PMID- 37631944 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230829 IS - 2076-393X (Print) IS - 2076-393X (Electronic) IS - 2076-393X (Linking) VI - 11 IP - 8 DP - 2023 Aug 17 TI - A Comparative Study of Immunogenicity, Antibody Persistence, and Safety of Three Different COVID-19 Boosters between Individuals with Comorbidities and the Normal Population. LID - 10.3390/vaccines11081376 [doi] LID - 1376 AB - Data on immunogenicity, immune response persistency, and safety of COVID-19 boosters in patients with comorbidities are limited. Therefore, we aimed to evaluate three different boosters' immunogenicity and safety in individuals with at least one underlying disease (UD) (obesity, hypertension, and diabetes mellitus) with healthy ones (HC) who were primed with two doses of the BBIBP-CorV vaccine and received a booster shot of the same priming vaccine or protein subunit vaccines, PastoCovac Plus or PastoCovac. One hundred and forty subjects including sixty-three ones with a comorbidity and seventy-seven healthy ones were enrolled. The presence of SARS-CoV-2 antibodies was assessed before the booster injection and 28, 60, 90, and 180 days after it. Moreover, the adverse events (AEs) were recorded on days 7 and 21 postbooster shot for evaluating safety outcomes. Significantly increased titers of antispike, antiRBD, and neutralizing antibodies were observed in both UD and HC groups 28 days after the booster dose. Nevertheless, the titer of antispike IgG and anti-RBD IgG was lower in the UD group compared to the HC group. The long-term assessment regarding persistence of humoral immune responses showed that the induced antibodies were detectable up to 180 days postbooster shots though with a declined titer in both groups with no significant differences (p > 0.05). Furthermore, no significant difference in antibody levels was observed between each UD subgroup and the HC group, except for neutralizing antibodies in the hypertension subgroup. PastoCovac Plus and PastoCovac boosters induced a higher fold rise in antibodies in UD individuals than BBIBP-CorV booster recipients. No serious AEs after the booster injection were recorded. The overall incidence of AEs after the booster injection was higher in the UD group than the HC group among whom the highest systemic rate of AEs was seen in the BBIBP-CorV booster recipients. In conclusion, administration of COVID-19 boosters could similarly induce robust and persistent humoral immune responses in individuals with or without UD primarily vaccinated with two doses of the BBIBP-CorV. Protein-based boosters with higher a higher fold rise in antibodies and lower AEs in individuals with comorbidities might be considered a better choice for these individuals. FAU - Ashrafian, Fatemeh AU - Ashrafian F AUID- ORCID: 0000-0001-8260-100X AD - Clinical Research Department, Pasteur Institute of Iran, Tehran 1316943551, Iran. FAU - Bagheri Amiri, Fahimeh AU - Bagheri Amiri F AUID- ORCID: 0000-0003-2943-2846 AD - Department of Epidemiology and Biostatistics, Research Centre for Emerging and Reemerging Infectious Diseases, Pasteur Institute of Iran, Tehran 1316943551, Iran. FAU - Bavand, Anahita AU - Bavand A AD - Clinical Research Department, Pasteur Institute of Iran, Tehran 1316943551, Iran. FAU - Zali, Mahsan AU - Zali M AD - Clinical Research Department, Pasteur Institute of Iran, Tehran 1316943551, Iran. FAU - Sadat Larijani, Mona AU - Sadat Larijani M AUID- ORCID: 0000-0003-3681-5319 AD - Clinical Research Department, Pasteur Institute of Iran, Tehran 1316943551, Iran. FAU - Ramezani, Amitis AU - Ramezani A AUID- ORCID: 0000-0003-3502-8524 AD - Clinical Research Department, Pasteur Institute of Iran, Tehran 1316943551, Iran. LA - eng GR - 2127/Pasteur Institute of Iran/ PT - Journal Article DEP - 20230817 PL - Switzerland TA - Vaccines (Basel) JT - Vaccines JID - 101629355 PMC - PMC10459403 OTO - NOTNLM OT - COVID-19 vaccine OT - antibody persistence OT - booster OT - underlying diseases COIS- The authors declare that they have no competing interest. EDAT- 2023/08/26 10:46 MHDA- 2023/08/26 10:47 PMCR- 2023/08/17 CRDT- 2023/08/26 01:34 PHST- 2023/06/25 00:00 [received] PHST- 2023/08/12 00:00 [revised] PHST- 2023/08/14 00:00 [accepted] PHST- 2023/08/26 10:47 [medline] PHST- 2023/08/26 10:46 [pubmed] PHST- 2023/08/26 01:34 [entrez] PHST- 2023/08/17 00:00 [pmc-release] AID - vaccines11081376 [pii] AID - vaccines-11-01376 [pii] AID - 10.3390/vaccines11081376 [doi] PST - epublish SO - Vaccines (Basel). 2023 Aug 17;11(8):1376. doi: 10.3390/vaccines11081376.