Langerhans cell deficiency in reticular dysgenesis.

Abstract:

:Reticular dysgenesis is a rare inherited immunodeficiency characterized by the lack of blood monocytes and neutrophils and low lymphocyte counts, contrasting with normal red blood cell counts and normal or decreased platelet counts. Whether dendritic cells or macrophages, both of which derive primarily from blood monocytes, are affected in this condition remains unknown. We studied 7 patients with reticular dysgenesis. Macrophages were present in normal numbers in the dermis and in the atrophic lymphoid tissues of these patients, proving that at least some subsets of macrophages can differentiate despite very low monocyte counts. By contrast, Langerhans cells, which are CD1a-positive epidermal dendritic cells, were absent in all (n = 5) patients before bone marrow transplantation. After bone marrow transplantation, Langerhans cells were present (n = 2), suggesting that the defect is not related to keratinocyte dysfunction. A split chimeric reconstitution, characterized by the presence of autologous blood monocytes able to differentiate in vitro into CD1a-positive dendritic cells, was observed in a patient who underwent successful engraftment. These results suggest that an intrinsic cell defect is unlikely and that a bone marrow-derived factor may be defective in reticular dysgenesis; it may be responsible for the Langerhans cell defect but not involved in macrophage differentiation.

journal_name

Blood

journal_title

Blood

authors

Emile JF,Geissmann F,Martin OC,Radford-Weiss I,Lepelletier Y,Heymer B,Espanol T,de Santes KB,Bertrand Y,Brousse N,Casanova JL,Fischer A

subject

Has Abstract

pub_date

2000-07-01 00:00:00

pages

58-62

issue

1

eissn

0006-4971

issn

1528-0020

journal_volume

96

pub_type

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