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The mechanism of bone marrow failure (BMF) in paroxysmal nocturnal hemoglobinuria (PNH) is not yet known. Because in PNH the biosynthesis of the glycolipid molecule glycosylphosphatidylinositol (GPI) is disrupted in hematopoietic stem and progenitor cells by a somatic mutation in the PIG-A gene, BMF might result from an autoimmune attack, whereby T cells target GPI in normal cells, whereas PIG-A mutant GPI-negative cells are spared. In a deliberate test of this hypothesis, we have demonstrated in PNH patients the presence of CD8(+) T cells reactive against antigen-presenting cells (APCs) loaded with GPI. These T cells were significantly more abundant in PNH patients than in healthy controls; their reactivity depended on CD1d expression and they increased upon coculture with CD1d-expressing, GPI-positive APCs. In GPI-specific T cells captured by CD1d dimer technology, we identified, through global T-cell receptor α (TCRα) analysis, an invariant TCRVα21 sequence, which was then found at frequencies higher than background in the TCR repertoire of 6 of 11 PNH patients. Thus, a novel, autoreactive, CD1d-restricted, GPI-specific T-cell population, enriched in an invariant TCRα chain, is expanded in PNH patients and may be responsible for BMF in PNH.

Original publication

DOI

10.1182/blood-2012-11-469353

Type

Journal article

Journal

Blood

Publication Date

04/04/2013

Volume

121

Pages

2753 - 2761

Keywords

Adult, Aged, Anemia, Aplastic, Antigen-Presenting Cells, Antigens, CD1d, Bone Marrow Diseases, Bone Marrow Failure Disorders, CD8-Positive T-Lymphocytes, Coculture Techniques, Dimerization, Female, Flow Cytometry, Gene Library, Glycosylphosphatidylinositols, Hemoglobinuria, Paroxysmal, Humans, K562 Cells, Male, Middle Aged, RNA, Messenger, Receptors, Antigen, T-Cell, alpha-beta, Young Adult