Literature DB >> 21108444

Expression patterns of fetal hemoglobin in sickle cell erythrocytes are both patient- and treatment-specific during childhood.

Emily Riehm Meier1, Colleen Byrnes, Maxine Weissman, Pierre Noel, Naomi L C Luban, Jeffery L Miller.   

Abstract

BACKGROUND: Treatment-associated fetal hemoglobin (HbF) expression patterns in children with sickle cell disease (SCD) have not been fully described. The objective of this study was to compare HbF expression profiles (HbF and F-cells) in the peripheral blood of pediatric SCD patients receiving hydroxyurea (HU), chronic transfusions (Tx) or no chronic therapy (Ctrl). PROCEDURE: Peripheral blood samples were collected from SCD patients between 1 month and 21 years of age and immunostained with anti-HbF and anti-HbA antibodies. Erythrocytes containing HbF (F-cells) were enumerated with this dual staining method. HbF was measured using chromatography (HPLC).
RESULTS: Blood from 44 Ctrl patients ≤ 4 years of age was compared with that from older children (50 Ctrl, 17 HU, 17 Tx). Among the older children, the percentage of both HbF and F-cells in the Tx group was significantly decreased compared to the control (HbF 5.4 ± 4.2% vs. 11.0 ± 7.2%, P = 0.003; F-cells 30.2 ± 16.3% vs. 43.8 ± 20.4%, P = 0.0071). While the distribution of F-cells was significantly increased in the HU group (56.3 ± 17.1% vs. 43.8 ± 20.4%, P = 0.016), the increase in HbF was less robust (14.7 ± 6.4% vs. 11.0 ± 7.2%, P = 0.051). Positive correlations of HbF and F-cell distributions were noted in all groups (P < 0.0001 for all groups). In serial samples from individual patients, relatively static patterns of HbF and F-cell distribution were noted.
CONCLUSION: Pediatric SCD patients possess distinct patterns of HbF switching and silencing in peripheral blood erythrocytes. Thereafter, erythrocyte HbF expression level and distribution are maintained with both patient- and treatment-specific patterns that may be useful for predicting the need or response to HbF-modulating therapy.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21108444      PMCID: PMC3299194          DOI: 10.1002/pbc.22643

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  22 in total

Review 1.  Stroke in sickle cell disease: demographic, clinical, and therapeutic considerations.

Authors:  K Ohene-Frempong
Journal:  Semin Hematol       Date:  1991-07       Impact factor: 3.851

2.  Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease.

Authors:  M Maier-Redelsperger; C T Noguchi; M de Montalembert; G P Rodgers; A N Schechter; A Gourbil; D Blanchard; J P Jais; R Ducrocq; J Y Peltier
Journal:  Blood       Date:  1994-11-01       Impact factor: 22.113

Review 3.  Levels of fetal hemoglobin necessary for treatment of sickle cell disease.

Authors:  C T Noguchi; G P Rodgers; G Serjeant; A N Schechter
Journal:  N Engl J Med       Date:  1988-01-14       Impact factor: 91.245

Review 4.  The biology of stress erythropoiesis and erythropoietin production.

Authors:  C E Bozzini; R M Alippi; A C Barceló; M I Conti; C Bozzini; C E Lezon; M I Olivera
Journal:  Ann N Y Acad Sci       Date:  1994-04-15       Impact factor: 5.691

5.  Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease.

Authors:  S J Marcus; T R Kinney; W H Schultz; E E O'Branski; R E Ware
Journal:  Am J Hematol       Date:  1997-01       Impact factor: 10.047

6.  Longitudinal follow up of elevated pulmonary artery pressures in children with sickle cell disease.

Authors:  Farzana D Pashankar; Judith Carbonella; Alia Bazzy-Asaad; Alan Friedman
Journal:  Br J Haematol       Date:  2008-12-01       Impact factor: 6.998

7.  Mortality in sickle cell disease. Life expectancy and risk factors for early death.

Authors:  O S Platt; D J Brambilla; W F Rosse; P F Milner; O Castro; M H Steinberg; P P Klug
Journal:  N Engl J Med       Date:  1994-06-09       Impact factor: 91.245

8.  Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Authors:  S Charache; M L Terrin; R D Moore; G J Dover; F B Barton; S V Eckert; R P McMahon; D R Bonds
Journal:  N Engl J Med       Date:  1995-05-18       Impact factor: 91.245

9.  Control of haemoglobin switching by a developmental clock?

Authors:  W G Wood; C Bunch; S Kelly; Y Gunn; G Breckon
Journal:  Nature       Date:  1985 Jan 24-30       Impact factor: 49.962

10.  Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Authors:  A K Brown; L A Sleeper; S T Miller; C H Pegelow; F M Gill; M A Waclawiw
Journal:  Arch Pediatr Adolesc Med       Date:  1994-08
View more
  7 in total

1.  Increased reticulocytosis during infancy is associated with increased hospitalizations in sickle cell anemia patients during the first three years of life.

Authors:  Emily Riehm Meier; Colleen Byrnes; Y Terry Lee; Elizabeth C Wright; Alan N Schechter; Naomi L C Luban; Jeffery L Miller
Journal:  PLoS One       Date:  2013-08-07       Impact factor: 3.240

Review 2.  Emerging science of hydroxyurea therapy for pediatric sickle cell disease.

Authors:  Nancy S Green; Sandra Barral
Journal:  Pediatr Res       Date:  2013-11-19       Impact factor: 3.756

3.  LIN28A expression reduces sickling of cultured human erythrocytes.

Authors:  Jaira F de Vasconcellos; Ross M Fasano; Y Terry Lee; Megha Kaushal; Colleen Byrnes; Emily R Meier; Molly Anderson; Antoinette Rabel; Raul Braylan; David F Stroncek; Jeffery L Miller
Journal:  PLoS One       Date:  2014-09-04       Impact factor: 3.240

4.  Shape oscillations of single blood drops: applications to human blood and sickle cell disease.

Authors:  Vahideh Ansari Hosseinzadeh; Carlo Brugnara; R Glynn Holt
Journal:  Sci Rep       Date:  2018-11-14       Impact factor: 4.379

5.  Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia.

Authors:  Alina Sadaf; Katie G Seu; Elizabeth Thaman; Rose Fessler; Diamantis G Konstantinidis; Holly A Bonar; Jennifer Korpik; Russell E Ware; Patrick T McGann; Charles T Quinn; Theodosia A Kalfa
Journal:  Front Physiol       Date:  2021-03-25       Impact factor: 4.566

6.  Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.

Authors:  Nancy S Green; Katherine L Ender; Farzana Pashankar; Catherine Driscoll; Patricia J Giardina; Craig A Mullen; Lorraine N Clark; Deepa Manwani; Jennifer Crotty; Sergey Kisselev; Kathleen A Neville; Carolyn Hoppe; Sandra Barral
Journal:  PLoS One       Date:  2013-02-07       Impact factor: 3.240

7.  Absolute Reticulocyte Count Acts as a Surrogate for Fetal Hemoglobin in Infants and Children with Sickle Cell Anemia.

Authors:  Emily Riehm Meier; Colleen Byrnes; Maxine Weissman; Y Terry Lee; Jeffery L Miller
Journal:  PLoS One       Date:  2015-09-14       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.