Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2019 Jun;104(6):1103-1105.
doi: 10.3324/haematol.2018.214908.

Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?

Affiliations
Editorial

Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?

Paquita Nurden et al. Haematologica. 2019 Jun.
No abstract available

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
GPV, a major target for autoantibodies in immune thrombocytopenia (ITP). (Left) Representation of a platelet showing the two principal receptor targets for platelet autoantibodies. Vollenberg et al., while confirming the abundance of autoantibodies detected by direct MAIPA in a series of 343 positive samples from among 1140 tested ITP patients, also showed a significant presence of antibodies to GPV. (Middle) The GPIb-IX-V complex showing the presence of anti-GPV antibody and highlighting binding or cleavage sites for thrombin and metalloproteases ADAM10 and ADAM17. Vollenberg et al. raise questions as to the consequences of bound autoantibodies on GPV structure, the cleavage of released soluble forms, and a potential desialylation of the subunits on platelet survival in ITP. (Right) The detection of both high avidity autoantibodies to GPV by MAIPA and additional low avidity antibodies by surface plasmon resonance (SPR) technology is intriguing, as both of these appear to contribute to the diagnosis of ITP.

Comment on

References

    1. Kiefel V, Santoso S, Kaufmann E, Mueller-Eckhardt C. Autoantibodies against platelet glycoprotein Ib/IX: a frequent finding in autoimmune thrombocytopenic purpura. Br J Haematol. 1991;79(2):256–262. - PubMed
    1. Noris P, Balduini CL. Inherited thrombocytopenias in the era of personalized medicine. Haematologica. 2015;100(2):145–148. - PMC - PubMed
    1. Bastida JM, Lozano ML, Benito R, et al. Introducing high-throughput sequencing into mainstream genetic diagnostic practice in inherited platelet disorders. Haematologica. 2018;103(1):148–162. - PMC - PubMed
    1. Vollenberg R, Jouni R, Norris PAA, et al. Glycoprotein V is a relevant immune target in patients with immune thrombocytopenia. Haematologica. 2019;104(6):1237–1243. - PMC - PubMed
    1. Ulsemer P, Strassel C, Baas MJ, et al. Biosynthesis and intracellular post-translational processing of normal and mutant platelet glycoprotein GPIb-IX. Biochem J. 2001;358(Pt 2):295–303. - PMC - PubMed

Substances