| Literature DB >> 9144467 |
H de la Salle1, E Houssaint, M A Peyrat, D Arnold, J Salamero, D Pinczon, S Stevanovic, H Bausinger, D Fricker, E Gomard, W Biddison, P Lehner, F UytdeHaag, M Sasportes, L Donato, H G Rammensee, J P Cazenave, D Hanau, M M Tongio, M Bonneville.
Abstract
Two siblings with a peptide TAP deficiency were recently described. Despite poor cell surface expression of HLA class I molecules, these patients were not unusually susceptible to viral infections. The majority of the cell surface-expressed class I molecules were HLA-B products as assessed by cytofluorometry and biochemical analysis. Analysis of two peptides eluted from the class I molecules expressed by TAP-deficient EBV B lymphoblastoid cell lines indicated that both were derived from cytosolic proteins and presented by HLA-B molecules. Peripheral alphabeta CD8+ T cells were present and their TCR repertoire was polyclonal. Most of the alphabeta CD8+ T cell clones studied (21 of 22) were nonreactive against cells expressing normal levels of the same HLA alleles as those of the TAP-deficient patients. However, it was possible to isolate one cytotoxic CD8+ alphabeta T cell clone recognizing the EBV protein LMP2 presented by HLA-B molecules on TAP-deficient cells. These observations suggest that in the TAP-deficient patients, CD8+ alphabeta T cells could mature and be recruited in immune responses to mediate HLA class I-restricted cytotoxic defense against viral infections. They also strengthen the physiologic importance of a TAP-independent processing pathway of the LMP2 protein, which was previously shown to contain several other TAP-independent epitopes.Entities:
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Year: 1997 PMID: 9144467
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422