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A class II-restricted cytotoxic T-cell clone recognizes a human minor histocompatibility antigen with a restricted tissue distribution.

Authors :
Holloway, Penny A.
Kaldenhoven, Niels
Kok-Schoemaker, Henriette M.
van Dijk, Mirjam
Otten, Hennie G.
Tilanus, Marcel
Postma, Saskia
Mutis, Tuna
Lokhorst, Henk M.
Bloem, Andries C.
Source :
British Journal of Haematology; Jan2005, Vol. 128 Issue 1, p73-81, 9p
Publication Year :
2005

Abstract

Following a human leucocyte antigen (HLA)-identical allogeneic stem cell transplantation (allo-SCT), minor histocompatibility antigens (mHags) play an important role in the induction of graft-versus-leukaemia (GvL) and graft-versus-myeloma (GvM). Many mHags show ubiquitous tissue expression and are associated with GvL and graft-versus-host disease. Here we describe a cytotoxic CD4<superscript>+</superscript> T lymphocyte line and a cytotoxic, CD4<superscript>+</superscript> T cell clone (CTC), 3AB11, which recognized a tissue-restricted mHag. This CTC was isolated from a multiple myeloma patient with clinical GvM following an HLA-matched allo-SCT. CTC 3AB11 was activated in aHLA-DP*0401 restricted fashion and the antigen was expressed by 27% of HLA-DP*0401 positive Epstein–Barr virus (EBV)-transformed B-cell lines (EBV-B). Tissue distribution analysis of antigen 3AB11 showed it to be expressed by patient-derived EBV-transformed B cell lines (EBVp), the myeloma plasma cell-line UM9 and monocytes. It was weakly expressed by peripheral blood-derived phytohaemagglutinin-induced T-cell blasts and absent on CD40L stimulated peripheral B (CD40L B) cells and stromal cells. The relatively high prevalence of the HLA class II-restricted 3AB11 antigen, together with its apparent haematopoietic-restricted expression, makes it an antigen of interest for cellular immunotherapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071048
Volume :
128
Issue :
1
Database :
Complementary Index
Journal :
British Journal of Haematology
Publication Type :
Academic Journal
Accession number :
15275752
Full Text :
https://doi.org/10.1111/j.1365-2141.2004.05283.x