Literature DB >> 2985012

[Severe combined immune deficiency with hypereosinophilia. Immunologic study of 5 cases].

F Le Deist, A Fischer, A Durandy, F Arnaud-Battandier, C Nezelof, M Hamet, Y de Prost, C Griscelli.   

Abstract

We herein report five new cases of severe combined immunodeficiency with hypereosinophilia, the so-called familial reticuloendotheliosis first described by Omenn. It is characterized by erythroderma, polyadenopathy, hepatosplenomegaly, severe and repeated infections, protracted diarrhoea with failure to thrive. There is marked eosinophilia as well as a profound immunodeficiency. The immunologic abnormalities consist of an increase in T cell number, a B cell lymphopenia and a complete lack of humoral and cellular immune responses to antigens. A deficiency of lymphocytes 5'-nucleotidase has been inconstantly found. Histologic findings are characteristic, consisting of severe T and B lymphocyte depletion in lymphoid organs with infiltration by histiocytes and, to a lesser extent, eosinophils. The outcome was uniformly fatal within the first year of life. Treatment by a combination of parenteral nutrition, steroids and epipodophyllotoxin was effective in obtaining the complete remission of clinical manifestations due to the histiocytic and eosinophilic infiltration in two patients. However, the treatment failed to correct the immunologic defect. These results indicate that the histiocytic infiltration is possibly not responsible for the immunologic detect observed in this condition.

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Year:  1985        PMID: 2985012

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  7 in total

Review 1.  Primary T-lymphocyte immunodeficiencies.

Authors:  A Fischer
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

2.  Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

Authors:  G de Saint-Basile; F Le Deist; J P de Villartay; N Cerf-Bensussan; O Journet; N Brousse; C Griscelli; A Fischer
Journal:  J Clin Invest       Date:  1991-04       Impact factor: 14.808

3.  Severe pulmonary vascular occlusive disease following bone marrow transplantation in Omenn syndrome.

Authors:  C Brückmann; W Lindner; R Roos; W Permanetter; R J Haas; S G Haworth; B H Belohradsky
Journal:  Eur J Pediatr       Date:  1991-02       Impact factor: 3.183

Review 4.  Autoimmunity in Primary Immunodeficiencies (PID).

Authors:  Grace T Padron; Vivian P Hernandez-Trujillo
Journal:  Clin Rev Allergy Immunol       Date:  2022-06-01       Impact factor: 8.667

5.  Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.

Authors:  F Rieux-Laucat; P Bahadoran; N Brousse; F Selz; A Fischer; F Le Deist; J P De Villartay
Journal:  J Clin Invest       Date:  1998-07-15       Impact factor: 14.808

6.  AIRE deficiency in thymus of 2 patients with Omenn syndrome.

Authors:  Patrizia Cavadini; William Vermi; Fabio Facchetti; Stefania Fontana; Seiho Nagafuchi; Evelina Mazzolari; Anna Sediva; Veronica Marrella; Anna Villa; Alain Fischer; Luigi D Notarangelo; Raffaele Badolato
Journal:  J Clin Invest       Date:  2005-03       Impact factor: 14.808

Review 7.  Omenn syndrome: a disorder of Rag1 and Rag2 genes.

Authors:  A Villa; S Santagata; F Bozzi; L Imberti; L D Notarangelo
Journal:  J Clin Immunol       Date:  1999-03       Impact factor: 8.317

  7 in total

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