Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment

Abstract Background The anti-tumor activity of anti-PD-1/PD-L1 therapies correlates with T cell infiltration in tumors. Thus, a major goal in oncology is to find strategies that enhance T cell infiltration and efficacy of anti-PD-1/PD-L1 therapy. TGF-β has been shown to contribute to T cell exclusio...

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Main Authors: Yoong Wearn Lim, Garry L. Coles, Savreet K. Sandhu, David S. Johnson, Adam S. Adler, Erica L. Stone
Format: Article
Language:English
Published: BMC 2021-05-01
Series:BMC Biology
Subjects:
Online Access:https://doi.org/10.1186/s12915-021-01034-z
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author Yoong Wearn Lim
Garry L. Coles
Savreet K. Sandhu
David S. Johnson
Adam S. Adler
Erica L. Stone
author_facet Yoong Wearn Lim
Garry L. Coles
Savreet K. Sandhu
David S. Johnson
Adam S. Adler
Erica L. Stone
author_sort Yoong Wearn Lim
collection DOAJ
description Abstract Background The anti-tumor activity of anti-PD-1/PD-L1 therapies correlates with T cell infiltration in tumors. Thus, a major goal in oncology is to find strategies that enhance T cell infiltration and efficacy of anti-PD-1/PD-L1 therapy. TGF-β has been shown to contribute to T cell exclusion, and anti-TGF-β improves anti-PD-L1 efficacy in vivo. However, TGF-β inhibition has frequently been shown to induce toxicity in the clinic, and the clinical efficacy of combination PD-L1 and TGF-β blockade has not yet been proven. To identify strategies to overcome resistance to PD-L1 blockade, the transcriptional programs associated with PD-L1 and/or TGF-β blockade in the tumor microenvironment should be further elucidated. Results We used single-cell RNA sequencing in a mouse model to characterize the transcriptomic effects of PD-L1 and/or TGF-β blockade on nearly 30,000 single cells in the tumor and surrounding microenvironment. Combination treatment led to upregulation of immune response genes, including multiple chemokine genes such as CCL5, in macrophages, and downregulation of extracellular matrix genes in fibroblasts. Analysis of publicly available tumor transcriptome profiles showed that the chemokine CCL5 was strongly associated with immune cell infiltration in various human cancers. Further investigation with in vivo models showed that intratumorally administered CCL5 enhanced cytotoxic lymphocytes and the anti-tumor activity of anti-PD-L1. Conclusions Taken together, our data could be leveraged translationally to complement or find alternatives to anti-PD-L1 plus anti-TGF-β combination therapy, for example through companion biomarkers, and/or to identify novel targets that could be modulated to overcome resistance.
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spelling doaj.art-00fd9007a4614376a1b047d12d4c34302022-12-21T22:31:21ZengBMCBMC Biology1741-70072021-05-0119111710.1186/s12915-021-01034-zSingle-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironmentYoong Wearn Lim0Garry L. Coles1Savreet K. Sandhu2David S. Johnson3Adam S. Adler4Erica L. Stone5GigaGen, Inc.GigaGen, Inc.GigaGen, Inc.GigaGen, Inc.GigaGen, Inc.GigaGen, Inc.Abstract Background The anti-tumor activity of anti-PD-1/PD-L1 therapies correlates with T cell infiltration in tumors. Thus, a major goal in oncology is to find strategies that enhance T cell infiltration and efficacy of anti-PD-1/PD-L1 therapy. TGF-β has been shown to contribute to T cell exclusion, and anti-TGF-β improves anti-PD-L1 efficacy in vivo. However, TGF-β inhibition has frequently been shown to induce toxicity in the clinic, and the clinical efficacy of combination PD-L1 and TGF-β blockade has not yet been proven. To identify strategies to overcome resistance to PD-L1 blockade, the transcriptional programs associated with PD-L1 and/or TGF-β blockade in the tumor microenvironment should be further elucidated. Results We used single-cell RNA sequencing in a mouse model to characterize the transcriptomic effects of PD-L1 and/or TGF-β blockade on nearly 30,000 single cells in the tumor and surrounding microenvironment. Combination treatment led to upregulation of immune response genes, including multiple chemokine genes such as CCL5, in macrophages, and downregulation of extracellular matrix genes in fibroblasts. Analysis of publicly available tumor transcriptome profiles showed that the chemokine CCL5 was strongly associated with immune cell infiltration in various human cancers. Further investigation with in vivo models showed that intratumorally administered CCL5 enhanced cytotoxic lymphocytes and the anti-tumor activity of anti-PD-L1. Conclusions Taken together, our data could be leveraged translationally to complement or find alternatives to anti-PD-L1 plus anti-TGF-β combination therapy, for example through companion biomarkers, and/or to identify novel targets that could be modulated to overcome resistance.https://doi.org/10.1186/s12915-021-01034-zPD-L1TGF-βTumor microenvironmentscRNA-seqImmuno-oncology
spellingShingle Yoong Wearn Lim
Garry L. Coles
Savreet K. Sandhu
David S. Johnson
Adam S. Adler
Erica L. Stone
Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
BMC Biology
PD-L1
TGF-β
Tumor microenvironment
scRNA-seq
Immuno-oncology
title Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
title_full Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
title_fullStr Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
title_full_unstemmed Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
title_short Single-cell transcriptomics reveals the effect of PD-L1/TGF-β blockade on the tumor microenvironment
title_sort single cell transcriptomics reveals the effect of pd l1 tgf β blockade on the tumor microenvironment
topic PD-L1
TGF-β
Tumor microenvironment
scRNA-seq
Immuno-oncology
url https://doi.org/10.1186/s12915-021-01034-z
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