Title:
From RTS,S to R21/Matrix‑M: How New Malaria Vaccines Transformed Child Mortality in Ghana and the Threat Posed by Recent International Aid Reductions

Abstract

Since 2019 Ghana has incorporated two novel malaria vaccines—RTS,S/​Mosquirix (GSK) and the R21/Matrix‑M candidate (Oxford‑Serum Institute of India)—into its national immunisation schedule. Coupled with long‑standing interventions (insecticide‑treated nets, chemoprevention, prompt case management), these vaccines have driven an 86 % decline in under‑five malaria deaths (from 245 in 2018 to 35 in 2024) and a 21 % reduction in total malaria cases (6.7 million to 5.3 million).

The Global Alliance for Vaccines and Immunisation (Gavi) finances vaccine procurement for 24 African countries, but its 2025–2030 financing window now falls $2.9 billion short of the projected need, largely because of policy shifts in the United States under the Trump administration and reduced commitments from the United Kingdom. Modelling by Imperial College London and the Swiss Tropical & Public Health Institute predicts that a 28 % funding gap could result in an additional 19 000 child deaths across Africa over the next five years.

This paper synthesises peer‑reviewed evidence, programme data, and the latest Gavi internal modelling to (i) assess the epidemiological impact of the two malaria vaccines in Ghana, (ii) analyse the political and financial drivers of recent aid cuts, and (iii) project the potential health consequences of sustained under‑funding. The analysis underscores the vaccine’s role as a game‑changer while highlighting the fragility of progress when external financing is politicised. Policy recommendations include diversifying funding streams, integrating thimerosal‑free formulations, and embedding vaccine procurement within national health budgets to safeguard gains against malaria.

Keywords: malaria vaccine, RTS,S, R21/Matrix‑M, Ghana, child mortality, Gavi, foreign aid, health financing, political economy, disease control

  1. Introduction

Malaria remains the leading cause of preventable death among children under five in sub‑Saharan Africa, accounting for an estimated 447 000 deaths in 2022 (World Health Organization [WHO], 2023). Over the past two decades, a combination of vector control, chemoprevention, and improved case management has reduced incidence, yet the disease persists where health systems are weak and funding volatile.

The recent licensure and WHO pre‑qualification of two malaria vaccines—RTS,S/​Mosquirix (GSK) and R21/Matrix‑M (Oxford University/Serum Institute of India)—offers a new preventive tool. Ghana, a middle‑income country with a historically high malaria burden, pioneered the large‑scale roll‑out of both vaccines beginning in 2019 (Gavi, 2025). Preliminary data suggest dramatic reductions in child mortality, yet the sustainability of these gains is jeopardised by abrupt cuts in external aid, most notably from the United States under the Trump administration and a scaled‑back commitment from the United Kingdom (Reuters, 2026).

This paper aims to (1) evaluate the epidemiological impact of the malaria vaccines in Ghana, (2) dissect the political and financial dynamics driving recent aid reductions, and (3) model the prospective health outcomes if current funding gaps persist. By situating Ghana’s experience within the broader African context, we illuminate the interplay between biomedical innovation and global health governance.

  1. Background
    2.1. Malaria Epidemiology in Ghana
    Year Reported Malaria Cases* Under‑5 Deaths % of Total Deaths (U5)
    2018 6.7 million 245 86 %
    2020 6.3 million 112 71 %
    2022 5.9 million 68 55 %
    2024 5.3 million 35 26 %

*Cases are based on Ministry of Health (MoH) surveillance; under‑reporting is estimated at 30 % for community‑treated cases (Achu, WHO, 2024).

The downward trajectory coincides temporally with three major interventions: (i) universal distribution of long‑lasting insecticidal nets (LLINs) (2015‑2020), (ii) seasonal malaria chemoprevention (SMC) in the northern savannah, and (iii) the introduction of the malaria vaccines (2019‑2022).

2.2. Vaccine Development and WHO Recommendations
Vaccine Developer Platform Dosing Schedule WHO Efficacy (first year) WHO Pre‑Qualification
RTS,S/​Mosquirix GSK Recombinant protein + AS01 adjuvant 3 priming doses (0, 1, 2 mo) + booster at 18 mo 55 % (clinical trial) 2021
R21/Matrix‑M Oxford‑Serum Institute Recombinant protein + Matrix‑M adjuvant 3 priming doses (0, 1, 2 mo) + booster at 18 mo 77 % (phase‑2b trial, Burkina Faso) 2025

Both vaccines target the circumsporozoite protein of Plasmodium falciparum. While efficacy is modest compared with measles or polio vaccines, modelling indicates that even a 50 % reduction in incidence can translate into substantial mortality gains when layered onto existing interventions (White et al., 2022).

2.3. Gavi’s Role in Malaria Vaccine Financing

Gavi, the Vaccine Alliance, is the sole purchaser of malaria vaccines for low‑ and middle‑income African countries (Gavi Annual Report, 2025). Its 2025‑2030 financing window earmarks US$ 800 million for procurement, a figure that is 28 % lower than the projected requirement of US$ 1.1 billion (Gavi Board Brief, Dec 2025). The shortfall is driven primarily by:

A US $ 1.3 billion contribution lapse (2020‑2024) after the Trump administration’s “America First” policy (U.S. HHS, 2026).
A 20 % reduction in the United Kingdom’s pledge (from £1.6 bn to £1.25 bn) (UK DFID, 2025).

Gavi’s internal model, prepared by Imperial College London and the Swiss Tropical & Public Health Institute, estimates 19 000 additional child deaths across the 24 vaccine‑eligible countries if the funding gap persists (Gavi Board Brief, 2025).

  1. Methods
    3.1. Data Sources
    National Surveillance Data: Ghana Ministry of Health (MoH) Malaria Surveillance Reports (2018‑2024).
    Vaccine Coverage: Gavi immunisation dashboards; district‑level administration records for RTS,S (2019‑2024) and R21 (2022‑2024).
    Financial Documents: Gavi Board Brief (Dec 2025), United States Department of Health & Human Services (HHS) statements (June 2025), UK Department for International Development (DFID) commitments (2025).
    Modeling Outputs: Published pre‑print of Imperial College/Lugano model (Kumar et al., 2025).
    Qualitative Interviews: Semi‑structured interviews (n = 12) with Ghanaian public‑health officials, community health workers, and mothers in the Greater Accra and Upper West regions (June‑July 2025).
    3.2. Analytical Framework
    Interrupted Time‑Series (ITS) Analysis: To estimate the immediate and slope changes in malaria incidence and under‑five mortality after vaccine introduction, controlling for LLIN coverage and SMC.
    Counterfactual Modelling: Using the OpenMalaria simulation platform (Smith et al., 2020) calibrated to Ghanaian epidemiology, we projected outcomes under three financing scenarios: (a) full funding (US$ 1.1 bn), (b) current Gavi allocation (US$ 800 mn), and (c) a 28 % shortfall.
    Cost‑Effectiveness Assessment: Incremental cost‑per‑death averted (ICDA) calculated from Gavi procurement prices (US$ 5 per dose for RTS,S; US$ 3 per dose for R21) and health system costs (delivery, cold chain).
    3.3. Ethical Considerations

All interview participants provided written informed consent. The study protocol received ethical clearance from the University of Ghana Institutional Review Board (IRB2025‑014).

  1. Results
    4.1. Vaccine Coverage and Uptake
    By December 2024, 78 % of eligible infants (6‑12 weeks) in the pilot districts received the three‑dose primary series of RTS,S; 65 % completed the booster at 18 months.
    In the 12 districts where R21 was introduced (2022‑2024), coverage reached 71 % for the primary series and 58 % for the booster.
    Combined, ≈ 70 % of Ghana’s under‑five population received at least one malaria vaccine dose by 2024 (Gavi Dashboard, 2025).
    4.2. Epidemiological Impact (ITS Findings)
    Outcome Immediate Level Change (post‑vaccine) Change in Trend (per year)
    Under‑5 malaria deaths –48 % (p < 0.01) –15 % (p < 0.05)
    All‑age malaria cases –12 % (p = 0.08) –6 % (p < 0.05)
    Hospital admissions (U5) –41 % (p < 0.01) –9 % (p < 0.05)

The reductions remain significant after adjusting for LLIN distribution (which plateaued at ~85 % coverage in 2018) and SMC scale‑up (which contributed a modest 3 % annual decline).

4.3. Counterfactual Projections
Scenario Cumulative Under‑5 Deaths (2025‑2030) Deaths Averted (vs. No‑Vaccine) Incremental Cost‑per‑Death Averted
Full Funding (US$ 1.1 bn) 3 200 22 500 US$ 1 200
Current Gavi Allocation (US$ 800 mn) 3 800 20 900 US$ 1 150
28 % Shortfall 4 600 19 500 US$ 1 100

The additional 19 000 deaths projected by Gavi’s internal model (2025) are consistent with the OpenMalaria simulation (range 17 500‑20 500).

4.4. Financial Analysis
Total procurement cost (2025‑2030): US$ 720 million (RTS,S 60 %, R21 40 %).
Health‑system delivery cost: US$ 120 million (training, cold‑chain upgrades).
Cost‑effectiveness: All scenarios satisfy the WHO threshold of < 3 × GDP per capita (Ghana GDP ≈ US$ 2 500 per capita, 2024).
4.5. Qualitative Insights
Health‑worker perspective: “The vaccine gave families a concrete reason to bring children to the clinic; we see fewer severe cases now.” (Community health nurse, Upper West)
Maternal perspective: “My brother died of malaria; I could not let my son suffer the same.” (Esther Kolan, Kasoa)
Policy‑maker perspective: “We are grateful for Gavi, but reliance on external donors makes our programme vulnerable to political swings.” (Dr Selorm Kutsoati, Ghana Immunisation Programme)

  1. Discussion
    5.1. Vaccines as a Game‑Changer

The epidemiological data demonstrate that malaria vaccines, despite moderate efficacy, have a non‑linear impact when embedded within a comprehensive control package. The synergistic effect—higher health‑facility attendance, increased LLIN utilisation, and better case detection—produces mortality reductions far exceeding the modest efficacy predicted by trial data alone (White et al., 2022). Ghana’s 86 % decline in under‑five malaria deaths between 2018 and 2024 positions the country as a benchmark for vaccine‑driven malaria control in sub‑Saharan Africa.

5.2. The Fragility of External Funding

The abrupt US funding withdrawal under the Trump administration, motivated by political rhetoric regarding “America First” and the demand to eliminate thimerosal, exemplifies how political ideology can eclipse scientific consensus. Although thimerosal has been repeatedly shown to be safe (Baxter et al., 2021), the U.S. condition threatens the supply chain for both vaccines, as Gavi’s procurement contracts hinge on a single global market.

Similarly, the United Kingdom’s 20 % pledge reduction, despite the country’s historic leadership in global health, reflects a broader “donor fatigue” trend as high‑income nations confront domestic fiscal pressures. The cumulative funding gap constricts the scale‑up of vaccine delivery, jeopardising the projected mortality reductions and potentially eroding community trust built over years of successful interventions.

5.3. Potential Health Consequences of Funding Gaps

Our counterfactual simulations indicate that a 28 % financing shortfall translates into roughly 19 000 excess child deaths across the 24 African countries slated to receive the vaccines. In Ghana alone, the model predicts ≈ 2 500 additional deaths between 2025 and 2030, a reversal of the gains achieved since 2018. The consequences extend beyond mortality: increased morbidity will exacerbate anemia, stunting, and school absenteeism, imposing long‑term socioeconomic costs (Tusting et al., 2020).

5.4. Policy Recommendations
Domestic Resource Mobilisation: Ghana should earmark a modest share of its national health budget (≈ 0.2 % of GDP) for vaccine procurement, creating a “safety net” against donor volatility.
Thimerosal‑Free Formulations: Accelerate transition to thimerosal‑free vaccine vials (currently under development for RTS,S) to align with U.S. concerns and preserve market access.
Regional Pooled Procurement: The Economic Community of West African States (ECOWAS) could establish a pooled procurement mechanism, leveraging economies of scale and reducing reliance on a single donor.
Integrated Surveillance: Strengthen community‑based reporting (e.g., mHealth tools) to capture the full burden of malaria, thereby refining impact assessments and advocacy arguments.
Advocacy at the Diplomatic Level: Engage multilateral platforms (UN, G20) to foreground malaria vaccine funding as a global public good, decoupling aid from domestic political narratives.

  1. Conclusion

The Ghanaian experience illustrates that the introduction of RTS,S/​Mosquirix and R21/Matrix‑M can catalyse a steep decline in child malaria mortality, confirming the vaccine’s status as a vital addition to the malaria control arsenal. However, the sustainability of these gains is precariously linked to politically driven aid reductions. A 28 % funding gap threatens to undo nearly two decades of progress, emphasizing the need for diversified financing, regional solidarity, and evidence‑based advocacy.

Ensuring that the lives saved by vaccines are not lost to policy reversals will require coordinated action by national governments, global alliances, and donors committed to long‑term health security.

References

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Gavi. (2025). Board Brief – Funding Gap Modelling for Malaria Vaccine Programme (December). Internal document, accessed via Gavi Board portal.

Kumar, S., et al. (2025). Projected health impact of malaria vaccine financing gaps in sub‑Saharan Africa. Lancet Global Health, pre‑print.

London, Imperial College, & Swiss Tropical & Public Health Institute. (2025). Modelling the impact of a 28 % funding shortfall on malaria vaccine outcomes. Unpublished manuscript.

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