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dc.contributor.authorToor, SM
dc.contributor.authorSasidharan, N
dc.contributor.authorPfister, G
dc.contributor.authorElkord, Eyad
dc.date.accessioned2019-03-18T07:52:28Z
dc.date.available2019-03-18T07:52:28Z
dc.date.issued2019en
dc.identifier.citationToor SM, Sasidharan Nair V, Pfister G, Elkord E. Effect of pembrolizumab on CD4(+) CD25(+) , CD4(+) LAP(+) and CD4(+) TIM-3(+) T cell subsets. Clin Exp Immunol. 2019 Jan 28.en
dc.identifier.pmid30693485en
dc.identifier.doi10.1111/cei.13264en
dc.identifier.urihttp://hdl.handle.net/10541/621611
dc.description.abstractTumor immune evasion involves the expansion of avidly proliferating immunosuppressive cells and inhibition of effector T cell proliferation. Immune checkpoints (IC) block the activation pathways of tumor-reactive T cells. IC pathways are often exploited by tumor cells to evade immune destruction, and blocking these pathways through IC inhibitors (ICI) has shown promising results in multiple malignancies. In this study, we investigated the effects of an ICI, pembrolizumab, on various T cell subsets in vitro. We compared the suppressive activity of CD4+ CD25+ regulatory T cells (conventional Treg ) with T cells expressing T cell immunoglobulin-3+ (TIM-3+ ) and latency-associated peptide (LAP)+ T cells. We found that LAP-expressing T cells were more suppressive than conventional Treg , but TIM-3-expressing T cells were not suppressive. Our results show that pembrolizumab does not modulate functions of Treg and mediates its immunostimulatory effects via the release of effector T cells from suppression. These findings may assist in the development of agents designed to intervene in IC pathways to overcome Treg resistance to ICI.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1111/cei.13264en
dc.titleEffect of pembrolizumab on CD4(+) CD25(+) , CD4(+) LAP(+) and CD4(+) TIM-3(+) T cell subsets.en
dc.typeArticleen
dc.contributor.departmentCancer Research Center, Qatar, Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, Doha, Qataren
dc.identifier.journalClinical and Experimental Immunologyen
dc.description.noteen]


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