Rituximab Monotherapy for Common Variable Immune Deficiency-Associated Granulomatous-Lymphocytic Interstitial Lung Disease

被引:28
|
作者
Ng, Julie [1 ]
Wright, Kyle [2 ]
Alvarez, Maura [1 ]
Hunninghake, Gary M. [1 ]
Wesemann, Duane R. [3 ,4 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Div Pulm & Crit Care, 75 Francis St, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, Div Rheumatol Immunol & Allergy, 75 Francis St, Boston, MA 02115 USA
[4] Harvard Med Sch, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
B cells; common variable immunodeficiency; granulomatous lymphocytic interstitial lung disease; rituximab; tertiary lymphoid tissue; LYMPHOID-TISSUE; CELLS;
D O I
10.1016/j.chest.2019.01.034
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Patients with common variable immunodeficiency (CVID) can develop granulomatous-lymphocytic interstitial lung disease (GLILD), which is associated with increased morbidity and mortality. Treating GLILD is a significant challenge because it is rare and can be pathologically heterogeneous. Here we describe two cases of patients with CVID-associated GLILD with biopsies demonstrating loosely organized tertiary lymphoid structures (TLSs). Based on the pivotal role that B cells play in TLS initiation and maintenance, we hypothesized that using rituximab monotherapy for B-cell depletion alone would be sufficient for the disruption of the pathologic process underlying GLILD. These two cases demonstrate that adapting a strategy of B cell depletion monotherapy may be effective in TLS-associated conditions such as GLILD.
引用
收藏
页码:E117 / E121
页数:5
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