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ISSN Approved Journal | | IMPACT FACTOR 8.16 | | eISSN: 2582-5542 | |  Free Crossref DOI 

Fast Publication within 2 days | | Low Article Processing Charges | | Peer Reviewed and Referred Journal

Research and review articles are invited for publication in September 2026 (Volume 27, Issue 3) Submit Paper

Increased plasma soluble major histocompatibility complex class I polypeptide-related sequence A/B (sMICA/B) and related biomarkers in patients with pancreatitis

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  • Increased plasma soluble major histocompatibility complex class I polypeptide-related sequence A/B (sMICA/B) and related biomarkers in patients with pancreatitis

Soichiro Uehara 1, *, Yuichi Fukuzawa 2, Tomohiko Matuyama 3 and Katshuhiro Gotoh 4

1 Departments of Gastroenterology, Evergreen Hospital, Hokkaido, Japan.
2 Department of Pharmacy, Hijirigaoka Hospital, Hokkaido, Japan.
3 Department of Pharmacy, Evergreen Hospital, Hokkaido, Japan.
4 Departments of Gastroenteronology, Hijirigaoka Hospital, Hokkaido, Japan.
 

Research Article

World Journal of Biology Pharmacy and Health Sciences, 2025, 23(01), 132–142

Article DOI: 10.30574/wjbphs.2025.23.1.0649

DOI url: https://doi.org/10.30574/wjbphs.2025.23.1.0649

Received on 29 May 2025; revised on 05 July 2025; accepted on 07 July 2025

Plasma soluble MHC class I chain-related gene (sMIC) A/B, sTAMRs (sTyro3, sAxl, and sMer), Gas6 and free-PROS1, ADAM 10/17, sFas, and severity markers (APACHE-II and SOFA) were measured in 55 cases (severe 14 and mild 41) of acute pancreatitis (AP), 20 cases of chronic pancreatitis (CP), and 20 cases of normal control (NC).
Methods: These markers were measured by ELISA-kit.
Results: sMICA/B, ADAM10/17, sFas, sTAMRs and both ligands were significantly higher in the pancreatitis group than in the NC. The non-survival SAP group showed the highest levels for these markers, and the peaks of sMICA/B levels were seen at the onset of disease in many cases and they damped. However, sMICA/B values in the non-survival SAP group showed another peak at onset and 14-30 days after onset.
The correlations between these markers among groups showed significant good correlations except for the non-survival SAP and CP groups. 
Regarding the correlations between sMICA/B and APACHE-Ⅱin the non-survival SAP and CP group were inconsistent, whereas significant correlations were observed in other pancreatitis groups. The correlations between APACHE-II, and Gas6 and free-PROS1 showed significant correlation with most of the groups, whereas free-PROS1 showed significant correlations with the severe group.
Conclusions: The higher the sMICA/B value, the higher the severity of the disease. In addition, non-survival SAP and CP suggested impaired efferocytosis. Furthermore, while Gas6 acts regardless of the symptoms of pancreatitis, free-PROS1 seems to act mainly in severe cases.
 

sMICA; sMICB; sFas; Gas6; PROS1; sTAMRs

https://wjbphs.com/sites/default/files/fulltext_pdf/WJBPHS-2025-0649.pdf

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Soichiro Uehara, Yuichi Fukuzawa, Tomohiko Matuyama and Katshuhiro Gotoh. Increased plasma soluble major histocompatibility complex class I polypeptide-related sequence A/B (sMICA/B) and related biomarkers in patients with pancreatitis. World Journal of Biology Pharmacy and Health Sciences, 2025, 23(01), 132-142. Article DOI: https://doi.org/10.30574/wjbphs.2025.23.1.0649.

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