Primary mediastinal B-cell lymphoma is a locally highly aggressive but poor
ly disseminating tumor composed of medium sized or large cells most probabl
y of thymic medullary origin. it has a mature B-cell phenotype, typically l
acks immunoglobulin expression and has variable defects in expression of HL
A-molecules. We present here a cell line, MedB-1, derived from such a tumor
. As is frequently found in mediastinal B-cell lymphomas in situ, MedB-1 is
CD10(-), CD19(+), CD21(-). CD22(+), CD23(+) CD25(-), CD37(+), CD38(-), CD3
9(+), CD40(+), CD54(+), CD95(+), Like the parental tumor, MedB-1 lacks HLA-
A,B,C alpha -chains and beta (2)microglobulin and expresses HLA-D molecules
at decreased levels. Both parental tumor and MedB-1 cells are clonally rel
ated as shown by immunoglobulin heavy chain gene rearrangement analysis, Un
like the parental tumor tissue, the MedB-1 cell line cytoplasmically expres
ses IgG/kappa in a very small subset of cells under standard culture condit
ions. MedB-1 does not contain any Epstein-Barr virus DNA, In a tissue adhes
ion assay MedB-1 cells showed an extensive binding to the medullary region
of normal thymus, Altogether, MedB-1 is a suitable tool for functional and
molecular analysis of this distinct lymphoma entity. (C) 2001 Wiley-Liss. I
nc.