The SCID mouse mutant: definition and potential use as a model for immune and hematological disorders

Hematol Cell Ther. 1997 Oct;39(5):213-21. doi: 10.1007/s00282-997-0213-2.

Abstract

Mice homozygous for a SCID mutation (SCID mice) are severely deficient in T and B lymphocytes. The absence of effector T and B cells has encouraged investigators to attempt engraftment of SCID mice with human fetal tissues, mature lymphocytes, hematopoietic progenitors and tumors. SCID mice can be reconstituted with human lymphocytes and are of interest for studying normal and abnormal lymphocyte development and function. SCID mice are also providing an in vivo model of infectious diseases. In addition, SCID mice readily support normal and pathologic human hematopoiesis differentiation and is useful for testing innovative hematological disease therapy. SCID mice with a fully functional human immune or hematopoietic system therefore seem to be extremely valuable for biomedical research.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Differentiation / immunology
  • Disease Models, Animal
  • Hematologic Diseases / physiopathology*
  • Humans
  • Immune System Diseases / physiopathology*
  • Lymphocytes / immunology
  • Mice
  • Mice, SCID
  • Severe Combined Immunodeficiency / blood
  • Severe Combined Immunodeficiency / immunology
  • Severe Combined Immunodeficiency / physiopathology*
  • Species Specificity