Volume 120, Issue 3 pp. 499-502

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

D. P. Inwald

D. P. Inwald

Portex Department of Anaesthesia, Intensive Therapy and Respiratory Medicine and

Immunobiology Unit, Institute of Child Health, and

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M. J. Peters

M. J. Peters

Portex Department of Anaesthesia, Intensive Therapy and Respiratory Medicine and

Immunobiology Unit, Institute of Child Health, and

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D. Walshe

D. Walshe

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

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A. Jones

A. Jones

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

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E. G. Davies

E. G. Davies

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

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N. J. Klein

N. J. Klein

Immunobiology Unit, Institute of Child Health, and

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First published: 24 December 2001
Citations: 22
Dr D. P. Inwald, Portex Department of Anaesthesia, Intensive Therapy and Respiratory Medicine, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.  E-mail: [email protected]

Abstract

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.

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