» Articles » PMID: 24466297

Detection of Circulating B Cells Producing Anti-GPIb Autoantibodies in Patients with Immune Thrombocytopenia

Overview
Journal PLoS One
Date 2014 Jan 28
PMID 24466297
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: We previously reported that an enzyme-linked immunospot (ELISPOT) assay for detecting anti-GPIIb/IIIa antibody-secreting B cells is a sensitive method for identifying patients with immune thrombocytopenia (ITP). Here we assessed the clinical significance of measuring circulating B cells producing antibodies to GPIb, another major platelet autoantigen.

Methods: Anti-GPIb and anti-GPIIb/IIIa antibody-producing B cells were simultaneously measured using ELISPOT assays in 32 healthy controls and 226 consecutive thrombocytopenic patients, including 114 with primary ITP, 25 with systemic lupus erythematosus (SLE), 30 with liver cirrhosis, 39 with post-hematopoietic stem cell transplantation (post-HSCT), and 18 non-ITP controls (aplastic anemia and myelodysplastic syndrome).

Results: There were significantly more circulating anti-GPIb and anti-GPIIb/IIIa antibody-producing B cells in primary ITP, SLE, liver cirrhosis, and post-HSCT patients than in healthy controls (P<0.05 for all comparisons). For diagnosing primary ITP, the anti-GPIb ELISPOT assay had 43% sensitivity and 89% specificity, whereas the anti-GPIIb/IIIa ELISPOT assay had 86% sensitivity and 83% specificity. When two tests were combined, the sensitivity was slightly improved to 90% without a reduction in specificity. In primary ITP patients, the anti-GPIb antibody response was associated with a low platelet count, lack of Helicobacter pylori infection, positive anti-nuclear antibody, and poor therapeutic response to intravenous immunoglobulin.

Conclusion: The ELISPOT assay for detecting anti-GPIb antibody-secreting B cells is useful for identifying patients with ITP, but its utility for diagnosing ITP is inferior to the anti-GPIIb/IIIa ELISPOT assay. Nevertheless, detection of the anti-GPIb antibody response is useful for subtyping patients with primary ITP.

Citing Articles

Impact of Thrombopoietin Receptor Agonists on Pathophysiology of Pediatric Immune Thrombocytopenia.

Evangelidis P, Tragiannidis K, Gavriilaki E, Tragiannidis A Curr Issues Mol Biol. 2025; 47(1).

PMID: 39852180 PMC: 11763769. DOI: 10.3390/cimb47010065.


Reference guide for the diagnosis of adult primary immune thrombocytopenia, 2023 edition.

Kashiwagi H, Kuwana M, Murata M, Shimada N, Takafuta T, Yamanouchi J Int J Hematol. 2023; 119(1):1-13.

PMID: 37957517 PMC: 10770234. DOI: 10.1007/s12185-023-03672-1.


Interferon-gamma FlowSpot assay for the measurement of the T-cell response to cytomegalovirus.

Ye Q, Wang J, Chen M, Nie W, Zhang H, Su X Heliyon. 2023; 9(6):e16792.

PMID: 37360105 PMC: 10285093. DOI: 10.1016/j.heliyon.2023.e16792.


Autoimmune Regulator Gene Polymorphisms and the Risk of Primary Immune Thrombocytopenic Purpura: A Case-Control Study.

Abdel Ghafar M, Elshora O, Allam A, Mashaal R, Hamous S, El-Khalik S Int J Mol Sci. 2023; 24(5).

PMID: 36902438 PMC: 10003684. DOI: 10.3390/ijms24055007.


B cell-activating factor is involved in thrombocytopenia in patients with liver cirrhosis.

Satoh T, Takiguchi H, Uojima H, Kubo M, Tanaka C, Yokoyama F Ann Hematol. 2022; 101(11):2433-2444.

PMID: 36098792 DOI: 10.1007/s00277-022-04973-x.


References
1.
Kuwana M, Kurata Y, Fujimura K, Fujisawa K, Wada H, Nagasawa T . Preliminary laboratory based diagnostic criteria for immune thrombocytopenic purpura: evaluation by multi-center prospective study. J Thromb Haemost. 2006; 4(9):1936-43. DOI: 10.1111/j.1538-7836.2006.02091.x. View

2.
George J, Woolf S, Raskob G, Wasser J, Aledort L, Ballem P . Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology. Blood. 1996; 88(1):3-40. View

3.
Cauwenberghs N, Schlammadinger A, Vauterin S, Cooper S, Descheemaeker G, Tornai I . Fc-receptor dependent platelet aggregation induced by monoclonal antibodies against platelet glycoprotein Ib or von Willebrand factor. Thromb Haemost. 2001; 85(4):679-85. View

4.
Murata M, Ware J, Ruggeri Z . Site-directed mutagenesis of a soluble recombinant fragment of platelet glycoprotein Ib alpha demonstrating negatively charged residues involved in von Willebrand factor binding. J Biol Chem. 1991; 266(23):15474-80. View

5.
Kuwana M, Kaburaki J, Okazaki Y, Miyazaki H, Ikeda Y . Two types of autoantibody-mediated thrombocytopenia in patients with systemic lupus erythematosus. Rheumatology (Oxford). 2006; 45(7):851-4. DOI: 10.1093/rheumatology/kel010. View