Absence of platelet CD40L identifies patients with X-linked hyper IgM syndrome

Author:

Inwald D P12,Peters M J12,Walshe D3,Jones A3,Davies E G3,Klein N J2

Affiliation:

1. Portex Department of Anaesthesia, Intensive Therapy and Respiratory Medicine and

2. Immunobiology Unit, Institute of Child Health

3. Department of Clinical Immunology, Great Ormond Street Hospital for Children NHS Trust, London, UK

Abstract

SUMMARY CD40 ligand (CD40L), a membrane protein expressed on activated T cells, plays a pivotal role in B cell proliferation and differentiation. Mutations in the CD40L gene are associated with a rare immunodeficiency state, X-linked hyper IgM syndrome (XLHIGM). Recently, platelets have been described as capable of expressing CD40L within minutes of stimulation. We have developed a rapid technique to determine expression of CD40L on activated platelets by flow cytometry in whole blood. We have demonstrated that this technique is useful in neonatal screening, in rapid diagnosis and in determining reconstitution by donor bone marrow post-transplantation.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference14 articles.

1. CD40 and its ligand in host defence;Noelle;Immunity,1996

2. The many roles of CD40 in cell-mediated inflammatory responses;Stout;Immunol Today,1996

3. CD40-mediated signalling in B cells. Balancing cell survival, growth, and death;Kehry;J Immunol,1996

4. Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM;Korthauer;Nature,1993

5. CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM;DiSanto;Nature,1993

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