Evidence map›Paper›PMID 41942985›Full record

ArticleCell communication and signaling : CCS2026

Ostreae Testa enhances anti-tumor immunity by activating T cells via antigen-presenting cell stimulation.

Ju A Shim, So Min Lee, Hyori Kim, Hyo-Jeong Cha, Yuna Jo, Jun Hong Park, Changwan Hong

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ju A ShimDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.
So Min LeeDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.
Hyori KimDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.
Hyo-Jeong ChaDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.
Yuna JoDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea. yoona30@pusan.ac.kr.
Jun Hong ParkDepartment of Physiology, College of Veterinary Medicine, Jeonbuk National University, Specialized Campus, 79 Gobong-ro, Iksan, Jeollabuk-do, 54596, Republic of Korea. jhpark77@jbnu.ac.kr.
Changwan HongDepartment of Anatomy, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea. chong@pusan.ac.kr.

Funding

National Research Foundation of Korea 2022R1C1C2005725National Research Foundation of Korea 2023R1A2C2002435
6 · The paper itself

Abstract

backgroundOysters are known for their rich nutritional profile and medicinal properties documented in traditional medicine. Their bioactive compounds exhibit antioxidant, anti-inflammatory, antimicrobial, and osteogenic activities, leading to widespread applications in food and medicine. Oyster shells—composed of > 90% calcium carbonate and various minerals and amino acids—are traditionally used as antacids in East Asia. Despite these recognized benefits, the mechanisms by which oyster shells modulate immune responses remain unclear. In this study, we elucidated the immunomodulatory effects of Ostreae Testa water (OTW) extract from oyster shells, focusing on OTW’s ability to modulate T cell responses.

methodsMouse splenocytes were treated with OTW extract, and T cell activation was assessed. The role of antigen-presenting cells (APCs), including dendritic cells (DCs) and macrophages, was assessed by analyzing cytokine profiles and cell-cell interactions. OTW extract-primed CD8+ T cells were assessed for anti-tumor responses in an in vivo solid tumor model.

resultsOTW extract treatment significantly enhanced T cell activation in mouse splenocytes. DCs and macrophages mediated this effect, facilitating the immune response via cytokine and direct interactions with T cells. Moreover, OTW extract-primed CD8+ T cells enhanced anti-tumor immune responses in the solid tumor model, demonstrating potent immunotherapeutic potential.

conclusionsOur findings demonstrate that OTW extract exhibits novel immune-enhancing properties by activating APCs and subsequently promoting T cell responses. These results underscore the therapeutic potential of OTW extract for improving immune function, particularly in the context of immunological disorders and cancer.

Indexed as

Antigen-Presenting CellsLymphocyte ActivationNeoplasmsOstreidaeT-LymphocytesAnimalsCytokinesDendritic CellsFemaleMacrophagesMiceMice, Inbred C57BLSpleenCytokinesAntigen presenting cellsAnti-tumor immunityCD8+ T cellsImmune responseOyster shell

Identifiers

PMID41942985
PMCPMC13217661

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.