HLA-Dw14 and HLA-DR3 haplotypes share a functional determinant recognized by a human alloreactive T-cell clone

• Published in: Human immunology Vol. 23; no. 1; pp. 59 - 70
• Main Authors: Lang, Bernhard, LoGalbo, Peter R., Sanchez, Berta, Winchester, Robert
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.1988
• Subjects: Amino Acid Sequence; Antibodies, Monoclonal; Clone Cells - immunology; Epitopes; Haplotypes; HLA-D Antigens - genetics; HLA-D Antigens - immunology; HLA-DR Antigens - genetics; HLA-DR Antigens - immunology; HLA-DR3 Antigen; Humans; Molecular Sequence Data; T-Lymphocytes - immunology; EBV; MHC; PBL; LCL; HLA; MoAb
• ISSN: 0198-8859; 1879-1166
• DOI: 10.1016/0198-8859(88)90018-3

In the process of studying the fine specificity of HLA class II molecules, we identified an alloreactive T-cell clone raised to a HLA-Dw14 homozygous cell line that was specifically stimulated by Dw14+ homozygous typing cells but negatively with cells expressing the HLA-Dw4, -Dw10, -Dw13, and -Dw15 subspecificities of DR4. Of interest, this clone was also equivalently activated by stimulation with all DR3 cells and cell lines tested. Negative responses were obtained using a panel of 87 non-DR3 and non-Dw14 cells, including cell lines of the Tenth Histocompatibility Workshop. A monoclonal antibody inhibition study revealed the relevant stimulating determinant to be on HLA-DR molecules in both Dw14- and DR3-positive cells. A comparison of the DRβ1-chain-inferred amino acid sequences suggests that formation of a topologically equivalent stimulating determinant would involve the participation of two noncontiguous regions of the third diversity region of DRβ1. The putative recognition conformation detected by the clone is most probably specified by the presence of a valine at position 86 and a nonnegatively charged residue at positions 70, 71, and 74, since these are the only residues where DR3 and Dw14 are distinguishable from all other HLA-DR types. These findings illustrate that the functional ability of class II molecules is not necessarily either illustrated or predicted by serologic typing or by simple consideration of amino acid sequence.