Literature DB >> 7843626

Serum levels of cytokines and soluble antigens in polytransfused patients with beta-thalassemia major: relationship to immune status.

G Lombardi1, R Matera, M M Minervini, N Cascavilla, P D'Arcangelo, M Carotenuto, G Di Giorgio, P Musto.   

Abstract

BACKGROUND: A series of immunological abnormalities has been described in patients with beta-thalassemia. The aim of this study was to investigate whether the measurement of serum levels of selected cytokines and soluble molecules (deriving from cell membrane antigens) involved in the immune response could be useful for a better definition of such alterations. PATIENTS AND METHODS: Serum levels of interleukin-2 (IL-2), IL-6, tumor necrosis factor (TNF), soluble (s) CD4, sCD8, sCD23 and sCD25 were measured using immunoenzymatic assays in 45 transfusion-dependent patients affected by beta-thalassemia major and correlated to conventional immunological indexes, such as peripheral lymphocyte subpopulations and circulating immunoglobulins.
RESULTS: Patients with beta-thalassemia major showed increased TNF, sCD8, sCD23 and sCD25 and lower sCD4 values compared to normal controls. IL-2 and IL-6 were found to be undetectable or within the normal range in all patients. Splenectomized patients presented lower levels of sCD8 and sCD23 than those observed in unsplenectomized ones. A series of correlations involving TNF, sCD8, sCD23, sCD25, serum immunoglobulins and some lymphocyte subpopulations was observed. In addition, serum markers of immune activation (TNF, sCD23, sCD25) correlated directly with the annual blood transfusion requirement. Despite this series of immunological anomalies, no patient had a history of repeated infectious episodes.
CONCLUSIONS: Polytransfused beta-thalassemic patients are characterized by a partial functional immunodeficiency determined by increased activity of CD8+ suppressor/cytotoxic lymphocytes and possibly reduced activity of the CD4+ helper/inducer subset. B-lymphocytes also appear highly activated. The allo-antigenic stimulation of transfusions seems to play a major role in the determination of these defects; however, this functional immunological imbalance does not seem to have any clinical relevance.

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Year:  1994        PMID: 7843626

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  6 in total

1.  Blood transfusions with high levels of contaminating soluble HLA-I correlate with levels of soluble CD8 in recipients' plasma; a new control factor in soluble HLA-I-mediated transfusion-modulated immunomodulation?

Authors:  Massimo Ghio; Paola Contini; Gianluca Ubezio; Filippo Ansaldi; Maurizio Setti; Gino Tripodi
Journal:  Blood Transfus       Date:  2012-12-21       Impact factor: 3.443

2.  Comparison of vascular complications between conventional treatment and bone marrow transplantation for children with beta-thalassemia disease.

Authors:  Alisa Limsuwan; Darin Tubtom; Samart Pakakasama; Ampiwan Chaunsumrit
Journal:  Pediatr Cardiol       Date:  2009-04-14       Impact factor: 1.655

3.  Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications.

Authors:  Bianca Maria Ricerca; Arturo Di Girolamo; Deborah Rund
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-12-28       Impact factor: 2.576

4.  Effect of Tumor Necrosis Factor-Alpha on Erythropoietin and Erythropoietin Receptor-Induced Erythroid Progenitor Cell Proliferation in β-Thalassemia/Hemoglobin E Patients.

Authors:  Dalina I Tanyong; Prapaporn Panichob; Wasinee Kheansaard; Suthat Fucharoen
Journal:  Turk J Haematol       Date:  2015-08-06       Impact factor: 1.831

5.  Evaluation of immune system in patients with transfusion-dependent beta-thalassemia in Rasoul-e-Akram Hospital in 2021: A descriptive cross-sectional study.

Authors:  Fahime Ehsanipour; Pooya Faranoush; Mohammad Reza Foroughi-Gilvaee; Negin Sadighnia; Morteza Fallahpour; Mona Motamedi; Afsoon Zandi; Zahra Safaei; Ashkan Zandi; Mohammad Faranoush
Journal:  Health Sci Rep       Date:  2022-10-03

Review 6.  Ineffective erythropoiesis in β -thalassemia.

Authors:  Jean-Antoine Ribeil; Jean-Benoit Arlet; Michael Dussiot; Ivan Cruz Moura; Geneviève Courtois; Olivier Hermine
Journal:  ScientificWorldJournal       Date:  2013-03-28
  6 in total

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