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An unusual case of severe combined immunodeficiency with hypereosinophilia
Author(s) -
Dams E. Th. M.,
MascartLemone F.,
Schandené L.,
van der Meer J. W. M.
Publication year - 1997
Publication title -
journal of internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.625
H-Index - 160
eISSN - 1365-2796
pISSN - 0954-6820
DOI - 10.1046/j.1365-2796.1997.00199.x
Subject(s) - hypereosinophilia , medicine , immunodeficiency , immunology , pathogenesis , eosinophilia , immune system
Dams ETHM, Mascart‐Lemone F, Schandené L, van der Meer JWM (University Hospital Nijmegen, Nijmegen, The Netherlands, and Hôpital Erasme, Brussels, Belgium). An unusual case of severe combined immunodeficiency with hypereosinophilia (Case Report). J Intern Med 1997; 242 : 267–9. Investigation of the cytokine profile in a 26‐year‐old man, suffering from combined immunodeficiency with hypereosinophilia, revealed high levels of interleukin‐4 and interleukin‐5 and relatively low levels of interleukin‐2 and interferon gamma, consistent with a T‐helper type 2 pattern, as has been reported in Omenn's syndrome. However, some distinct clinical and immunological features suggest that this case may represent a unique disease with specific pathogenesis.