| Literature DB >> 28422754 |
Ryan M McCormack1, Eva P Szymanski2, Amy P Hsu2, Elena Perez1, Kenneth N Olivier3, Eva Fisher1, E Brook Goodhew1, Eckhard R Podack1, Steven M Holland2.
Abstract
Perforin-2 is a highly conserved pore-forming protein encoded by macrophage expressed gene 1 (MPEG1). A number of studies have shown that Perforin-2-deficient mice are unable to survive following a bacterial challenge that is nonlethal in WT mice. There is also recent evidence that Mpeg1+/- heterozygous mice display an intermediate killing ability compared with Mpeg1 WT and Mpeg1-/- mice. Despite these in vivo findings, to date, no perforin-2 deficiencies have been associated with human disease. Here, we report four patients with persistent nontuberculous mycobacterial infection who had heterozygous MPEG1 mutations. In vitro, neutrophils, macrophages, and B cells from these patients were unable to kill Mycobacterium avium as efficiently as normal controls. CRISPR mutagenesis validated the deleterious antibacterial activity of these mutations. These data suggest that perforin-2 haploinsufficiency may contribute to human susceptibility to infections with intracellular bacteria.Entities:
Keywords: Genetics; Infectious disease
Year: 2017 PMID: 28422754 PMCID: PMC5396519 DOI: 10.1172/jci.insight.89635
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708