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Interferon Cytokine Res., 15, 939, 10.1089\u002Fjir.1995.15.939\nDijkmans, 1990, Chicken macrophage activation by interferon: do birds lack the molecular homologue of mammalian interferon-γ?, Vet. Immunol. Immunopathol., 26, 319, 10.1016\u002F0165-2427(90)90116-A\nGreen, 1982, Analysis of nitrate, nitrite, and [15N]nitrite in biological fluids, Anal. Biochem., 126, 131, 10.1016\u002F0003-2697(82)90118-X\nHarroch, 1994, Induction by interleukin-6 of interferon regulatory factor 1 (IRF-1) gene expression through the palindromic interferon response element pIRE and cell type-dependent control of IRF-1 binding to DNA, EMBO J., 13, 1942, 10.1002\u002Fj.1460-2075.1994.tb06463.x\nKawade, 1986, Quantitation of neutralization of interferon by antibody, Methods Enzymol., 119, 558, 10.1016\u002F0076-6879(86)19076-8\nKohase, 1983, Temperature-sensitive mutant of Newcastle disease virus affecting interferon induction, J. Gen. Virol., 64, 1469, 10.1099\u002F0022-1317-64-7-1469\nKohase, 1986, Purification and characterization of chick interferon induced by viruses, J. Gen. Virol., 67, 215, 10.1099\u002F0022-1317-67-1-215\nLaemmli, 1970, Cleavage of structural proteins during the assembly of the head of bacteriophage T4, Nature, 227, 680, 10.1038\u002F227680a0\nLowenthal, 1994, Development of T cell immune responsiveness in the chicken, Immunol. Cell Biol., 72, 115, 10.1038\u002Ficb.1994.18\nLowenthal, 1995, Production of interferon-γ by chicken T cells, J. Interferon Cytokine Res., 15, 933, 10.1089\u002Fjir.1995.15.933\nMuller, 1994, Functional role of type I and type II interferons in antiviral defense, Science, 264, 1918, 10.1126\u002Fscience.8009221\nProwse, 1989, Interferon release as a measure of the T-cell response to coccidial antigens in chickens, Avian Pathol., 18, 619, 10.1080\u002F03079458908418637\nRubinstein, 1981, Convenient assay for interferons, J. 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Med., 120, 413, 10.1084\u002Fjem.120.3.413\nSanchez-Madrid, 1983, A human leukocyte differentiation antigen family with distinct alpha subunits and a common beta subunit: the lymphocyte function associated antigen (LFA-1), the C3bi complement receptor (OKM1\u002FMac-1), and the p150, 95 molecule, J. Exp. Med., 158, 1785, 10.1084\u002Fjem.158.6.1785\nSchulman, 1978, A better cell line for making hybridomas secreting specific antibodies, Nature, 276, 269, 10.1038\u002F276269a0\nSchwartz, 1971, Preparation of purified lymphocyte suspensions using Tris-NH4Cl-buffer, Exp. Med. and Surg., 29, 1\nSpooner, 1984, Cross reaction of monoclonal antibodies to human MHC class I and class II products with bovine lymphocyte subpoplations, Tissue Antigens, 24, 270, 10.1111\u002Fj.1399-0039.1984.tb02137.x\nSzer, 1985, Monoclonal antibody to human cytotoxic-suppressor T-lymphocytes cross-reacts with canine lymphocytes and inhibits cell mediated lympholysis of canine cells, Exp. Hematol., 13, 641\nThierfelder, 1974, Haemopoietic stem cells of rats but not of mice express Thy-1.1 alloantigen, Nature, 269, 691, 10.1038\u002F269691a0\nTiellaud, 1982, Monoclonal antibodies as a tool for phylogenetic studies of major histocompatibility antigens and β2-microglobulin, Immunogenetics, 15, 377, 10.1007\u002FBF00364261\nUsinger, 1981, Two molecularly independent surface receptors identify bovine T lymphocytes, J. Immunol. Methods, 45, 209, 10.1016\u002F0022-1759(81)90299-4\nWilliams, 1976, Many cells in rat bone marrow have cell surface Thy-1 antigen, Eur. J. Immunol., 6, 526, 10.1002\u002Feji.1830060716\nWood, 1983, Anti-Leu3\u002FT4 antibodies react with cells of monocyte\u002Fmacrophage and Langerhans lineage, J. Immunol., 131, 212\nZweig, 1984, Monoclonal antibodies directed against human Ia antigens detect an evolutionary conserved epitope on guinea pig Ia antigens with unique functional properties, J. 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Immunol., 72, 274\nGorrell, 1988, Lymphocyte phenotypes in the abomasal mucosa of sheep infected with Haemonchus contortus, Parasite Immunol., 10, 661, 10.1111\u002Fj.1365-3024.1988.tb00252.x\nHein, 1990, Differential peripheral expansion and in vivo antigen reactivity of αβ and γδ T cells emigrating from the early fetal lamb thymus, Eur. J. Immunol., 20, 1805, 10.1002\u002Feji.1830200827\nKambara, 1993, The effect of age and dietary protein on immunity and resistance in lambs vaccinated with Trichostrongylus colubriformis, Int. J. Parasitol., 23, 471, 10.1016\u002F0020-7519(93)90035-W\nMackay, 1988, Sheep leucocyte molecules: a review of their distribution, structure and possible function, Vet. Immunol. Immunopathol., 19, 1, 10.1016\u002F0165-2427(88)90042-6\nMackay, 1992, Altered patterns of T cell migration through lymph nodes and skin following antigen challenge, Eur. J. Immunol., 22, 2205, 10.1002\u002Feji.1830220904\nMacKay, 1985, Characterization of two sheep lymphocyte differentiation antigens SBU-T1 and SBU-T6, Immunology, 55, 729\nMaddox, 1985, Surface antigens, SBU-T4 and SBU-T8, of sheep lymphocyte subsets defined by monoclonal antibodies, Immunology, 55, 739\nManton, 1962, The influence of age on naturally acquired resistance to Haemonchus conttortus in lambs, Res. Vet. Sci., 3, 308, 10.1016\u002FS0034-5288(18)34905-1\nMcClure, 1991, Effects of Freund's adjuvants on local, draining and circulating lymphocyte populations in sheep, Immunol. Cell Biol., 69, 361, 10.1038\u002Ficb.1991.52\nMcClure, 1992, A serial study of rejection of Trichostrongylus colubriformis by immune sheep, Int. J. 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2017, Induction of haem oxygenase-1 increases infection of dog macrophages by L. infantum, Parasite Immunol., 10.1111\u002Fpim.12494","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fpim.12494",{"doi":1275},"10.1111\u002Fpim.12494",{"id":1277,"text":1278,"url":1279,"identifiers":1280},"11b4cf2b-bbed-478f-b9ff-c6a0a9ed9b42","Araujo, 2011, Immunological changes in canine peripheral blood leukocytes triggered by immunization with first or second generation vaccines against canine visceral leishmaniasis, Vet Immunol Immunopathol, 141, 64, 10.1016\u002Fj.vetimm.2011.02.007","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS016524271100050X",{"doi":1281},"10.1016\u002Fj.vetimm.2011.02.007",{"id":18,"text":1283,"url":18,"identifiers":1284},"Arce, 2013, Re-emergence of leishmaniasis in Spain: community outbreak in Madrid, Spain, 2009 to 2012, Euro Surveill, 18, 20546, 10.2807\u002F1560-7917.ES2013.18.30.20546",{"doi":1285},"10.2807\u002F1560-7917.ES2013.18.30.20546",{"id":1287,"text":1288,"url":1289,"identifiers":1290},"a78041a5-fcb1-45b3-9135-7384529e30bf","Ashford, 1996, Leishmaniasis reservoirs and their significance in control, Clin Dermatol, 14, 523, 10.1016\u002F0738-081X(96)00041-7","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002F0738081X96000417",{"doi":1291},"10.1016\u002F0738-081x(96)00041-7",{"id":1293,"text":1294,"url":1295,"identifiers":1296},"2a65bbfd-cd62-4991-923f-8a09bab43675","Brodskyn, 2000, Virulent or avirulent (dhfr-ts-) Leishmania major elicit predominantly a type-1 cytokine response by human cells in vitro, Clinical and experimental immunology, 119, 299, 10.1046\u002Fj.1365-2249.2000.01122.x","https:\u002F\u002Facademic.oup.com\u002Fcei\u002Farticle\u002F119\u002F2\u002F299\u002F6461744",{"doi":1297},"10.1046\u002Fj.1365-2249.2000.01122.x",{"id":1299,"text":1300,"url":1301,"identifiers":1302},"f709583f-dc67-4c18-8076-6d36b3f6fd2b","Carneiro, 2016, The Role of Nitric Oxide and Reactive Oxygen Species in the Killing of Leishmania braziliensis by Monocytes from Patients with Cutaneous Leishmaniasis, PLoS One, 11, 10.1371\u002Fjournal.pone.0148084","https:\u002F\u002Fdx.plos.org\u002F10.1371\u002Fjournal.pone.0148084",{"doi":1303},"10.1371\u002Fjournal.pone.0148084",{"id":18,"text":1305,"url":18,"identifiers":1306},"Chicharro, 2013, Molecular typing of Leishmania infantum isolates from a leishmaniasis outbreak in Madrid, Spain, 2009 to 2012, Euro Surveill, 18, 20545, 10.2807\u002F1560-7917.ES2013.18.30.20545",{"doi":1307},"10.2807\u002F1560-7917.ES2013.18.30.20545",{"id":18,"text":1309,"url":18,"identifiers":1310},"Cortes, 2018, Elucidating in vitro and in vivo phenotypic behaviour of L. infantum\u002FL. major natural hybrids, Parasitology, 1",{},{"id":200,"text":1312,"url":202,"identifiers":1313},"de Almeida, 2017, Induction of heme oxygenase-1 increases infection of dog macrophages by L. infantum, Parasite Immunol.",{"doi":204},{"id":1315,"text":1316,"url":1317,"identifiers":1318},"dd990331-0304-401e-8ba9-ca253ce3c2ae","Ding, 1988, Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production, J Immunol, 141, 2407, 10.4049\u002Fjimmunol.141.7.2407","https:\u002F\u002Fjournals.aai.org\u002Fjimmunol\u002Farticle\u002F141\u002F7\u002F2407\u002F21525\u002FRelease-of-reactive-nitrogen-intermediates-and",{"doi":1319},"10.4049\u002Fjimmunol.141.7.2407",{"id":1321,"text":1322,"url":1323,"identifiers":1324},"145b2f55-2078-4fef-9fb5-64373d6e51d1","Dominguez-Bernal, 2012, Mitigating an undesirable immune response of inherent susceptibility to cutaneous leishmaniosis in a mouse model: the role of the pathoantigenic HISA70 DNA vaccine, Vet Res, 43, 59, 10.1186\u002F1297-9716-43-59","https:\u002F\u002Fveterinaryresearch.biomedcentral.com\u002Farticles\u002F10.1186\u002F1297-9716-43-59",{"doi":1325},"10.1186\u002F1297-9716-43-59",{"id":1327,"text":1328,"url":1329,"identifiers":1330},"e982edac-7373-427f-94b5-917d23a6ab97","Dominguez-Bernal, 2015, HisAK70: progress towards a vaccine against different forms of leishmaniosis, Parasites & vectors, 8, 629, 10.1186\u002Fs13071-015-1246-y","https:\u002F\u002Fparasitesandvectors.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs13071-015-1246-y",{"doi":1331},"10.1186\u002Fs13071-015-1246-y",{"id":1333,"text":1334,"url":1335,"identifiers":1336},"746ea168-2508-4866-9ab7-0359460e9d30","Dominguez-Bernal, 2014, Characterisation of the ex vivo virulence of Leishmania infantum isolates from Phlebotomus perniciosus from an outbreak of human leishmaniosis in Madrid, Spain, Parasites & vectors, 7, 499, 10.1186\u002Fs13071-014-0499-1","https:\u002F\u002Fparasitesandvectors.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs13071-014-0499-1",{"doi":1337},"10.1186\u002Fs13071-014-0499-1",{"id":1339,"text":1340,"url":1341,"identifiers":1342},"3b0a3396-c034-4082-ade4-9c283732d0a2","Faria, 2012, Toll-like receptors in leishmania infections: guardians or promoters?, J Parasitol Res, 2012, 10.1155\u002F2012\u002F930257","http:\u002F\u002Fwww.hindawi.com\u002Fjournals\u002Fjpr\u002F2012\u002F930257\u002F",{"doi":1343},"10.1155\u002F2012\u002F930257",{"id":1345,"text":1346,"url":1347,"identifiers":1348},"239e9538-8a49-440c-979e-d61627e908ed","Fernandez-Cotrina, 2013, Experimental model for reproduction of canine visceral leishmaniosis by Leishmania infantum, Veterinary parasitology, 192, 118, 10.1016\u002Fj.vetpar.2012.10.002","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS0304401712005481",{"doi":1349},"10.1016\u002Fj.vetpar.2012.10.002",{"id":1351,"text":1352,"url":1353,"identifiers":1354},"f2693598-ede1-4aa0-9463-7b2b8a373522","Gantt, 2001, Oxidative responses of human and murine macrophages during phagocytosis of Leishmania chagasi, J Immunol, 167, 893, 10.4049\u002Fjimmunol.167.2.893","https:\u002F\u002Fjournals.aai.org\u002Fjimmunol\u002Farticle\u002F167\u002F2\u002F893\u002F33962\u002FOxidative-Responses-of-Human-and-Murine",{"doi":1355},"10.4049\u002Fjimmunol.167.2.893",{"id":1357,"text":1358,"url":1359,"identifiers":1360},"1a401bac-71e8-4698-a332-6aa50d8ad3d3","Gonzalez, 2017, Detection of high Leishmania infantum loads in Phlebotomus perniciosus captured in the leishmaniasis focus of southwestern Madrid region (Spain) by real time PCR, Acta tropica, 171, 68, 10.1016\u002Fj.actatropica.2017.03.023","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS0001706X1631049X",{"doi":1361},"10.1016\u002Fj.actatropica.2017.03.023",{"id":1363,"text":1364,"url":1365,"identifiers":1366},"ad438437-3268-4444-aee4-2ab4edc83c9f","Gradoni, 2015, Canine Leishmania vaccines: Still a long way to go, Veterinary parasitology, 208, 94, 10.1016\u002Fj.vetpar.2015.01.003","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0304401715000072",{"doi":1367},"10.1016\u002Fj.vetpar.2015.01.003",{"id":18,"text":1369,"url":1370,"identifiers":1371},"Gupta, 2013, Mechanisms of immune evasion in leishmaniasis, Adv Appl Microbiol, 82, 155, 10.1016\u002FB978-0-12-407679-2.00005-3","https:\u002F\u002Fdoi.org\u002F10.1016\u002Fb978-0-12-407679-2.00005-3",{"mag":1372,"pmc":1373,"openalex":1374,"pm":1375,"doi":1376},"1490606958","3697132","W1490606958","23415155","10.1016\u002Fb978-0-12-407679-2.00005-3",{"id":1378,"text":1379,"url":1380,"identifiers":1381},"26ef8236-0439-41fa-85d2-81d34a697198","Horrillo, 2019, Clinical aspects of visceral leishmaniasis caused by L. infantum in adults, Ten years of experience of the largest outbreak in Europe: what have we learned? Parasites & vectors, 12, 359","https:\u002F\u002Fparasitesandvectors.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs13071-019-3628-z",{"doi":1382},"10.1186\u002Fs13071-019-3628-z",{"id":1384,"text":1385,"url":1386,"identifiers":1387},"3261f919-2f6a-4c6d-982a-74fc2e34f6b6","Horrillo, 2015, Atypical presentation in adults in the largest community outbreak of leishmaniasis in Europe (Fuenlabrada, Spain), Clin Microbiol Infect, 21, 269, 10.1016\u002Fj.cmi.2014.10.017","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS1198743X14000792",{"doi":1388},"10.1016\u002Fj.cmi.2014.10.017",{"id":1390,"text":1391,"url":1392,"identifiers":1393},"e96dc23a-6ba5-442a-ad38-84a803937d3e","Hurrell, 2016, Different Leishmania Species Drive Distinct Neutrophil Functions, Trends Parasitol, 32, 392, 10.1016\u002Fj.pt.2016.02.003","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS1471492216000362",{"doi":1394},"10.1016\u002Fj.pt.2016.02.003",{"id":1396,"text":1397,"url":1398,"identifiers":1399},"65487264-92f7-4c90-be3c-75edaf94ac43","Jimenez, 2014, Could wild rabbits (Oryctolagus cuniculus) be reservoirs for Leishmania infantum in the focus of Madrid, Spain?, Veterinary parasitology, 202, 296, 10.1016\u002Fj.vetpar.2014.03.027","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002FS0304401714002027",{"doi":1400},"10.1016\u002Fj.vetpar.2014.03.027",{"id":1402,"text":1403,"url":1404,"identifiers":1405},"c3f121f9-d451-4877-808a-bc0631651128","Kassai, 1988, Standardized nomenclature of animal parasitic diseases (SNOAPAD), Veterinary parasitology, 29, 299, 10.1016\u002F0304-4017(88)90148-3","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0304401788901483",{"doi":1406},"10.1016\u002F0304-4017(88)90148-3",{"id":200,"text":1408,"url":202,"identifiers":1409},"Li, 2012, Differences in iNOS and arginase expression and activity in the macrophages of rats are responsible for the resistance against T. gondii infection, PLoS One, 7",{"doi":204},{"id":1411,"text":1412,"url":1413,"identifiers":1414},"1c5b4975-0580-48d6-a866-0f8eb28ef575","Martin-Martin, 2015, Natural transmission of Leishmania infantum through experimentally infected Phlebotomus perniciosus highlights the virulence of Leishmania parasites circulating in the human visceral leishmaniasis outbreak in Madrid, Spain, Vet Res, 46, 138, 10.1186\u002Fs13567-015-0281-1","http:\u002F\u002Fwww.veterinaryresearch.org\u002Fcontent\u002F46\u002F1\u002F138",{"doi":1415},"10.1186\u002Fs13567-015-0281-1",{"id":1417,"text":1418,"url":1419,"identifiers":1420},"e8eacf49-cd63-4999-a3f0-d1e16e871649","Martínez-Rodrigo, 2019, Strength and medium-term impact of HisAK70 immunization in dogs: Vaccine safety and biomarkers of effectiveness for ex vivo Leishmania infantum infection, Comparative Immunology, Microbiology and Infectious Diseases., 10.1016\u002Fj.cimid.2019.05.009","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0147957119300888",{"doi":1421},"10.1016\u002Fj.cimid.2019.05.009",{"id":1423,"text":1424,"url":1425,"identifiers":1426},"de7d022e-ecfe-439b-968a-02798708b86b","Mas, 2020, Properties of virulence emergence of Leishmania infantum isolates from Phlebotomus perniciosus collected during the human leishmaniosis outbreak in Madrid, Spain. Hepatic histopathology and immunological parameters as virulence markers in the mouse model, Transbound Emerg Dis., 10.1111\u002Ftbed.13733","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Ftbed.13733",{"doi":1427},"10.1111\u002Ftbed.13733",{"id":1429,"text":1430,"url":1431,"identifiers":1432},"40b052df-9083-4c33-aacb-848ae66e5a14","Mauel, 1991, Nitrogen and oxygen metabolites and the killing of Leishmania by activated murine macrophages, Res Immunol, 142, 577, 10.1016\u002F0923-2494(91)90106-S","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F092324949190106S",{"doi":1433},"10.1016\u002F0923-2494(91)90106-s",{"id":1435,"text":1436,"url":1437,"identifiers":1438},"ccf2052d-b0f1-402d-a74a-3c0dd1da447d","Meddeb-Garnaoui, 2009, Effects of tropism and virulence of Leishmania parasites on cytokine production by infected human monocytes, Clinical and experimental immunology, 155, 199, 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Population study of DLA-D alleles using a panel of homozygous typing cells, Tissue Antigens, 21, 360, 10.1111\u002Fj.1399-0039.1983.tb00185.x\nStamenkovic, 1989, A B-lymphocyte activation molecule related to the nerve growth factor receptor and induced by cytokines in carcinomas, EMBO J., 8, 1403, 10.1002\u002Fj.1460-2075.1989.tb03521.x\nStorb, 1997, Stable mixed hematopoietic chimerism in DLA-identical littermate dogs given sublethal total body irradiation before and pharmacological immunosuppression after marrow transplantation, Blood, 89, 3048, 10.1182\u002Fblood.V89.8.3048\nStorb, 1999, Stable mixed hematopoietic chimerism in dogs given donor antigen, CTLA4Ig, and 100 cGy total body irradiation before and pharmacologic immunosuppression after marrow transplant, Blood, 94, 2523, 10.1182\u002Fblood.V94.7.2523.419k18_2523_2529\nWekerle, 2002, Tolerance through bone marrow transplantation with costimulation blockade (Review), Transpl. 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Domest. Anim., 43, 212, 10.1111\u002Fj.1439-0531.2007.00879.x\nBrandes, 2005, Professional antigen-presentation function by human gammadelta T cells, Science, 309, 264, 10.1126\u002Fscience.1110267\nBreathnach, 2005, Equine herpesvirus-1 infection induces IFN-gamma production by equine T lymphocyte subsets, Vet. Immunol. Immunopathol., 103, 207, 10.1016\u002Fj.vetimm.2004.09.024\nCharerntantanakul, 2006, Immune responses and protection by vaccine and various vaccine adjuvant candidates to virulent porcine reproductive and respiratory syndrome virus, Vet. Immunol. Immunopathol., 109, 99, 10.1016\u002Fj.vetimm.2005.07.026\nCheng, 2008, Mouse gammadelta T cells are capable of expressing MHC class II molecules, and of functioning as antigen-presenting cells, J. Neuroimmunol., 203, 3, 10.1016\u002Fj.jneuroim.2008.06.007\nCoombs, 2006, Cytokine responses to EHV-1 infection in immune and non-immune ponies, Vet. Immunol. 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Immunopathol., 104, 105, 10.1016\u002Fj.vetimm.2004.11.004\nHagberg, 2008, Characterization of bovine lymphocytes stimulated in vitro by Dictyocaulus viviparus homogenate, Parasite Immunol., 30, 342, 10.1111\u002Fj.1365-3024.2008.01031.x\nKydd, 1994, Distribution of equid herpesvirus-1 (EHV-1) in respiratory tract associated lymphoid tissue: implications for cellular immunity, Equine Vet. J., 26, 470, 10.1111\u002Fj.2042-3306.1994.tb04052.x\nKydd, 1994, Distribution of equid herpesvirus-1 (EHV-1) in the respiratory tract of ponies: implications for vaccination strategies, Equine Vet. J., 26, 466, 10.1111\u002Fj.2042-3306.1994.tb04051.x\nKydd, 2006, The equine immune response to equine herpesvirus-1: the virus and its vaccines, Vet. Immunol. Immunopathol., 111, 15, 10.1016\u002Fj.vetimm.2006.01.005\nKydd, 2003, Pre-infection frequencies of equine herpesvirus-1 specific, cytotoxic T lymphocytes correlate with protection against abortion following experimental infection of pregnant mares, Vet. Immunol. Immunopathol., 96, 207, 10.1016\u002Fj.vetimm.2003.08.004\nLunn, 2000, Immunological basis of vaccination, AAEP Proc., 46, 1\nMoretta, 2004, Unravelling natural killer cell function: triggering and inhibitory human NK receptors, EMBO J., 23, 255, 10.1038\u002Fsj.emboj.7600019\nMoser, 2006, Gammadelta T cells: an alternative type of professional APC, Trends Immunol., 27, 112, 10.1016\u002Fj.it.2006.01.002\nPaillot, 2005, Equine interferon gamma synthesis in lymphocytes after in vivo infection and in vitro stimulation with EHV-1, Vaccine, 23, 4541, 10.1016\u002Fj.vaccine.2005.03.048\nPaillot, 2006, Characterisation of CTL and IFN-gamma synthesis in ponies following vaccination with a NYVAC-based construct coding for EHV-1 immediate early gene, followed by challenge infection, Vaccine, 24, 1490, 10.1016\u002Fj.vaccine.2005.10.019\nPedersen, 2002, Identification of monoclonal antibodies that cross-react with cytokines from different animal species, Vet. Immunol. 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