IRF8 mutations and human dendritic-cell immunodeficiency.

  title={IRF8 mutations and human dendritic-cell immunodeficiency.},
  author={Sophie Hambleton and Sandra Salem and Jacinta Bustamante and Venetia Bigley and St{\'e}phanie Boisson-Dupuis and Joana Azevedo and Anny Fortin and Muzlifah Haniffa and Lourdes Ceron-Gutierrez and Chris M Bacon and Geetha S Menon and C{\'e}line Trouillet and David McDonald and Peter F Carey and Florent Ginhoux and Laia Alsina and Timothy J. Zumwalt and Xiao-fei Kong and Dinakantha Kumararatne and Karina Butler and Marjorie Hubeau and Jacqueline Feinberg and Saleh Zaid Al-Muhsen and Andrew Cant and Laurent Abel and Damien Chaussabel and Rainer Doffinger and Eduardo Talesnik and Anete Sevciovic Grumach and Alberto Jos{\'e} da Silva Duarte and Katia Abarca and Dewton de Moraes-Vasconcelos and David R Burk and Albert M Berghuis and Fr{\'e}d{\'e}ric Geissmann and Matthew Collin and J. Hugo P{\'e}rez Casanova and Philippe Gros},
  journal={The New England journal of medicine},
  volume={365 2},
BACKGROUND The genetic analysis of human primary immunodeficiencies has defined the contribution of specific cell populations and molecular pathways in the host defense against infection. Disseminated infection caused by bacille Calmette-Guérin (BCG) vaccines is an early manifestation of primary immunodeficiencies, such as severe combined immunodeficiency. In many affected persons, the cause of disseminated BCG disease is unexplained. METHODS We evaluated an infant presenting with features of… CONTINUE READING
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