| Literature DB >> 30910977 |
Christian Männe1, Akiko Takaya2, Yuzuru Yamasaki1, Mathias Mursell1, Shintaro Hojyo1, Tsung-Yen Wu1, Jana Sarkander1, Mairi A McGrath1, Rebecca Cornelis1, Stefanie Hahne1, Qingyu Cheng1,3, Tadafumi Kawamoto4, Falk Hiepe1,3, Stefan H E Kaufmann5, Tomoko Yamamoto6, Andreas Radbruch1, Koji Tokoyoda7.
Abstract
Serum IgG, which is mainly generated from IgG-secreting plasma cells in the bone marrow (BM), protects our body against various pathogens. We show here that the protein SiiE of Salmonella is both required and sufficient to prevent an efficient humoral immune memory against the pathogen by selectively reducing the number of IgG-secreting plasma cells in the BM. Attenuated SiiE-deficient Salmonella induces high and lasting titers of specific and protective Salmonella-specific IgG and qualifies as an efficient vaccine against Salmonella A SiiE-derived peptide with homology to laminin β1 is sufficient to ablate IgG-secreting plasma cells from the BM, identifying laminin β1 as a component of niches for IgG-secreting plasma cells in the BM, and furthermore, qualifies it as a unique therapeutic option to selectively ablate IgG-secreting plasma cells in autoimmune diseases and multiple myeloma.Entities:
Keywords: Salmonella; bone marrow; immunoglobulin G; niche; plasma cells
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Year: 2019 PMID: 30910977 PMCID: PMC6462062 DOI: 10.1073/pnas.1818242116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205