Literature DB >> 6704540

Cobalamin (vitamin B12) and B12 binding proteins in hypereosinophilic syndromes and secondary eosinophilia.

J Zittoun, J P Farcet, J Marquet, C Sultan, R Zittoun.   

Abstract

Serum cobalamin (vitamin B12) and unsaturated B12 binding capacity (UBBC) have been measured in 24 cases of hypereosinophilia: 16 were cases of hypereosinophilic syndrome (HES) and 8 of secondary eosinophilia. The two groups were similar with respect to absolute eosinophil counts. Serum cobalamin and UBBC were found to be markedly increased in most cases of HES and normal in secondary eosinophilia. This elevation of UBBC was mainly related to the increase of R binders (transcobalamins I and III). The elevated serum cobalamin and R binders in HES were due neither to a higher intracellular content of R binders nor to an increased release of these binders from eosinophils of HES. Pure fractions of eosinophils obtained from HES and secondary eosinophilia did not exhibit any difference in vitamin B12 binders. On the other hand, neutrophil-rich fractions from the same patients showed a higher content of intracellular B12 binding proteins than pure eosinophil fractions, irrespective of the cause of eosinophilia. These findings suggest that the increased serum vitamin B12 and UBBC could reflect an expanded pool of both eosinophils and neutrophils in HES and, thus, provide an additional argument for the inclusion of this syndrome in the group of myeloproliferative disorders.

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Year:  1984        PMID: 6704540

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  5 in total

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Authors:  R Christen; R Morant; J Schneider; R Jenni; J Fehr
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4.  Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion.

Authors:  Hava T Ladinsky; Araceli Elizalde; Robyn Schickler; Paola B Dees; Melissa L Crenshaw; John W Sleasman
Journal:  Pediatr Allergy Immunol       Date:  2014-03-16       Impact factor: 6.377

5.  Megaloblastic anemia and immune abnormalities in a patient with methionine synthase deficiency.

Authors:  J Zittoun; A Fischer; J Marquet; J L Pérignon; A Lagrue; C Griscelli
Journal:  Acta Paediatr Scand       Date:  1987-11
  5 in total

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