<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Parra-Lopez CA</submitter><funding>NIAID NIH HHS</funding><funding>PHS HHS</funding><pagination>e100639</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4077652</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(7)</volume><pubmed_abstract>Malaria is transmitted by Plasmodium-infected anopheles mosquitoes. Widespread resistance of mosquitoes to insecticides and resistance of parasites to drugs highlight the urgent need for malaria vaccines. The most advanced malaria vaccines target sporozoites, the infective form of the parasite. A major target of the antibody response to sporozoites are the repeat epitopes of the circumsporozoite (CS) protein, which span almost one half of the protein. Antibodies to these repeats can neutralize sporozoite infectivity. Generation of protective antibody responses to the CS protein (anti-CS Ab) requires help by CD4 T cells. A CD4 T cell epitope from the CS protein designated T* was previously identified by screening T cells from volunteers immunized with irradiated P. falciparum sporozoites. T</pubmed_abstract><journal>PloS one</journal><pubmed_title>An unstable Th epitope of P. falciparum fosters central memory T cells and anti-CS antibody responses.</pubmed_title><pmcid>PMC4077652</pmcid><funding_grant_id>R37 AI038996</funding_grant_id><funding_grant_id>R56 AI038996</funding_grant_id><funding_grant_id>AI38996</funding_grant_id><funding_grant_id>U19-57319</funding_grant_id><funding_grant_id>R01 AI038996</funding_grant_id><pubmed_authors>Calvo-Calle JM</pubmed_authors><pubmed_authors>Vargas LE</pubmed_authors><pubmed_authors>Pulido-Calixto C</pubmed_authors><pubmed_authors>Stern LJ</pubmed_authors><pubmed_authors>Bernal-Estevez D</pubmed_authors><pubmed_authors>Salazar LM</pubmed_authors><pubmed_authors>Yin L</pubmed_authors><pubmed_authors>Parra-Lopez CA</pubmed_authors></additional><is_claimable>false</is_claimable><name>An unstable Th epitope of P. falciparum fosters central memory T cells and anti-CS antibody responses.</name><description>Malaria is transmitted by Plasmodium-infected anopheles mosquitoes. Widespread resistance of mosquitoes to insecticides and resistance of parasites to drugs highlight the urgent need for malaria vaccines. The most advanced malaria vaccines target sporozoites, the infective form of the parasite. A major target of the antibody response to sporozoites are the repeat epitopes of the circumsporozoite (CS) protein, which span almost one half of the protein. Antibodies to these repeats can neutralize sporozoite infectivity. Generation of protective antibody responses to the CS protein (anti-CS Ab) requires help by CD4 T cells. A CD4 T cell epitope from the CS protein designated T* was previously identified by screening T cells from volunteers immunized with irradiated P. falciparum sporozoites. T</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2026-05-03T23:24:01.354Z</modification><creation>2019-03-26T23:26:21Z</creation></dates><accession>S-EPMC4077652</accession><cross_references><pubmed>24983460</pubmed><doi>10.1371/journal.pone.0100639</doi></cross_references></HashMap>