Publication date: Nov 11, 2024
To assess the immunogenicity and safety of two-dose regimen of inactivated COVID-19 vaccines in patients with pulmonary tuberculosis (PTB), and explored the potential benefits of additional dose. 182 PTB patients were randomly (1:1) assigned to the standard-dose group to receive three standard doses of inactivated COVID-19 vaccines, or the double-dose boosting group to receive two standard doses plus a double dose, with a 28-day interval. 40 healthy controls were assigned to receive two doses of inactivated COVID-19 vaccines 28 days apart. The primary endpoint was neutralizing antibodies 28 days after the second vaccination. Two doses of inactivated COVID-19 vaccines induced comparable neutralizing antibodies in PTB patients and the healthy controls, with GMTs against ancestral SARS-CoV-2 of 36. 8 vs 31. 4 (p = 0. 4618) and seroconversion rates of 83. 9% vs 87. 5% (p = 0. 6965). In the PTB patients, a third dose at day 56 led to a modest increase in neutralizing antibodies compared to the second dose, with a GMT fold increase of 1. 3-1. 8. Most adverse reactions were mild pain at the injection site. Inactivated COVID-19 vaccine was safe and immunogenic in PTB patients, and two-dose immunization could induce moderate level of humoral responses similar to the healthy adults. www. clinicaltrials. gov identifier: NCT05148949.
Concepts | Keywords |
---|---|
28days | clinical trial |
Expert | COVID-19 |
Inactivated | immunogenicity |
Nct05148949 | inactivated COVID-19 vaccines |
Vaccines | Pulmonary tuberculosis |
safety |
Semantics
Type | Source | Name |
---|---|---|
disease | MESH | pulmonary tuberculosis |
disease | MESH | seroconversion |
disease | IDO | site |
disease | MESH | COVID-19 |