z-logo
Premium
Expression of cancer/testis antigens in cutaneous T cell lymphomas
Author(s) -
Häffner Andreas C.,
Tassis Anatoli,
Zepter Karoline,
Storz Monique,
Tureci Oezlem,
Burg Günter,
Nestle Frank Oliver
Publication year - 2001
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.1643
Subject(s) - mycosis fungoides , lymphoma , antigen , cutaneous t cell lymphoma , immunohistochemistry , medicine , pathology , cancer , immunotherapy , peripheral t cell lymphoma , serology , t cell , antibody , immunology , immune system
Cancer/testis‐antigens (CTA), a novel and expanding family of immunogenic proteins detected by serological screening of recombinant cDNA expression libraries, encompass promising candidate targets for T‐cell based immunotherapy. We screened kryo‐preserved tissue of cutaneous T cell lymphoma (CTCL, n =36) such as mycosis fungoides (MF, n =17), pleomorphic cutaneous T‐cell lymphoma ( n =8) and Sezary's syndrome (SS, n = 11) as well as a non‐malignant entity (small plaques parapsoriasis, SPP, n =5), for the expression of CTA by RT‐PCR and Northern blot hybridization. From a panel of eleven CTA (MAGE‐1, MAGE‐C1, MAGE‐3, BAGE, GAGE, SSX‐1, SSX‐2, SSX4, SCP‐1, NY‐ESO‐1 and TS85) (HOM‐Tes‐85), mRNA expression could be detected for SCP‐1 in 8/17 MF and 6/8 pleomorphic CTCL patients but was completely absent in small plaques parapsoriasis. SS patients had a more heterogeneous antigen expression pattern: Gage (1/11), MAGE‐1 (3/11), MAGE‐3 (6/11), MAGE‐C1 (5/11), NY‐ESO‐1 (7/11) and TS85 (5/11), with expression of MAGE‐3 confirmed by immunohistochemistry. CTA could provide defined targets for antigen‐based vaccination in a high percentage of cases with CTCL. SCP‐1 might serve as an additional diagnostic indicator in early and clinically indistinct lesions suspicious for cutaneous T‐cell lymphoma. © 2001 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom