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Research Article Free access | 10.1172/JCI332

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.

F Rieux-Laucat, P Bahadoran, N Brousse, F Selz, A Fischer, F Le Deist, and J P De Villartay

Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

Find articles by Rieux-Laucat, F. in: JCI | PubMed | Google Scholar

Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Unité INSERM 429, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex 15, France. rieux@necker.fr

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Published July 15, 1998 - More info

Published in Volume 102, Issue 2 on July 15, 1998
J Clin Invest. 1998;102(2):312–321. https://doi.org/10.1172/JCI332.
© 1998 The American Society for Clinical Investigation
Published July 15, 1998 - Version history
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Abstract

Omenn's syndrome is an inherited human combined immunodeficiency condition characterized by the presence of a large population of activated and tissue-infiltrating T cells. Analysis of the TCRB repertoire revealed a highly restricted TCRBV usage in three patients. More strikingly, T cell clones from the three patients expressed TCRB chains with VDJ junction similarities, suggesting a common antigenic specificity. Analysis of the TCRA repertoire in one patient also revealed a restricted TCRAV usage. Finally, analysis of the TCRBV repertoire of tissue-infiltrating T cells in one patient suggested nonrandom tissue migration. These results suggest that the oligoclonal expansion of T cells observed in Omenn's syndrome could be the consequence of autoimmune proliferation generated by a profound defect in lymphocyte development.

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