Multiple defects in innate and adaptive immunologic function in NOD/LtSz-scid mice

J Immunol. 1995 Jan 1;154(1):180-91.

Abstract

The scid mutation was backcrossed ten generations onto the NOD/Lt strain background, resulting in an immunodeficient stock (NOD/LtSz-scid/scid) with multiple defects in adaptive as well as nonadaptive immunologic function. NOD/LtSz-scid/scid mice lack functional lymphoid cells and show little or no serum Ig with age. Although NOD/(Lt-)+/+ mice develop T cell-mediated autoimmune, insulin-dependent diabetes mellitus, NOD/LtSz-scid/scid mice are both insulitis- and diabetes-free throughout life. However, because of a high incidence of thymic lymphomas, the mean lifespan of this congenic stock is only 8.5 mo under specific pathogen-free conditions. After i.v. injection of human CEM T-lymphoblastoid cells, splenic engraftment of these cells was fourfold greater in NOD/LtSz-scid/scid mice than in C.B17/Sz-scid/scid mice. Although C.B-17Sz-scid/scid mice exhibit robust NK cell activity, this activity is markedly reduced in both NOD/(Lt-)+/+ and NOD/LtSz-scid/scid mice. Presence of a functionally less mature macrophage population in NOD/LtSz-scid/scid vs C.B-17Sz-scid/scid mice is indicated by persistence in the former of the NOD/Lt strain-specific defect in LPS-stimulated IL-1 secretion by marrow-derived macrophages. Although C.B-17Sz-scid/scid and C57BL/6Sz-scid/scid mice have elevated serum hemolytic complement activity compared with their respective +/+ controls, both NOD/(LtSz-)+/+ and NOD/LtSz-scid/scid mice lack this activity. Age-dependent increases in serum Ig levels (> 1 micrograms/ml) were observed in only 2 of 30 NOD/LtSz-scid/scid mice vs 21 of 29 C.B-17/Sz-scid/scid animals. The multiple defects in innate and adaptive immunity unique to the NOD/LtSz-scid/scid mouse provide an excellent in vivo environment for reconstitution with human hematopoietic cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Agammaglobulinemia / genetics
  • Agammaglobulinemia / immunology
  • Age Factors
  • Animals
  • Complement System Proteins / analysis
  • Crosses, Genetic
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / immunology
  • Female
  • Humans
  • Immunity, Cellular
  • Immunity, Innate
  • Immunologic Deficiency Syndromes / genetics
  • Immunologic Deficiency Syndromes / immunology*
  • Immunophenotyping
  • Interleukin-1 / metabolism
  • Killer Cells, Natural / immunology
  • Leukocyte Count
  • Lipopolysaccharides / pharmacology
  • Longevity
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / pathology
  • Lymphoma / genetics
  • Lymphoma / virology
  • Macrophage Activation / drug effects
  • Macrophages / immunology
  • Macrophages / pathology
  • Male
  • Mice
  • Mice, Inbred NOD / genetics
  • Mice, Inbred NOD / immunology*
  • Mice, Mutant Strains / genetics
  • Mice, Mutant Strains / immunology*
  • Mice, SCID / genetics
  • Mice, SCID / immunology*
  • Poly I-C / pharmacology
  • Severe Combined Immunodeficiency / genetics
  • Skin Transplantation / immunology
  • T-Lymphocytes / transplantation
  • Thymus Neoplasms / genetics
  • Thymus Neoplasms / virology
  • Transplantation, Heterologous

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • Complement System Proteins
  • Poly I-C