Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-23T21:43:04.221Z Has data issue: false hasContentIssue false

Optimising COVID-19 vaccine efficacy by ensuring nutritional adequacy

Published online by Cambridge University Press:  28 January 2021

Margaret P. Rayman
Affiliation:
Department of Nutritional Sciences, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK
Philip C. Calder*
Affiliation:
Faculty of Medicine, University of Southampton, Southampton, UK NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK
Rights & Permissions [Opens in a new window]

Abstract

Type
Letter to the Editor
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society

Now that a number of COVID-19 vaccines are being employed to control the current pandemic, we are concerned about the likelihood of a poor response in the frail or malnourished elderly which would reduce the effectiveness of the vaccination campaigns.

Older people have a weakened immune response(Reference Pawelec, Larbi and Derhovanessian1,Reference Agarwal and Busse2) and are known to respond less well than middle-aged adults to many vaccines including the seasonal influenza vaccine(Reference Goodwin, Viboud and Simonsen3,Reference Pera, Campos and Lopez4) . We note that the Oxford vaccine trial recruited older participants with ‘few comorbidities, [who] might not be representative of the general older population, including those living in residential care settings or older than 80 years’(Reference Ramasamy, Minassian and Ewer5). Both the 56–69 and ≥70-year-old groups showed a lower IgG response and lower neutralising antibody titres to a single dose of the Oxford vaccine than did the 18–55-year-olds(Reference Ramasamy, Minassian and Ewer5). Hence, in the real-world setting, weaker older people may not gain the desired clinical protection from the vaccine and resource may be wasted. Poor vaccination responses in older people are related not only to frailty(Reference Yao, Hamilton and Weng6) which cannot be easily remedied, but also to deficiencies in micronutrients, which can be addressed.

An effective immune response requires an adequate host nutritional status(Reference Calder7). In recognising this, the European Food Safety Authority has authorised nutrient function health claims for vitamins A (including β-carotene), B6, B9 (folate), B12, C and D, and the minerals Zn, Se, Fe and Cu based on scientific assessment of their contributions to the normal functioning of the immune system(8). Each of these micronutrients, as well as vitamin E, has been shown to have multiple key roles in supporting the immune system and reducing the risk of infections. This is detailed in recent comprehensive reviews that attest the importance of individual micronutrients to the immune response and explain the multiple mechanisms of action involved(Reference Gombart, Pierre and Maggini9,Reference Calder10) . Human studies, particularly in the elderly, have associated impairments in immune markers to low status of micronutrients such as vitamin B6, vitamin C, Zn and Fe (for references, see Gombart et al. (Reference Gombart, Pierre and Maggini9) and Calder(Reference Calder7,Reference Calder10) ). Such immune impairments have been linked to poor vaccine responses. For example, a systematic review and meta-analysis of nine studies involving 2367 individuals found lower seroprotection rates to influenza A virus subtype H3N2 and to influenza B virus in those who were vitamin D deficient(Reference Lee, Lin and Lei11). By contrast, randomised controlled trials of supplemental micronutrients (e.g. vitamin B6, vitamin E, Zn and Se) in older people report enhancements in many of the immune biomarkers measured (for references, see Gombart et al. (Reference Gombart, Pierre and Maggini9) and Calder(Reference Calder10)). In surveying the literature in this field, it appears that vitamins C, D and E together with Zn and Se are needed by the immune system in excess of amounts that can usually be achieved through diet alone(Reference Gombart, Pierre and Maggini9,Reference Calder10) . As an example, Se status above that required for optimal selenoprotein function has been associated with better cure rate from COVID-19(Reference Zhang, Taylor and Bennett12).

A cause-and-effect relationship between micronutrient status and vaccination responses has been demonstrated through randomised controlled trials. Such trials in older people have shown better responses to vaccination after an intervention. For example, a randomised controlled trial of ≥5 servings of fruits and vegetables per d compared with ≤2 servings in people aged 65–85 years reported a better response to pneumococcal vaccination in the group consuming the higher amount of fruits and vegetables(Reference Gibson, Edgar and Neville13). A study of vitamin E demonstrated improvement in response to some vaccines in individuals aged over 65 years given 60 or 200 mg vitamin E/d compared with those in the placebo group(Reference Meydani, Meydani and Blumberg14). Se supplementation (50 or 100 μg/d) in adults in the UK with low Se status improved some aspects of their immune response to a poliovirus vaccine and also reduced the emergence of mutant viral strains(Reference Broome, McArdle and Kyle15).

Nutritional deficiency and malnutrition are common in the elderly. In a systematic review of intake and deficiency of eight trace elements in adults ≥ 60 years in seven Western countries, consistent nutritional insufficiency was found for Se, Zn, iodine and Cu(Reference Vural, Avery and Kalogiros16). Notably, Zn deficiency was observed in 31 and 49 % of community-based women and men, respectively, and in 50 and 66 % of women and men in institutional care(Reference Vural, Avery and Kalogiros16). Se intake was similarly compromised with deficiency found in 49 % of women and 37 % of men in the community and in 44 % of women and 27 % of men in institutions(Reference Vural, Avery and Kalogiros16). Significant proportions of both populations showed insufficiency for Fe, iodine and Cu(Reference Vural, Avery and Kalogiros16). Specific to the UK, the 2019 National Diet and Nutrition Survey showed ‘a sustained worsening of the dietary intakes and chronic shortages of several of the nutrients involved in supporting the normal immune functions’; these included vitamins A, B12, C and D and the trace minerals Zn, Se and Cu(Reference Richardson and Lovegrove17). Such micronutrient deficiencies may limit the effectiveness of the COVID vaccines.

We propose that a nutritional supplement (e.g. containing vitamins A, B6, B9, B12, C, D and E and the minerals Zn, Cu, Se and Fe) should be provided free of charge to all those aged over 70 years for a period of weeks before and after they receive the vaccine. The additional cost of providing a supplement of those nutrients important to immune function that are likely to be insufficient or deficient in the elderly would be a small investment to better assure a robust vaccine response. It is possible to buy a multivitamin and mineral supplement, retail, for around £1·50 (US$2) per forty-five tablets. A 45-d supply of the supplement, purchased wholesale, would provide great potential gain and would add only a modest cost to any vaccination programme: the US Government negotiated price of the Pfizer vaccine is US$20 per dose (i.e. US$40 per full treatment), the Moderna vaccine is costed at US$10–$50 per dose with the European Union negotiating a cost of up to US$25 per dose (i.e. US$50 per full treatment), while the cost of the Astra Zeneca vaccine to the US Government is US$4 per dose (i.e. US$8 per full treatment)(Reference Cao18).

References

Pawelec, G, Larbi, A & Derhovanessian, E (2010) Senescence of the human immune system. J Comp Pathol 142, Suppl. 1, S39S44.CrossRefGoogle ScholarPubMed
Agarwal, S & Busse, PJ (2010) Innate and adaptive immunosenescence. Ann Allergy Asthma Immunol 104, 183190.CrossRefGoogle ScholarPubMed
Goodwin, K, Viboud, C & Simonsen, L (2006) Antibody response to influenza vaccination in the elderly: a quantitative review. Vaccine 24, 11591169.CrossRefGoogle ScholarPubMed
Pera, A, Campos, C, Lopez, N, et al. (2015) Immunosenescence: implications for response to infection and vaccination in older people. Maturitas 82, 5055.CrossRefGoogle ScholarPubMed
Ramasamy, MN, Minassian, AM, Ewer, KJ, et al. (2021) Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled phase 2/3 trial. Lancet 396, 19791993.CrossRefGoogle Scholar
Yao, X, Hamilton, RG, Weng, N-P, et al. (2011) Frailty is associated with impairment of vaccine-induced antibody response and increase in post-vaccination influenza infection in community-dwelling older adults. Vaccine 39, 50155021.CrossRefGoogle Scholar
Calder, PC (2013) Feeding the immune system. Proc Nutr Soc 72, 299309.CrossRefGoogle ScholarPubMed
European Commission of the European Union (2020) EU Register of nutrition and health claims made on foods. https://ec.europa.eu/food/safety/labelling_nutrition/claims/register/public/?event=register.home (accessed July 2020).Google Scholar
Gombart, AF, Pierre, A & Maggini, S (2020) A review of micronutrients and the immune system – working in harmony to reduce the risk of infection. Nutrients 12, 236.CrossRefGoogle Scholar
Calder, PC (2020) Nutrition, immunity and COVID-19. BMJ Nutr Prev Health 3, e000085.CrossRefGoogle ScholarPubMed
Lee, M-D, Lin, C-H, Lei, W-T, et al. (2018) Does vitamin D deficiency affect the immunogenic responses to influenza vaccination? A systematic review and meta-analysis. Nutrients 10, 409.CrossRefGoogle ScholarPubMed
Zhang, J, Taylor, EW, Bennett, K, et al. (2020) Association between regional selenium status and reported outcome of COVID-19 cases in China. Am J Clin Nutr 111, 12971299.CrossRefGoogle ScholarPubMed
Gibson, A, Edgar, JD, Neville, CE, et al. (2012) Effect of fruit and vegetable consumption on immune function in older people: a randomized controlled trial. Am J Clin Nutr 96, 14291436.CrossRefGoogle ScholarPubMed
Meydani, SN, Meydani, M, Blumberg, JB, et al. (1997) Vitamin E supplementation and in vivo immune response in healthy elderly subjects. JAMA 277, 13801386.CrossRefGoogle ScholarPubMed
Broome, CS, McArdle, F, Kyle, JAM, et al. (2004) An increase in selenium intake improves immune function and poliovirus handling in adults with marginal selenium status. Am J Clin Nutr 80, 154162.CrossRefGoogle ScholarPubMed
Vural, Z, Avery, A, Kalogiros, DI, et al. (2020) Trace mineral intake and deficiencies in older adults living in the community and institutions: a systematic review. Nutrients 12, 107.CrossRefGoogle ScholarPubMed
Richardson, DP & Lovegrove, JA (2020) Nutritional status of micronutrients as a possible and modifiable risk factor for COVID-19: a UK perspective. Br J Nutr (epublication ahead of print version 20 August 2020).Google ScholarPubMed
Cao, S (2020) COVID-19 Vaccine Prices Revealed From Pfizer, Moderna, and AstraZeneca. https://observer.com/2020/11/covid19-vaccine-price-pfizer-moderna-astrazeneca-oxford/ (accessed January 2021).Google Scholar