TY - JOUR
T1 - Consistent neutralization of circulating omicron sub-variants by hybrid immunity up to 6 months after booster vaccination
AU - Cheung, Allen K. L.
AU - Lu, Yingying
AU - Zhu, Yufang
AU - Fung, Tsz Yan
AU - Zheng, Yulan
AU - Zheng, Zhihua
AU - Hong, Peng
N1 - Funding Information:
This study was supported by Health and Medical Research Fund (18170032 to AKLC), Research Grant Council (T12‐712/21‐R to AKLC), Pneumoconiosis Compensation Fund Board (2022 to AKLC), Shenzhen Science and Technology Innovation Commission (JCYJ20220530144608020 to Y. L.), and Science and Technology Department of Tibet (XZ202201ZY0050G to P. H.). Funding sources have no role in the study and manuscript preparation.
Publisher Copyright:
© 2023 Wiley Periodicals LLC.
PY - 2023/4
Y1 - 2023/4
N2 - The current COVID-19 vaccination program requires frequent booster vaccination to maintain sufficient neutralization levels against immune evasive SARS-CoV-2 variants. However, prior studies found more potent and durable immune response in convalescing individuals, raising the possibility of less frequent booster vaccination for them. Here, we conducted a longitudinal immunological study based on two prospective cohorts of booster vaccinated convalescing COVID-19 patients or healthcare workers (HCW) without COVID-19 history in Xiangyang, China. Comparing to 1-month post-boosting, pseudovirus neutralization titers (pVNT50) of ancestral Wuhan-Hu-1 and circulating omicron sub-variants BA.5, BF.7, BA.4.6, BA.2.75, and BA.2.75.2 spikes were stable or even increased in convalescing samples at 6-month post-boosting, when HCW samples showed substantial drop of neutralization titers across the spectrum. Variant-to-Wuhan-Hu-1 pVNT50 ratios showed no significant variation during the 17 months from pre-vaccination to 6-month post-boosting in convalescing individuals, indicating that the high durability of hybrid immunity was likely sustained by continuously improving neutralization potency that compensated immune decay. Our data provide mechanistic insight into prior epidemiological findings that vaccine-elicited humoral immune response was more durable in convalescing individuals than those without SARS-CoV-2 infection, and suggest further research into potential extension of boosting intervals for convalescing individuals.
AB - The current COVID-19 vaccination program requires frequent booster vaccination to maintain sufficient neutralization levels against immune evasive SARS-CoV-2 variants. However, prior studies found more potent and durable immune response in convalescing individuals, raising the possibility of less frequent booster vaccination for them. Here, we conducted a longitudinal immunological study based on two prospective cohorts of booster vaccinated convalescing COVID-19 patients or healthcare workers (HCW) without COVID-19 history in Xiangyang, China. Comparing to 1-month post-boosting, pseudovirus neutralization titers (pVNT50) of ancestral Wuhan-Hu-1 and circulating omicron sub-variants BA.5, BF.7, BA.4.6, BA.2.75, and BA.2.75.2 spikes were stable or even increased in convalescing samples at 6-month post-boosting, when HCW samples showed substantial drop of neutralization titers across the spectrum. Variant-to-Wuhan-Hu-1 pVNT50 ratios showed no significant variation during the 17 months from pre-vaccination to 6-month post-boosting in convalescing individuals, indicating that the high durability of hybrid immunity was likely sustained by continuously improving neutralization potency that compensated immune decay. Our data provide mechanistic insight into prior epidemiological findings that vaccine-elicited humoral immune response was more durable in convalescing individuals than those without SARS-CoV-2 infection, and suggest further research into potential extension of boosting intervals for convalescing individuals.
KW - COVID-19 vaccines
KW - SARS-CoV-2 variants
KW - humoral immune response
KW - immunization program
KW - neutralizing antibodies
UR - https://onlinelibrary.wiley.com/toc/10969071/2023/95/4
UR - http://www.scopus.com/inward/record.url?scp=85153852955&partnerID=8YFLogxK
U2 - 10.1002/jmv.28694
DO - 10.1002/jmv.28694
M3 - Journal article
SN - 0146-6615
VL - 95
JO - Journal of Medical Virology
JF - Journal of Medical Virology
IS - 4
M1 - e28694
ER -