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. 2022 Mar;10(3):e326-e328.
doi: 10.1016/S2214-109X(21)00593-3.

Response to additional COVID-19 vaccine doses in people who are immunocompromised: a rapid review

Affiliations

Response to additional COVID-19 vaccine doses in people who are immunocompromised: a rapid review

Edward P K Parker et al. Lancet Glob Health. 2022 Mar.
No abstract available

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Conflict of interest statement

The authors acknowledge the contributions of all members of the WHO Strategic Advisory Group of Experts (SAGE) on Immunization and the SAGE Working Group on COVID-19 Vaccines. EPKP is a consultant for the SAGE Working Group on COVID-19 vaccines. SD, MM, KLO’B, JH, and AW-S are staff of WHO. The authors alone are responsible for the views expressed in this article and they do not necessarily represent the views, decisions, or policies of the institutions with which they are affiliated. SK and HN are members of SAGE. DCK is a member of the SAGE Working Group on COVID-19 vaccines.

Figures

Figure
Figure
Antibody response rate following an additional COVID-19 vaccine dose in people who are immunocompromised (A) Cumulative antibody response rates before and after an additional dose in different patient subgroups across 13 studies with paired data. Lines link estimates from individual study populations. The same participants were measured before and after the additional dose. (B) Antibody response rates following an additional dose among patients with low or no detectable antibodies after the standard primary series (19 estimates from 17 studies). Note that antibody response criteria and patient characteristics varied among studies, restricting comparability (see appendix pp 3–5 for details). Estimates for subgroups receiving mRNA and vectored vaccines were extracted separately where possible. *Denominator includes patients who did not receive an additional dose but responded after the primary vaccine series. †Post-vaccination data available for a subset of the cohort.

References

    1. Williamson EJ, Walker AJ, Bhaskaran K, et al. Factors associated with COVID-19-related death using OpenSAFELY. Nature. 2020;584:430–436. - PMC - PubMed
    1. Yang X, Sun J, Patel RC, et al. Associations between HIV infection and clinical spectrum of COVID-19: a population level analysis based on US National COVID Cohort Collaborative (NC3) data. Lancet HIV. 2021;8:e690–e700. - PMC - PubMed
    1. Lee ARYB, Wong SY, Chai LYA, et al. Efficacy of COVID-19 vaccines in immunocompromised patients: a systematic review and meta-analysis. medRxiv. 2021 doi: 10.1101/2021.09.28.21264126. published online Oct 1. (preprint). - DOI - PMC - PubMed
    1. Young-Xu Y, Korves C, Roberts J, et al. Coverage and estimated effectiveness of mRNA COVID-19 vaccines among US veterans. JAMA Netw Open. 2021;4 - PMC - PubMed
    1. Whitaker HJ, Tsang RSM, Byford R, et al. Pfizer-BioNTech and Oxford AstraZeneca COVID-19 vaccine effectiveness and immune response among individuals in clinical risk groups. J Infect. 2022 doi: 10.1016/j.jinf.2021.12.044. published online Jan 3. - DOI - PMC - PubMed

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