|Allorecognition in the Tasmanian devil (Sarcophilus harrisii), an endangered marsupial species with limited genetic diversity.|
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|PMID: 21811598 Owner: NLM Status: MEDLINE|
|Tasmanian devils (Sarcophilus harrisii) are on the verge of extinction due to a transmissible cancer, devil facial tumour disease (DFTD). This tumour is an allograft that is transmitted between individuals without immune recognition of the tumour cells. The mechanism to explain this lack of immune recognition and acceptance is not well understood. It has been hypothesized that lack of genetic diversity at the Major Histocompatibility Complex (MHC) allowed the tumour cells to grow in genetically similar hosts without evoking an immune response to alloantigens. We conducted mixed lymphocyte reactions and skin grafts to measure functional MHC diversity in the Tasmanian devil population. The limited MHC diversity was sufficient to produce measurable mixed lymphocyte reactions. There was a wide range of responses, from low or no reaction to relatively strong responses. The highest responses occurred when lymphocytes from devils from the east of Tasmania were mixed with lymphocytes from devils from the west of Tasmania. All of the five successful skin allografts were rejected within 14 days after surgery, even though little or no MHC I and II mismatches were found. Extensive T-cell infiltration characterised the immune rejection. We conclude that Tasmanian devils are capable of allogeneic rejection. Consequently, a lack of functional allorecognition mechanisms in the devil population does not explain the transmission of a contagious cancer.|
|Alexandre Kreiss; Yuanyuan Cheng; Frank Kimble; Barrie Wells; Shaun Donovan; Katherine Belov; Gregory M Woods|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2011-07-21|
|Title: PloS one Volume: 6 ISSN: 1932-6203 ISO Abbreviation: PLoS ONE Publication Date: 2011|
|Created Date: 2011-08-03 Completed Date: 2011-12-05 Revised Date: 2013-06-28|
Medline Journal Info:
|Nlm Unique ID: 101285081 Medline TA: PLoS One Country: United States|
|Languages: eng Pagination: e22402 Citation Subset: IM|
|Menzies Research Institute Tasmania, University of Tasmania, Tasmania, Australia. firstname.lastname@example.org|
|APA/MLA Format Download EndNote Download BibTex|
Graft Rejection / immunology
Lymphocyte Culture Test, Mixed
Major Histocompatibility Complex / genetics
Marsupialia / genetics*, immunology*
Sequence Analysis, Protein
Skin Transplantation / immunology
Journal ID (nlm-ta): PLoS One
Journal ID (publisher-id): plos
Journal ID (pmc): plosone
Publisher: Public Library of Science, San Francisco, USA
Kreiss et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Received Day: 27 Month: 5 Year: 2011
Accepted Day: 21 Month: 6 Year: 2011
collection publication date: Year: 2011
Electronic publication date: Day: 21 Month: 7 Year: 2011
Volume: 6 Issue: 7
E-location ID: e22402
PubMed Id: 21811598
Publisher Id: PONE-D-11-09605
|Allorecognition in the Tasmanian Devil (Sarcophilus harrisii), an Endangered Marsupial Species with Limited Genetic Diversity Alternate Title:Allorecognition in the Tasmanian Devil|
|Gregory M. Woods1|
|Matthias G. von Herrathedit1||
1Menzies Research Institute Tasmania, University of Tasmania, Tasmania, Australia
2Faculty of Veterinary Science, University of Sydney, New South Wales, Australia
3School of Medicine, University of Tasmania, Tasmania, Australia
4Royal Hobart Hospital, Department of Pathology, Tasmania, Australia
|La Jolla Institute of Allergy and Immunology, United States of America
|Correspondence: * E-mail: email@example.com
Contributed by footnote: Conceived and designed the experiments: AK KB GMW. Performed the experiments: AK YC FK BW. Analyzed the data: AK YC KB SD GMW. Wrote the paper: AK GMW. Read and commented on the manuscript: AK YC FK BW SD KB GMW.
Devil facial tumour disease (DFTD) is a transmissible Schwann cell cancer of Tasmanian devils (Sarcophilus harrisii) , , . The cancer cells are passed from animal to animal during the process of biting, which most frequently occurs on the head and neck. Metastases to distant organs are common and affected devils die within months after tumours become apparent , . This disease was noted in 1996 in the far northeast of Tasmania, and has since spread to over half of the devil's range , . The far northwestern areas of Tasmania still remain disease free, although it is predicted that DFTD will affect all devil habitat within the decade. It is possible that extinction of the species will occur within 20 years .
Despite being a cell allograft, DFTD tumours do not evoke an immune response , and there is no evidence of lymphocyte infiltration into the tumour masses . In vertebrates, organ, tissue or cell transplants are rejected by the immune system, unless the recipient is severely immunocompromised or both recipient and donor share identical Major Histocompatibility Complex (MHC) genes (e.g. homozygous twins) . MHC genes were originally identified in mammalian cells, encoding specialised glycoproteins expressed on the cell surface of almost all nucleated cells. These genes were first related to foreign tissue (allograft) transplantation, but are now known to be essential in the immune recognition of pathogens and tumour cells , . There are two main MHC subgroups that have different immunological functions, MHC I and MHC II. MHC I molecules are composed of a polymorphic α-chain associated with a non-polymorphic β2-microglobulin. Its role is to present intracellular antigens to CD8+ T-cells. These molecules are present on all nucleated cells. MHC II molecules are composed of a polymorphic α-chain attached to a polymorphic β-chain, and present extracellular antigens to CD4+ T-cells. Under normal conditions, MHC II is only located on the cell surface of professional antigen presenting cells, such as dendritic cells and macrophages (reviewed in , ). Tasmanian devils have a competent immune system , , but the devil population has been through genetic bottlenecks and lacks MHC diversity , .
MHC molecules regulate the immunological mechanisms of tissue graft rejection and provoke vigorous T-cell responses against incompatible cells , . Different effector processes may reject the allografts, but the main mediators are CD8+ T-cells and CD4+ T-cells. Allopeptides presented to CD8+ T-cells by MHC I molecules stimulate the differentiation of cytotoxic T-cells, which kill nucleated cells expressing MHC I in the graft. Alloantigens presented by MHC II molecules activate helper T-cells, which differentiate and produce cytokines that damage the tissue graft. Allograft rejection mediated by CD4+ and CD8+ T cells is deemed acute rejection, as it can usually occur within eight to 12 days after the transplant. This form of rejection is primarily due to mismatching of MHC loci , .
A predictive in vitro test for T-cell recognition of allogeneic MHC molecules is the mixed lymphocyte reaction (MLR) . This experiment has been used in clinical analyses of allogeneic impact of MHC I and II mismatches between live donors (e.g. kidney donors) and recipients. Donors with poor MLR responses against the recipient have lower incidence of graft rejection , . MLR experiments can be performed with cultured lymphocytes from both donor and recipient and the resultant proliferation will correspond to differences in the MHC alleles of both individuals (two-way MLR). By inactivating the mononuclear cells from the donor (by X-irradiation or chemical mitotic inhibition), only the recipient response is evaluated (one-way MLR).
Skin grafting between unrelated individuals has been performed to test MHC disparity in a wild mammal, the cheetah (Acynonyx jubatus). Captive cheetahs were unable to quickly recognize alloantigens as foreign and reject the skin grafts . More recently, wild-living Namibian cheetahs were shown to have low levels of MHC variation, although this did not appear to impair their immune response against infectious diseases , . To date, a lack of MHC diversity has been the primary reason given for the lack of rejection of allograft tumours by Tasmanian devils. It has been proposed that devils have a similar range of MHC antigens as the tumours , , and therefore do not see the tumours as foreign. Acceptance, or delayed rejection, of skin allografts would help to confirm the theory that impoverished MHC diversity is responsible for a lack of tumour allograft recognition , . To determine whether this limited MHC diversity is sufficiently low to permit allograft transplantation, we characterised levels of functional MHC variation by two-way MLR and skin grafts experiments.
All experiments describing the use of animals were undertaken with approval and under inspection of the Animal Ethics Committee of University of Tasmania, permit numbers A9491 and A11052. Captive devils were housed in groups of two or three in 100 m2 enclosures. Animals were fed possum or wallaby meat once a day and water ad libitum. All procedures (blood collection, skin graft surgery, biopsy and bandage removal) were performed with the animals under general anaesthesia and all efforts were made to minimise pain or discomfort.
Fifteen Tasmanian devils from five areas in eastern Tasmania (Nugent, Epping, Mount William National Park, Forestier Peninsula and Bronte Park) and nine devils from four regions in western Tasmania (Woolnorth, Temma, Granville Harbour and Milkshake Hills) were used. Figure 1 shows a map of Tasmania with the geographical locations of all devils used for MLR and skin graft experiments. The DFTD-affected area is also illustrated. Whole blood was collected into lithium heparin tubes from the jugular vein while under general anaesthesia. Mononuclear cells were harvested using density gradient centrifugation as described previously . Cells were diluted to a concentration of 106 cells/mL in RPMI 1640 incomplete medium (CSL Limited 05182301) supplemented with 10% pooled devil plasma, 2 mM of glutamine (Sigma G7513) and 15 mg of gentamicin (Pfizer 61022010).
MLR experiments were conducted in U-bottomed 96 well plates (Iwaki 3870-096), mixing 100 µL of a mononuclear cell suspension from one devil with 100 µL of a mononuclear cell suspension from another devil. Background controls consisted of 200 µL of mononuclear cells from individual devils incubated alone and positive controls consisted of mononuclear cells of individual devils incubated with 50 µg/mL of Concanavalin A (Con A, Sigma C7275). Mixed lymphocyte cultures were incubated at 37°C and 5% CO2 for 144 hours. Mitogen controls were incubated under the same conditions for 96 hours. Eighteen hours prior the harvesting, cultures were pulsed with 1 µCi tritiated thymidine (Amersham Pharmacia Biotech TRA 310) to assess proliferation. Cells were harvested onto a filter paper and dried overnight at room temperature. Uptake of thymidine by proliferating cells was measured by radiation emittance using a scintillation counter (Pharmacia, 1214 Rackbeta). Results were obtained in counts per minute (CPM) and stimulation indices (SI) were calculated with the formula: SI = Average CPM of mixed culture/Average CPM of control cultures. Mitogen stimulated culture controls were calculated by dividing the average of incorporated thymidine in stimulated cultures by non-stimulated cultures. All SI controls were considered to be one in the MLR experiments, as no proliferation was characterised in autologous cultures. All experiments were conducted in triplicates. MLR results were considered strong when SI >10, moderate when 5<SI<10 and low or no reaction when SI<5. To compare differences in MLR stimulation indices between groups and between ‘eastern versus eastern’, ‘western versus western’ and ‘eastern versus western’, results were log transformed and analysed with nonparametric Mann Whitney test with non-Gaussian distribution.
Seven unrelated captive devils of eastern Tasmania were used for two-way skin grafting experiments (one of the animals was used for two procedures). All devils were three year old females, except TD 187, which was a three year old male. Table 1 shows the pairing and origin of devils for each procedure. Surgeries were performed in two devils simultaneously. Animals were pre-medicated with acepromazine (0.2 mg/Kg) and morphine (1 mg/Kg) injected subcutaneously. For further analgesia, xylocaine 1% was injected in the subcutaneous tissue around the surgery site (not exceeding 20 mg/Kg). General anaesthesia was induced by isofluorane delivered via an endotracheal tube. The hair of the surgery site (the dorsal area of the animal) was clipped and shaved and the site disinfected with a solution of chlorexidine and cetrimide. The surgery field was covered with a sterile fenestrated drape.
A square (3×8 cm) was drawn on the skin of the mid-dorsal region of each devil and a dermatome knife with a sterile blade was used to ‘shave’ 1 mm thick dermis and epidermis of the demarcated skin. This loose piece of skin was divided into approximately two equal pieces (approximately 3×4 cm) and one of them slid in to the cranial wound (autograft). The other piece (allograft) was placed in sterile Hartmann's solution, until the same procedure had been performed on the other devil. The allograft skin pieces were then placed in the caudal position of the wound. Surgical glue was placed on the borders of the grafts to secure the skin. A sterile dressing was applied to the surgical wound and the thoracic and chest areas were covered with cotton wool and elastic bandages under firm pressure. Bandages were changed on Day 7 and removed on Day 14. Pain relief medication (meloxicam 0.05 mg/Kg) was administered in the food for three to five days after skin graft surgery.
On Days 7, 14 and 21 the grafts were visually inspected for signs of rejection. The grafts were photographed and a punch biopsy (3–4 mm) was taken from the grafts and fixed in 10% buffered formalin solution for one to four weeks. After fixation, skin biopsy punches were processed and paraffin embedded. Four to six sections (3 µm thickness) were cut onto 3-aminotriethoxysilane (Sigma A7222) coated slides for haematoxylin and eosin staining and the same number of sections was prepared for immunohistochemistry.
Skin biopsies were labelled for T-cells with a rabbit anti-human CD3 antibody (Dako A0452). Isotype controls included non-specific rabbit immunoglobulin fraction (Dako X0903) and negative controls were labelled without the primary antibody (replaced with antibody diluent, Dako S0809). Sections of devil lymph nodes were used as positive controls.
Tissue sections were deparaffinised in xylene and rehydrated through graded alcohol solutions to water and boiled in citrate buffer solution (pH 6) in an electric pressure cooker for 10 minutes at medium heat. Slides were left to cool to 35°C and placed in PBS. Endogenous peroxidase activity was quenched by incubating sections with a solution of 3% H2O2 for 15 minutes and non-specific protein binding was blocked with serum-free protein block solution (Dako X0909) for 30 minutes. The antibody was diluted (1∶800) with antibody diluent and placed onto the slides for 60 minutes. Antibody binding was detected by placing a biotinylated link universal followed by streptavidin and horseradish peroxidase (30 minutes each) (LSAB kit, Dako K0690). A solution of diaminobenzidine (Dako K3466) was placed onto the slides for ten minutes to allow for brown colour development of positive cells and then washed with distilled water. Sections were briefly counterstained with haematoxylin for 40 seconds, dehydrated through graded alcohol solutions to xylene and coverslipped.
Histology and CD3-labelled sections were examined for signs of immunological rejection and a pathological score adapted from a previous study in human hand transplantation  was given to each section. Table S1 describes the criteria used to determine immune rejection.
The seven individuals used for skin graft experiments were genotyped at MHC I α chain and MHC II β chain loci through nucleotide sequencing. Genomic DNA samples were extracted from fresh or frozen whole blood using MoBio UltraClean BloodSpin Kit. The α1 domain of MHC I genes and β1 domain of MHC II genes were amplified by PCR using previously published primers and PCR conditions , . PCR amplifications were performed on a Bio-Rad MJ Mini Personal Thermal Cycler and the Platinum Taq DNA Polymerase High Fidelity Kit (Invitrogen 11304-011) was used to ensure the lowest error rate. PCR products were isolated by running 1.8% agarose TBE gels using Bioline HyperLadder IV as size marker and purified from the gel using UltraClean 15 DNA Purification Kit (MoBio 12100-300). Purified DNA fragments were cloned in a pGEM-T Easy Vector (Promega A1360) /JM109 High Efficiency Competent Cells (Promega L1001) cloning system. Twenty-four clones were picked for each sample. Plasmids were extracted using UltraClean 6 Minute Mini Plasmid Prep Kit (MoBio 12300-250) and sequenced in two directions with T7 and SP6 primers at the Australian Genome Research Facility. Two independent PCRs were performed for each individual, and only sequence variants found in more than one PCR amplification were included in the subsequent analyses to minimize nucleotide errors yielded during PCR, cloning and sequencing. The sequencing results were quality-checked in Sequencher 4.1.4 (Gene Codes) and aligned with previously identified devil MHC alleles  in BioEdit using the ClustalW alignment tool , .
To confirm that the mononuclear cell suspensions were able to proliferate, all suspensions were incubated with the mitogen Con A. Each of these controls resulted in high SI, indicating that experiment conditions were optimum (data not shown). There was a wide range of MLR responses among all groups, from SI<1 to SI>100. Figure 2a summarises the MLR proliferations among the eastern groups. The MLRs from devils from Mount William National Park showed the highest SI, whereas the MLRs from devils from Nugent had the lowest responses. Figure 2b illustrates the MLR responses among the western groups. The MLRs from devils from Granville Harbour and Woolnorth had the highest proliferations, whereas MLRs from devils from Milkshake Hills and Temma had the lowest responses. Because DFTD is spreading from eastern to western areas of Tasmania, we investigated the functional MHC diversity between devils from these two areas. Figure 2c shows that the MLR responses from west versus east devils were significantly higher than the MLR responses from east versus east devils and west versus west devils. In order to compare these results more effectively, the SI was characterised as either strong (SI>10), moderate (5<SI<10) or low or no reaction (SI<5). Most MLRs between devils from east and west yielded strong responses. Figure 3 illustrates the intensity of MLR responses among all groups.
Skin graft surgeries were performed to test whether allogeneic tissue from an unrelated devil would be immunologically accepted by the recipient devil. Five of the eight skin allografts and six of the eight autografts engrafted successfully, as determined by macroscopic and histological assessment. The remaining three allografts and two autografts showed pathological changes characteristic of mechanical trauma, resulting in failure of these tissues to engraft. The main histological alterations in these unsuccessful grafts were necrosis associated with polymorphonuclear cell infiltration, surface parakeratosis and fibrin deposition.
All successful grafts appeared indistinguishable from the autografts at Day 7. Four of five engrafted allografts had macroscopic changes associated with immune rejection 14 days following the surgery. These changes consisted of scaly lesions, coagulative exudates and brown to black coloration of the allografted skin. For one allograft, these macroscopic changes were not visible until 17 days after the procedure. Microscopically, immune rejection was characterised as Grade II, III or IV rejection (moderate, severe or very severe, respectively). Typical alterations were moderate to severe perivascular and interstitial CD3 infiltration, dermal and epidermal lymphocytic exocytosis, usually accompanied by apoptotic keratinocytes and epidermal necrosis. Spongiosis was a common finding. Most of these alterations were recognised 14 days after the surgery, and progressed to very severe rejection on Day 21. In three cases, there was total loss of the allografted skin, hence a biopsy could not be taken. Table 2 summarises the results for all surgeries (Table S2 describes the pathological changes of the allografts in detail) and Figure 4 shows the macroscopic and microscopic appearance of a representative result from one experiment.
MHC genotyping and MLR results for animals used for the skin graft surgeries are summarized in Table 3 and Table 4. TD 190 and TD 199 have exactly the same set of MHC I and II alleles. TD 188 and TD 189 have three (two MHC I and one MHC II) allelic mismatches, resulting in amino acid variations at two peptide binding sites in MHC I α1 domain. The other two pairs of individuals both have four MHC allele mismatches but no different amino acid substitutions at peptide binding sites were identified.
The presence of a histocompatibility system should prevent the establishment of transmissible cancers in vertebrates , . Despite this, in addition to DFTD, two other naturally transmissible tumours in mammals exist. Canine transmissible venereal tumour (CTVT) , which affects members of the Canidae family. A transmissible sarcoma in captive Syrian hamsters (Mesocrycetus auratus), which was either artificially or spontaneously transmitted by social interactions . CTVT down-regulates MHC antigens  and secretes immunosuppressive molecules  to escape the immune system. Syrian hamsters bearing transmissible sarcomas originated from a single family , suggesting that they were highly monomorphic at the MHC loci. The mechanism of DFTD tumour acceptance is still unclear. Low MHC variation between devils is the most accepted hypothesis to explain the susceptibility of the species to this cancer .
Even though Tasmanian devils lack MHC diversity , it is becoming apparent that devils are capable of allogeneic responses. Our previous work showed low MLR responses using pooled lymphocytes as stimulators . It is likely that different (or rare) MHC antigens were ‘diluted out’ and not present in enough quantity to stimulate proliferation of the responder cells. The present experiments produced responses throughout the devil range, although some MLR experiments yielded low or no proliferations, suggesting that these devils share most MHC antigens. Importantly, some high responses were identified in the MHC-impoverished eastern population, in which DFTD has spread rapidly. The greatest MLR responses were found between eastern and western devils, which possess differences in the MHC nucleotide sequence . We confirmed this by sequencing MHC I and II alleles from two western devils (data not shown). These animals had three MHC I and two MHC II alleles that were not present in the eastern population analysed. This indicates that allelic and antigenic differences might be behind the higher allogeneicity between the two populations. The MLR results suggest that unaltered allogeneic cells should initiate an immune response in most recipient devils, irrespective of the origin of the animal.
All successful allografts were acutely rejected, despite low MLR responses in three out of the four skin graft pairs and little or no mismatches in MHC I and II alleles. The rejection of the foreign tissue was usually visible macroscopically and microscopically by 14 days after the procedure. The grafts could only be assessed every seven days, as procedures with live devils require general anaesthesia. In this context, the onset of rejection occurred between seven and 14 days, which is within the normal range (8–12 days) , . The low MLR responses and the combined MHC I and II genotyping would suggest that a slower rejection should have occurred. This was not the case, suggesting that little mismatches can activate an allogeneic response in devils. Indeed, allografts in animal models may only require a single amino acid difference between donor and recipient to be rejected , . In addition, other genetic (such as cytokine genes and killer cell immunoglobulin-like receptor haplotypes) and non-genetic (such as age, source of skin and size of the graft) factors may also affect the transplant outcome , , . In human transplantation, allografts from fully matched unrelated donors can still be rejected, unless the recipient receives immunosuppressive therapy , . The advantage of using skin transplants is that the outcome of the experiments is easily visualised. The disadvantage is that skin is a very immunogenic tissue and might be rejected more rapidly than other organs , . Skin harbours cells expressing MHC I and II, plus minor histocompatibility complex molecules, all of which can act as alloantigens and trigger rejection. Nonetheless, it is clear that little antigenic or allelic mismatches are sufficient to trigger rapid rejection of foreign tissue between unrelated devils.
The florid T-cell infiltration observed in the skin allografts contrasts with the absence of tumour infiltrating lymphocytes in DFTD tumours , . Down-regulation of the MHC machinery is a well-known mechanism that tumour cells, including CTVT, utilise to escape destruction by T-cells , , , . The expression of MHC I and II proteins by DFTD tumour cells still needs to be resolved. DFTD tumour cells express MHC I and II at mRNA level , but it is unknown whether this is translated into functional proteins. Preliminary experiments in our laboratory indicate that DFTD tumour cells do not express MHC II on the cell surface (unpublished data). It has not been possible to test for MHC I expression, due to the lack of specific antibodies. In tumours with changed MHC profile, NK cells are activated and promote the killing of abnormal cells . Although devils possess the expected range of immune cells , NK cell function has still to be explored in the Tasmanian devil. Tumours can utilise other mechanisms to evade immune recognition. Increased resistance to cytotoxic molecules, such as perforin , decreased tumour antigen expression  and secretion of immunosuppressive factors, such as IL-4, IL-10 and transforming growth factor-β1 ,  are alternative (or concurrent) mechanisms of immune escape.
The devil population is under threat because an allogeneic tumour cell clone is being transferred between animals without immune recognition. The host is immunocompetent , , but the population has undergone bottlenecks in the past and lacks genetic and MHC diversity , , . This homogeneity in the population, however, is not sufficient to allow allotransplantation between unrelated devils. DFTD tumour cells are likely to have evolved adaptive mechanisms to survive unhindered in the tissues of the new host.
Skin graft scoring used for the Tasmanian devil skin grafts.
Click here for additional data file (pone.0022402.s001.doc)
Histopathological alterations of skin allografts of Tasmanian devils.
Click here for additional data file (pone.0022402.s002.doc)
Competing Interests: The authors have declared that no competing interests exist.
Funding: The Australian Research Council (LP0989727 ARC) and Dr Eric Guiler Tasmanian Devil Research Grant provided financial support for this project. AK and KB were funded by an ARC linkage grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors are thankful to Mrs. Ginny Ralph and the devil keepers for help with the animals, and to the Department of Primary Industries, Water and Environment of Tasmania, for support for this project. The authors are very grateful to Dr. Sarah Peck, Dr. Colette Harmsen and Dr. Kim Scogvold, who performed the anaesthesia and post-operative care of all devils. Dr. David Challis and Dr. David Obendorf provided advice on the histological interpretation of skin grafts, and Mrs. Narelle Phillips provided technical support with skin graft sections.
|1.||Murchison EP,Tovar C,Hsu A,Bender HS,Kheradpour P,et al. Year: 2010The Tasmanian devil transcriptome reveals Schwann cell origins of a clonally transmissible cancer.Science327848720044575|
|2.||Pearse AM,Swift K. Year: 2006Allograft theory: transmission of devil facial-tumour disease.Nature43954916452970|
|3.||Tovar C,Obendorf D,Murchison EP,Papenfuss AT,Kreiss A,et al. Year: 2011Tumor-Specific Diagnostic Marker for Transmissible Facial Tumors of Tasmanian Devils: Immunohistochemistry Studies.Vet Pathol|
|4.||Loh R,Bergfeld J,Hayes D,O'Hara A,Pyecroft S,et al. Year: 2006The pathology of devil facial tumor disease (DFTD) in Tasmanian devils (Sarcophilus harrisii).Vet Path4389089517099145|
|5.||McCallum H,Tompkins DM,Jones M,Lachish S,Marvanek S,et al. Year: 2007Distribution and impacts of Tasmanian devil facial tumor disease.Ecohealth4318325|
|6.||Hawkins CE,Baars C,Hesterman H,Hocking GJ,Jones ME,et al. Year: 2006Emerging disease and population decline of an island endemic, the Tasmanian devil Sarcophilus harrisii.Biological Conservation131307324|
|7.||Woods GM,Kreiss A,Belov K,Siddle HV,Obendorf DL,et al. Year: 2007The immune response of the Tasmanian Devil (Sarcophilus harrisii) and Devil Facial Tumour Disease.Ecohealth4338345|
|8.||Loh R,Hayes D,Mahjoor A,O'Hara A,Pyecroft S,et al. Year: 2006The immunohistochemical characterization of devil facial tumor disease (DFTD) in the Tasmanian Devil (Sarcophilus harrisii).Vet Path4389690317099146|
|9.||Berlanda M,Di Cocco P,Mazzotta C,Rizza V,D'Angelo M,et al. Year: 2008Clinical operational tolerance after kidney transplantation: a short literature review.Transplant Proc401847185118675067|
|10.||Klein J. Year: 1986The natural history of the major histocompatibility complex.New York, USAJohn Wiley & Sons|
|11.||Kumanovics A,Takada T,Lindahl KF. Year: 2003Genomic organization of the mammalian MHC.Annu Rev Immunol2162965712500978|
|12.||Jensen PE. Year: 2007Recent advances in antigen processing and presentation.Nat Immunol81041104817878914|
|13.||Ackerman AL,Cresswell P. Year: 2004Cellular mechanisms governing cross-presentation of exogenous antigens.Nat Immunol567868415224093|
|14.||Kreiss A,Fox N,Bergfeld J,Quinn SJ,Pyecroft S,et al. Year: 2008Assessment of cellular immune responses of healthy and diseased Tasmanian devils (Sarcophilus harrisii).Dev Comp Immunol3254455317988737|
|15.||Kreiss A,Wells B,Woods GM. Year: 2009The humoral immune response of the Tasmanian devil (Sarcophilus harrisii) against horse red blood cells.Vet Immunol Immunopathol13013513719264365|
|16.||Siddle HV,Kreiss A,Eldridge MD,Noonan E,Clarke CJ,et al. Year: 2007Transmission of a fatal clonal tumor by biting occurs due to depleted MHC diversity in a threatened carnivorous marsupial.Proc Natl Acad Sci U S A104162211622617911263|
|17.||Siddle HV,Marzec J,Cheng Y,Jones M,Belov K. Year: 2010MHC gene copy number variation in Tasmanian devils: implications for the spread of a contagious cancer.Proc Biol Sci2772001200620219742|
|18.||Sherman LA,Chattopadhyay S. Year: 1993The molecular basis of allorecognition.Annu Rev Immunol113854028476567|
|19.||Hernandez-Fuentes MP,Baker RJ,Lechler RI. Year: 1999The alloresponse.Rev Immunogenet128229611256420|
|20.||Game DS,Warrens AN,Lechler RI. Year: 2001Rejection mechanisms in transplantation.Wien Klin Wochenschr11383283811732119|
|21.||Game DS,Lechler RI. Year: 2002Pathways of allorecognition: implications for transplantation tolerance.Transpl Immunol1010110812216939|
|22.||Derks RA,Burlingham WJ. Year: 2005In vitro parameters of donor-antigen-specific tolerance.Curr Opin Immunol1756056416084707|
|23.||Nishigaki F,Nozaki M,Nakamura A,Taniguchi M,Kobayashi K,et al. Year: 1990[Significance of histocompatibility tests].Rinsho Byori381511562139476|
|24.||Jeras M. Year: 2002The role of in vitro alloreactive T-cell functional tests in the selection of HLA matched and mismatched haematopoietic stem cell donors.Transpl Immunol1020521412216951|
|25.||O'Brien SJ,Roelke ME,Marker L,Newman A,Winkler CA,et al. Year: 1985Genetic basis for species vulnerability in the cheetah.Science227142814342983425|
|26.||Castro-Prieto A,Wachter B,Sommer S. Cheetah Paradigm Revisited: MHC Diversity in the World's Largest Free-Ranging Population.Mol Biol Evol281455146821183613|
|27.||Munson L,Terio KA,Worley M,Jago M,Bagot-Smith A,et al. Year: 2005Extrinsic factors significantly affect patterns of disease in free-ranging and captive cheetah (Acinonyx jubatus) populations.J Wildl Dis4154254816244064|
|28.||Belov K. Year: 2011The role of the Major Histocompatibility Complex in the spread of contagious cancers.Mamm Genome22839020963591|
|29.||Fassati A,Mitchison NA. Year: 2010Testing the theory of immune selection in cancers that break the rules of transplantation.Cancer Immunol Immunother5964365120033157|
|30.||Kanitakis J,Petruzzo P,Jullien D,Badet L,Dezza MC,et al. Year: 2005Pathological score for the evaluation of allograft rejection in human hand (composite tissue) allotransplantation.Eur J Dermatol1523523816048749|
|31.||Siddle HV,Sanderson C,Belov K. Year: 2007Characterization of major histocompatibility complex class I and class II genes from the Tasmanian devil (Sarcophilus harrisii).Immunogenetics5975376017673996|
|32.||Hall T. Year: 1999Bioedit: a user friendly biological sequence alignment editor and analysis program for windows 95/98/NT.Nucleic Acids Symp Ser419598|
|33.||Thompson JD,Higgins DG,Gibson TJ. Year: 1994CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.Nucleic Acids Res22467346807984417|
|34.||Rinkevich B. Year: 2004Primitive immune systems: are your ways my ways?Immunol Rev198253515199952|
|35.||Stoner DS,Weissman IL. Year: 1996Somatic and germ cell parasitism in a colonial ascidian: possible role for a highly polymorphic allorecognition system.Proc Natl Acad Sci U S A9315254152598986797|
|36.||Cohen D. Year: 1985The canine transmissible venereal tumor: a unique result of tumor progression.Adv Cancer Res43751123887857|
|37.||Ashbel R. Year: 1945Spontaneous Transmissible Tumours in the Syrian Hamster.Nature3942607|
|38.||Cohen D,Shalev A,Krup M. Year: 1984Lack of beta 2-microglobulin on the surface of canine transmissible venereal tumor cells.J Natl Cancer Inst723954016363791|
|39.||Hsiao YW,Liao KW,Chung TF,Liu CH,Hsu CD,et al. Year: 2008Interactions of host IL-6 and IFN-gamma and cancer-derived TGF-beta1 on MHC molecule expression during tumor spontaneous regression.Cancer Immunol Immunother571091110418259750|
|40.||Adler JH. Year: 1989The origin of the golden hamster as a laboratory animal.Isr J Med Sci252062092651351|
|41.||Medawar PB. Year: 1944The behaviour and fate of skin autografts and skin homografts in rabbits: A report to the War Wounds Committee of the Medical Research Council.J Anat7817619917104960|
|42.||Richters CD,Hoekstra MJ,du Pont JS,Kreis RW,Kamperdijk EW. Year: 2005Immunology of skin transplantation.Clin Dermatol2333834216023928|
|43.||Vokaer B,Van Rompaey N,Lemaitre PH,Lhomme F,Kubjak C,et al. Critical role of regulatory T cells in Th17-mediated minor antigen-disparate rejection.J Immunol1853417342520733201|
|44.||Cho PS,Lo DP,Wikiel KJ,Rowland HC,Coburn RC,et al. Year: 2007Establishment of transplantable porcine tumor cell lines derived from MHC-inbred miniature swine.Blood1103996400417702898|
|45.||Krichen H,Khazen D,Sfar I,Ben Abdallah T,Bardi R,et al. Year: 2011Genetic polymorphisms of inflammatory molecules in tunisian kidney transplantation.Transplant Proc4343343621440726|
|46.||Shaw BE,Arguello R,Garcia-Sepulveda CA,Madrigal JA. Year: 2010The impact of HLA genotyping on survival following unrelated donor haematopoietic stem cell transplantation.Br J Haematol15025125820560963|
|47.||Wachtel SS,Silvers WK. Year: 1971Tolerance induction in adult mice with tumor homografts.Transplantation1261644932698|
|48.||Pascual Santos J,Hernandez Marrero D. Year: 2010[Immunosuppression for living donor renal allograft recipients].Nefrologia30Suppl 2808421183966|
|49.||Sasaki N,Idica A,Hall B,Terasaki PI. Year: 2008Using the mimetic epitope concept to find a possible way to widen the graft-survival difference between matched and mismatched renal transplants.Clin Transpl241252|
|50.||Chen HD,Silvers WK. Year: 1983Influence of Langerhans cells on the survival of H-Y incompatible skin grafts in rats.J Invest Dermatol8120236345684|
|51.||Ferrone S,Marincola FM. Year: 1995Loss of HLA class I antigens by melanoma cells: molecular mechanisms, functional significance and clinical relevance.Immunol Today164874947576053|
|52.||Maeurer MJ,Gollin SM,Storkus WJ,Swaney W,Karbach J,et al. Year: 1996Tumor escape from immune recognition: loss of HLA-A2 melanoma cell surface expression is associated with a complex rearrangement of the short arm of chromosome 6.Clin Cancer Res26416529816214|
|53.||Rivoltini L,Barracchini KC,Viggiano V,Kawakami Y,Smith A,et al. Year: 1995Quantitative correlation between HLA class I allele expression and recognition of melanoma cells by antigen-specific cytotoxic T lymphocytes.Cancer Res55314931577541714|
|54.||Ikeda H,Lethe B,Lehmann F,van Baren N,Baurain JF,et al. Year: 1997Characterization of an antigen that is recognized on a melanoma showing partial HLA loss by CTL expressing an NK inhibitory receptor.Immunity61992089047241|
|55.||Kreiss A,Obendorf DL,Hemsley S,Canfield PJ,Woods GM. Year: 2009A histological and immunohistochemical analysis of lymphoid tissues of the Tasmanian devil.Anat Rec (Hoboken)29261162019382223|
|56.||Lehmann C,Zeis M,Schmitz N,Uharek L. Year: 2000Impaired binding of perforin on the surface of tumor cells is a cause of target cell resistance against cytotoxic effector cells.Blood9659460010887123|
|57.||Lee KH,Panelli MC,Kim CJ,Riker AI,Bettinotti MP,et al. Year: 1998Functional dissociation between local and systemic immune response during anti-melanoma peptide vaccination.J Immunol161418341949780192|
|58.||Sarris AH,Kliche KO,Pethambaram P,Preti A,Tucker S,et al. Year: 1999Interleukin-10 levels are often elevated in serum of adults with Hodgkin's disease and are associated with inferior failure-free survival.Ann Oncol1043344010370786|
|59.||Hsiao YW,Liao KW,Hung SW,Chu RM. Year: 2004Tumor-infiltrating lymphocyte secretion of IL-6 antagonizes tumor-derived TGF-beta 1 and restores the lymphokine-activated killing activity.J Immunol1721508151414734728|
|60.||Jones ME,Paetkau D,Geffen E,Moritz C. Year: 2004Genetic diversity and population structure of Tasmanian devils, the largest marsupial carnivore.Molecular Ecology132197220915245394|
Table 1 Origin and pairing of Tasmanian devils used for skin graft experiments.
|Tasmanian devil ID||Origin|
|TD 190 and TD 199||Nugent and Epping|
|TD 187 and TD 200||Nugent and Mount William National Park|
|TD 188 and TD 189||Forestier Peninsula and Nugent|
|TD 190 and TD 191||Nugent and Forestier Peninsula|
Table 2 Outcome of skin allografts.
|Tasmanian devil ID||Day 7||Day 14||Day 21|
|TD 190||Grade II||Grade IV||Necrotic skin, biopsy not done|
|TD 199||No evidence of rejection||Grade III||Grade IV|
|TD 187||Unable to determine rejection||Grade IV||Necrotic skin, biopsy not done|
|TD 188||No evidence of rejection||Grade III||Grade IV|
|TD 191||No evidence of rejection||Grade III||Necrotic skin, biopsy not done|
TD 190 was the only devil that showed an early rejection response at Day 7. All five devils had Grade III to Grade IV rejection at Day 14 and Day 21.
Table 3 MHC genotyping of Tasmanian devils used for skin graft experiments.
|Tasmanian devil ID||MHC I α1 sequence variants||MHC II β1 sequence variants|
|TD 190||SahaI*27, 28, 32, 35, 49||SahaDAB*01, 03, 05|
|TD 199||SahaI*27, 28, 32, 35, 49||SahaDAB*01, 03, 05|
|TD 187||SahaI*28, 32, 35, 49, 57||SahaDAB*01, 03, 05, 12|
|TD 200||SahaI*27, 28, 32, 35, 49||SahaDAB*01, 03, 05, 11|
|TD 188||SahaI*27, 32, 35, 49||SahaDAB*01, 03, 05, 15|
|TD 189||SahaI*27, 32, 35, 48||SahaDAB*01, 03, 05, 11, 15|
|TD 191||SahaI*28, 32, 34, 48, 49||SahaDAB*01, 03, 05, 13|
TD 190 and TD 199 shared all MHC I and II alleles. The remaining devil pairs had two to three MHC I allelic mismatches and one to two MHC II allelic mismatches.
Table 4 Amino acid difference count at peptide binding sites and MLR results within skin graft devil pairs.
|Tasmanian devil ID||Amino acid difference count at peptide binding sites at MHC I α1||Amino acid difference count at peptide binding sites at MHC II β1||Mixed lymphocyte reaction (SI)|
|TD 190 and TD 199||0||0||1|
|TD 187 and TD 200||0||0||1|
|TD 188 and TD 189||2||0||17|
|TD 190 and TD 191||0||0||5|
TD 188 and TD 189 had two amino acid differences at peptide binding sites at MHC I α1 and had a strong MLR response. The other three pairs did not have amino acid difference count at peptide binding sites at MHC I α1 or MHC II β1 and had low MLR responses.
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