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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Public Health</journal-id>
<journal-title>Frontiers in Public Health</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Public Health</abbrev-journal-title>
<issn pub-type="epub">2296-2565</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpubh.2023.1237011</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Public Health</subject>
<subj-group>
<subject>Opinion</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Issues related to the approval of the R21/Matrix-M malaria vaccine for use in Nigeria and Ghana</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Dzi</surname> <given-names>Kevin T. J.</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/2303709/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>D&#x000E9;partement de la formation et recherche, Institut des humanit&#x000E9;s en m&#x000E9;decine (IHM), Centre hospitalier universitaire vaudois et Universite de Lausanne</institution>, <addr-line>Lausanne</addr-line>, <country>Switzerland</country></aff>
<aff id="aff2"><sup>2</sup><institution>Facult&#x000E9; de Biologie et de M&#x000E9;decine, Universit&#x000E9; de Lausanne</institution>, <addr-line>Lausanne</addr-line>, <country>Switzerland</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Juarez Antonio Sim&#x000F5;es Quaresma, Federal University of Par&#x000E1;, Brazil</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Godwin W. Nchinda, Chantal BIYA International Reference Center (CBIRC), Cameroon; Michael Fokuo Ofori, University of Ghana, Ghana</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Kevin T. J. Dzi <email>kevin.dzi&#x00040;unil.ch</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>04</day>
<month>10</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>11</volume>
<elocation-id>1237011</elocation-id>
<history>
<date date-type="received">
<day>08</day>
<month>06</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>18</day>
<month>09</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2023 Dzi.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Dzi</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license></permissions> 
<kwd-group>
<kwd>public health</kwd>
<kwd>malaria</kwd>
<kwd>vaccine efficacy and effectiveness</kwd>
<kwd>malaria control and elimination</kwd>
<kwd>epidemic</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="10"/>
<page-count count="3"/>
<word-count count="1596"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Infectious Diseases: Epidemiology and Prevention</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Malaria is a potentially fatal parasitic illness prevalent in tropical areas, primarily transmitted to individuals through the bites of female Anopheles mosquitoes that are infected. Individuals in the demographic categories of infants and children below the age of 5, pregnant women, travelers, and individuals diagnosed with HIV or AIDS are more susceptible to acquiring a severe infection (<xref ref-type="bibr" rid="B1">1</xref>). Malaria still causes a significant number of deaths annually in low-income countries.</p>
<p>Over the course of time, numerous research institutions, universities, biotech companies, and pharmaceutical companies have dedicated their efforts toward developing a malaria vaccine to safeguard individuals, particularly children, residing in Africa, where the disease exhibits the highest prevalence.</p>
<p>The Oxford University Malaria Vaccine (R21/Matrix-M vaccine) was recently approved for use in Ghana (<xref ref-type="bibr" rid="B2">2</xref>) and provisionally approved for use in Nigeria (<xref ref-type="bibr" rid="B3">3</xref>) for malaria protection in children. Many other African countries are currently assessing the trial data of the vaccine to determine whether they will approve the vaccine to be used in their own countries. The purpose of this review is to examine some rationales for the necessity of integrating the recently approved malaria vaccine with pre-existing control strategies in Ghana and Nigeria.</p>
<p>The World Health Organization (WHO) first announced the availability of a vaccine against malaria caused by <italic>Plasmodium falciparum</italic> in 2021. This vaccine, known as RTS,S/AS01 (Mosquirix), has an efficacy of only 30%, suggesting that many children are still at risk of contracting malaria in countries where the vaccines are administered (<xref ref-type="bibr" rid="B4">4</xref>). Recently, a phase IIb trial of the vaccine R21/Matrix-M developed by Oxford University showed an increased level of efficacy of 77% (<xref ref-type="bibr" rid="B5">5</xref>). Compared to the Mosquirix vaccine, which was approved by the WHO in 2021, this is an improvement; however, it is still less effective than other standard childhood vaccines, such as those for polio (90&#x02013;99% efficacy) and measles (97% efficacy) (<xref ref-type="bibr" rid="B4">4</xref>). Both Ghana and Nigeria have approved or provisionally approved the use of the R21/Matrix-M vaccine, recognizing its potential benefits for children. However, the vaccine&#x00027;s efficacy is slightly lower than that of other commonly used vaccines for children, leaving many youngsters vulnerable to infection.</p>
<p>I argue that, in combination with vaccination efforts, it is crucial to maintain and possibly increase the intensity of existing malaria control measures to achieve greater protection for more children and eventually the eradication of the disease in the African region. Enforcing existing control measures is a key part of the solution to preventing more children from contracting the disease, whilst the rollout of the vaccine is taking place in nations that have approved the vaccine, and deliberations are going on in other countries to determine the approval of the vaccine.</p>
<p>Some of the malaria control measures I propose should be reinforced, including those recommended by the Center for Disease Control that have been put in place in the past few years through the ministries of public health in different countries. This includes case management (diagnosing and treating people with malaria), the distribution of insecticide-treated nets (ITNs), indoor residual spraying (IRS), and intermittent preventive treatment of malaria in pregnant women, and infancy, amongst others (<xref ref-type="bibr" rid="B6">6</xref>).</p>
<p>In Ghana and Nigeria, their malaria control programmes have previously implemented these measures, and they should persist in reinforcing them during the implementation of the vaccine rollout. The National Malaria Strategic Plans (NMSPs) have traditionally served as the fundamental framework for setting objectives and targets related to malaria control and elimination in Nigeria, and between 2014 and 2020, they identified the measures listed above as intervention areas to reduce malaria cases in Nigeria (<xref ref-type="bibr" rid="B7">7</xref>). In Ghana, the distribution of ITNs was carried out on a nationwide basis in 2004. Additionally, various control measures, including the IRS and others, are presently being implemented with the aim of effectively managing the spread of malaria (<xref ref-type="bibr" rid="B8">8</xref>).</p>
<p>The enthusiasm surrounding a vaccine may result in a reduction in the reinforcement of prevention measures such as those listed above.</p>
<p>Given that the R21/Matrix-M vaccine has received approval in only a limited number of countries and that Africa continues to bear the highest burden of reported malaria cases globally, it is imperative to strengthen existing malaria control programmes and other preventive measures, especially in countries where the vaccine has not yet been approved. This is necessary as it may take considerable time for the vaccine to receive approval and be implemented in all African countries. In both Nigeria and Ghana, where the vaccine has obtained approval, the vaccination process for all children may face potential delays due to reported challenges in vaccine distribution within the African context. These challenges include inadequate infrastructure for vaccine storage and difficulties in accessing individuals residing in remote areas (<xref ref-type="bibr" rid="B9">9</xref>).</p>
<p>Additional measures include the provision of vaccine-related education. Historically, erroneous beliefs have frequently resulted in suboptimal vaccination programme implementation (<xref ref-type="bibr" rid="B9">9</xref>), demonstrating the necessity of conducting effective campaigns. One illustrative example relates to the difficulties encountered in the northern region of Nigeria in 2003, when a significant portion of the population exhibited reluctance toward accepting the polio vaccine, resulting in significantly lower rates of vaccine coverage (<xref ref-type="bibr" rid="B10">10</xref>).</p>
<p>The approval of the R21/Matrix-M vaccine in Ghana and Nigeria is a huge breakthrough in malaria control in these countries and Africa in general, but there is still a long way to go before malaria is eradicated from Africa. Apart from the fact that the vaccine&#x00027;s efficacy is lower than that of other childhood vaccines, it will take some time for all African nations to approve the vaccine for use in their countries and subsequently execute vaccination campaigns with optimal efficiency. In addition to embracing the vaccine, African governments must continue to prioritize additional measures of prevention and management to ensure the greatest number of their inhabitants are protected from malaria. In addition to putting these processes into action, consistent assessments and follow-ups are required to determine their effectiveness.</p>
<sec id="s1">
<title>Summary</title>
<p>To eliminate malaria worldwide, the R21/Matrix-M malaria vaccine must be used alongside current control measures.</p></sec>
<sec sec-type="author-contributions" id="s2">
<title>Author contributions</title>
<p>The author confirms being the sole contributor of this work and has approved it for publication.</p></sec>
</body>
<back>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of interest</title>
<p>The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s3">
<title>Publisher&#x00027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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