IMMUNOPEROXIDASE STAINING OF NON-HODGKINS-LYMPHOMAS FOR T-CELL LINEAGE ASSOCIATED ANTIGENS IN PARAFFIN SECTIONS - COMPARISON OF THE PERFORMANCE-CHARACTERISTICS OF 4 COMMERCIALLY AVAILABLE ANTIBODY PREPARATIONS
Pj. Kurtin et Pc. Roche, IMMUNOPEROXIDASE STAINING OF NON-HODGKINS-LYMPHOMAS FOR T-CELL LINEAGE ASSOCIATED ANTIGENS IN PARAFFIN SECTIONS - COMPARISON OF THE PERFORMANCE-CHARACTERISTICS OF 4 COMMERCIALLY AVAILABLE ANTIBODY PREPARATIONS, The American journal of surgical pathology, 17(9), 1993, pp. 898-904
Paraffin sections of 133 cases of non-Hodgkin's lymphoma (69 B-cell ty
pe and 64 T-cell type) were stained in a labeled streptavidin biotin i
mmunoperoxidase technique with a panel of antibodies that recognized T
-lymphocyte associated antigens. This study was done to determine the
sensitivity and specificity of these reagents for phenotyping T-cell l
ymphomas. UCHL-1, polyclonal anti-CD3, Leu-22, and OPD4 stained 78%, 7
2%, 91%, and 69% of the cases of T-cell lymphomas, respectively. The p
henotype of L-26 negative and CD3 or UCHL-1 positive accurately predic
ted T-cell phenotype in 95% (60 of 63) of the T-cell lymphomas and was
not seen in any of the cases of B-cell lymphoma. Although Leu-22 was
the most sensitive T-cell-associated marker in this series, its lack o
f specificity for T-lymphocytes limited its usefulness as part of a ro
utine panel designed to distinguish between T-cell and B-cell lymphoma
s. In conjunction with other reports, this study supports the use of t
he T-cell markers CD3 and UCHL-1 in combination with the B-cell-associ
ated marker L-26 to phenotype most efficiently non-Hodgkin's lymphomas
in paraffin sections.