WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12. - Archive ouverte HAL Access content directly
Journal Articles Blood Year : 2005

WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.

Karl Balabanian
Lysiane Laurent
  • Function : Author
Olivier Verola
  • Function : Author
Celeste Lebbe
Delphine Kerob
  • Function : Author
Alain Dupuy
  • Function : Author
Olivier Hermine
Jean-François Nicolas
  • Function : Author
Véronique Latger-Cannard
  • Function : Author
  • PersonId : 758461
  • IdRef : 142792950
Danièle Bensoussan
Pierre Bordigoni
  • Function : Author
Françoise Baleux
Françoise Le Deist
  • Function : Author
Fernando Arenzana-Seisdedos
  • Function : Author
  • PersonId : 853031

Abstract

The WHIM syndrome is a rare immunodeficiency disorder characterized by warts, hypogammaglobulinemia, infections, and myelokathexis. Dominant heterozygous mutations of the gene encoding CXCR4, a G-protein-coupled receptor with a unique ligand, CXCL12, have been associated with this pathology. We studied patients belonging to 3 different pedigrees. Two siblings inherited a CXCR4 mutation encoding a novel C-terminally truncated receptor. Two unrelated patients were found to bear a wild-type CXCR4 open reading frame. Circulating lymphocytes and neutrophils from all patients displayed similar functional alterations of CXCR4-mediated responses featured by a marked enhancement of G-protein-dependent responses. This phenomenon relies on the refractoriness of CXCR4 to be both desensitized and internalized in response to CXCL12. Therefore, the aberrant dysfunction of the CXCR4-mediated signaling constitutes a common biologic trait of WHIM syndromes with different causative genetic anomalies. Responses to other chemokines, namely CCL4, CCL5, and CCL21, were preserved, suggesting that, in clinical forms associated with a wild-type CXCR4 open reading frame, the genetic anomaly might target an effector with some degree of selectivity for the CXCL12/CXCR4 axis. We propose that the sustained CXCR4 activity in patient cells accounts for the immune-hematologic clinical manifestations and the profusion of warts characteristic of the WHIM syndrome.
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Dates and versions

pasteur-00166808 , version 1 (10-08-2007)

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Karl Balabanian, Bernard Lagane, José Luis Pablos, Lysiane Laurent, Thierry Planchenault, et al.. WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.. Blood, 2005, 105 (6), pp.2449-57. ⟨10.1182/blood-2004-06-2289⟩. ⟨pasteur-00166808⟩

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