| Literature DB >> 21576700 |
Manuella L Gomes Ochtrop1, Sigune Goldacker, Annette M May, Marta Rizzi, Ruth Draeger, Dieter Hauschke, Claudia Stehfest, Klaus Warnatz, Heike Goebel, Katja Technau-Ihling, Martin Werner, Ulrich Salzer, Hermann Eibel, Michael Schlesier, Hans Hartmut Peter.
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.Entities:
Mesh:
Year: 2011 PMID: 21576700 DOI: 10.1182/blood-2010-11-321695
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113