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In most individuals, circulating neutrophils comprise distinct fractions of CD177\u2010expressing (CD177\n                    <jats:sup>+<\/jats:sup>\n                    ) and non\u2010expressing (CD177\n                    <jats:sup>\u2212<\/jats:sup>\n                    ) cells, which differ functionally and influence disease outcomes. Currently, CD177 is considered a dynamic activation marker ultimately expressed by most neutrophils. Here, we show that, instead, CD177\n                    <jats:sup>\u2212<\/jats:sup>\n                    \u2010neutrophils represent a stable subpopulation that never acquires CD177. CD177\n                    <jats:sup>+<\/jats:sup>\n                    \u2010 to CD177\n                    <jats:sup>\u2212<\/jats:sup>\n                    \u2010neutrophil ratios persist over time in individuals, regardless of circadian rhythms or inflammation. Neutrophils remain CD177\n                    <jats:sup>\u2212<\/jats:sup>\n                    during in vitro stimulation and are morphologically similar to CD177\n                    <jats:sup>+<\/jats:sup>\n                    \u2010cells, but differ markedly regarding protein composition. Following stem cell transplantation, the host bone marrow defines the CD177\u2010pattern of mature neutrophils. Functionally, CD177\n                    <jats:sup>\u2212<\/jats:sup>\n                    neutrophils display pro\u2010tumoral properties, including elevated arginase expression and enhanced tumor\u2010supporting activity, are enriched in human head\u2010and\u2010neck cancer tissues, and associated with adverse clinical outcomes. Hence, CD177\u2010expression or \u2010absence defines stable human neutrophil subtypes with distinct functions.\n                  <\/jats:p>","DOI":"10.1002\/advs.76236","type":"journal-article","created":{"date-parts":[[2026,6,22]],"date-time":"2026-06-22T10:31:12Z","timestamp":1782124272000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["CD177 Deficiency Defines a Stable Subtype of Human Neutrophil Granulocytes with Tumor Promoting Activity"],"prefix":"10.1002","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8277-3052","authenticated-orcid":false,"given":"Marcel","family":"Jung","sequence":"first","affiliation":[{"name":"Institute For Experimental Immunology and Imaging University Hospital University of Duisburg\u2010Essen  Essen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexander","family":"Beer","sequence":"additional","affiliation":[{"name":"Institute For Experimental Immunology and Imaging University Hospital University of Duisburg\u2010Essen  Essen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Susmita","family":"Ghosh","sequence":"additional","affiliation":[{"name":"Leibniz\u2010Institut F\u00fcr Analytische Wissenschaften \u2013 ISAS \u2013 e.V.  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