A combination of molecular genotyping and protein biochemistry methods was
used to assess the HLA-A, -B, -C genotyping and expression of six tumor cel
l lines. Four cell lines had been previously HLA typed by conventional sero
logic methods. Two could not be typed by serology because deficient in the
surface expression of HLA-A, -B, -C molecules. As shown herein, all the 25
alleles carried by the six tested cell lines were typed at the DNA level. I
n addition, discrepancies between the previous serologic and the present DN
A typing results were detected in 9 of the 21 tested serologic specificitie
s. Typing at the protein level by isoelectric focusing and allele-specific
monoclonal antibodies confirmed the DNA typing data. Our results exemplify
the limits of the serologic typing procedures and demonstrate that molecula
r methods are highly desirable to conduct functional experiments and identi
fy HLA losses in neoplastic cells at single allele level.