<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(6)</volume><submitter>Krejsa CM</submitter><pubmed_abstract>Rituximab, a monoclonal antibody targeting CD20 on B cells, is currently used to treat many subtypes of B cell lymphomas. However, treatment is not curative and response rates are variable. Recombinant interleukin-21 (rIL-21) is a cytokine that enhances immune effector function and affects both primary and transformed B cell differentiation. We hypothesized that the combination of rIL-21 plus rituximab would be a more efficacious treatment for B cell malignancies than rituximab alone. We cultured human and cynomolgus monkey NK cells with rIL-21 and found that their activity was increased and proteins associated with antibody dependent cytotoxicity were up-regulated. Studies in cynomolgus monkeys modeled the effects of rIL-21 on rituximab activity against CD20 B cells. In these studies, rIL</pubmed_abstract><journal>PloS one</journal><pagination>e67256</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3692496</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.</pubmed_title><pmcid>PMC3692496</pmcid><pubmed_authors>Roque R</pubmed_authors><pubmed_authors>Ren HP</pubmed_authors><pubmed_authors>Bannink KM</pubmed_authors><pubmed_authors>Sivakumar PV</pubmed_authors><pubmed_authors>Kindsvogel W</pubmed_authors><pubmed_authors>Shiota F</pubmed_authors><pubmed_authors>Heipel M</pubmed_authors><pubmed_authors>Johnson R</pubmed_authors><pubmed_authors>Chin L</pubmed_authors><pubmed_authors>Foster D</pubmed_authors><pubmed_authors>Henderson K</pubmed_authors><pubmed_authors>Clegg C</pubmed_authors><pubmed_authors>Hughes SD</pubmed_authors><pubmed_authors>Waggie K</pubmed_authors><pubmed_authors>Wagener F</pubmed_authors><pubmed_authors>Barahmand-Pour F</pubmed_authors><pubmed_authors>Krejsa CM</pubmed_authors><pubmed_authors>Heffernan J</pubmed_authors><pubmed_authors>Ponce R</pubmed_authors><pubmed_authors>Hill J</pubmed_authors><pubmed_authors>Holly RD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.</name><description>Rituximab, a monoclonal antibody targeting CD20 on B cells, is currently used to treat many subtypes of B cell lymphomas. However, treatment is not curative and response rates are variable. Recombinant interleukin-21 (rIL-21) is a cytokine that enhances immune effector function and affects both primary and transformed B cell differentiation. We hypothesized that the combination of rIL-21 plus rituximab would be a more efficacious treatment for B cell malignancies than rituximab alone. We cultured human and cynomolgus monkey NK cells with rIL-21 and found that their activity was increased and proteins associated with antibody dependent cytotoxicity were up-regulated. Studies in cynomolgus monkeys modeled the effects of rIL-21 on rituximab activity against CD20 B cells. In these studies, rIL</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-06-01T12:27:40.767Z</modification><creation>2025-06-01T12:27:40.767Z</creation></dates><accession>S-EPMC3692496</accession><cross_references><pubmed>23825648</pubmed><doi>10.1371/journal.pone.0067256</doi></cross_references></HashMap>