<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Cobos C</submitter><pubmed_abstract>A decline in the prevalence of parasites such as hookworms appears to be correlated with the rise in non-communicable inflammatory conditions in people from high- and middle-income countries. This correlation has led to studies that have identified proteins produced by hookworms that can suppress inflammatory bowel disease (IBD) and asthma in animal models. Hookworms secrete a family of abundant netrin-domain containing proteins referred to as AIPs (Anti-Inflammatory Proteins), but there is no information on the structure-function relationships. Here we have applied a downsizing approach to the hookworm AIPs to derive peptides of 20 residues or less, some of which display anti-inflammatory effects when co-cultured with human peripheral blood mononuclear cells and oral therapeutic activity in a chemically induced mouse model of acute colitis. Our results indicate that a conserved helical region is responsible, at least in part, for the anti-inflammatory effects. This helical region has potential in the design of improved leads for treating IBD and possibly other inflammatory conditions.</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>934852</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9524151</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Peptides derived from hookworm anti-inflammatory proteins suppress inducible colitis in mice and inflammatory cytokine production by human cells.</pubmed_title><pmcid>PMC9524151</pmcid><pubmed_authors>Field MA</pubmed_authors><pubmed_authors>Daly NL</pubmed_authors><pubmed_authors>Giacomin PR</pubmed_authors><pubmed_authors>Navarro S</pubmed_authors><pubmed_authors>Loukas A</pubmed_authors><pubmed_authors>Ryan RYM</pubmed_authors><pubmed_authors>Ruscher R</pubmed_authors><pubmed_authors>Ratnatunga CN</pubmed_authors><pubmed_authors>Pickering DA</pubmed_authors><pubmed_authors>Wilson DT</pubmed_authors><pubmed_authors>Eichenberger RM</pubmed_authors><pubmed_authors>Jones L</pubmed_authors><pubmed_authors>Zhao G</pubmed_authors><pubmed_authors>Cobos C</pubmed_authors><pubmed_authors>Miles JJ</pubmed_authors><pubmed_authors>Bansal PS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Peptides derived from hookworm anti-inflammatory proteins suppress inducible colitis in mice and inflammatory cytokine production by human cells.</name><description>A decline in the prevalence of parasites such as hookworms appears to be correlated with the rise in non-communicable inflammatory conditions in people from high- and middle-income countries. This correlation has led to studies that have identified proteins produced by hookworms that can suppress inflammatory bowel disease (IBD) and asthma in animal models. Hookworms secrete a family of abundant netrin-domain containing proteins referred to as AIPs (Anti-Inflammatory Proteins), but there is no information on the structure-function relationships. Here we have applied a downsizing approach to the hookworm AIPs to derive peptides of 20 residues or less, some of which display anti-inflammatory effects when co-cultured with human peripheral blood mononuclear cells and oral therapeutic activity in a chemically induced mouse model of acute colitis. Our results indicate that a conserved helical region is responsible, at least in part, for the anti-inflammatory effects. This helical region has potential in the design of improved leads for treating IBD and possibly other inflammatory conditions.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-31T15:56:04.817Z</modification><creation>2025-04-04T12:46:14.995Z</creation></dates><accession>S-EPMC9524151</accession><cross_references><pubmed>36186812</pubmed><doi>10.3389/fmed.2022.934852</doi></cross_references></HashMap>