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Devil facial tumor disease (DFTD) is renowned for its successful evasion of the host immune system. Down regulation of the major histocompatabilty complex class I molecule (MHC-I) on the DFTD cells is a primary mechanism of immune escape. Immunization trials on captive Tasmanian devils have previously demonstrated that an immune response against DFTD can be induced, and that immune-mediated tumor regression can occur. However, these trials were limited by their small sample sizes. Here, we describe the results of two DFTD immunization trials on cohorts of devils prior to their wild release as part of the Tasmanian Government's Wild Devil Recovery project. 95% of the devils developed anti-DFTD antibody responses. Given the relatively large sample sizes of the trials (N = 19 and N = 33), these responses are likely to reflect those of the general devil population. DFTD cells manipulated to express MHC-I were used as the antigenic basis of the immunizations in both trials. Although the adjuvant composition and number of immunizations differed between trials, similar anti-DFTD antibody levels were obtained. The first trial comprised DFTD cells and the adjuvant combination of ISCOMATRIX™, polyIC, and CpG with up to four immunizations given at monthly intervals. This compared to the second trial whereby two immunizations comprising DFTD cells and the adjuvant combination ISCOMATRIX™, polyICLC (Hiltonol®) and imiquimod were given a month apart, providing a shorter and, therefore, more practical protocol. Both trials incorporated a booster immunization given up to 5 months after the primary course. A key finding was that devils in the second trial responded more quickly and maintained their antibody levels for longer compared to devils in the first trial. The different adjuvant combination incorporating the RNAase resistant polyICLC and imiquimod used in the second trial is likely to be responsible. The seroconversion in the majority of devils in these anti-DFTD immunization trials was remarkable, especially as DFTD is hallmarked by its immune evasion mechanisms. Microsatellite analyzes of MHC revealed that some MHC-I microsatellites correlated to stronger immune responses. These trials signify the first step in the long-term objective of releasing devils with immunity to DFTD into the wild. ; Ruth Pye, Amanda Patchett, Elspeth McLennan, Russell Thomson, Scott Carver . A. Bruce Lyons . et al.

We present the results of a process to attempt to identify 100 questions that, if answered, would make a substantial difference to terrestrial and marine landscape restoration in Europe. Representatives from a wide range of European governmental and non-governmental conservation organisations, universities, independent ecologists and land managers compiled 677 questions relating to all aspects of European landscape restoration for nature and people. The questions were shortlisted by an email vote, followed by a two-day workshop, to produce the final list of 100 questions. Many of the final questions evolved through a process of modification and combination as the workshop progressed. The questions are divided into eight sections: conservation of biodiversity; connectivity, migration and translocations; delivering and evaluating restoration; natural processes; ecosystem services; social and cultural aspects of restoration; policy and governance; and economics. We anticipate that these questions will help identify new directions for researchers and policy-makers and assist funders and programme managers in allocating funds and planning projects, resulting in improved understanding and implementation of landscape-scale ecological restoration in Europe.