Antibodies to cryptic epitopes on HLA class I and class II heavy chains bound to single antigen beads: Clinically relevant?


Journal

Transplant immunology
ISSN: 1878-5492
Titre abrégé: Transpl Immunol
Pays: Netherlands
ID NLM: 9309923

Informations de publication

Date de publication:
12 2021
Historique:
received: 14 07 2021
revised: 08 10 2021
accepted: 08 10 2021
pubmed: 18 10 2021
medline: 19 2 2022
entrez: 17 10 2021
Statut: ppublish

Résumé

Cell surface HLA class I consists of trimers, i.e., alpha - heavy chain, beta - 2 - microglobulin, and a peptide, termed closed conformers (CC) on non-activated lymphocytes. HLA class I and class II may also exist, respectively, as alpha-chain only or alpha and beta - chain only on activated cells termed open conformers (OC). We extend previous studies using an OC-specific monoclonal antibody that demonstrate LABScreen HLA class I and II single antigen beads (SABs) contain a mixture of open and closed conformers. LIFECODES SABs have bound CC only. More HLA class I and class II LABScreen SABs were reactive than LIFECODES SABs due to the presence of OC on LABScreen SABs. We hypothesized that antibody against OC on HLA B antigens would not be detected in cell based cross matches (XMs) with typical lymphocyte targets since anti-HLA OC antibodies would not react with native HLA CC on the cell surface. To test this hypothesis, we performed flow cytometry XM (FCXM) assays with sera of sufficient strength that most laboratories would likely predict positive FCXMs. Sera that reacted strongly with LABScreen SABs (>13,000 MFI) but weakly or not at all with LIFECODES SABs (<1000 MFI) gave negative T and B cell FCXMs. In contrast, sera that reacted with LIFECODES SABs (>13,000 MFI) but weakly with LABScreen SABs (<2100 MFI) exhibited positive FCXMs. Detection of antibodies directed against OC in SAB assays, may lead to inappropriate listing of unacceptable antigens, a decision not to XM or pre-or post - transplant desensitization procedures.

Identifiants

pubmed: 34656784
pii: S0966-3274(21)00122-2
doi: 10.1016/j.trim.2021.101482
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Epitopes 0
HLA Antigens 0
Isoantibodies 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101482

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Mepur H Ravindranath (MH)

Department. of Hematology and Oncology, Children's Hospital, Los Angeles, CA 90027, United States of America.

Edward J Filippone (EJ)

Division of Nephrology, Dept. of Medicine, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19145, United States of America.

Carly J Amato-Menker (CJ)

Department of Immunology and Microbial Pathogenesis, West Virginia University, School of Medicine, Morgantown, WV 26506, United States of America.

Fernando A Arosa (FA)

Health Sciences Research Center (CICS-UBI) & Department of Medical Sciences, University of Beira Interior, Covilhã 6200-506, Portugal. Electronic address: arosa@fcsaude.ubi.pt.

Ballabh Das (B)

Department of Pathology, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, United States of America. Electronic address: Ballabh.Das@downstate.edu.

Yijun Ou (Y)

Department of Pathology, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, United States of America. Electronic address: Yijun.Ou@downstate.edu.

Allen J Norin (AJ)

Department of Medicine and Cell Biology, Transplant Immunology and Immunogenetics, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, United States of America. Electronic address: Allen.Norin@downstate.edu.

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Classifications MeSH