Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis

Background Vaccine supply shortages are of global concern. We hypothesise that intradermal (ID) immunisation as an alternative to standard routes might augment vaccine supply utilisation without loss of vaccine immunogenicity and efficacy. Methods We conducted a systematic review and meta-analysis s...

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Autores:
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
eng
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/13284
Acceso en línea:
https://doi.org/10.1016/j.tmaid.2020.101868
http://hdl.handle.net/20.500.12010/13284
Palabra clave:
Drug administration routes
Intradermal injection
Intramuscular injection
Subcutaneous injection
Antibody response
Immunisation
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
Rights
License
Abierto (Texto Completo)
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oai_identifier_str oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/13284
network_acronym_str UTADEO2
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dc.title.spa.fl_str_mv Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
title Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
spellingShingle Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
Drug administration routes
Intradermal injection
Intramuscular injection
Subcutaneous injection
Antibody response
Immunisation
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
title_short Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
title_full Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
title_fullStr Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
title_full_unstemmed Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
title_sort Fractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysis
dc.subject.spa.fl_str_mv Drug administration routes
Intradermal injection
Intramuscular injection
Subcutaneous injection
Antibody response
Immunisation
topic Drug administration routes
Intradermal injection
Intramuscular injection
Subcutaneous injection
Antibody response
Immunisation
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
dc.subject.lemb.spa.fl_str_mv Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
description Background Vaccine supply shortages are of global concern. We hypothesise that intradermal (ID) immunisation as an alternative to standard routes might augment vaccine supply utilisation without loss of vaccine immunogenicity and efficacy. Methods We conducted a systematic review and meta-analysis searching Medline, Embase and Web of Science databases. Studies were included if: licensed, currently available vaccines were used; fractional dose of ID was compared to IM or SC immunisation; primary immunisation schedules were evaluated; immunogenicity, safety data and/or cost were reported. We calculated risk differences (RD). Studies were included in meta-analysis if: a pre-defined immune correlate of protection was assessed; WHO-recommend schedules and antigen doses were used in the control group; the same schedule was applied to both ID and control groups (PROSPERO registration no. CRD42020151725). Results The primary search yielded 5,873 articles, of which 156 articles were included; covering 12 vaccines. Non-inferiority of immunogenicity with 20-60% of antigen used with ID vaccines was demonstrated for influenza (H1N1: RD -0·01; 95% CI -0·02, 0·01; I 2 = 55%, H2N3: RD 0·00; 95% CI -0·01, 0·01; I2 = 0%, B: RD -0·00; 95% CI -0·02, 0·01; I2 = 72%), rabies (RD 0·00; 95% CI -0·02, 0·02; I2 = 0%), and hepatitis B vaccines (RD -0·01; 95% CI -0·04, 0·02; I2 = 20%). Clinical trials on the remaining vaccines yielded promising results, but are scarce. Conclusions There is potential for inoculum/antigen dose-reduction by using ID immunisation as compared to standard routes of administration for some vaccines (e.g. influenza, rabies). When suitable, vaccine trials should include an ID arm.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-09-15T19:56:43Z
dc.date.available.none.fl_str_mv 2020-09-15T19:56:43Z
dc.date.created.none.fl_str_mv 2020
dc.type.local.spa.fl_str_mv Artículo
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
format http://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.issn.spa.fl_str_mv 1477-8939
dc.identifier.other.spa.fl_str_mv https://doi.org/10.1016/j.tmaid.2020.101868
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/13284
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.1016/j.tmaid.2020.101868
identifier_str_mv 1477-8939
url https://doi.org/10.1016/j.tmaid.2020.101868
http://hdl.handle.net/20.500.12010/13284
dc.language.iso.spa.fl_str_mv eng
language eng
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dc.rights.local.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
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dc.format.extent.spa.fl_str_mv 82 páginas
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dc.source.spa.fl_str_mv reponame:Expeditio Repositorio Institucional UJTL
instname:Universidad de Bogotá Jorge Tadeo Lozano
instname_str Universidad de Bogotá Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
reponame_str Expeditio Repositorio Institucional UJTL
collection Expeditio Repositorio Institucional UJTL
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spelling 2020-09-15T19:56:43Z2020-09-15T19:56:43Z20201477-8939https://doi.org/10.1016/j.tmaid.2020.101868http://hdl.handle.net/20.500.12010/13284https://doi.org/10.1016/j.tmaid.2020.101868Background Vaccine supply shortages are of global concern. We hypothesise that intradermal (ID) immunisation as an alternative to standard routes might augment vaccine supply utilisation without loss of vaccine immunogenicity and efficacy. Methods We conducted a systematic review and meta-analysis searching Medline, Embase and Web of Science databases. Studies were included if: licensed, currently available vaccines were used; fractional dose of ID was compared to IM or SC immunisation; primary immunisation schedules were evaluated; immunogenicity, safety data and/or cost were reported. We calculated risk differences (RD). Studies were included in meta-analysis if: a pre-defined immune correlate of protection was assessed; WHO-recommend schedules and antigen doses were used in the control group; the same schedule was applied to both ID and control groups (PROSPERO registration no. CRD42020151725). Results The primary search yielded 5,873 articles, of which 156 articles were included; covering 12 vaccines. Non-inferiority of immunogenicity with 20-60% of antigen used with ID vaccines was demonstrated for influenza (H1N1: RD -0·01; 95% CI -0·02, 0·01; I 2 = 55%, H2N3: RD 0·00; 95% CI -0·01, 0·01; I2 = 0%, B: RD -0·00; 95% CI -0·02, 0·01; I2 = 72%), rabies (RD 0·00; 95% CI -0·02, 0·02; I2 = 0%), and hepatitis B vaccines (RD -0·01; 95% CI -0·04, 0·02; I2 = 20%). Clinical trials on the remaining vaccines yielded promising results, but are scarce. Conclusions There is potential for inoculum/antigen dose-reduction by using ID immunisation as compared to standard routes of administration for some vaccines (e.g. influenza, rabies). When suitable, vaccine trials should include an ID arm.82 páginasapplication/pdfengreponame:Expeditio Repositorio Institucional UJTLinstname:Universidad de Bogotá Jorge Tadeo LozanoDrug administration routesIntradermal injectionIntramuscular injectionSubcutaneous injectionAntibody responseImmunisationSíndrome respiratorio agudo graveCOVID-19SARS-CoV-2CoronavirusFractional dose of intradermal compared to intramuscular and subcutaneous vaccination - A systematic review and meta-analysisArtículohttp://purl.org/coar/resource_type/c_2df8fbb1Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Schnyder, Jenny L.Pijper, Cornelis A. DeGarcia Garrido, Hannah M.Daams, Joost G.Goorhuis, AbrahamStijnis, CornelisSchaumburg, FriederGrobusch, Martin P.ORIGINALFractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdfFractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdfVer artículoapplication/pdf4152885https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13284/1/Fractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdf27975058bae59ae9eac0d7b8c34d1059MD51open accessLICENSElicense.txtlicense.txttext/plain; charset=utf-82938https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13284/2/license.txtabceeb1c943c50d3343516f9dbfc110fMD52open accessTHUMBNAILFractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdf.jpgFractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdf.jpgIM Thumbnailimage/jpeg12601https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13284/3/Fractional-dose-of-intradermal-compared-to-intramuscul_2020_Travel-Medicine-.pdf.jpgc5b2714468a87db093d909f07dedb71cMD53open access20.500.12010/13284oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/132842020-09-15 14:56:44.015open accessRepositorio Institucional - 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