Combined Immunodeficiency Evolving into Predominant CD4+ Lymphopenia Caused by Somatic Chimerism in JAK3-Reference-Cited by-同舟云学术

Combined Immunodeficiency Evolving into Predominant CD4+ Lymphopenia Caused by Somatic Chimerism in JAK3

Published:2014-09-10 Issue:8 Volume:34 Page:941-953
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Ban Sol A.,Salzer Elisabeth,Eibl Martha M.,Linder Angela,Geier Christoph B.,Santos-Valente Elisangela,Garncarz Wojciech,Lion Thomas,Ott Raphael,Seelbach Christoph,Boztug Kaan,Wolf Hermann M.

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/content/pdf/10.1007/s10875-014-0088-2.pdf

Reference49 articles.

1. From the Centers for Disease Control. Unexplained CD4+ T-lymphocyte depletion, persons without evident HIV infection, JAMA, 268 (1992) 1254–1255.

2. Walker UA, Warnatz K. Idiopathic CD4 lymphocytopenia. Curr Opin Rheumatol. 2006;18:389–95.

3. Zonios DI, Falloon J, Bennett JE, Shaw PA, Chaitt D, Baseler MW, et al. Idiopathic CD4+ lymphocytopenia: natural history and prognostic factors. Blood. 2008;112:287–94.

4. Smith DK, Neal JJ, Holmberg SD. Unexplained opportunistic infections and CD4+ T-lymphocytopenia without HIV infection. An investigation of cases in the United States. The centers for disease control idiopathic CD4+ T-lymphocytopenia task force. N Engl J Med. 1993;328:373–9.

5. Zhou H, Glimcher LH. Human MHC class II gene transcription directed by the carboxyl terminus of CIITA, one of the defective genes in type II MHC combined immune deficiency. Immunity. 1995;2:545–53.

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