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Risk of vaccine preventable diseases in UK migrants: A serosurvey and concordance analysis.

Gogoi, M; Martin, CA; Bird, PW; Wiselka, MJ; Gardener, J; Ellis, K; Renals, V; Lewszuk, AJ; Hargreaves, S; Pareek, M (2024) Risk of vaccine preventable diseases in UK migrants: A serosurvey and concordance analysis. J Migr Health, 9. p. 100217. ISSN 2666-6235 https://doi.org/10.1016/j.jmh.2024.100217
SGUL Authors: Hargreaves, Sally

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Abstract

BACKGROUND: Vaccine preventable diseases (VPDs) such as measles and rubella cause significant morbidity and mortality globally every year. The World Health Organization (WHO), reported vaccine coverage for both measles and rubella to be 71 % in 2019, indicating an immunity gap. Migrants in the EU/EEA may be at high risk of VPDs due to under-immunisation and poor living conditions. However, there are limited data on VPD seroprotection rates amongst migrants living in the United Kingdom (UK). METHODS: We conducted an exploratory cross-sectional serosurvey amongst a sample of adult migrants living in Leicester, UK to: (a) determine seroprotection rates for measles, varicella zoster, and rubella in this group; (b) identify risk factors associated with seronegativity and, (c) understand if self-reported vaccine or diseases history is an effective measure of seroprotection. Participants gave a blood sample and completed a questionnaire asking basic demographic details and vaccine and disease history for the three VPDs. We summarised the data using median and interquartile range (IQR) for non-parametric continuous variables and count and percentage for categorical variables. We used logistic regression to establish predictors of seroprotection against these diseases. We examined the reliability of self-reported vaccination/disease history for prediction of seroprotection through a concordance analysis. RESULTS: 149 migrants were included in the analysis. Seroprotection rates were: varicella zoster 98 %, rubella 92.6 % and measles 89.3 %. Increasing age was associated with seroprotection (OR 1.07 95 % CI 1.01-1.13 for each year increase in age). Migrants from Africa and the Middle East (aOR 15.16 95 % CI 1.31 - 175.06) and South/East Asia and Pacific regions (aOR 15.43 95 %CI 2.38 - 100.00) are significantly more likely to be seroprotected against measles as compared to migrants from Europe and Central Asia. The proportions of migrants unsure about their vaccination and disease history combined were 53.0 % for measles; 57.7 % for rubella; 43.0 % for varicella. There was no agreement between self-reported vaccination/disease history and serostatus. CONCLUSION: Our findings suggest lower levels of seroprotection against measles in migrants living in Leicester, UK, with younger migrants and those from Europe and Central Asia more likely to lack seroprotection. A high proportion of surveyed migrants were unaware of their vaccination/disease history and self-reported vaccine/disease was a poor predictor of seroprotection against VPDs which is important for clinical decision-making regarding catch-up vaccination in this population. Our results, although derived from a small sample, suggest that there may be gaps in seroimmunity for certain VPDs in particular migrant populations. These findings should inform future qualitative studies investigating barriers to vaccine uptake in migrants and population-level seroprevalence studies aimed at determining individualised risk profiles based on demographic and migration factors.

Item Type: Article
Additional Information: © 2024 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Keywords: Measles, Migrant, Rubella, Seroprotection, Vaccination, Vaccine preventable diseases, Varicella, Migrant, Vaccination, Seroprotection, Vaccine preventable diseases, Measles, Varicella, Rubella
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: J Migr Health
ISSN: 2666-6235
Language: eng
Dates:
DateEvent
1 March 2024Published
25 February 2024Published Online
22 February 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/V027549/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
NIHR300072National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
SBF005\1111Academy of Medical Scienceshttp://dx.doi.org/10.13039/501100000691
MRC/N013638/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
PubMed ID: 38455071
Web of Science ID: WOS:001202860400001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116475
Publisher's version: https://doi.org/10.1016/j.jmh.2024.100217

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