| Literature DB >> 31060706 |
Julie Ng1, Kyle Wright2, Maura Alvarez1, Gary M Hunninghake1, Duane R Wesemann3.
Abstract
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.Entities:
Keywords: B cells; common variable immunodeficiency; granulomatous lymphocytic interstitial lung disease; rituximab; tertiary lymphoid tissue
Mesh:
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Year: 2019 PMID: 31060706 PMCID: PMC6689079 DOI: 10.1016/j.chest.2019.01.034
Source DB: PubMed Journal: Chest ISSN: 0012-3692 Impact factor: 9.410