scholarly journals Defective recruitment and activation of ZAP-70 in common variable immunodeficiency patients with T cell defects

2000 ◽  
Vol 30 (9) ◽  
pp. 2632-2638 ◽  
Author(s):  
Marianna Boncristiano ◽  
M. Bernardetta Majolini ◽  
Mario M. D'Elios ◽  
Sonia Pacini ◽  
Silvia Valensin ◽  
...  
2010 ◽  
Vol 126 (3) ◽  
pp. 671-675 ◽  
Author(s):  
Nagaja Capitani ◽  
Amedeo Amedei ◽  
Silvia Rossi Paccani ◽  
Andrea Matucci ◽  
Alessandra Vultaggio ◽  
...  

1993 ◽  
Vol 33 ◽  
pp. S24-S28 ◽  
Author(s):  
Jon S Jaffe ◽  
Eli Eisenstein ◽  
Michael C Sneller ◽  
Warren Strober

Blood ◽  
2011 ◽  
Vol 118 (2) ◽  
pp. 309-318 ◽  
Author(s):  
Manuella L. Gomes Ochtrop ◽  
Sigune Goldacker ◽  
Annette M. May ◽  
Marta Rizzi ◽  
Ruth Draeger ◽  
...  

Abstract In common variable immunodeficiency (CVID) defects in early stages of B-cell development, bone marrow (BM) plasma cells and T lymphocytes have not been studied systematically. Here we report the first morphologic and flow cytometric study of B- and T-cell populations in CVID BM biopsies and aspirates. Whereas the hematopoietic compartment showed no major lineage abnormalities, analysis of the lymphoid compartment exhibited major pathologic alterations. In 94% of the patients, BM plasma cells were either absent or significantly reduced and correlated with serum immunoglobulin G levels. Biopsies from CVID patients had significantly more diffuse and nodular CD3+ T lymphocyte infiltrates than biopsies from controls. These infiltrates correlated with autoimmune cytopenia but not with other clinical symptoms or with disease duration and peripheral B-cell counts. Nodular T-cell infiltrates correlated significantly with circulating CD4+CD45R0+ memory T cells, elevated soluble IL2-receptor and neopterin serum levels indicating an activated T-cell compartment in most patients. Nine of 25 patients had a partial block in B-cell development at the pre-B-I to pre-B-II stage. Because the developmental block correlates with lower transitional and mature B-cell counts in the periphery, we propose that these patients might form a new subgroup of CVID patients.


2009 ◽  
Vol 49 (9) ◽  
pp. 1329-1338 ◽  
Author(s):  
Marion Malphettes ◽  
Laurence Gérard ◽  
Maryvonnick Carmagnat ◽  
Gaël Mouillot ◽  
Nicolas Vince ◽  
...  

2008 ◽  
Vol 87 (1) ◽  
pp. 46-52 ◽  
Author(s):  
W. RUDNICKA ◽  
N. ENGLISH ◽  
J. FARRANT ◽  
M. E NORTH ◽  
A. E. BRYANT ◽  
...  

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