Establishment of immunity against Epstein‐Barr virus infection in a patient with CHARGE/complete DiGeorge syndrome after peripheral blood lymphocyte transfusion

CHARGE syndrome is a rare congenital malformation syndrome which may share symptoms with DiGeorge syndrome. Complete DiGeorge syndrome (cDGS) is a severe form of DiGeorge syndrome, characterized by a CD3+ T‐cell count of

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Bibliographische Detailangaben
Veröffentlicht in:	Pediatric transplantation 2019-06, Vol.23 (4), p.e13424-n/a
Hauptverfasser:	Hosaka, Sho, Kobayashi, Chie, Saito, Hirota, Imai-Saito, Ayako, Suzuki, Ryoko, Iwabuchi, Atsushi, Kato, Yoshiaki, Jimbo, Takahiro, Watanabe, Nobuyuki, Onodera, Masafumi, Imadome, Ken‐Ichi, Masumoto, Kouji, Nanmoku, Toru, Fukushima, Takashi, Kosaki, Kenjiro, Sumazaki, Ryo, Takada, Hidetoshi
Format:	Artikel
Sprache:	eng
Schlagworte:	Blood transfusion CD3 antigen CD3 Complex - metabolism Cell Proliferation CHARGE syndrome CHARGE Syndrome - therapy CHD7 mutation Concanavalin A Concanavalin A - pharmacology Congenital defects Copy number Cyclosporine - administration & dosage Cyclosporins Diarrhea Diarrhea - therapy DiGeorge syndrome DiGeorge Syndrome - complications DiGeorge Syndrome - immunology Epstein-Barr virus Epstein-Barr Virus Infections - immunology Epstein-Barr Virus Infections - prevention & control Fatal Outcome Genomes Graft vs Host Disease Graft-versus-host reaction Herpesvirus 4, Human - genetics Histocompatibility antigen HLA HLA Antigens - chemistry Humans immune reconstitution Immunity Infant, Newborn Lymphocyte Transfusion Male Methotrexate Methotrexate - administration & dosage Mutation Peripheral blood peripheral blood lymphocyte transfusion Phenotype Phytohemagglutinins - chemistry Prophylaxis Seroconversion Siblings T-Lymphocytes - cytology Thymic hypoplasia
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Beschreibung
Zusammenfassung:	CHARGE syndrome is a rare congenital malformation syndrome which may share symptoms with DiGeorge syndrome. Complete DiGeorge syndrome (cDGS) is a severe form of DiGeorge syndrome, characterized by a CD3+ T‐cell count of
ISSN:	1397-3142 1399-3046
DOI:	10.1111/petr.13424