scholarly journals Progress and development of platelet antibody detection

2020 ◽  
Vol 59 (1) ◽  
pp. 102705 ◽  
Author(s):  
L. Porcelijn ◽  
E. Huiskes ◽  
M. de Haas
Blood ◽  
1979 ◽  
Vol 54 (5) ◽  
pp. 1101-1108
Author(s):  
PL Cimo ◽  
SA Gerber

2-Aminoethylisothiouronium bromide (AET) increases the sensitivity of blood cells to complement-mediated immune lysis. We compared the sensitivities of untreated or AET-treated platelets to immune lysis induced by different types of platelet antibody in the 51Cr platelet lysis test. AET platelets were 8–16 times more sensitive to autoantibody and alloantibody, but 8–16 times less sensitive to drug- dependent antibody. AET-platelets bound similar amounts of alloantibody but less drug-dependent antibody, and they lysed at higher complement dilutions than did untreated platelets. AET-platelets detected 10 of 25 autoantibodies, 9 of 9 alloantibodies, and 5 of 8 drug-dependent antibodies. Untreated platelets detected 1 of 25, 6 of 9, and 7 of 8 of these respective platelet antibodies. The use of AET-platelets in the 51Cr platelet lysis test increases its sensitivity for detecting non- drug-dependent platelet antibodies. AET-platelets resemble paroxysmal nocturnal hemoglobinuria (PNH) platelets in their enhanced sensitivity to complement-mediated lysis. They differ from PNH platelets in their insensitivity to immune lysis induced by drug-dependent antibodies and, in this respect, are similar to Bernard-Soulier syndrome platelets.


Platelets ◽  
2014 ◽  
Vol 26 (5) ◽  
pp. 421-424 ◽  
Author(s):  
Julie Di Cristofaro ◽  
Coralie Frassati ◽  
Rolande Montagnie ◽  
Agnes Basire ◽  
Yves Merieux ◽  
...  

Author(s):  
A. E. G. Kr. von dem Borne ◽  
W. H. Ouwehand ◽  
C. M. van Dalen

1988 ◽  
Vol 28 (1) ◽  
pp. 1-7 ◽  
Author(s):  
J. Freedman ◽  
M. B. Garvey ◽  
A. Hornstein ◽  
Z. Salomon De Friedberg ◽  
V. Blanchette

Blood ◽  
1979 ◽  
Vol 54 (5) ◽  
pp. 1101-1108 ◽  
Author(s):  
PL Cimo ◽  
SA Gerber

Abstract 2-Aminoethylisothiouronium bromide (AET) increases the sensitivity of blood cells to complement-mediated immune lysis. We compared the sensitivities of untreated or AET-treated platelets to immune lysis induced by different types of platelet antibody in the 51Cr platelet lysis test. AET platelets were 8–16 times more sensitive to autoantibody and alloantibody, but 8–16 times less sensitive to drug- dependent antibody. AET-platelets bound similar amounts of alloantibody but less drug-dependent antibody, and they lysed at higher complement dilutions than did untreated platelets. AET-platelets detected 10 of 25 autoantibodies, 9 of 9 alloantibodies, and 5 of 8 drug-dependent antibodies. Untreated platelets detected 1 of 25, 6 of 9, and 7 of 8 of these respective platelet antibodies. The use of AET-platelets in the 51Cr platelet lysis test increases its sensitivity for detecting non- drug-dependent platelet antibodies. AET-platelets resemble paroxysmal nocturnal hemoglobinuria (PNH) platelets in their enhanced sensitivity to complement-mediated lysis. They differ from PNH platelets in their insensitivity to immune lysis induced by drug-dependent antibodies and, in this respect, are similar to Bernard-Soulier syndrome platelets.


Author(s):  
Carolina Bonet Bub ◽  
Beatriz Moraes Martinelli ◽  
Thayná Mendonça Avelino ◽  
Ana Cláudia Gonçalez ◽  
Maria de Lourdes Barjas-Castro ◽  
...  

2021 ◽  
Vol 4 (1) ◽  
pp. 006-012
Author(s):  
Lin Jeong-Shi ◽  
Lee Li-Hsuan ◽  
Liu Hsueng-Mei ◽  
Chen Ying-Ju ◽  
Chiou Tzeon-Jye

Background: Interleukin-6 (IL-6) promotes antibody production. The objective of this study was to investigate whether IL-6 C-572G single nucleotide polymorphisms (SNP) and clinical factors are associated with positive platelet antibody test. Materials and methods: Thirty platelet recipients with platelet antibodies (responders) and 20 platelet recipients without platelet antibodies (non-responders) were randomly selected. The -572 C>G (rs 1800796) SNPs in the promoter region of IL-6 gene were genotyped by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) method. Solid phase red cell adherence assay (SPRCA) was used for platelet antibody detection. Results: Age, sex, percentage patients with benign diseases, and percentage of patients with homozygotes for the C allele at position -572 of the IL-6 gene were similar between responders and non-responders. Although the amounts of platelets pheresis transfused to patients with hematologic diseases were higher than those of non-hematologic diseases (47.2 ± 54.2 vs. 17.4 ± 13.8 units, p = 0.019), detection rate of platelet antibodies was lower in patients with hematologic diseases than that in patients with non-hematologic diseases (42.3% vs. 79.2%, p = 0.01). Conclusion: There was no association between IL-6 C-572G gene polymorphism and positive reactivity in solid phase platelet antibody detection method in platelet recipients.


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