2021
DOI: 10.4103/ijmr.ijmr_4431_20
|View full text |Cite
|
Sign up to set email alerts
|

Comparison of the immunogenicity & protective efficacy of various SARS-CoV-2 vaccine candidates in non-human primates

Abstract: Background & objectives: The COVID-19 pandemic has emerged as a global public health crisis and research groups worldwide are engaged in developing vaccine candidates to curb its transmission, with a few vaccines having progressed to advanced stages of clinical trials. The aim of this systematic review was to compare immunogenicity and protective efficacy of various SARS-CoV-2 vaccine candidates tested in non-human primate (NHP) models. Methods: Lit… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

1
6
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 28 publications
(7 citation statements)
references
References 51 publications
1
6
0
Order By: Relevance
“…BNT162b2 induced marked levels of EIA antibodies as early as one week after the first dose; however, detectable EIA antibodies developed two weeks after the first dose, and the level increased after the second dose of NVX-CoV2373. Similar EIA IgG antibody development was reported after mRNA vaccination, and a delay in the IgG response was reported following inoculation with NVX-CoV2373 [31][32][33]. This is related to the different profiles of cytokines and chemokines following inoculation with BNT162b2 and NVX-CoV2373, with higher levels of CXCL13 after first dose of inoculation with BNT162b2 and higher levels of Th2 chemokines (CCL17 and CCL11) in muscle tissues and sera on Day 1 of the second dose of NVX-CoV2373.…”
Section: Discussionsupporting
confidence: 74%
“…BNT162b2 induced marked levels of EIA antibodies as early as one week after the first dose; however, detectable EIA antibodies developed two weeks after the first dose, and the level increased after the second dose of NVX-CoV2373. Similar EIA IgG antibody development was reported after mRNA vaccination, and a delay in the IgG response was reported following inoculation with NVX-CoV2373 [31][32][33]. This is related to the different profiles of cytokines and chemokines following inoculation with BNT162b2 and NVX-CoV2373, with higher levels of CXCL13 after first dose of inoculation with BNT162b2 and higher levels of Th2 chemokines (CCL17 and CCL11) in muscle tissues and sera on Day 1 of the second dose of NVX-CoV2373.…”
Section: Discussionsupporting
confidence: 74%
“…In our study, all vaccinated pregnant women received inactivated vaccines. Compared with mRNA COVID‐19 vaccines, inactivated vaccines may have lower immunogenicity 33 …”
Section: Discussionmentioning
confidence: 99%
“…Compared with mRNA COVID-19 vaccines, inactivated vaccines may have lower immunogenicity. 33 The main strength of this study was the longitudinal followup setting, which allowed us to obtain data regarding both maternal and newborn health. Additionally, COVID-19 vaccination information was obtained from each participant's electronic vaccination record, thus exposure misclassification is unlikely.…”
Section: Discussionmentioning
confidence: 99%
“…In our study, all vaccinated pregnant women received inactivated vaccines. Compared with mRNA vaccines, inactivated vaccines may have lower immunogenicity 40 …”
Section: Discussionmentioning
confidence: 99%