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Regression of devil facial tumour disease following immunotherapy in immunised Tasmanian devils

Regression of devil facial tumour disease following immunotherapy in immunised Tasmanian devils
Regression of devil facial tumour disease following immunotherapy in immunised Tasmanian devils
Devil facial tumour disease (DFTD) is a transmissible cancer devastating the Tasmanian devil (Sarcophilus harrisii) population. The cancer cell is the ‘infectious’ agent transmitted as an allograft by biting. Animals usually die within a few months with no evidence of antibody or immune cell responses against the DFTD allograft. This lack of anti-tumour immunity is attributed to an absence of cell surface major histocompatibility complex (MHC)-I molecule expression. While the endangerment of the devil population precludes experimentation on large experimental groups, those examined in our study indicated that immunisation and immunotherapy with DFTD cells expressing surface MHC-I corresponded with effective anti-tumour responses. Tumour engraftment did not occur in one of the five immunised Tasmanian devils, and regression followed therapy of experimentally induced DFTD tumours in three Tasmanian devils. Regression correlated with immune cell infiltration and antibody responses against DFTD cells. These data support the concept that immunisation of devils with DFTD cancer cells can successfully induce humoral responses against DFTD and trigger immune-mediated regression of established tumours. Our findings support the feasibility of a protective DFTD vaccine and ultimately the preservation of the species.
2045-2322
Tovar, Cesar
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Pye, Ruth J.
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Kreiss, Alexandre
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Cheng, Yuanyuan
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Brown, Gabriella K.
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Darby, Jocelyn
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Malley, Roslyn C.
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Siddle, Hannah V. T.
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Skjødt, Karsten
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Kaufman, Jim
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Silva, Anabel
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Baz Morelli, Adriana
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Papenfuss, Anthony T.
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Corcoran, Lynn M.
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Murphy, James M.
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Pearse, Martin J.
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Belov, Katherine
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Lyons, A. Bruce
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Woods, Gregory M.
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Tovar, Cesar
4f690817-bccc-4123-92e7-63730ff14221
Pye, Ruth J.
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Kreiss, Alexandre
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Cheng, Yuanyuan
5ecff653-5fa6-45f3-ae30-61d4e955f3ac
Brown, Gabriella K.
80217ac2-f985-4463-be58-c9614898b537
Darby, Jocelyn
c702daae-1a87-4b2a-be3c-9380e7bd4a59
Malley, Roslyn C.
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Siddle, Hannah V. T.
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Skjødt, Karsten
9692db3f-9512-4106-b006-6a312a3715f5
Kaufman, Jim
c2afcfb2-dc2b-45af-8c80-83ad341aa78f
Silva, Anabel
badcf564-61a8-4710-be32-dc97bdee3454
Baz Morelli, Adriana
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Papenfuss, Anthony T.
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Corcoran, Lynn M.
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Murphy, James M.
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Pearse, Martin J.
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Belov, Katherine
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Lyons, A. Bruce
fe7b8829-9c3f-496d-926f-d9687aefbb3a
Woods, Gregory M.
5e97f157-aaa1-4e46-b718-c75bcf2fe611

Tovar, Cesar, Pye, Ruth J., Kreiss, Alexandre, Cheng, Yuanyuan, Brown, Gabriella K., Darby, Jocelyn, Malley, Roslyn C., Siddle, Hannah V. T., Skjødt, Karsten, Kaufman, Jim, Silva, Anabel, Baz Morelli, Adriana, Papenfuss, Anthony T., Corcoran, Lynn M., Murphy, James M., Pearse, Martin J., Belov, Katherine, Lyons, A. Bruce and Woods, Gregory M. (2017) Regression of devil facial tumour disease following immunotherapy in immunised Tasmanian devils. Scientific Reports, 7, [43827]. (doi:10.1038/srep43827).

Record type: Article

Abstract

Devil facial tumour disease (DFTD) is a transmissible cancer devastating the Tasmanian devil (Sarcophilus harrisii) population. The cancer cell is the ‘infectious’ agent transmitted as an allograft by biting. Animals usually die within a few months with no evidence of antibody or immune cell responses against the DFTD allograft. This lack of anti-tumour immunity is attributed to an absence of cell surface major histocompatibility complex (MHC)-I molecule expression. While the endangerment of the devil population precludes experimentation on large experimental groups, those examined in our study indicated that immunisation and immunotherapy with DFTD cells expressing surface MHC-I corresponded with effective anti-tumour responses. Tumour engraftment did not occur in one of the five immunised Tasmanian devils, and regression followed therapy of experimentally induced DFTD tumours in three Tasmanian devils. Regression correlated with immune cell infiltration and antibody responses against DFTD cells. These data support the concept that immunisation of devils with DFTD cancer cells can successfully induce humoral responses against DFTD and trigger immune-mediated regression of established tumours. Our findings support the feasibility of a protective DFTD vaccine and ultimately the preservation of the species.

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Accepted/In Press date: 1 February 2017
e-pub ahead of print date: 9 March 2017
Published date: 9 March 2017
Organisations: Biological Sciences, Academic

Identifiers

Local EPrints ID: 407990
URI: http://eprints.soton.ac.uk/id/eprint/407990
ISSN: 2045-2322
PURE UUID: dee047da-d99a-4284-abe5-c482d5fdaad7
ORCID for Hannah V. T. Siddle: ORCID iD orcid.org/0000-0003-2906-4385

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Date deposited: 06 May 2017 01:04
Last modified: 16 Mar 2024 04:18

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Contributors

Author: Cesar Tovar
Author: Ruth J. Pye
Author: Alexandre Kreiss
Author: Yuanyuan Cheng
Author: Gabriella K. Brown
Author: Jocelyn Darby
Author: Roslyn C. Malley
Author: Karsten Skjødt
Author: Jim Kaufman
Author: Anabel Silva
Author: Adriana Baz Morelli
Author: Anthony T. Papenfuss
Author: Lynn M. Corcoran
Author: James M. Murphy
Author: Martin J. Pearse
Author: Katherine Belov
Author: A. Bruce Lyons
Author: Gregory M. Woods

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