Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.

The association of B7-1/CD28 between antigen presenting cells (APCs) and T-cells provides a second signal to proliferate and activate T-cell immunity at the induction phase. Many reports indicate that tumor cells transfected with B7-1 induced augmented antitumor immunity at the induction phase by mi...

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Main Authors: Xiao-Lin Li, Marjolein Sluijter, Elien M Doorduijn, Shubha P Kale, Harris McFerrin, Yong-Yu Liu, Yan Li, Madhusoodanan Mottamal, Xin Yao, Fengkun Du, Baihan Gu, Kim Hoang, Yen H Nguyen, Nichelle Taylor, Chelsea R Stephens, Thorbald van Hall, Qian-Jin Zhang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4226464?pdf=render
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author Xiao-Lin Li
Marjolein Sluijter
Elien M Doorduijn
Shubha P Kale
Harris McFerrin
Yong-Yu Liu
Yan Li
Madhusoodanan Mottamal
Xin Yao
Fengkun Du
Baihan Gu
Kim Hoang
Yen H Nguyen
Nichelle Taylor
Chelsea R Stephens
Thorbald van Hall
Qian-Jin Zhang
author_facet Xiao-Lin Li
Marjolein Sluijter
Elien M Doorduijn
Shubha P Kale
Harris McFerrin
Yong-Yu Liu
Yan Li
Madhusoodanan Mottamal
Xin Yao
Fengkun Du
Baihan Gu
Kim Hoang
Yen H Nguyen
Nichelle Taylor
Chelsea R Stephens
Thorbald van Hall
Qian-Jin Zhang
author_sort Xiao-Lin Li
collection DOAJ
description The association of B7-1/CD28 between antigen presenting cells (APCs) and T-cells provides a second signal to proliferate and activate T-cell immunity at the induction phase. Many reports indicate that tumor cells transfected with B7-1 induced augmented antitumor immunity at the induction phase by mimicking APC function; however, the function of B7-1 on antitumor immunity at the effector phase is unknown. Here, we report direct evidence of enhanced T-cell antitumor immunity at the effector phase by the B7-1 molecule. Our experiments in vivo and in vitro indicated that reactivity of antigen-specific monoclonal and polyclonal T-cell effectors against a Lass5 epitope presented by RMA-S cells is increased when the cells expressed B7-1. Use of either anti-B7-1 or anti-CD28 antibodies to block the B7-1/CD28 association reduced reactivity of the T effectors against B7-1 positive RMA-S cells. Transfection of Lass5 cDNA into or pulse of Lass5 peptide onto B7-1 positive RMA-S cells overcomes the requirement of the B7-1/CD28 signal for T effector response. To our knowledge, the data offers, for the first time, strong evidence that supports the requirement of B7-1/CD28 secondary signal at the effector phase of antitumor T-cell immunity being dependent on the density of an antigenic peptide.
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spelling doaj.art-f19ef3458ca444f3bfe66781882d6c972022-12-21T18:09:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e10819210.1371/journal.pone.0108192Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.Xiao-Lin LiMarjolein SluijterElien M DoorduijnShubha P KaleHarris McFerrinYong-Yu LiuYan LiMadhusoodanan MottamalXin YaoFengkun DuBaihan GuKim HoangYen H NguyenNichelle TaylorChelsea R StephensThorbald van HallQian-Jin ZhangThe association of B7-1/CD28 between antigen presenting cells (APCs) and T-cells provides a second signal to proliferate and activate T-cell immunity at the induction phase. Many reports indicate that tumor cells transfected with B7-1 induced augmented antitumor immunity at the induction phase by mimicking APC function; however, the function of B7-1 on antitumor immunity at the effector phase is unknown. Here, we report direct evidence of enhanced T-cell antitumor immunity at the effector phase by the B7-1 molecule. Our experiments in vivo and in vitro indicated that reactivity of antigen-specific monoclonal and polyclonal T-cell effectors against a Lass5 epitope presented by RMA-S cells is increased when the cells expressed B7-1. Use of either anti-B7-1 or anti-CD28 antibodies to block the B7-1/CD28 association reduced reactivity of the T effectors against B7-1 positive RMA-S cells. Transfection of Lass5 cDNA into or pulse of Lass5 peptide onto B7-1 positive RMA-S cells overcomes the requirement of the B7-1/CD28 signal for T effector response. To our knowledge, the data offers, for the first time, strong evidence that supports the requirement of B7-1/CD28 secondary signal at the effector phase of antitumor T-cell immunity being dependent on the density of an antigenic peptide.http://europepmc.org/articles/PMC4226464?pdf=render
spellingShingle Xiao-Lin Li
Marjolein Sluijter
Elien M Doorduijn
Shubha P Kale
Harris McFerrin
Yong-Yu Liu
Yan Li
Madhusoodanan Mottamal
Xin Yao
Fengkun Du
Baihan Gu
Kim Hoang
Yen H Nguyen
Nichelle Taylor
Chelsea R Stephens
Thorbald van Hall
Qian-Jin Zhang
Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
PLoS ONE
title Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
title_full Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
title_fullStr Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
title_full_unstemmed Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
title_short Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase.
title_sort limited density of an antigen presented by rma s cells requires b7 1 cd28 signaling to enhance t cell immunity at the effector phase
url http://europepmc.org/articles/PMC4226464?pdf=render
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