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The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency

Congenital or acquired cellular deficiencies in humans have the potential to reveal much about normal hematopoiesis and immune function. We show that a recently described syndrome of monocytopenia, B and NK lymphoid deficiency additionally includes the near absence of dendritic cells. Four subjects...

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Detalles Bibliográficos
Autores principales: Bigley, Venetia, Haniffa, Muzlifah, Doulatov, Sergei, Wang, Xiao-Nong, Dickinson, Rachel, McGovern, Naomi, Jardine, Laura, Pagan, Sarah, Dimmick, Ian, Chua, Ignatius, Wallis, Jonathan, Lordan, Jim, Morgan, Cliff, Kumararatne, Dinakantha S., Doffinger, Rainer, van der Burg, Mirjam, van Dongen, Jacques, Cant, Andrew, Dick, John E., Hambleton, Sophie, Collin, Matthew
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039861/
https://www.ncbi.nlm.nih.gov/pubmed/21242295
http://dx.doi.org/10.1084/jem.20101459
Descripción
Sumario:Congenital or acquired cellular deficiencies in humans have the potential to reveal much about normal hematopoiesis and immune function. We show that a recently described syndrome of monocytopenia, B and NK lymphoid deficiency additionally includes the near absence of dendritic cells. Four subjects showed severe depletion of the peripheral blood HLA-DR(+) lineage(−) compartment, with virtually no CD123(+) or CD11c(+) dendritic cells (DCs) and very few CD14(+) or CD16(+) monocytes. The only remaining HLA-DR(+) lineage(−) cells were circulating CD34(+) progenitor cells. Dermal CD14(+) and CD1a(+) DC were also absent, consistent with their dependence on blood-derived precursors. In contrast, epidermal Langerhans cells and tissue macrophages were largely preserved. Combined loss of peripheral DCs, monocytes, and B and NK lymphocytes was mirrored in the bone marrow by complete absence of multilymphoid progenitors and depletion of granulocyte-macrophage progenitors. Depletion of the HLA-DR(+) peripheral blood compartment was associated with elevated serum fms-like tyrosine kinase ligand and reduced circulating CD4(+)CD25(hi)FoxP3(+) T cells, supporting a role for DC in T reg cell homeostasis.