Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis.
Adult
Amino Acid Sequence
Animals
Antibodies, Bacterial
/ immunology
Antibodies, Monoclonal
/ immunology
B-Lymphocytes
/ immunology
Bacterial Proteins
/ chemistry
Epitopes
/ chemistry
Humans
Immunologic Memory
Male
Membrane Transport Proteins
/ immunology
Mice, Inbred BALB C
Models, Molecular
Mycobacterium tuberculosis
/ immunology
Protein Structure, Secondary
Structure-Activity Relationship
THP-1 Cells
Tuberculosis
/ blood
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
27 01 2021
27 01 2021
Historique:
received:
03
05
2020
accepted:
04
01
2021
entrez:
28
1
2021
pubmed:
29
1
2021
medline:
4
2
2021
Statut:
epublish
Résumé
Mycobacterium tuberculosis (Mtb) exposure drives antibody responses, but whether patients with active tuberculosis elicit protective antibodies, and against which antigens, is still unclear. Here we generate monoclonal antibodies from memory B cells of one patient to investigate the B cell responses during active infection. The antibodies, members of four distinct B cell clones, are directed against the Mtb phosphate transporter subunit PstS1. Antibodies p4-36 and p4-163 reduce Mycobacterium bovis-BCG and Mtb levels in an ex vivo human whole blood growth inhibition assay in an FcR-dependent manner; meanwhile, germline versions of p4-36 and p4-163 do not bind Mtb. Crystal structures of p4-36 and p4-170, complexed to PstS1, are determined at 2.1 Å and 2.4 Å resolution, respectively, to reveal two distinctive PstS1 epitopes. Lastly, a prophylactic p4-36 and p4-163 treatment in Mtb-infected Balb/c mice reduces bacterial lung burden by 50%. Our study shows that inhibitory anti-PstS1 B cell responses arise during active tuberculosis.
Identifiants
pubmed: 33504803
doi: 10.1038/s41467-021-20930-0
pii: 10.1038/s41467-021-20930-0
pmc: PMC7840946
doi:
Substances chimiques
Antibodies, Bacterial
0
Antibodies, Monoclonal
0
Bacterial Proteins
0
Epitopes
0
Membrane Transport Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
602Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 207487/C/17/Z
Pays : United Kingdom
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