<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mulamba C</submitter><funding>European &amp; Developing Countries Clinical Trials Partnership (EDCTP)</funding><pagination>1589061</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12460233</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16</volume><pubmed_abstract>Transmission-blocking vaccines are among the novel tools under development for malaria control and elimination. Understanding the human immune response to the sexual stages of &lt;i>Plasmodium falciparum&lt;/i> is essential for progressing transmission-blocking vaccine development. A serosurvey was conducted in Tanzania, from May to August 2022 among 290 participants, consisting of 114 children (5-12 years), 44 adolescents (13-17 years), and 132 adults (18-45 years). The participants were tested for malaria parasites using quantitative polymerase chain reaction, and standardized enzyme-linked immunosorbent assays were performed to detect the presence of IgG antibodies against transmission-blocking target antigens-Pfs230D1M, Pfs48/45, and Pfs25. A set of 10 plasma samples that were reactive to Pf</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Seroprevalence of antibodies to &amp;lt;i&amp;gt;Plasmodium falciparum&amp;lt;/i&amp;gt; transmission-blocking target proteins Pfs230D1M and Pfs48/45 in Tanzanian populations of diverse malaria transmission intensity.</pubmed_title><pmcid>PMC12460233</pmcid><funding_grant_id>RIA2016V-1649</funding_grant_id><pubmed_authors>Mulamba C</pubmed_authors><pubmed_authors>Miura K</pubmed_authors><pubmed_authors>Long CA</pubmed_authors><pubmed_authors>Mtaka I</pubmed_authors><pubmed_authors>Kamage J</pubmed_authors><pubmed_authors>Williams C</pubmed_authors><pubmed_authors>Lazaro LO</pubmed_authors><pubmed_authors>Kreppel K</pubmed_authors><pubmed_authors>Mekhaiel D</pubmed_authors><pubmed_authors>Nkumama I</pubmed_authors><pubmed_authors>Odufuwa OG</pubmed_authors><pubmed_authors>Olotu AI</pubmed_authors><pubmed_authors>Kalinga WF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Seroprevalence of antibodies to &amp;lt;i&amp;gt;Plasmodium falciparum&amp;lt;/i&amp;gt; transmission-blocking target proteins Pfs230D1M and Pfs48/45 in Tanzanian populations of diverse malaria transmission intensity.</name><description>Transmission-blocking vaccines are among the novel tools under development for malaria control and elimination. Understanding the human immune response to the sexual stages of &lt;i>Plasmodium falciparum&lt;/i> is essential for progressing transmission-blocking vaccine development. A serosurvey was conducted in Tanzania, from May to August 2022 among 290 participants, consisting of 114 children (5-12 years), 44 adolescents (13-17 years), and 132 adults (18-45 years). The participants were tested for malaria parasites using quantitative polymerase chain reaction, and standardized enzyme-linked immunosorbent assays were performed to detect the presence of IgG antibodies against transmission-blocking target antigens-Pfs230D1M, Pfs48/45, and Pfs25. A set of 10 plasma samples that were reactive to Pf</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-03T21:40:40.891Z</modification><creation>2026-05-02T03:08:08.433Z</creation></dates><accession>S-EPMC12460233</accession><cross_references><pubmed>41019048</pubmed><doi>10.3389/fimmu.2025.1589061</doi></cross_references></HashMap>