<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Walker IS</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) proteins are expressed on the surface of infected erythrocytes, mediating parasite sequestration in the vasculature. PfEMP1 is a major target of protective antibodies, but the features of the antibody response are poorly defined.&lt;h4>Methods&lt;/h4>In Malawian children with cerebral or uncomplicated malaria, we characterized the antibody response to 39 recombinant PfEMP1 Duffy binding like (DBL) domains or cysteine-rich interdomain regions (CIDRs) in detail, including measures of antibody classes, subclasses, and engagement with Fcγ receptors and complement. Using elastic net regularized logistic regression, we identified a combination of seven antibody targets and Fc features that best distinguished between child</pubmed_abstract><journal>BMC medicine</journal><pagination>388</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11396342</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A systems serology approach to identifying key antibody correlates of protection from cerebral malaria in Malawian children.</pubmed_title><pmcid>PMC11396342</pmcid><pubmed_authors>Takashima E</pubmed_authors><pubmed_authors>Alemu A</pubmed_authors><pubmed_authors>Mandala W</pubmed_authors><pubmed_authors>Damelang T</pubmed_authors><pubmed_authors>Seydel KB</pubmed_authors><pubmed_authors>Hasang W</pubmed_authors><pubmed_authors>Harawa V</pubmed_authors><pubmed_authors>Rambhatla JS</pubmed_authors><pubmed_authors>Opi DH</pubmed_authors><pubmed_authors>Tsuboi T</pubmed_authors><pubmed_authors>Chung AW</pubmed_authors><pubmed_authors>Dini S</pubmed_authors><pubmed_authors>Jensen ATR</pubmed_authors><pubmed_authors>Rogerson SJ</pubmed_authors><pubmed_authors>Simpson JA</pubmed_authors><pubmed_authors>Walker IS</pubmed_authors><pubmed_authors>Taylor TE</pubmed_authors><pubmed_authors>Aitken EH</pubmed_authors><pubmed_authors>Duffy MF</pubmed_authors></additional><is_claimable>false</is_claimable><name>A systems serology approach to identifying key antibody correlates of protection from cerebral malaria in Malawian children.</name><description>&lt;h4>Background&lt;/h4>Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) proteins are expressed on the surface of infected erythrocytes, mediating parasite sequestration in the vasculature. PfEMP1 is a major target of protective antibodies, but the features of the antibody response are poorly defined.&lt;h4>Methods&lt;/h4>In Malawian children with cerebral or uncomplicated malaria, we characterized the antibody response to 39 recombinant PfEMP1 Duffy binding like (DBL) domains or cysteine-rich interdomain regions (CIDRs) in detail, including measures of antibody classes, subclasses, and engagement with Fcγ receptors and complement. Using elastic net regularized logistic regression, we identified a combination of seven antibody targets and Fc features that best distinguished between child</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-06-02T22:20:42.726Z</modification><creation>2025-04-04T18:53:21.417Z</creation></dates><accession>S-EPMC11396342</accession><cross_references><pubmed>39267089</pubmed><doi>10.1186/s12916-024-03604-8</doi></cross_references></HashMap>