Literature DB >> 20345392

Prevalence of allo-immunization anti-HLA and anti-integrin alphaIIbbeta3 in Glanzmann Thromboasthenia patients.

C Santoro1, A Rago, F Biondo, L Conti, F Pulcinelli, L Laurenti, M P Perrone, E Baldacci, A Leporace, M G Mazzucconi.   

Abstract

SUMMARY: Platelet transfusions, main therapy of Glanzmann Thromboasthenia (GT), can induce an allo-immunization against human leucocyte antigen and integrin alphaIIbbeta3. We have investigated in our GT patients the rate of allo-immunization and of refractoriness to platelet transfusions. From 1975 until December 2005, we have followed 17 GT patients: 14 type 1, 3 variant type; nine females, eight males; median age at diagnosis 9.8 years (range 1-44.5); median age at the time of the study 35.5 years (range 23.6-68.5). In our patients, 121 bleeding episodes occurred (24 severe, 37 moderate, and 60 mild). Ten major and 22 minor surgical procedures have been performed. Two spontaneous deliveries and three caesarian sections with five live births were performed; moreover, one late foetal loss occurred, and one voluntary abortion was performed. Sixteen of 17 patients have been transfused at least once in life with platelets and/or red blood cells (RBC). All transfused patients have been investigated for the presence of anti-HLA and anti-integrin alphaIIbbeta3 allo-antibodies. The positiveness of allo-antibodies has been demonstrated in 4/16 transfused patients (25%): isolated for anti-HLA in two; isolated for anti-integrin alphaIIbbeta3 in one; and combined in one. In spite of the presence of allo-antibodies, platelet transfusions have always been effective and the haemostasis was not compromised.

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Year:  2010        PMID: 20345392     DOI: 10.1111/j.1365-2516.2010.02230.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  8 in total

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Review 2.  Clinical use and the Italian demand for activated prothrombin complex and activated recombinant factor VII concentrates.

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Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

3.  The international, prospective Glanzmann Thrombasthenia Registry: treatment modalities and outcomes of non-surgical bleeding episodes in patients with Glanzmann thrombasthenia.

Authors:  Giovanni Di Minno; Rainer B Zotz; Roseline d'Oiron; Niels Bindslev; Matteo Nicola Dario Di Minno; Man-Chiu Poon
Journal:  Haematologica       Date:  2015-05-22       Impact factor: 9.941

4.  The international, prospective Glanzmann Thrombasthenia Registry: treatment and outcomes in surgical intervention.

Authors:  Man-Chiu Poon; Roseline d'Oiron; Rainer B Zotz; Niels Bindslev; Matteo Nicola Dario Di Minno; Giovanni Di Minno
Journal:  Haematologica       Date:  2015-05-22       Impact factor: 9.941

5.  Molecular analysis of a patient with type I Glanzmann thrombasthenia and clinical impact of the presence of anti-αIIbβ3 alloantibodies.

Authors:  Hirokazu Kashiwagi; Kazunobu Kiyomizu; Tsuyoshi Kamae; Tsuyoshi Nakazawa; Seiji Tadokoro; Shuji Takiguchi; Yuichiro Doki; Yuzuru Kanakura; Yoshiaki Tomiyama
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6.  Menstrual and obstetrical bleeding in women with inherited platelet receptor defects-A systematic review.

Authors:  Marieke C Punt; Pauline C E Schuitema; Kitty W M Bloemenkamp; Idske C L Kremer Hovinga; Karin P M van Galen
Journal:  Haemophilia       Date:  2020-01-31       Impact factor: 4.287

Review 7.  Glanzmann Thrombasthenia: Perspectives from Clinical Practice on Accurate Diagnosis and Optimal Treatment Strategies.

Authors:  Natalie Mathews; Georges-Etienne Rivard; Arnaud Bonnefoy
Journal:  J Blood Med       Date:  2021-06-11

8.  In silico analysis of structural modifications in and around the integrin αIIb genu caused by ITGA2B variants in human platelets with emphasis on Glanzmann thrombasthenia.

Authors:  Xavier Pillois; Pierre Peters; Karin Segers; Alan T Nurden
Journal:  Mol Genet Genomic Med       Date:  2018-01-31       Impact factor: 2.183

  8 in total

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