Mouse strains with defined genetic defects engineered by the method of
targeted gene disruption and homologous recombination have furthered
our understanding of immune functions at the single gene level. More i
mportantly, these mutant 'gene knockout' mice are powerful in vivo too
ls to dissect the complex mechanisms of lymphocyte development and fun
ction, complementing our broadening knowledge of congenital and acquir
ed human immunodeficiencies.