| First Author | Spalinger MR | Year | 2019 |
| Journal | Mucosal Immunol | Volume | 12 |
| Issue | 6 | Pages | 1336-1347 |
| PubMed ID | 31501515 | Mgi Jnum | J:293503 |
| Mgi Id | MGI:6452896 | Doi | 10.1038/s41385-019-0201-1 |
| Citation | Spalinger MR, et al. (2019) Loss of PTPN22 abrogates the beneficial effect of cohousing-mediated fecal microbiota transfer in murine colitis. Mucosal Immunol 12(6):1336-1347 |
| abstractText | Fecal microbiota transfer (FMT) is a very efficient approach for the treatment of severe and recurring C. difficile infections. However, the beneficial effect of FMT in other disorders such as ulcerative colitis (UC) or Crohn's disease remains unclear. Furthermore, it is currently unknown how disease-associated genetic variants in donors or recipients influence the effect of FMT. We found that bacteria-transfer from wild-type (WT) donors via cohousing was efficient in inducing recovery from colitis in WT mice, but not in mice deficient in protein-tyrosine phosphatase non-receptor type 22 (PTPN22), a known risk gene for several chronic inflammatory diseases. Also cohousing of PTPN22-deficient mice with diseased WT mice failed to induce faster recovery. Our data indicate that the genetic background of the donor and the recipient influences the outcome of microbiota transfer, and offers a potential explanation why transfer of fecal microbes from some, but not all donors is efficient in UC patients. |
