By using clones of murine T cells reactive with alloantigens as well as soluble antigens, it has been possible to demonstrate that Ia antigens, Ir gene phenomena (defined as the ability of immune T cells to recognize antigen), and mixed lymphocyte reaction (MLR)-stimulating determinants encoded within the I-A subregion are different manifestations associated with same product. These studies utilized the I-A(b) mutant mouse B6. C-H-2(bm12) (bm12), whose defect in the normal expression of the cell surface products of the I-A(b) subregion can be partially circumvented through trans-complementation by deriving hybrids between bm12 and mice expressing normal I-A subregion products. Such mice [e.g., (bm 12 x B10.A)F1] express several serologically normal I-A(b) products but have defects in certain I-A subregion gene products normally expressed on cells of H-2(a) x H-2(b) heterozygote mice that are used as restricting elements for antigen recognition by antigen-reactive T cell clones or recognized as alloantigens by alloreactive T cell clones. This defect in cell surface expression of certain normal I-A(b) products on the mutant bm12 cells has allowed us to suggest that there exist trans-complementing products H-2(a) x H-2(b) heterozygote mice consisting of A(b)(α)A(k)β) and A(k)(α)A(b)(β) that restrict antigen recognition by cloned T cells, stimulate MLR responses by cloned T cells, and react with certain anti-Ia antisera.
|Original language||English (US)|
|Number of pages||5|
|Journal||Proceedings of the National Academy of Sciences of the United States of America|
|Issue number||3 I|
|State||Published - Jan 1 1981|
ASJC Scopus subject areas