Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.

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 prim...

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Main Authors: Cecile M Krejsa, Rick D Holly, Mark Heipel, Ken M Bannink, Rebecca Johnson, Richard Roque, Jane Heffernan, Julie Hill, Lay Chin, Felecia Wagener, Faith Shiota, Katherine Henderson, Pallavur V Sivakumar, Hong-Ping Ren, Fariba Barahmand-Pour, Don Foster, Chris Clegg, Wayne Kindsvogel, Rafael Ponce, Steven D Hughes, Kim Waggie
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3692496?pdf=render
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spelling doaj-75eba1524ef24901bc6062fdb1f8b56a2020-11-24T21:50:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6725610.1371/journal.pone.0067256Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.Cecile M KrejsaRick D HollyMark HeipelKen M BanninkRebecca JohnsonRichard RoqueJane HeffernanJulie HillLay ChinFelecia WagenerFaith ShiotaKatherine HendersonPallavur V SivakumarHong-Ping RenFariba Barahmand-PourDon FosterChris CleggWayne KindsvogelRafael PonceSteven D HughesKim WaggieRituximab, 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-21 activated innate immune effectors, increased ADCC and mobilized B cells into peripheral blood. When rIL-21 was combined with rituximab, deeper and more durable B cell depletion was observed. In another series of experiments, IL-21 was shown to have direct antiproliferative activity against a subset of human lymphoma cell lines, and combination of murine IL-21 with rituximab yielded significant survival benefits over either agent alone in xenogeneic mouse tumor models of disseminated lymphoma. Therefore, our results do suggest that the therapeutic efficacy of rituximab may be improved when used in combination with rIL-21.http://europepmc.org/articles/PMC3692496?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Cecile M Krejsa
Rick D Holly
Mark Heipel
Ken M Bannink
Rebecca Johnson
Richard Roque
Jane Heffernan
Julie Hill
Lay Chin
Felecia Wagener
Faith Shiota
Katherine Henderson
Pallavur V Sivakumar
Hong-Ping Ren
Fariba Barahmand-Pour
Don Foster
Chris Clegg
Wayne Kindsvogel
Rafael Ponce
Steven D Hughes
Kim Waggie
spellingShingle Cecile M Krejsa
Rick D Holly
Mark Heipel
Ken M Bannink
Rebecca Johnson
Richard Roque
Jane Heffernan
Julie Hill
Lay Chin
Felecia Wagener
Faith Shiota
Katherine Henderson
Pallavur V Sivakumar
Hong-Ping Ren
Fariba Barahmand-Pour
Don Foster
Chris Clegg
Wayne Kindsvogel
Rafael Ponce
Steven D Hughes
Kim Waggie
Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
PLoS ONE
author_facet Cecile M Krejsa
Rick D Holly
Mark Heipel
Ken M Bannink
Rebecca Johnson
Richard Roque
Jane Heffernan
Julie Hill
Lay Chin
Felecia Wagener
Faith Shiota
Katherine Henderson
Pallavur V Sivakumar
Hong-Ping Ren
Fariba Barahmand-Pour
Don Foster
Chris Clegg
Wayne Kindsvogel
Rafael Ponce
Steven D Hughes
Kim Waggie
author_sort Cecile M Krejsa
title Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
title_short Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
title_full Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
title_fullStr Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
title_full_unstemmed Interleukin-21 enhances rituximab activity in a cynomolgus monkey model of B cell depletion and in mouse B cell lymphoma models.
title_sort interleukin-21 enhances rituximab activity in a cynomolgus monkey model of b cell depletion and in mouse b cell lymphoma models.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
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-21 activated innate immune effectors, increased ADCC and mobilized B cells into peripheral blood. When rIL-21 was combined with rituximab, deeper and more durable B cell depletion was observed. In another series of experiments, IL-21 was shown to have direct antiproliferative activity against a subset of human lymphoma cell lines, and combination of murine IL-21 with rituximab yielded significant survival benefits over either agent alone in xenogeneic mouse tumor models of disseminated lymphoma. Therefore, our results do suggest that the therapeutic efficacy of rituximab may be improved when used in combination with rIL-21.
url http://europepmc.org/articles/PMC3692496?pdf=render
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