T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency

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 aspirate...

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Veröffentlicht in:Blood 2011-07, Vol.118 (2), p.309-318
Hauptverfasser: Ochtrop, Manuella L. Gomes, Goldacker, Sigune, May, Annette M., Rizzi, Marta, Draeger, Ruth, Hauschke, Dieter, Stehfest, Claudia, Warnatz, Klaus, Goebel, Heike, Technau-Ihling, Katja, Werner, Martin, Salzer, Ulrich, Eibel, Hermann, Schlesier, Michael, Peter, Hans Hartmut
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Sprache:eng
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Zusammenfassung: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.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2010-11-321695