{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T22:21:51Z","timestamp":1790461311733,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2025,4,9]],"date-time":"2025-04-09T00:00:00Z","timestamp":1744156800000},"content-version":"vor","delay-in-days":8,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Allergy Immunology"],"published-print":{"date-parts":[[2025,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Invasive fungal disease (IFD) is a common complication observed in inborn errors of immunodeficiency (IEI) patients, and little is known about the overall prevalence of IFD in IEI patients. We aimed to summarize the fungal spectrum and outcomes of IFDs in a Chinese cohort of hospitalized patients with IEI.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>In this retrospective study, 607 IEI patients hospitalized from January 2018 to June 2022 were included. Demographic, clinical, and fungal infection data and IEI patient characteristics were collected and analyzed according to the IEI classification.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      One hundred and two IEI patients were diagnosed with proven or probable IFD. The overall prevalence of IFD was 17% (102\/607). There were 29 different genotypes, among which\n                      <jats:italic>CYBB<\/jats:italic>\n                      (25%),\n                      <jats:italic>CD40LG<\/jats:italic>\n                      (9%), and\n                      <jats:italic>RAG1<\/jats:italic>\n                      (7%) mutations were the most common. Most IFD infections (87\/102) were caused by one fungus. Invasive\n                      <jats:italic>Aspergillus<\/jats:italic>\n                      ,\n                      <jats:italic>Pneumocystis jirovecii<\/jats:italic>\n                      pneumonia, and\n                      <jats:italic>Penicillium<\/jats:italic>\n                      infections were more commonly observed in patients with congenital defects in phagocytes, immunodeficiencies affecting cellular and humoral immunity, and defects in innate immunity, respectively. Most IFDs observed in IEI patients were single\u2010site infections, most of which were lung infections (74%). Seventeen patients were diagnosed with disseminated IFDs, nine of which were caused by\n                      <jats:italic>Penicillium<\/jats:italic>\n                      . All patients received antifungal treatments. Eight patients (8%) died within 3\u2009months of IFD diagnosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>IFD occurrence suggests the presence of immunity impairment. The IFD fungal profile may indicate different types of IEI. Early recognition of immunodeficiency and optimal timing of antifungal therapy can reduce fatality in IEI patients.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/pai.70074","type":"journal-article","created":{"date-parts":[[2025,4,10]],"date-time":"2025-04-10T01:15:16Z","timestamp":1744247716000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Invasive fungal disease in a large cohort of hospitalized children with inborn errors of immunity in China"],"prefix":"10.1111","volume":"36","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1489-1951","authenticated-orcid":false,"given":"Haiqiao","family":"Zhang","sequence":"first","affiliation":[{"name":"Shanghai Institute of Infectious Disease and Biosecurity Fudan University  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mi","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Clinical Immunology 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