The T-cell activation markers CD30 and OX40/CD134 are expressed in nonoverlapping subsets of peripheral T-cell lymphoma

Citation
D. Jones et al., The T-cell activation markers CD30 and OX40/CD134 are expressed in nonoverlapping subsets of peripheral T-cell lymphoma, BLOOD, 93(10), 1999, pp. 3487-3493
Citations number
54
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BLOOD
ISSN journal
00064971 → ACNP
Volume
93
Issue
10
Year of publication
1999
Pages
3487 - 3493
Database
ISI
SICI code
0006-4971(19990515)93:10<3487:TTAMCA>2.0.ZU;2-5
Abstract
The tumor necrosis factor (TNF) receptor family includes several important markers of activation in T cells. We examined expression patterns of two T- cell-associated members of these receptors, namely CD30 and OX40/CD134, in 148 cases of T-cell lymphoma to identify possible objective immunohistochem ical criteria for subclassification of these tumors. CD30 expression was ch aracteristic of tumors with an anaplastic (46/47 cases [98%]) or large-cell (10/21 [48%]) morphology and was seen in only scattered cells in other tum or types, In contrast, large numbers of OX40/CD134(+) tumors cells were typ ical of angioimmunoblastic lymphoma (15/16 [94%]), angiocentric lymphoma (4 /4), a subset of large-cell lymphomas (10/21 [48%]), and lymphomas with a p rominent histiocytic component (6/7 [86%]). Strong OX40/ CD134 and CD30 coe xpression was seen in only 4% of tumors, typically those with an anaplastic /Hodgkin's-like appearance. OX40/CD134 expression was characteristic of tum ors composed of activated CD4(+) T cells and was not seen in small-cell T-c ell lymphomas, lymphoblastic lymphomas, or other tumor types, including B-c ell lymphomas or carcinomas. These results suggest that immunostaining for OX40/CD134 may be helpful in subclassification of peripheral T-cell lymphom as and that the patterns of TNF receptor family expression in these tumors may parallel those seen within nonneoplastic helper T-cell subsets. (C) 199 9 by The American Society of Hematology.