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      Safety and Efficacy of the Covid-19 Vaccine in children andor adolescents: A meta-analysis

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          Abstract

          Dear Editor, Since 2019, the COVID-19 epidemic has raged worldwide, with children and adolescents accounting for a quarter of the world's population being greatly threatened. The safety and effectiveness of the COVID-19 vaccine for children have been examined. At present, clinical trials of COVID-19 vaccines for children are gradually increasing. The most common ones are attenuated and inactivated vaccines.The efficacy and safety of many randomized clinical trials (RCTs) and observational trials of the COVID-19 vaccine in children have been published through a systematic search of common databases between 2019, and November 8, 2021. We read with great interest the report in this Journal by Martinón-Torres et al. who found that SARS-CoV-2 infections have occurred in immunocompromised children and young people with no increased risk of severe disease.1 Even without an increased risk of contracting covid-19 in immunocompromised children and young adults. However, a meta-analysis of the safety and efficacy of Covid-19 vaccines in children and/or adolescents is still warranted. An extensive literature search was performed in PubMed, Web of Science, EMBASE, Elsevier ScienceDirect, and Cochrane Library to find all compliant articles published from January 1, 2020, to November 8, 2021. The following keywords were used on the search strategy: “COVID-19”, “2019-nCoV”, “SARS-CoV-2”, “2019 novel coronavirus”, “coronavirus disease 2019”, “severe acute respiratory syndrome coronavirus 2”, “children”, “child”, “adolescent”, and “teenager”. The reference lists, cited in the included studies and reviews, were eligible as exploratory targets to identify extensive articles.The inclusion criteria included: (1) adult COVID-19 children/adolescents confirmed by reverse transcriptase-polymerase chain reaction (rt-PCR); (2) peer-reviewed original articles in English; (3) individual study populations being at least fifteen cases; (4) the key available data tabulated data or effect (95% confidence interval (CI)), must be clearly stated. Case reports, repeated articles, review papers, and preprints were eliminated. Single-group rates and corresponding 95% CIs were used to assess the association between children/adolescents and the COVID-19 vaccine in a whole random-effects meta-analysis model. The model includes effectiveness rates, adverse effects rates, and injection site pain rates in the COVID-19 group. The I2 statistic was used to quantify the heterogeneity of the effects among the included studies. A sensitivity analysis was perform to determine the robustness of the results. The "META" package of the R software (version 4.1.1) was applied. A significant association was not recognized until the two-tailed P<0.05. A total of 9 articles involving 264674 patients were identified, including 7 RCTs and 2 observational studies. Table 1 describes the detailed characteristics of the effectiveness and safety studies. 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 Seven studies have shown that the overall effectiveness of the COVID-19 vaccine is 96.09% (95% confidence interval [CI]:93.35–98.90, p<0.01) (Figure. 1 A), of the attenuated vaccine is 95.05% (95% [CI]:90.21-100.16, p<0.01) (Figure. 1A), and the inactivated vaccine 97.32% (95% [CI];95.17-99.52, p>0.01) (Figure.1A). Safety is important for children. In 5 studies, we found that the adverse reaction was 0.59 (95% [CI]; 0.45-0.73, p<0.01) (Figure.1B). The adverse reaction of the attenuated vaccine was 0.78 (95% [CI]: 0.62-0.94, p<0.01) (Figure.1B), the adverse reaction of the inactivated vaccine was 0.47 (95% [CI]: 0.19-0.75, p<0.01) (Figure.1B) The adverse reactions of inactivated vaccines are significantly less than that of attenuated vaccines. We also counted the pain at the injection site. In 7 studies, the pain at the injection site was 0.58 (95% [CI]: 0.43-0.72, p <0.01) (Figure.1C), the injection pain of the attenuated vaccine was 0.78 (95% [CI]:0.60-0.95, p<0.01) (Figure. 1C), the injection pain of the inactivated vaccine was 0.30(95 % [CI]: 0.17-0.43, p<0.01)(Figure. 1C), the injection of inactivated vaccine is less painful and more friendly to children and adolescents. Table 1 The basic information of the included literature. Table 1 Study Population Study type Country Intervention All person controls Vaccine efficacy(95%CI) Injection-site pain Adverse reactions E.B.Walter.et.al2 5-11years Randomized controlled trial United States BNT162b2 mRNA 2268 750 90.7% (95% CI, 67.7- 98.3) 1093 / /Robert W. Frenck.et.al.3 12-15years Randomized controlled trial United States BNT162b2 mRNA 2260 1129 100% (95% CI, 78.1 to 100) 939 / Samantha M. Olson.et.al.4 12-18years Randomized controlled trial United States Pfizer-BioNTech mRNA.2doses 464 285 93% (95% CI = 83%-97%) / / Anne M. Hause.et.al.5 12-17years observational study United States BNT162b2 mRNA 66550 / / 41927 46585 Aharona Glatman-Freedman.et.al.6 12-15years observational study Israel BNT162b2 mRNA 187707 / 91.5% (95% CI 88.2%–93.9% / / Kashif Ali.et.al.7 12-17years Randomized controlled trial United States mRNA-1273 3732 1243 98.8(95%CI= 97.0 to 99.7) 2290 2140 Bihua Han.et.al8 3–17 years Randomized controlled trial China CoronaVac 333 114 96•8% [95%CI= 93•1-98•8] 35 59 Fengcai Zhu.et.al.9 6-17years Randomized controlled trial China Recombinant Adenovirus Type-5–Vectored Coronavirus 150 50 98.0% (95%CI= 93.0–99.5) 50 82 ShengLi Xia.et.al.10 3–17years Randomized controlled trial China BBIBP-CorV 810 90 100% 53 229 Figure 1 Forest plot of Vaccine efficacy(95%CI), njection-site pain, and Adverse reactions. Figure 1 In conclusion, our research shows that the current COVID-19 vaccine for children is effective and safe, and is more effective than the adult COVID-19 vaccine. There is a gap between the effectiveness of attenuated and inactivated vaccines, and the effectiveness of inactivated vaccines is the highest. We found that the inactivated vaccine is less painful at the injection site and is more friendly to children and adolescents. More carefully designed further studies based on risk factor adjusted estimates are necessary to confirm our findings. Funding This study was supported by Hangzhou Science and Technology Bureau fund (No. 20191203B96;No. 20191203B105;No. 20191231Y039); Youth Fund of Zhejiang Academy of Medical Sciences (No. 2019Y009); Medical and Technology Project of Zhejiang Province (No. 2020362651, No.2021KY890); Clinical Research Fund of Zhejiang Medical Association (No. 2020ZYC-A13); Hangzhou Health and Family Planning Technology Plan Key Projects (No.2017ZD02);Hangzhou Medical and Health Technology Project (No. 0020290592). Zhejiang Traditional Chinese Medicine Scientific Research Fund Project(No.2022ZB280). Data Sharing Statement All the data and materials mentioned in the manuscript are available. Ethics Approval and Consent to Participate This study was approved by the ethics committee of Affiliated Hospital of Hangzhou Normal University. This study was carried out according to the Declaration of Helsinki. Disclosure of interest The authors declare no competing interests.

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          Most cited references10

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          Safety and immunogenicity of an inactivated SARS-CoV-2 vaccine, BBIBP-CorV: a randomised, double-blind, placebo-controlled, phase 1/2 trial

          Background The ongoing COVID-19 pandemic warrants accelerated efforts to test vaccine candidates. We aimed to assess the safety and immunogenicity of an inactivated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine candidate, BBIBP-CorV, in humans. Methods We did a randomised, double-blind, placebo-controlled, phase 1/2 trial at Shangqiu City Liangyuan District Center for Disease Control and Prevention in Henan Province, China. In phase 1, healthy people aged 18–80 years, who were negative for serum-specific IgM/IgG antibodies against SARS-CoV-2 at the time of screening, were separated into two age groups (18–59 years and ≥60 years) and randomly assigned to receive vaccine or placebo in a two-dose schedule of 2 μg, 4 μg, or 8 μg on days 0 and 28. In phase 2, healthy adults (aged 18–59 years) were randomly assigned (1:1:1:1) to receive vaccine or placebo on a single-dose schedule of 8 μg on day 0 or on a two-dose schedule of 4 μg on days 0 and 14, 0 and 21, or 0 and 28. Participants within each cohort were randomly assigned by stratified block randomisation (block size eight) and allocated (3:1) to receive vaccine or placebo. Group allocation was concealed from participants, investigators, and outcome assessors. The primary outcomes were safety and tolerability. The secondary outcome was immunogenicity, assessed as the neutralising antibody responses against infectious SARS-CoV-2. This study is registered with www.chictr.org.cn, ChiCTR2000032459. Findings In phase 1, 192 participants were enrolled (mean age 53·7 years [SD 15·6]) and were randomly assigned to receive vaccine (2 μg [n=24], 4 μg [n=24], or 8 μg [n=24] for both age groups [18–59 years and ≥60 years]) or placebo (n=24). At least one adverse reaction was reported within the first 7 days of inoculation in 42 (29%) of 144 vaccine recipients. The most common systematic adverse reaction was fever (18–59 years, one [4%] in the 2 μg group, one [4%] in the 4 μg group, and two [8%] in the 8 μg group; ≥60 years, one [4%] in the 8 μg group). All adverse reactions were mild or moderate in severity. No serious adverse event was reported within 28 days post vaccination. Neutralising antibody geometric mean titres were higher at day 42 in the group aged 18–59 years (87·7 [95% CI 64·9–118·6], 2 μg group; 211·2 [158·9–280·6], 4 μg group; and 228·7 [186·1–281·1], 8 μg group) and the group aged 60 years and older (80·7 [65·4–99·6], 2 μg group; 131·5 [108·2–159·7], 4 μg group; and 170·87 [133·0–219·5], 8 μg group) compared with the placebo group (2·0 [2·0–2·0]). In phase 2, 448 participants were enrolled (mean age 41·7 years [SD 9·9]) and were randomly assigned to receive the vaccine (8 μg on day 0 [n=84] or 4 μg on days 0 and 14 [n=84], days 0 and 21 [n=84], or days 0 and 28 [n=84]) or placebo on the same schedules (n=112). At least one adverse reaction within the first 7 days was reported in 76 (23%) of 336 vaccine recipients (33 [39%], 8 μg day 0; 18 [21%], 4 μg days 0 and 14; 15 [18%], 4 μg days 0 and 21; and ten [12%], 4 μg days 0 and 28). One placebo recipient in the 4 μg days 0 and 21 group reported grade 3 fever, but was self-limited and recovered. All other adverse reactions were mild or moderate in severity. The most common systematic adverse reaction was fever (one [1%], 8 μg day 0; one [1%], 4 μg days 0 and 14; three [4%], 4 μg days 0 and 21; two [2%], 4 μg days 0 and 28). The vaccine-elicited neutralising antibody titres on day 28 were significantly greater in the 4 μg days 0 and 14 (169·5, 95% CI 132·2–217·1), days 0 and 21 (282·7, 221·2–361·4), and days 0 and 28 (218·0, 181·8–261·3) schedules than the 8 μg day 0 schedule (14·7, 11·6–18·8; all p<0·001). Interpretation The inactivated SARS-CoV-2 vaccine, BBIBP-CorV, is safe and well tolerated at all tested doses in two age groups. Humoral responses against SARS-CoV-2 were induced in all vaccine recipients on day 42. Two-dose immunisation with 4 μg vaccine on days 0 and 21 or days 0 and 28 achieved higher neutralising antibody titres than the single 8 μg dose or 4 μg dose on days 0 and 14. Funding National Program on Key Research Project of China, National Mega projects of China for Major Infectious Diseases, National Mega Projects of China for New Drug Creation, and Beijing Science and Technology Plan.
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            Safety, Immunogenicity, and Efficacy of the BNT162b2 Covid-19 Vaccine in Adolescents

            Background Until very recently, vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had not been authorized for emergency use in persons younger than 16 years of age. Safe, effective vaccines are needed to protect this population, facilitate in-person learning and socialization, and contribute to herd immunity. Methods In this ongoing multinational, placebo-controlled, observer-blinded trial, we randomly assigned participants in a 1:1 ratio to receive two injections, 21 days apart, of 30 μg of BNT162b2 or placebo. Noninferiority of the immune response to BNT162b2 in 12-to-15-year-old participants as compared with that in 16-to-25-year-old participants was an immunogenicity objective. Safety (reactogenicity and adverse events) and efficacy against confirmed coronavirus disease 2019 (Covid-19; onset, ≥7 days after dose 2) in the 12-to-15-year-old cohort were assessed. Results Overall, 2260 adolescents 12 to 15 years of age received injections; 1131 received BNT162b2, and 1129 received placebo. As has been found in other age groups, BNT162b2 had a favorable safety and side-effect profile, with mainly transient mild-to-moderate reactogenicity (predominantly injection-site pain [in 79 to 86% of participants], fatigue [in 60 to 66%], and headache [in 55 to 65%]); there were no vaccine-related serious adverse events and few overall severe adverse events. The geometric mean ratio of SARS-CoV-2 50% neutralizing titers after dose 2 in 12-to-15-year-old participants relative to 16-to-25-year-old participants was 1.76 (95% confidence interval [CI], 1.47 to 2.10), which met the noninferiority criterion of a lower boundary of the two-sided 95% confidence interval greater than 0.67 and indicated a greater response in the 12-to-15-year-old cohort. Among participants without evidence of previous SARS-CoV-2 infection, no Covid-19 cases with an onset of 7 or more days after dose 2 were noted among BNT162b2 recipients, and 16 cases occurred among placebo recipients. The observed vaccine efficacy was 100% (95% CI, 75.3 to 100). Conclusions The BNT162b2 vaccine in 12-to-15-year-old recipients had a favorable safety profile, produced a greater immune response than in young adults, and was highly effective against Covid-19. (Funded by BioNTech and Pfizer; C4591001 ClinicalTrials.gov number, NCT04368728 .)
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              Evaluation of the BNT162b2 Covid-19 Vaccine in Children 5 to 11 Years of Age

              Background Safe, effective vaccines against coronavirus disease 2019 (Covid-19) are urgently needed in children younger than 12 years of age. Methods A phase 1, dose-finding study and an ongoing phase 2–3 randomized trial are being conducted to investigate the safety, immunogenicity, and efficacy of two doses of the BNT162b2 vaccine administered 21 days apart in children 6 months to 11 years of age. We present results for 5-to-11-year-old children. In the phase 2–3 trial, participants were randomly assigned in a 2:1 ratio to receive two doses of either the BNT162b2 vaccine at the dose level identified during the open-label phase 1 study or placebo. Immune responses 1 month after the second dose of BNT162b2 were immunologically bridged to those in 16-to-25-year-olds from the pivotal trial of two 30-μg doses of BNT162b2. Vaccine efficacy against Covid-19 at 7 days or more after the second dose was assessed. Results During the phase 1 study, a total of 48 children 5 to 11 years of age received 10 μg, 20 μg, or 30 μg of the BNT162b2 vaccine (16 children at each dose level). On the basis of reactogenicity and immunogenicity, a dose level of 10 μg was selected for further study. In the phase 2–3 trial, a total of 2268 children were randomly assigned to receive the BNT162b2 vaccine (1517 children) or placebo (751 children). At data cutoff, the median follow-up was 2.3 months. In the 5-to-11-year-olds, as in other age groups, the BNT162b2 vaccine had a favorable safety profile. No vaccine-related serious adverse events were noted. One month after the second dose, the geometric mean ratio of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) neutralizing titers in 5-to-11-year-olds to those in 16-to-25-year-olds was 1.04 (95% confidence interval [CI], 0.93 to 1.18), a ratio meeting the prespecified immunogenicity success criterion (lower bound of two-sided 95% CI, >0.67; geometric mean ratio point estimate, ≥0.8). Covid-19 with onset 7 days or more after the second dose was reported in three recipients of the BNT162b2 vaccine and in 16 placebo recipients (vaccine efficacy, 90.7%; 95% CI, 67.7 to 98.3). Conclusions A Covid-19 vaccination regimen consisting of two 10-μg doses of BNT162b2 administered 21 days apart was found to be safe, immunogenic, and efficacious in children 5 to 11 years of age. (Funded by BioNTech and Pfizer; ClinicalTrials.gov number, NCT04816643 .)
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                Author and article information

                Journal
                J Infect
                J Infect
                The Journal of Infection
                The British Infection Association. Published by Elsevier Ltd.
                0163-4453
                1532-2742
                31 January 2022
                31 January 2022
                Affiliations
                [a ]Hangzhou Institute of Cardiovascular Diseases, Affiliated Hospital of Hangzhou Normal University, Hangzhou, 310015, China
                [b ]Hangzhou Normal University, Hangzhou, 311121, China
                [c ]School of Public Health, Hangzhou Medical College, Hangzhou, 311300, China
                [d ]Department of Molecular & Cellular Physiology, Shinshu University School of Medicine, 3900803, Japan
                [e ]Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, China
                Author notes
                [* ]Corresponding Author:
                Article
                S0163-4453(22)00050-0
                10.1016/j.jinf.2022.01.032
                8802164
                f73e35fd-d3d7-488e-a5f8-12de54e6c5ab
                © 2022 The British Infection Association. Published by Elsevier Ltd. All rights reserved.

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                Infectious disease & Microbiology
                Infectious disease & Microbiology

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