Reasons why DBA/2 mice are resistant to malarial infection: expansion of CD3int B220+ gammadelta T cells with double-negative CD4- CD8- phenotype in the liver

Immunology. 2006 Jan;117(1):127-35. doi: 10.1111/j.1365-2567.2005.02273.x.

Abstract

DBA/2 (H-2(d)) mice are known to be more resistant than C57BL/6 (B6, H-2(b)) mice to the non-lethal 17XNL strain of Plasmodium yoelii. This is a very strange phenomenon because the functions of conventional T cells, especially CD8(+) T cells, are known to be somewhat lower in DBA/2 mice than in other strains of mice. We examined herein how immune responses differed between DBA/2 mice and B6 mice during malarial infection. DBA/2 mice and (DBA/2 x B6)F(1) (BDF(1), H-2(b/d)) mice were found to have milder parasitaemia and to recover more quickly from malarial infection than B6 mice. These DBA/2 and BDF(1) mice were also found to experience a marked expansion of interleukin (IL)-2Rbeta(+) CD3(int) cells and gammadelta T cells in the liver, especially in the recovery phase. The expansion of unconventional T cells (i.e. B220(+) T cells) was also marked in DBA/2 and BDF(1) mice. The majority of B220(+) T cells were gammadelta T cells and these T cells were double-negative CD4(-) CD8(-). More importantly, the production of immunoglobulin M (IgM)-type anti-DNA autoantibody was also higher in DBA/2 and BDF(1) mice than in B6 mice. In conjunction with data on cytokine production, these results indicate that primitive T and B cells, namely autoreactive extrathymic T cells and autoantibody-producing B cells, may be much more activated in DBA/2 mice and therefore resistant to the non-lethal 17XNL strain of P. yoelii.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Antinuclear / biosynthesis
  • Antibodies, Monoclonal / immunology
  • CD3 Complex / analysis
  • Cytokines / biosynthesis
  • Immunity, Innate
  • Immunoglobulin M / biosynthesis
  • Immunophenotyping
  • Leukocyte Common Antigens / analysis
  • Liver / immunology*
  • Malaria / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Parasitemia / immunology
  • Plasmodium yoelii*
  • Receptors, Antigen, T-Cell, gamma-delta / analysis
  • Receptors, Antigen, T-Cell, gamma-delta / immunology
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Spleen / immunology
  • T-Lymphocyte Subsets / immunology*

Substances

  • Antibodies, Antinuclear
  • Antibodies, Monoclonal
  • CD3 Complex
  • Cytokines
  • Immunoglobulin M
  • Receptors, Antigen, T-Cell, gamma-delta
  • Leukocyte Common Antigens