<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saito M</submitter><funding>Genesis Oncology Trust</funding><funding>University of Otago</funding><pagination>1991-2002</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9294030</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>148(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Progression of cervical intraepithelial neoplasia (CIN) to higher grade disease is associated with persistent human papillomavirus (HPV) infection and an absence of immune-mediated regression. However, the immune microenvironment that distinguishes progression from persistent or regressing lesions has not been well defined.&lt;h4>Methods&lt;/h4>A total of 69 patients under the age of 25 with high-risk HPV-positive cytology and biopsy-confirmed p16-positive CIN2 were included in the study. Biopsies were stained using 20 antibodies to a range of immune markers. Based on a 2-year follow-up, samples were analysed in "progressor" (CIN3 +) or "persister/regressor" (CIN1, 2 or normal) groups.&lt;h4>Results&lt;/h4>Progression was most strongly associated with Blimp-1 positive cell staining </pubmed_abstract><journal>Journal of cancer research and clinical oncology</journal><pubmed_title>Blimp-1 is a prognostic indicator for progression of cervical intraepithelial neoplasia grade 2.</pubmed_title><pmcid>PMC9294030</pmcid><funding_grant_id>2016</funding_grant_id><pubmed_authors>Simcock B</pubmed_authors><pubmed_authors>Sykes P</pubmed_authors><pubmed_authors>Rajesh A</pubmed_authors><pubmed_authors>Innes C</pubmed_authors><pubmed_authors>Hibma M</pubmed_authors><pubmed_authors>Saito M</pubmed_authors><pubmed_authors>Fitzgerald P</pubmed_authors><pubmed_authors>van der Griend R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Blimp-1 is a prognostic indicator for progression of cervical intraepithelial neoplasia grade 2.</name><description>&lt;h4>Background&lt;/h4>Progression of cervical intraepithelial neoplasia (CIN) to higher grade disease is associated with persistent human papillomavirus (HPV) infection and an absence of immune-mediated regression. However, the immune microenvironment that distinguishes progression from persistent or regressing lesions has not been well defined.&lt;h4>Methods&lt;/h4>A total of 69 patients under the age of 25 with high-risk HPV-positive cytology and biopsy-confirmed p16-positive CIN2 were included in the study. Biopsies were stained using 20 antibodies to a range of immune markers. Based on a 2-year follow-up, samples were analysed in "progressor" (CIN3 +) or "persister/regressor" (CIN1, 2 or normal) groups.&lt;h4>Results&lt;/h4>Progression was most strongly associated with Blimp-1 positive cell staining </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-06T19:45:38.465Z</modification><creation>2025-04-06T19:45:38.465Z</creation></dates><accession>S-EPMC9294030</accession><cross_references><pubmed>35386001</pubmed><doi>10.1007/s00432-022-03993-4</doi></cross_references></HashMap>