A new alloantigenic system associated with the Mls locus in the mouse

J Immunol. 1976 Mar;116(3):835-41.

Abstract

An antiserum prepared by injecting C3H/HeJ mice with CBA/J tissue has been shown to react with cell surface components that are not part of any previously described system of serologically detectable alloantigens. The antiserum, which is designated AST-101, acts selectively in cytotoxic tests carried out with lymphoid cells, killing B cells, but not T cells. Phagocytic cells found in peritoneal exudates are also killed by AST-101 and complement in vitro; the sensitivity of other cell types has not been determined. Strain distribution does not indicate any association of the AST-101 system with H-2, Ly, or Thy systems; genetic analysis reveals close linkage with the mouse minor MLC-stimulating (Mls) locus. Serologic analysis also points to a close association between antigens reactive with AST-101 and the products of the Mls genes.

Publication types

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

MeSH terms

  • Animals
  • Chromosome Mapping*
  • Epitopes
  • Hemolytic Plaque Technique
  • Immune Sera / isolation & purification
  • Immunity, Cellular
  • Isoantigens / analysis*
  • Lectins / pharmacology
  • Lipopolysaccharides / pharmacology
  • Lymph Nodes / immunology
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred CBA
  • Mice, Inbred Strains
  • Spleen / immunology

Substances

  • Epitopes
  • Immune Sera
  • Isoantigens
  • Lectins
  • Lipopolysaccharides