Asymptomatic Malaria Infection and the Immune Response to the 2-Dose Ad26.ZEBOV, MVA-BN-Filo Ebola Vaccine Regimen in Adults and Children

David Ishola, Osman Mohamed Bah, Foday Suma Bangalie, Agnes Bangura, Ifeolu David, Gibrilla Fadlu Deen, Augustin Fombah, Abdulai Berber Jalloh, Abu Bakarr Kamara, Ibrahim Franklyn Kamara, Michael Kamara, Bailah Leigh, Foday Morovia, Baimba Rogers, Mohamed Samai, Alimamy Serry-Bangura, Mahmud Sheku, Ibrahim Swaray, Dickson Anumendem, Auguste GaddahViki Bockstal, Babajide Keshinro, Cynthia Robinson, Muhammed Afolabi, Pauline Akoo, Philip Ayieko, Frank Baiden, Katherine Gallagher, Brian Greenwood, David Ishola, Brian Kohn, Dickens Kowuor, Bolarinde Lawal, Brett Lowe, Daniela Manno, Lazarus Odeny, Tuda Otieno, Kwabena Owusu-Kyei, Elizabeth Smout, Daniel Tindanbil, Deborah Watson-Jones

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Background

Malaria infection affects the immune response to some vaccines. As Ebola virus (EBOV) outbreaks have occurred mainly in malaria-endemic countries, we have assessed whether asymptomatic malaria affects immune responses to the 2-dose Ad26.ZEBOV, MVA-BN-Filo Ebola vaccine regimen.

Methods

In this sub-study of the EBOVAC-Salone Ebola vaccine trial in Sierra Leone, malaria microscopy was performed at the time of Ebola vaccination. Participants with symptomatic malaria were treated before vaccination. Ebola vaccine responses were assessed post-dose 1 (day 57) and post-dose 2 (day 78) by the EBOV glycoprotein FANG enzyme-linked immunosorbent assay (ELISA), and responses expressed as geometric mean concentrations (GMCs). Geometric mean ratios (GMRs) of the GMCs in malaria-positive versus malaria-negative participants were derived with 95% confidence intervals (CIs).

Results

A total of 587 participants were studied, comprising 188 adults (≥18 years) and 399 children (in age groups of 12–17, 4–11, and 1–3 years). Asymptomatic malaria was observed in 47.5% of adults and 51.5% of children on day 1. Post-dose 1, GMCs were lower in 1–3-year-old malaria-positive compared with malaria-negative children (age group–specific GMR, .56; 95% CI, .39–.81) but not in older age groups. Post-dose 2, there was no consistent effect of malaria infection across the different age groups but there was a trend toward a lower response (GMR, .82; 95% CI, .67–1.02).

Conclusions

The Ad26.ZEBOV, MVA-BN-Filo Ebola vaccine regimen is immunogenic in participants with asymptomatic malaria. Therefore, it is not necessary to screen for asymptomatic malaria infection prior to vaccination with this regimen.

Original languageEnglish
Pages (from-to)1585-1593
Number of pages9
JournalClinical Infectious Diseases
Volume75
Issue number9
Early online date30 May 2022
DOIs
Publication statusE-pub ahead of print - 30 May 2022
Externally publishedYes

Keywords

  • Ebola vaccination
  • immune suppression
  • malaria

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