No evidence of MMR induced trained immunity to prevent SARS COV2 : results from a multi-centre RCT

dc.contributor.authorDelany-Moretlwe, Sinead
dc.contributor.authorDehbi, Hakim-Moulay
dc.contributor.authorSikazwe, Izukanji
dc.contributor.authorKyei, George
dc.contributor.authorKoram, Kwadwo
dc.contributor.authorDubberke, Erik
dc.contributor.authorMwelase, Noluthando
dc.contributor.authorHague, Dominic;
dc.contributor.authorBekker, Linda-Gail
dc.contributor.authorYun, Linda
dc.contributor.authorNel, Annalene
dc.contributor.authorDu Toit, Leon
dc.contributor.authorBiccard, Bruce
dc.contributor.authorGill, Katherine
dc.contributor.authorChipeta, Chikumbutso
dc.contributor.authorMngadi, Kathryn T.
dc.contributor.authorLebina, Limakatso
dc.contributor.authorDassaye, Reshmi
dc.contributor.authorAsari, Villeshni
dc.contributor.authorFry, Samantha H.
dc.contributor.authorTurton, Edwin
dc.contributor.authorAhmed, Khatija
dc.contributor.authorKusi, Kwadwo
dc.contributor.authorAdu-Amankwah, Susan
dc.contributor.authorChilengi, Roma
dc.contributor.authorChilekwa, Joyce Chinyama
dc.contributor.authorLovat, Laurence
dc.contributor.authorMcGuckin, Dermot
dc.contributor.authorCaverly, Emilia
dc.contributor.authorPoliti, Mary
dc.contributor.authorSwan, Ben
dc.contributor.authorDeSchryver, Anne
dc.contributor.authorMckinnon, Sherry
dc.contributor.authorGupta, Ananya
dc.contributor.authorJones, Gemma
dc.contributor.authorFreemantle, Nicholas
dc.contributor.authorKhader, Shabaana
dc.contributor.authorRees, Helen
dc.contributor.authorNetea, Mihai G.
dc.contributor.authorMoonesinghe, S. Ramani
dc.contributor.authorAvidan, Michael S.
dc.date.accessioned2025-11-12T08:00:04Z
dc.date.available2025-11-12T08:00:04Z
dc.date.issued2025-09-16
dc.descriptionDATA AVAILABILITY STATEMENT : The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
dc.description.abstractBACKGROUND : Measles-containing vaccines (MCV), by training innate immune cells, are hypothesized to prevent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19). METHODS : In this international, double-blind, placebo-controlled trial, we randomly assigned adults, 18 years and older, to receive MCV or saline. The primary outcome was polymerase chain reaction (PCR) confirmed symptomatic COVID-19, up to 60 days after intervention. Secondary outcomes were PCR-confirmed symptomatic COVID-19 and serologically confirmed SARS-CoV-2 infection, up to 150 days after intervention. RESULTS : Of 3411 randomised participants, the modified intention-to-treat population included 1607 in the MCV and 1545 in the saline group. The estimated risk of symptomatic COVID-19 by 60 days was 1.5% in the MCV and 1.2% in the saline group (risk difference, 0.3 percentage points, 95% CI, -0.5 to 1.1; p=0.52). At 150 days, these percentages were 4.1% (65/1585) and 4.1% (64/1544) in the MCV and saline groups, respectively (risk difference, 0.04 percentage points, 95% CI, -1.4 to 1.3; p=0.95). Based on serology results available at 0 and 150 days, 10.6% (100/945) of participants in the MCV and 10.3% (98/951) in the saline group had infection with SARS-CoV-2 over the course of the trial (risk difference, 0.3 percentage points, 95% CI, -2.6 to 3.1; p=0.84). Three patients were hospitalised with COVID-19 disease in the MCV and one in the saline group. CONCLUSIONS : Administering MCVs to stimulate trained immunity did not prevent COVID-19 or SARS-CoV2 infection. Stimulating trained immunity might not be useful for preventing respiratory illness during future pandemics. CLINICAL TRIAL REGISTRATION : https://clinicaltrials.gov/, identifier NCT04333732.
dc.description.departmentMedical Microbiology
dc.description.librarianhj2025
dc.description.sdgSDG-03: Good health and well-being
dc.description.sponsorshipSupport for this work from the COVID-19 Therapeutics Accelerator and the South African Medical Research Council with funds received from the Department of Science and Innovation.
dc.description.urihttps://www.frontiersin.org/journals/immunology
dc.identifier.citationDelany-Moretlwe, S., Dehbi, H.-M., Sikazwe, I., Kyei, G., Koram, K., Dubberke, E., Mwelase, N., Hague, D., Bekker, L.-G., Yun, L., Nel, A., Du Toit, L., Biccard, B., Gill, K., Chipeta, C., Mngadi, K.T., Lebina, L., Dassaye, R., Asari, V., Fry, S.H., Turton, E., Ahmed, K., Kusi, K., Adu-Amankwah, S., Chilengi, R., Chilekwa, J.C., Lovat, L., McGuckin, D., Caverly, E., Politi, M., Swan, B., DeSchryver, A., McKinnon, S., Gupta, A., Jones, G., Freemantle, N., Khader, S., Rees, H., Netea, M.G., Moonesinghe, S.R. & Avidan, M.S. (2025) No evidence of MMR induced trained immunity to prevent SARS COV2: results from a multi- centre RCT. Frontiers in Immunology 16:1588190: 1-9. doi: 10.3389/fimmu.2025.1588190.
dc.identifier.issn1664-3224 (online)
dc.identifier.other10.3389/fimmu.2025.1588190
dc.identifier.urihttp://hdl.handle.net/2263/105243
dc.language.isoen
dc.publisherFrontiers Media
dc.rights© 2025 Delany-Moretlwe, Dehbi, Sikazwe, Kyei, Koram, Dubberke, Mwelase, Hague, Bekker, Yun, Nel, Toit, Biccard, Gill, Chipeta, Mngadi, Lebina, Dassaye, Asari, Fry, Turton, Ahmed, Kusi, Adu-Amankwah, Chilengi, Chilekwa, Lovat, McGuckin, Caverly, Politi, Swan, DeSchryver, McKinnon, Gupta, Jones, Freemantle, Khader, Rees, Netea, Moonesinghe and Avidan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
dc.subjectMeasles-containing vaccines (MCV)
dc.subjectSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
dc.subjectCOVID-19 pandemic
dc.subjectCoronavirus disease 2019 (COVID-19)
dc.subjectPolymerase chain reaction (PCR)
dc.subjectTrained immunity
dc.subjectMeasles
dc.subjectMumps
dc.subjectPrevention
dc.subjectRubella
dc.titleNo evidence of MMR induced trained immunity to prevent SARS COV2 : results from a multi-centre RCT
dc.typeArticle

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