Literature DB >> 9332313

Immune function in patients with beta thalassaemia receiving the orally active iron-chelating agent deferiprone.

R Loebstein1, I Dalal, E Nisbet-Brown, M Berkovitch, N Meydan, D Andrews, M D Loubser, G Koren, C M Roifman, N F Olivieri.   

Abstract

Short-term deferiprone may reduce body iron in some patients with thalassaemia major. Concerns regarding potential immunosuppressive effects of deferiprone have been raised from results of animal studies and case reports in humans. We studied immune function in 57 thalassaemia patients: 36 treated with deferiprone (L1; CP020) and 21 treated with desferrioxamine (DFO). Circulating B lymphocytes were increased in all patient groups. No differences were detected between treatment groups in percentages of circulating lymphocytes, concentrations of IgG, IgM or IgA, specific antibody titres, complement levels, or in vitro lymphocyte proliferation. No clinically important infections were observed in any patient. These data suggest that no clinical or laboratory changes consistent with immuno-suppression or immunodeficiency are observed during deferiprone therapy.

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Year:  1997        PMID: 9332313     DOI: 10.1046/j.1365-2141.1997.2463064.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  3 in total

Review 1.  Deferiprone: a review of its clinical potential in iron overload in beta-thalassaemia major and other transfusion-dependent diseases.

Authors:  J A Barman Balfour; R H Foster
Journal:  Drugs       Date:  1999-09       Impact factor: 9.546

2.  Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier.

Authors:  Paolo Ricchi; Patrizia Cinque; Alfonso Lanza Galeota; Tiziana Di Matola; Massimiliano Ammirabile; Luciano Prossomariti
Journal:  Int J Hematol       Date:  2008-12-25       Impact factor: 2.490

3.  Serum immunoglobulin levels in splenectomized and non- splenectomized patients with major Beta-thalassemia.

Authors:  Mojgan Kiani-Amin; Mohammadmehdi Daneshi; Parviz Ayazi; Shima Mohammadian; Nima Rezaei
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

  3 in total

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