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A randomized, double-blind study on the safety and immunogenicity of rTSST-1 variant vaccine: phase 2 results.

Authors :
Schoergenhofer C
Gelbenegger G
Hasanacevic D
Schöner L
Steiner MM
Firbas C
Buchtele N
Derhaschnig U
Tanzmann A
Model N
Larcher-Senn J
Drost M
Eibl MM
Roetzer A
Jilma B
Source :
EClinicalMedicine [EClinicalMedicine] 2024 Jan 05; Vol. 67, pp. 102404. Date of Electronic Publication: 2024 Jan 05 (Print Publication: 2024).
Publication Year :
2024

Abstract

Background: Toxic shock syndrome toxin-1 (TSST-1) is a superantigen produced by Staphylococcus aureus that causes the life-threatening toxic shock syndrome. The development of a safe and immunogenic vaccine against TSST-1 remains an unmet medical need. We investigated the safety, tolerability and immunogenicity of a recombinant TSST-1 variant vaccine (rTSST-1v) after 1-3 injections in healthy volunteers.<br />Methods: In this randomised, double-blind, adjuvant-controlled, parallel-group, phase 2 trial, healthy adults aged 18-64 were randomly allocated to undergo 1-3 injections of either 10 or 100 μg rTSST-1v or Al(OH) <subscript>3</subscript> . The primary endpoint was safety and tolerability of rTSST-1v in the intention-to-treat population. The per-protocol population was used for the immunogenicity analysis. The trial is registered with EudraCT#: 2015-003714-24; ClinicalTrials.gov#: NCT02814708.<br />Findings: Between April and November 2017,140 subjects were enrolled and 126 completed the trial. rTSST-1v showed a good safety and tolerability profile. A total of 855 systemic adverse events occurred, 280 of which were suspected related adverse events, without dose dependency. Two participants were discontinued early because of allergic reactions. Seroconversion occurred in >81% of subjects within 3 months of the first immunisation which was sustained until 18 months after the third immunisation in over 70% of subjects in the pooled low-dose group and in over 85% in the pooled high-dose group.<br />Interpretation: rTSST-1v in cumulative doses of up to 300 μg was safe, well-tolerated and highly immunogenic. Two immunisations with 100 μg rTSST-1v provided the most persistent immune response and may be evaluated in future trials.<br />Funding: Biomedizinische Forschung & Bio-Produkte AG funded this study.<br />Competing Interests: GG, CS, CF, MMS, NB, UD, AT, and BJ declare no competing interests. Martha M. Eibl was the owner of Biomedizinische Forschung & Bio-Produkte AG. DH, LS, NM, and AR are employees of the study funder Biomedizinische Forschung & Bio-Produkte AG, a biotechnology company engaged in the development of BioMed rTSST-1v.<br /> (© 2024 Published by Elsevier Ltd.)

Details

Language :
English
ISSN :
2589-5370
Volume :
67
Database :
MEDLINE
Journal :
EClinicalMedicine
Publication Type :
Academic Journal
Accession number :
38274114
Full Text :
https://doi.org/10.1016/j.eclinm.2023.102404