The Bw4 public epitope of HLA-B molecules confers reactivity with natural killer cell clones that express NKB1, a putative HLA receptor.
Open Access
- 1 March 1995
- journal article
- Published by Rockefeller University Press in The Journal of Experimental Medicine
- Vol. 181 (3) , 1133-1144
- https://doi.org/10.1084/jem.181.3.1133
Abstract
Although inhibition of natural killer (NK) cell-mediated lysis by the class I HLA molecules of target cells is an established phenomenon, knowledge of the features of class I molecules which induce this effect remains rudimentary. Using class I alleles HLA-B*1502 and B*1513 which differ only at residues 77-83 which define the Bw4 and Bw6 serological epitopes, we tested the hypothesis that the presence of the Bw4 epitope on class I molecules determines recognition by NKB1+ NK cells. HLA-B*1513 possesses the Bw4 epitope, whereas B*1502 has the Bw6 epitope. Lysis by NKB1+ NK cell clones of transfected target cells expressing B*1513 as the only HLA-A, -B, or -C molecule was inhibited, whereas killing of transfectants expressing B*1502 was not. Addition of an an anti-NKB1 monoclonal antibody reconstituted lysis of the targets expressing B*1513, but did not affect killing of targets bearing B*1502. The inhibitory effect of B*1513 could be similarly prevented by the addition of an anti-class I monoclonal antibody. These results show that the presence of the Bw4 epitope influences recognition of HLA-B molecules by NK cells that express NKB1, and suggest that the NKB1 molecule may act as a receptor for Bw4+ HLA-B alleles. Sequences outside of the Bw4 region must also affect recognition by NKB1+ NK cells, because lysis of transfectants expressing HLA-A*2403 or A*2501, which possess the Bw4 epitope but are in other ways substantially different from HLA-B molecules, was not increased by addition of the anti-NKB1 antibody. Asparagine 86, the single site of N-linked glycosylation on class I molecules, is in close proximity to the Bw4/Bw6 region. The glycosylation site of the Bw4-positive molecule B*5801 was mutated, and the mutant molecules tested for inhibition of NKB1+ NK cells. Inhibition that could be reversed by addition of the anti-NKB1 monoclonal antibody was observed, showing the presence of the carbohydrate moiety is not essential for class I recognition by NKB1+ NK cell clones.Keywords
This publication has 45 references indexed in Scilit:
- The Structure and Evolution of the HLA-Bw4 and Bw6 AntigensTissue Antigens, 2008
- NK3-specific natural killer cells are selectively inhibited by Bw4-positive HLA alleles with isoleucine 80.The Journal of Experimental Medicine, 1994
- NKB1: a natural killer cell receptor involved in the recognition of polymorphic HLA-B molecules.The Journal of Experimental Medicine, 1994
- The HLA‐B73 antigen has a most unusual structure that defines a second lineage of HLA‐B allelesTissue Antigens, 1994
- HLA‐B15: A widespread and diverse family of HLA‐B allelesTissue Antigens, 1994
- Structural heterogeneity in HLA-B70, a high-frequency antigen of black populations *Tissue Antigens, 1993
- Specificity of HLA class I antigen recognition by human NK clones: evidence for clonal heterogeneity, protection by self and non-self alleles, and influence of the target cell type.The Journal of Experimental Medicine, 1993
- Reptilian class I major histocompatibility complex genes reveal conserved elements in class I structureImmunogenetics, 1992
- Identification of self peptides bound to purified HLA-B27Nature, 1991
- Expression of T Cell Antigen Receptor Heterodimers in a Lipid-Linked FormScience, 1990