<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sutton PL</submitter><funding>NIAID NIH HHS</funding><pagination>3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2818648</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Plasmodium falciparum re-emerged in Iquitos, Peru in 1994 and is now hypoendemic (&lt; 0.5 infections/person/year). Purportedly non-immune individuals with discrete (non-overlapping) P. falciparum infections can be followed using this population dynamic. Previous work demonstrated a strong association between this population's antibody response to PfMSP1-19KD and protection against febrile illness and parasitaemia. Therefore, some selection for PfMSP1-19KD allelic diversity would be expected if the protection is to allele-specific sites of PfMSP1-19KD. Here, the potential for allele-specific polymorphisms in this population is investigated, and the allele-specificity of antibody responses to PfMSP1-19KD are determined.&lt;h4>Methods&lt;/h4>The 42KD region in PfMSP1 was genotyped </pubmed_abstract><journal>Malaria journal</journal><pubmed_title>The Plasmodium falciparum merozoite surface protein-1 19 KD antibody response in the Peruvian Amazon predominantly targets the non-allele specific, shared sites of this antigen.</pubmed_title><pmcid>PMC2818648</pmcid><funding_grant_id>R01 AI064831</funding_grant_id><pubmed_authors>Sutton PL</pubmed_authors><pubmed_authors>Branch OH</pubmed_authors><pubmed_authors>Clark EH</pubmed_authors><pubmed_authors>Silva C</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Plasmodium falciparum merozoite surface protein-1 19 KD antibody response in the Peruvian Amazon predominantly targets the non-allele specific, shared sites of this antigen.</name><description>&lt;h4>Background&lt;/h4>Plasmodium falciparum re-emerged in Iquitos, Peru in 1994 and is now hypoendemic (&lt; 0.5 infections/person/year). Purportedly non-immune individuals with discrete (non-overlapping) P. falciparum infections can be followed using this population dynamic. Previous work demonstrated a strong association between this population's antibody response to PfMSP1-19KD and protection against febrile illness and parasitaemia. Therefore, some selection for PfMSP1-19KD allelic diversity would be expected if the protection is to allele-specific sites of PfMSP1-19KD. Here, the potential for allele-specific polymorphisms in this population is investigated, and the allele-specificity of antibody responses to PfMSP1-19KD are determined.&lt;h4>Methods&lt;/h4>The 42KD region in PfMSP1 was genotyped </description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jan</publication><modification>2026-04-07T15:40:39.329Z</modification><creation>2019-03-27T00:28:26Z</creation></dates><accession>S-EPMC2818648</accession><cross_references><pubmed>20047674</pubmed><doi>10.1186/1475-2875-9-3</doi></cross_references></HashMap>