Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kappaB activation

Immunol Rev. 2005 Feb:203:21-37. doi: 10.1111/j.0105-2896.2005.00221.x.

Abstract

The nuclear factor (NF)-kappaB family of transcription factors serves vital roles in a wide array of cell functions. An increasing number of human genetic lesions that result in defined disease entities are linked to inappropriate activation of NF-kappaB. The resulting aberrant NF-kappaB function can lead to cellular defects that ultimately impair normal developmental processes, host immune defenses, or both. Molecular defects that lie upstream in cell-signaling pathways and rely upon NF-kappaB activation tend to give a more specific phenotype, whereas those closer to the actual NF-kappaB proteins have broader defects. A detailed study of these diseases can provide insight into the biochemistry of NF-kappaB activation as well as the role of NF-kappaB in human health.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Genetic Diseases, Inborn / genetics*
  • Genetic Diseases, Inborn / immunology
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Mutation / genetics*
  • NF-kappa B / metabolism*

Substances

  • NF-kappa B