| Title: |
Vaccination schedule and age influence impaired responsiveness to hepatitis B vaccination: a randomized trial in Central Asia |
| Authors: |
Heisig, Janyn; Nurmatov, Zuridin; Riese, Peggy; Trittel, Stephanie; Sattarova, Gulsunai J.; Temirbekova, Saikal N.; Zhumagulova, Gulnara Zh.; Nuridinova, Zhanylai N.; Derkenbaeva, Aysuluu; Arykbaeva, Bubuzhan K.; Dzhangaziev, Bakyt I.; Prokein, Jana; Klopp, Norman; Illig, Thomas; Guzmán, Carlos A.; Kasymov, Omor T.; Akmatov, Manas K.; Pessler, Frank |
| Publisher Information: |
Springer Science and Business Media LLC |
| Publication Year: |
2024 |
| Description: |
Background Vaccination against hepatitis B virus (HBV) is the most cost-efficient measure to prevent infection. Still, vaccination coverage among adults in Central Asia, including Kyrgyzstan, remains suboptimal and data about immune responses to HBV vaccination are lacking. HBV vaccination is given as three injections, whereby the 2nd and 3rd doses are given 1 and 6 months after the 1st (0-1-6 scheme). However, compliance with the 3rd dose is low in Kyrgyzstan, presumably due to the long time interval between the 2nd and 3rd doses, suggesting that a shortened vaccination schedule could result in better adherence and increased seroconversion. Method We conducted a randomized trial of individuals aged 17–66 years comparing the 0-1-6 scheme against a shorter 0-1-3 scheme. Primary outcome measures were post-vaccination titers and the percentage of participants with protective post-vaccination titers (≥ 10 mIU/ml). Results Compliance with completeness of blood draws and administered 3rd vaccine dose was better with the 0-1-3 scheme than with the 0-1-6 scheme. In both study arms combined, younger age (< 40 years) was associated with better vaccine protection. The 0-1-6 scheme resulted in higher post-vaccination titers (52 versus 15 mIU/ml, p = 0.002) and a higher seroprotection rate (85% versus 64%, p = 0.01) than the 0-1-3 scheme, whereby post-vaccination titers correlated negatively with age in the 0-1-3 scheme. Conclusion The 0-1-6 scheme should continue to be the preferred HBV vaccination schedule, but interventions to improve compliance with the 3rd vaccine dose are needed. Trial registration: Research Registry, researchregistry10361, Registered 04 June 2024, Retrospectively registered, https://www.researchregistry.com/browse-the-registry#home/registrationdetails/665ed4e94d638f00294d35df/ |
| Document Type: |
other/unknown material |
| Language: |
unknown |
| DOI: |
10.21203/rs.3.rs-5427492/v1 |
| Availability: |
http://dx.doi.org/10.21203/rs.3.rs-5427492/v1; https://www.researchsquare.com/article/rs-5427492/v1; https://www.researchsquare.com/article/rs-5427492/v1.html |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.9DE7E043 |
| Database: |
BASE |