Common variable immunodeficiency (CVID) is the most frequent symptomatic primary immunodeficiency disease, characterized by low levels of circulating immunoglobulins and recurrent bacterial infections, particularly of the respiratory tract. T cell dysfunction is often present, and lymphoproliferative and autoimmune disorders as well as haematological cytopenias are frequently observed. In this study, we report a polyclonal expansion of large granular lymphocytes (LGL) in a substantial proportion of CVID patients, associated with splenomegaly, increased numbers of CD8(+) T cells, inverted CD4 : CD8 T cell ratios and neutropenia. CVID patients who had both increased numbers of LGL and granulocytopenia had elevated levels of soluble Fas ligand (sFasL). Our observations indicate that CVID may be added to the list of inflammatory diseases associated with increased numbers of LGL. Furthermore, our findings suggest common pathogenic mechanisms of granulocytopenia in CVID and lymphoproliferative disease of granular lymphocytes.
Polyclonal expansion of large granular lymphocytes in common variable immunodeficiency - association with neutropenia.
常见变异型免疫缺陷中大颗粒淋巴细胞的多克隆扩增——与中性粒细胞减少症相关
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作者:Holm A M, Tjønnfjord G, Yndestad A, Beiske K, Müller F, Aukrust P, Frøland S S
| 期刊: | Clinical and Experimental Immunology | 影响因子: | 3.800 |
| 时间: | 2006 | 起止号: | 2006 Jun;144(3):418-24 |
| doi: | 10.1111/j.1365-2249.2006.03086.x | 研究方向: | 细胞生物学 |
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