHumansVirus ReplicationEpstein-Barr virusnasal mucosaorganoids

Identifiers

PMID41633691
PMCPMC12867614

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