<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Honda F</submitter><funding>Japan Agency for Medical Research and Development</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Our previous studies reveal that CCL18-CCR8 chemokine axis is upregulated in patients of immunoglobulin G4-related disease (IgG4-RD), suggesting that the CCL18-CCR8 axis is implicated in the etiology of IgG4-RD, although whether this axis has a potential as a therapeutic target remains unclear. Our purpose was to clarify the pathogenic roles and therapeutic potential of the murine CCL8 (analog of human CCL18)-CCR8 axis by using an animal model of IgG4-RD (LAT Y136F knockin mice; LAT mice).&lt;h4>Methods&lt;/h4>We compared the infiltration of inflammatory cells and the fibrosis of the salivary glands of 6-week-old LAT mice and littermate mice. The expressions of Ccl8 and Ccr8 were also compared. Next, we investigated the therapeutic effects of intravenous administration of anti</pubmed_abstract><journal>Arthritis research &amp; therapy</journal><pagination>214</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8364087</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pathogenic roles and therapeutic potential of the CCL8-CCR8 axis in a murine model of IgG4-related sialadenitis.</pubmed_title><pmcid>PMC8364087</pmcid><pubmed_authors>Tsuboi H</pubmed_authors><pubmed_authors>Kawano M</pubmed_authors><pubmed_authors>Ono Y</pubmed_authors><pubmed_authors>Asano K</pubmed_authors><pubmed_authors>Honda F</pubmed_authors><pubmed_authors>Yamada K</pubmed_authors><pubmed_authors>Malissen B</pubmed_authors><pubmed_authors>Ito K</pubmed_authors><pubmed_authors>Kondo Y</pubmed_authors><pubmed_authors>Malissen M</pubmed_authors><pubmed_authors>Abe S</pubmed_authors><pubmed_authors>Matsumoto I</pubmed_authors><pubmed_authors>Takahashi H</pubmed_authors><pubmed_authors>Tanaka M</pubmed_authors><pubmed_authors>Sumida T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pathogenic roles and therapeutic potential of the CCL8-CCR8 axis in a murine model of IgG4-related sialadenitis.</name><description>&lt;h4>Background&lt;/h4>Our previous studies reveal that CCL18-CCR8 chemokine axis is upregulated in patients of immunoglobulin G4-related disease (IgG4-RD), suggesting that the CCL18-CCR8 axis is implicated in the etiology of IgG4-RD, although whether this axis has a potential as a therapeutic target remains unclear. Our purpose was to clarify the pathogenic roles and therapeutic potential of the murine CCL8 (analog of human CCL18)-CCR8 axis by using an animal model of IgG4-RD (LAT Y136F knockin mice; LAT mice).&lt;h4>Methods&lt;/h4>We compared the infiltration of inflammatory cells and the fibrosis of the salivary glands of 6-week-old LAT mice and littermate mice. The expressions of Ccl8 and Ccr8 were also compared. Next, we investigated the therapeutic effects of intravenous administration of anti</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2025-04-04T21:28:52.407Z</modification><creation>2022-02-11T08:14:21.742Z</creation></dates><accession>S-EPMC8364087</accession><cross_references><pubmed>34391459</pubmed><doi>10.1186/s13075-021-02597-6</doi></cross_references></HashMap>