Healthy Donors Exhibit a CD4 T Cell Repertoire Specific to the Immunogenic Human Hormone H2-Relaxin before Injection.
Autoantigens
/ genetics
CD4-Positive T-Lymphocytes
/ physiology
Cell Line
Enzyme-Linked Immunospot Assay
Epitope Mapping
Epitopes, T-Lymphocyte
/ genetics
HLA-DR Antigens
/ metabolism
Healthy Volunteers
Humans
Immune Tolerance
Interferon-gamma
/ metabolism
Lymphocyte Activation
Protein Binding
Relaxin
/ genetics
T-Cell Antigen Receptor Specificity
Journal
Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R
Informations de publication
Date de publication:
15 06 2019
15 06 2019
Historique:
received:
18
06
2018
accepted:
11
04
2019
pubmed:
19
5
2019
medline:
7
3
2020
entrez:
19
5
2019
Statut:
ppublish
Résumé
H2-relaxin (RLN2) is a two-chain peptide hormone structurally related to insulin with a therapeutic potential in multiple indications. However, multiple injections of human RLN2 induced anti-RLN2 Abs in patients, hampering its clinical development. As T cell activation is required to produce Abs, we wondered whether T cells specific for RLN2 might be already present in the human blood before any injection. We therefore quantified the RLN2-specific T cell repertoire using PBMCs collected from healthy donors. CD4 T cells were stimulated in multiple replicates by weekly rounds of stimulation by dendritic cells loaded with RLN2, and their specificity was assessed by IFN-γ ELISPOT. The number of specific T cell lines was used to estimate the frequency of circulating T cells. In vitro T cell response was demonstrated in 18 of the 23 healthy donors, leading to the generation of 70 independent RLN2-specific T cell lines. The mean frequency of RLN2-specific CD4 T cells was similar to that of T cells specific for known immunogenic therapeutic proteins. Using overlapping peptides, we identified multiple T cell epitopes hosted in the N-terminal parts of the α- and β-chains and common to multiple donors, in agreement with their capacity to bind to multiple HLA-DR molecules. Our results provide important clues to the immunogenicity of RLN2 and highlight the weak central immune tolerance induced against this self-hormone.
Identifiants
pubmed: 31101669
pii: jimmunol.1800856
doi: 10.4049/jimmunol.1800856
doi:
Substances chimiques
Autoantigens
0
Epitopes, T-Lymphocyte
0
HLA-DR Antigens
0
RLN2 protein, human
0
Interferon-gamma
82115-62-6
Relaxin
9002-69-1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3507-3513Informations de copyright
Copyright © 2019 by The American Association of Immunologists, Inc.