Antiviral antibody responses to systemic administration of an oncolytic RNA virus: the impact of standard concomitant anticancer chemotherapies.


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:
07 2021
Historique:
accepted: 05 07 2021
entrez: 24 7 2021
pubmed: 25 7 2021
medline: 12 1 2022
Statut: ppublish

Résumé

Oncolytic reovirus therapy for cancer induces a typical antiviral response to this RNA virus, including neutralizing antibodies. Concomitant treatment with cytotoxic chemotherapies has been hypothesized to improve the therapeutic potential of the virus. Chemotherapy side effects can include immunosuppression, which may slow the rate of the antiviral antibody response, as well as potentially make the patient more vulnerable to viral infection. Reovirus neutralizing antibody data were aggregated from separate phase I clinical trials of reovirus administered as a single agent or in combination with gemcitabine, docetaxel, carboplatin and paclitaxel doublet or cyclophosphamide. In addition, the kinetics of individual antibody isotypes were profiled in sera collected in these trials. These data demonstrate preserved antiviral antibody responses, with only moderately reduced kinetics with some drugs, most notably gemcitabine. All patients ultimately produced an effective neutralizing antibody response. Patients' responses to infection by reovirus are largely unaffected by the concomitant drug treatments tested, providing confidence that RNA viral treatment or infection is compatible with standard of care treatments.

Sections du résumé

BACKGROUND
Oncolytic reovirus therapy for cancer induces a typical antiviral response to this RNA virus, including neutralizing antibodies. Concomitant treatment with cytotoxic chemotherapies has been hypothesized to improve the therapeutic potential of the virus. Chemotherapy side effects can include immunosuppression, which may slow the rate of the antiviral antibody response, as well as potentially make the patient more vulnerable to viral infection.
METHOD
Reovirus neutralizing antibody data were aggregated from separate phase I clinical trials of reovirus administered as a single agent or in combination with gemcitabine, docetaxel, carboplatin and paclitaxel doublet or cyclophosphamide. In addition, the kinetics of individual antibody isotypes were profiled in sera collected in these trials.
RESULTS
These data demonstrate preserved antiviral antibody responses, with only moderately reduced kinetics with some drugs, most notably gemcitabine. All patients ultimately produced an effective neutralizing antibody response.
CONCLUSION
Patients' responses to infection by reovirus are largely unaffected by the concomitant drug treatments tested, providing confidence that RNA viral treatment or infection is compatible with standard of care treatments.

Identifiants

pubmed: 34301814
pii: jitc-2021-002673
doi: 10.1136/jitc-2021-002673
pmc: PMC8728387
pii:
doi:

Substances chimiques

Antibodies, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical Research Council
ID : MR/L023091/1
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: No, there are no competing interests.

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Auteurs

Victoria Roulstone (V)

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

David Mansfield (D)

Radiotherapy and Imaging, The Institute of Cancer Research, London, UK david.mansfield@icr.ac.uk.

Robert J Harris (RJ)

St John's Institute of Dermatology, Guy's Hospital, London, UK.

Katie Twigger (K)

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

Christine White (C)

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

Johann de Bono (J)

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

James Spicer (J)

St John's Institute of Dermatology, Guy's Hospital, London, UK.

Sophia N Karagiannis (SN)

St John's Institute of Dermatology, Guy's Hospital, London, UK.

Richard Vile (R)

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

Hardev Pandha (H)

Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.

Alan Melcher (A)

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

Kevin Harrington (K)

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

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