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6533b7d5fe1ef96bd12650e2

RESEARCH PRODUCT

Tissue microenvironment dictates the fate and tumor-suppressive function of type 3 ILCs

Sara H. BurkhardIsabel OhsChristoph S.n. KloseSebastian J. ArnoldKathrin NussbaumAndreas DiefenbachFlorian MairBurkhard BecherSonia Tugues

subject

0301 basic medicinemedicine.medical_treatmentImmunology314610 Medicine & healthBiology10263 Institute of Experimental ImmunologyArticle31103 medical and health sciencesMiceRAR-related orphan receptor gammaCell Line TumormedicineImmunology and AllergyAnimalsLymphocytesskin and connective tissue diseasesTranscription factorResearch ArticlesMice Knockout2403 ImmunologyInnate lymphoid cellNeoplasms ExperimentalNuclear Receptor Subfamily 1 Group F Member 3PhenotypeCell biologybody regionsKiller Cells NaturalMice Inbred C57BL030104 developmental biologyCytokineCellular MicroenvironmentCell cultureTumor progressionInterleukin 122723 Immunology and AllergyCytokines570 Life sciences; biologyTranscription Factors

description

Nussbaum et al. found that tumor suppression through innate lymphoid cells (ILCs) cannot be predicted solely based on the ILC phenotype and lineage but that their immune properties are shaped both by their ontogeny and by the tissue microenvironment they reside in.

yearjournalcountryeditionlanguage
2017-01-01
10.5167/uzh-140357https://www.zora.uzh.ch/id/eprint/140357/
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