CD4 T cell dynamics shape the immune response to combination oncolytic herpes virus and BRAF inhibitor therapy for melanoma.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
03 2022
Historique:
accepted: 04 03 2022
entrez: 26 3 2022
pubmed: 27 3 2022
medline: 15 4 2022
Statut: ppublish

Résumé

Combination herpes simplex virus (HSV) oncolytic virotherapy and BRAF inhibitors (BRAFi) represent promising immunogenic treatments for BRAF mutant melanoma, but an improved understanding of the immunobiology of combinations is needed to improve on the benefit of immune checkpoint inhibitors (ICI). Using a BRAF Adding BRAFi treatment to HSV improved anti-tumor effects in vivo but not in vitro. Immune characterization showed HSV or dual therapy led to fewer intratumoral Treg, although with a more activated phenotype, together with more effector CD8 +T cells. Tocky analysis further showed that HSV/BRAFi dual treatment reduced the Tocky signal (reflecting engagement with cognate antigen), in both Treg and conventional subsets of CD4+, but not in CD8 +cells. However, a higher percentage of Treg than of conventional CD4 +maintained frequent engagement with antigens on treatment, reflecting a predominance of suppressive over effector function within the CD4 +compartment. The only T cell subset which correlated with a reduction in tumor growth was within Tocky signal positive conventional CD4+, supporting their therapeutic role. Targeting CD25 high, antigen-engaged Treg with a depleting anti-CD25 ICI, achieved complete cures in 100% of mice with triple therapy. Transcriptomic analysis confirmed reduction in Foxp3 on addition of anti-CD25 to HSV/BRAFi, as well as increases in expression of genes reflecting interferon signaling and cytotoxic activity. Combination HSV/BRAFi is an immunogenic therapy for BRAF mutant melanoma, but cannot fully control tumors. Dual therapy results in changes in T cell dynamics within tumors, with relatively maintained antigen signaling in Treg compared with conv CD4+. Antigen-engaged CD4 +effectors correlate with tumor growth control, and depletion of Treg by addition of an anti-CD25 ICI, releasing suppression of conventional CD4 +effectors by Treg, enhances survival and activates immune signaling within tumors.

Sections du résumé

BACKGROUND
Combination herpes simplex virus (HSV) oncolytic virotherapy and BRAF inhibitors (BRAFi) represent promising immunogenic treatments for BRAF mutant melanoma, but an improved understanding of the immunobiology of combinations is needed to improve on the benefit of immune checkpoint inhibitors (ICI).
METHODS
Using a BRAF
RESULTS
Adding BRAFi treatment to HSV improved anti-tumor effects in vivo but not in vitro. Immune characterization showed HSV or dual therapy led to fewer intratumoral Treg, although with a more activated phenotype, together with more effector CD8 +T cells. Tocky analysis further showed that HSV/BRAFi dual treatment reduced the Tocky signal (reflecting engagement with cognate antigen), in both Treg and conventional subsets of CD4+, but not in CD8 +cells. However, a higher percentage of Treg than of conventional CD4 +maintained frequent engagement with antigens on treatment, reflecting a predominance of suppressive over effector function within the CD4 +compartment. The only T cell subset which correlated with a reduction in tumor growth was within Tocky signal positive conventional CD4+, supporting their therapeutic role. Targeting CD25 high, antigen-engaged Treg with a depleting anti-CD25 ICI, achieved complete cures in 100% of mice with triple therapy. Transcriptomic analysis confirmed reduction in Foxp3 on addition of anti-CD25 to HSV/BRAFi, as well as increases in expression of genes reflecting interferon signaling and cytotoxic activity.
CONCLUSIONS
Combination HSV/BRAFi is an immunogenic therapy for BRAF mutant melanoma, but cannot fully control tumors. Dual therapy results in changes in T cell dynamics within tumors, with relatively maintained antigen signaling in Treg compared with conv CD4+. Antigen-engaged CD4 +effectors correlate with tumor growth control, and depletion of Treg by addition of an anti-CD25 ICI, releasing suppression of conventional CD4 +effectors by Treg, enhances survival and activates immune signaling within tumors.

Identifiants

pubmed: 35338089
pii: jitc-2021-004410
doi: 10.1136/jitc-2021-004410
pmc: PMC8961178
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Cancer Research UK
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Galabina Bozhanova (G)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Jehanne Hassan (J)

Imperial College London, London, UK.

Lizzie Appleton (L)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.
Imperial College London, London, UK.

Victoria Jennings (V)

Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, UK.

Shane Foo (S)

Radiotherapy & Imaging, The Institute of Cancer Research, London, UK.

Martin McLaughlin (M)

Institute of Cancer Research, London, UK.

Charleen Ml Chan Wah Hak (CM)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Emmanuel C Patin (EC)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Eva Crespo-Rodriguez (E)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Gabby Baker (G)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Edward Armstrong (E)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Matthew Chiu (M)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Hardev Pandha (H)

Oncology, University of Surrey, Guildford, UK.

Adel Samson (A)

Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, UK.

Victoria Roulstone (V)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Joan Kyula (J)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Richard Vile (R)

Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Fiona Errington-Mais (F)

Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, UK.

Malin Pedersen (M)

Translational Immunotherapy/Targeted Therapy Teams, The Institute of Cancer Research, London, UK.

Kevin Harrington (K)

Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.

Masahiro Ono (M)

Imperial College London, London, UK.

Alan Melcher (A)

Institute of Cancer Research, London, UK alan.melcher@icr.ac.uk.

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Classifications MeSH