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Immunogenicity and safety of heterologous versus homologous prime-boost schedules with an adenoviral vectored and mRNA COVID-19 vaccine: a systematic review.
Lv, Jingjing; Wu, Hui; Xu, Junjie; Liu, Jiaye.
  • Lv J; Expanded Program Immunization Division of Shandong Provincial Center for Disease Control and Prevention, Shandong Provincial Key Laboratory of Infectious Disease Control and Prevention, Jinan, 250014, China.
  • Wu H; Nosocomial Infection Control Department, Shenzhen University General Hospital, Shenzhen, 518071, China.
  • Xu J; Clinical Research Academy, Peking University Shenzhen Hospital, Peking University, Shenzhen, 518036, China.
  • Liu J; School of Public Health, Shenzhen University Health Science Center, No. 1066 Xueyuan Avenue, Shenzhen, 518060, China. liujiaye1984@163.com.
Infect Dis Poverty ; 11(1): 53, 2022 May 13.
Article in English | MEDLINE | ID: covidwho-1846871
ABSTRACT

BACKGROUND:

Heterologous prime-boost with ChAdOx1 nCoV-19 vector vaccine (ChAd) and a messenger RNA vaccine (BNT or mRNA-1273) has been widely facilitating mass coronavirus disease 2019 (COVID-19) immunisation. This review aimed to synthesize immunogenicity and reactogenicity of heterologous immunisations with ChAd and BNT (mRNA-1273) vaccine compared with homologous ChAd or BNT (mRNA-1273) immunisation.

METHODS:

PubMed, Web of Science, and Embase databases were searched from inception to March 7, 2022. Immunogenicity involving serum antibodies against different SAS-CoV-2 fragments, neutralizing antibody, or spike-specific T cells response were compared. Any, local and systemic reactions were pooled by meta-analysis for comparison.

RESULTS:

Of 14,571 records identified, 13 studies (3024 participants) were included for analysis. Compared with homologous BNT/BNT vaccination, heterologous ChAd/BNT schedule probably induced noninferior anti-spike protein while higher neutralizing antibody and better T cells response. Heterologous ChAd/BNT (mRNA-1273) immunisation induced superior anti-spike protein and higher neutralizing antibody and better T cells response compared with homologous ChAd/ChAd vaccination. Heterologous ChAd/BNT (mRNA-1273) had similar risk of any reaction (RR = 1.30, 95% CI 0.86-1.96) while higher risk of local reactions (RR = 1.65, 95% CI 1.27-2.15) and systemic reactions (RR = 1.49, 95% CI 1.17-1.90) compared with homologous ChAd/ChAd vaccination. There was a higher risk of local reactions (RR = 1.16, 95% CI 1.03-1.31) in heterologous ChAd/BNT (mRNA-1273) vaccination compare with homologous BNT/BNT but a similar risk of any reaction (RR = 1.03, 95% CI 0.79-1.34) and systemic reactions (RR = 0.89, 95% CI 0.60-1.30).

CONCLUSIONS:

Heterologous ChAd/BNT schedule induced at least comparable immunogenicity compared with homologous BNT/BNT and better immunogenicity compared with homologous ChAd/ChAd vaccination. The synthetical evidence supported the general application of heterologous prime-boost vaccination using ChAd and BNT COVID-19 vaccines.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study / Reviews / Systematic review/Meta Analysis Topics: Vaccines Limits: Humans Language: English Journal: Infect Dis Poverty Year: 2022 Document Type: Article Affiliation country: S40249-022-00977-x

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study / Reviews / Systematic review/Meta Analysis Topics: Vaccines Limits: Humans Language: English Journal: Infect Dis Poverty Year: 2022 Document Type: Article Affiliation country: S40249-022-00977-x