Comparison of antibody persistency through one year between one-dose and two-dose regimens of Ad5-nCoV vaccine for COVID-19
This post-hoc analysis compared the receptor-binding domain (RBD)-specific and pseudovirus neutralizing antibodies against the wild-type SARS-CoV-2 strain elicited by one or two doses (56-d interval) of Ad5-nCoV vaccine regimen (NCT04341389 and NCT04566770). Both trials had low-dose and high-dose groups. Propensity score matching was used to adjust the baseline between one- and two-dose regimens. To predict the decrease in antibody titers 1 y after vaccination, half-lives of RBD-binding antibodies and pseudovirus neutralizing antibodies were computed. We obtained 34 and 29 pairs of participants in the low- and high-dose groups based on the propensity score matching. The two-dose regimen of Ad5-nCoV increased the peaking level of neutralizing antibodies compared to the one-dose regimen at day 28, but the responses of the neutralizing antibodies were not consistent with those of the RBD antibodies. Half-lives of the RBD-binding antibodies in the two-dose Ad5-nCoV regimen (202-209 days) were longer than those in the one-dose regimen (136-137 d); half-lives of the pseudovirus neutralizing antibody in the one-dose Ad5-nCoV regimen (177 d) were longer than those in the two-dose regimen (116-131 d). The predicted positive rates of RBD-binding antibodies in the one-dose regimen (34.1%-38.3%) would be lower than those in the two-dose Ad5-nCoV regimen (67.0%-84.0%), while the positive rates of pseudovirus neutralizing antibodies in the one-dose regimen (65.4%-66.7%) would be higher than those in the two-dose regimen (48.3%-58.0%). The two-dose Ad5-nCoV regimen with a 56-d interval had no effect on the persistence of neutralizing antibodies but slowed decay trend of RBD-binding antibodies.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:19 |
---|---|
Enthalten in: |
Human vaccines & immunotherapeutics - 19(2023), 2 vom: 01. Aug., Seite 2230760 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Feng, Jia-Lu [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 12.07.2023 Date Revised 18.07.2023 published: Print ClinicalTrials.gov: NCT04341389, NCT04566770 Citation Status MEDLINE |
---|
doi: |
10.1080/21645515.2023.2230760 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM359296629 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM359296629 | ||
003 | DE-627 | ||
005 | 20231226210621.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1080/21645515.2023.2230760 |2 doi | |
028 | 5 | 2 | |a pubmed24n1197.xml |
035 | |a (DE-627)NLM359296629 | ||
035 | |a (NLM)37428653 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Feng, Jia-Lu |e verfasserin |4 aut | |
245 | 1 | 0 | |a Comparison of antibody persistency through one year between one-dose and two-dose regimens of Ad5-nCoV vaccine for COVID-19 |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 12.07.2023 | ||
500 | |a Date Revised 18.07.2023 | ||
500 | |a published: Print | ||
500 | |a ClinicalTrials.gov: NCT04341389, NCT04566770 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a This post-hoc analysis compared the receptor-binding domain (RBD)-specific and pseudovirus neutralizing antibodies against the wild-type SARS-CoV-2 strain elicited by one or two doses (56-d interval) of Ad5-nCoV vaccine regimen (NCT04341389 and NCT04566770). Both trials had low-dose and high-dose groups. Propensity score matching was used to adjust the baseline between one- and two-dose regimens. To predict the decrease in antibody titers 1 y after vaccination, half-lives of RBD-binding antibodies and pseudovirus neutralizing antibodies were computed. We obtained 34 and 29 pairs of participants in the low- and high-dose groups based on the propensity score matching. The two-dose regimen of Ad5-nCoV increased the peaking level of neutralizing antibodies compared to the one-dose regimen at day 28, but the responses of the neutralizing antibodies were not consistent with those of the RBD antibodies. Half-lives of the RBD-binding antibodies in the two-dose Ad5-nCoV regimen (202-209 days) were longer than those in the one-dose regimen (136-137 d); half-lives of the pseudovirus neutralizing antibody in the one-dose Ad5-nCoV regimen (177 d) were longer than those in the two-dose regimen (116-131 d). The predicted positive rates of RBD-binding antibodies in the one-dose regimen (34.1%-38.3%) would be lower than those in the two-dose Ad5-nCoV regimen (67.0%-84.0%), while the positive rates of pseudovirus neutralizing antibodies in the one-dose regimen (65.4%-66.7%) would be higher than those in the two-dose regimen (48.3%-58.0%). The two-dose Ad5-nCoV regimen with a 56-d interval had no effect on the persistence of neutralizing antibodies but slowed decay trend of RBD-binding antibodies | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Ad5-nCoV | |
650 | 4 | |a RBD-binding antibody | |
650 | 4 | |a exponential decay model | |
650 | 4 | |a persistence of immunity | |
650 | 4 | |a power-law model | |
650 | 4 | |a pseudovirus neutralizing antibody | |
650 | 7 | |a Ad5-nCoV vaccine |2 NLM | |
650 | 7 | |a 5AHC3V2UQS |2 NLM | |
650 | 7 | |a Antibodies, Neutralizing |2 NLM | |
650 | 7 | |a Antibodies, Viral |2 NLM | |
650 | 7 | |a COVID-19 Vaccines |2 NLM | |
700 | 1 | |a Wang, Wen-Juan |e verfasserin |4 aut | |
700 | 1 | |a Jin, Peng-Fei |e verfasserin |4 aut | |
700 | 1 | |a Zheng, Hui |e verfasserin |4 aut | |
700 | 1 | |a Jin, Lai-Run |e verfasserin |4 aut | |
700 | 1 | |a Xia, Xin |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xiao-Yin |e verfasserin |4 aut | |
700 | 1 | |a Li, Zhuo-Pei |e verfasserin |4 aut | |
700 | 1 | |a Li, Jing-Xin |e verfasserin |4 aut | |
700 | 1 | |a Zhu, Feng-Cai |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Human vaccines & immunotherapeutics |d 2012 |g 19(2023), 2 vom: 01. Aug., Seite 2230760 |w (DE-627)NLM21576823X |x 2164-554X |7 nnns |
773 | 1 | 8 | |g volume:19 |g year:2023 |g number:2 |g day:01 |g month:08 |g pages:2230760 |
856 | 4 | 0 | |u http://dx.doi.org/10.1080/21645515.2023.2230760 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 19 |j 2023 |e 2 |b 01 |c 08 |h 2230760 |