The Chimeric antigen receptor T cell target Claudin 6 is a marker for early organ-specific epithelial progenitors and is expressed in some pediatric solid tumor entities

dc.contributor.authorSeidmann, Larissa
dc.contributor.authorWingerter, Arthur
dc.contributor.authorMetzig, Marie Oliver
dc.contributor.authorBornas, Angelina
dc.contributor.authorEl Malki, Khalifa
dc.contributor.authorUstjanzew, Arsenij
dc.contributor.authorOrtmüller, Franziska
dc.contributor.authorKamyshanskiy, Yevgeniy
dc.contributor.authorKindler, Thomas
dc.contributor.authorLaible, Mark
dc.contributor.authorMohr, Xenia
dc.contributor.authorHenninger, Nicole
dc.contributor.authorRusso, Alexandra
dc.contributor.authorBeck, Olaf
dc.contributor.authorAlt, Francesca
dc.contributor.authorWehling, Pia
dc.contributor.authorRoth, Wilfried
dc.contributor.authorParet, Claudia
dc.contributor.authorFaber, Jörg
dc.date.accessioned2026-07-01T10:09:02Z
dc.date.issued2025
dc.description.abstractThe oncofetal membrane protein Claudin 6 (CLDN6) is an attractive target for T cell-based therapies. There is a lack of detailed analyses on the age-dependent expression of CLDN6 in normal tissues is lacking, which limits the expansion of CLDN6 CAR-T cell clinical trials to pediatric populations. Methods: We analyzed CLDN6 expression in extracranial solid tumors and normal tissues of children using RNA-sequencing data from over 500 pediatric solid tumor samples, qRT-PCR and immunohistochemistry (IHC) in more than 100 fresh-frozen tumor samples and, approximately, 250 formalin-fixed paraffin-embedded (FFPE) samples. We examined normal tissue expression via qRT-PCR in 32 different infant tissues and via IHC in roughly 290 tissues from donors across four age groups, as well as in fetal autopsy samples. Results: In fetal tissues, we detected CLDN6 expression primarily in the epithelial cells of several organs, including the skin, lungs, kidneys, intestinal tract, and pancreas, but not in undifferentiated blastemal cells. Postnatally, we found CLDN6-positive epithelial progenitors only during the first few weeks of life. In older-age groups, isolated clusters of CLDN6-positive progenitors were present, but in scarce quantities. In tumor tissues, we found strong and homogeneous CLDN6 expression in desmoplastic small round cell tumors and germ cell tumors. Wilms tumors demonstrated heterogeneous CLDN6 expression, notably absent in the blastemal component. Conclusions: These findings highlight an organ-specific presence of CLDN6-positive epithelial precursors that largely disappear in terminally differentiated epithelia within weeks after birth. Therefore, our data support CLDN6 as a viable therapeutic target in pediatric patients and justify their inclusion in basket studies for anti-CLDN6-based therapies.en_GB
dc.identifier.doihttps://doi.org/10.25358/openscience-15704
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/15725
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleThe Chimeric antigen receptor T cell target Claudin 6 is a marker for early organ-specific epithelial progenitors and is expressed in some pediatric solid tumor entitiesen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.netprice2778,11
jgu.apc.price2972,58
jgu.apc.taxrate7
jgu.dfg.year2025
jgu.identifier.uuida0676bcb-0ff9-4439-8dec-405099f09b24
jgu.journal.issue6
jgu.journal.titleCancers
jgu.journal.volume17
jgu.nationalcurrency.eur2778,11
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative920
jgu.publisher.doi10.3390/cancers17060920
jgu.publisher.eissn2072-6694
jgu.publisher.nameMDPI
jgu.publisher.placeBasel
jgu.publisher.year2025
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaftende_DE
jgu.type.contenttypeScientific articleen_GB
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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