BACKGROUND: Epitopes of human leukocyte antigen (HLA) are the sites to which the antibodies bind. We identify here 103 HLA class I epitopes shared by groups of class I antigens. In particular, our emphasis was on identifying epitopes exclusive to the C-locus antigens or interlocus epitopes among A, B, and C antigens. The use of monoclonal antibodies or alloantibodies eluted from HLA recombinant single antigen cell lines tested with a panel of single antigen beads have proved very useful in the identification of the epitopes. METHODS: Alloantibodies absorbed onto then eluted from HLA single antigen cell lines and monoclonal antibodies were tested with a panel of 95 A-, B-, and C- single antigen beads and the HLA specificities determined. Each epitope was defined by amino acids shared exclusively by the positive antigens for each antibody. RESULTS: In addition to the 58 A and B class I epitopes identified in an earlier study, we add 45 more new A, B, C epitopes including, for the first time, epitopes found on C locus antigens. CONCLUSION: Beads bearing single antigens tested with monoclonal or eluted alloantibodies proved very powerful in identifying epitopes shared among HLA antigens. These epitopes are the targets of the antibodies. Antibody specificities to non-donor-specific antigens, often found in sera of transplant patients, can now be understood as reactions to epitopes shared with the donor specific antigens. The importance of identifying these epitopes is that they may be the "transplantation antigens" responsible for antibody-mediated transplant rejection.
BACKGROUND: Epitopes of human leukocyte antigen (HLA) are the sites to which the antibodies bind. We identify here 103 HLA class I epitopes shared by groups of class I antigens. In particular, our emphasis was on identifying epitopes exclusive to the C-locus antigens or interlocus epitopes among A, B, and C antigens. The use of monoclonal antibodies or alloantibodies eluted from HLA recombinant single antigen cell lines tested with a panel of single antigen beads have proved very useful in the identification of the epitopes. METHODS: Alloantibodies absorbed onto then eluted from HLA single antigen cell lines and monoclonal antibodies were tested with a panel of 95 A-, B-, and C- single antigen beads and the HLA specificities determined. Each epitope was defined by amino acids shared exclusively by the positive antigens for each antibody. RESULTS: In addition to the 58 A and B class I epitopes identified in an earlier study, we add 45 more new A, B, C epitopes including, for the first time, epitopes found on C locus antigens. CONCLUSION: Beads bearing single antigens tested with monoclonal or eluted alloantibodies proved very powerful in identifying epitopes shared among HLA antigens. These epitopes are the targets of the antibodies. Antibody specificities to non-donor-specific antigens, often found in sera of transplant patients, can now be understood as reactions to epitopes shared with the donor specific antigens. The importance of identifying these epitopes is that they may be the "transplantation antigens" responsible for antibody-mediated transplant rejection.
Authors: Robert O Endres; Steven H Kleinman; Danielle M Carrick; Whitney R Steele; David J Wright; Philip J Norris; Darrell Triulzi; Ram Kakaiya; Michael P Busch Journal: Transfusion Date: 2010-02-11 Impact factor: 3.157
Authors: Nathan Holman; Jason T Weinfurter; Trevor R Harsla; Roger W Wiseman; Aaron J Belli; Anthony J Michaels; Keith A Reimann; Robert I DeMars; Matthew R Reynolds Journal: PLoS One Date: 2017-07-18 Impact factor: 3.240
Authors: Roman Reindl-Schwaighofer; Andreas Heinzel; Guido A Gualdoni; Laurent Mesnard; Frans H J Claas; Rainer Oberbauer Journal: Transpl Int Date: 2019-11-28 Impact factor: 3.782
Authors: Suzanne Bezstarosti; Cynthia S M Kramer; Marry E I Franke-van Dijk; Manon Vergunst; Kim H Bakker; Merve Uyar-Mercankaya; Rico Buchli; Dave L Roelen; Johan W de Fijter; Frans H J Claas; Sebastiaan Heidt Journal: Front Immunol Date: 2022-01-07 Impact factor: 7.561