CBC.37 monoclonal antibody (mAb) was generated using balb/c mice immunized
with CEM T cell line. It was selected because of its strong reactivity on T
lymphocytes on paraffin tissue sections. The anti-CD7 specificity of CBC.3
7 mAb was assessed by immunohistochemistry, cross-blocking, and cross-immun
oprecipitation experiments using CBC.37 and the anti-CD7 mAb DK24. CBC.37 m
Ab immunoprecipitated a 40-kDa. protein. Cross-blocking and cross-immunopre
cipitation experiments demonstrated that the two antibodies recognized the
same molecule. Immunostaining of a large number of reactive lymph nodes and
B and T cell lymphomas confirms that CBC.37 mAb was directed against T cel
ls. As expected, on reactive lymph nodes the staining pattern was comparabl
e to that of CD3. Among the 110 T cell lymphomas examined all T lymphoblast
ic lymphomas were positive (15+115; 100%). As a result of the frequent loss
of CD7 antigen, only 25+/95 (26%) of peripheral T cell neoplasms were foun
d to be positive for CBC.37. A marked reduction in the number of CBC.37-pos
itive T cells was observed in 7 of the 60 cases of benign inflammatory derm
atoses studied (approximate to 12%). CBC.37 was unreactive with all healthy
and neoplastic non-lymphoid samples examined. Because the lack of CD7 expr
ession in T cell lymphomas is of diagnostic value, CBC.37 mAb in associatio
n with other anti-T cell antibodies working on paraffin sections could be o
f particular value in asserting the diagnosis of T cell lymphomas in routin
e histopathology.