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Role of dendritic cells in immunity against avian coccidiosis

Published online by Cambridge University Press:  01 November 2017

M. SHOAIB ,
S. XIAOKAI ,
M. UL-HASAN ,
A. ZAFAR ,
A. RIAZ ,
S. UMAR ,
M. ALI SHAH  and
L. XIANGRUI
M. SHOAIB
Affiliation:
Department of Pathobiology, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
S. XIAOKAI
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, 1 Weigang, Nanjing, Jiangsu 210095, PR China
M. UL-HASAN
Affiliation:
Department of Pathobiology, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
A. ZAFAR
Affiliation:
Department Clinical Sciences, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
A. RIAZ
Affiliation:
Department of Pathobiology, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
S. UMAR
Affiliation:
Department of Pathobiology, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
M. ALI SHAH*
Affiliation:
Department of Pathobiology, Faculty of Veterinary & Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Pakistan
L. XIANGRUI
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, 1 Weigang, Nanjing, Jiangsu 210095, PR China
*
Corresponding author: [email protected]
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Abstract

Dendritic cells (DC) are central regulators of immune responses and professional antigen-presenting cells (APCs) with the unique ability to induce both innate immune responses and a highly specific acquired immunity. DC communicates through chemical and mechanical signals in the initiation and maintenance of immune responses. DC forms immunological synapses with T-cells thus pulling T-cells strings and leading to activation of T-cells. Owing to their properties, DC are often called ‘nature's adjuvants’ and thus have become an important component of any vaccination strategy. Coccidiosis is a major intestinal disease caused by Eimeria spp., affecting economically valuable livestock animals such as chickens and turkeys. Economic losses are associated with decreased productivity in afflicted poultry. Vaccination strategies involving DC have been developed owing to the special properties of these cells in coordinating innate and adaptive immune responses. Vaccination of chickens with exosomes isolated from DC containing parasite antigens (Ags) represents a promising alternative strategy to control avian coccidiosis. In recent years, emergence of new chicken DC has opened a new horizon for the development of new vaccines and DC derived vaccine could be a possible strategy to control coccidiosis in field. This review summarises the current state of knowledge of DC and their specific functions in immunity against avian coccidiosis.

Keywords

dendritic cellsEimeriaimmunityavian coccidiosisvaccines
Type
Reviews
Information
World's Poultry Science Journal , Volume 73 , Issue 4 , December 2017 , pp. 737 - 746
Copyright
Copyright © World's Poultry Science Association 2017 

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References

ABID, S.A., AZEEM, T. and UMAR, S. (2016) Emerging threat of necrotic enteritis in poultry and its control without use of antibiotics: a review. Journal of Plant and Animal Sciences 26: 1556-1667.Google Scholar
AHMAD, T.A., EL-SAYED, B.A. and EL-SAYED, L.H. (2016) Development of immunization trials against Eimeria spp. Trials in Vaccinology 5: 38-47.CrossRefGoogle Scholar
ALINE, F., BOUT, D., AMIGORENA, S., ROINGEARD, P. and DIMIER, P. (2004) Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T. gondii infection. Infection and Immunity 72: 4127-4137.Google Scholar
ATIBA, E.M., TEMU, V.W., LADO, M.M. and SAYRE, B. (2016) Meat quality characteristics of goat (Capra hircus) artificially infected with Haemonchus contortus and fed high and low protein diets. Science Letters 4: 203-209.Google Scholar
CABY, M.P., LANKAR, D., VINCENDEAU-SCHERRER, C., RAPOSO, G. and BONNEROT, C. (2005) Exosomal-like vesicles are present in human blood plasma. International Immunology 17: 879-887.Google Scholar
CHAPMAN, H.D., CHERRY, T.E., DANFORTH, H.D., RICHARDS, G., SHIRLEY, M.W. and WILLIAMS, R.B. (2002) Sustainable coccidiosis control in poultry production: the role of live vaccines. International Journal for Parasitology 32: 617-629.CrossRefGoogle ScholarPubMed
CLARKE, L., FODEY, T.L., CROOKS, S.R., MOLONEY, M., O'MAHONY, J., DELAHAUT, P., O'KENNEDY, R. and DANAHER, M. (2014) A review of coccidiostats and the analysis of their residues in meat and other food. Meat Science 97: 358-374.Google Scholar
COLINO, J. and SNAPPER, C.M. (2006) Exosomes from bone marrow DC pulsed with diphtheria toxoid preferentially induce type 1 antigen-specific IgG responses in naive recipients in the absence of free antigen. Journal of Immunology 177: 3757-3762.CrossRefGoogle ScholarPubMed
DALLOUL, R.A. and LILLEHOJ, H.S. (2005) Recent advances in immunomodulation and vaccination strategies against coccidiosis. Avian Diseases 49: 1-8.CrossRefGoogle ScholarPubMed
DEL-CACHO, E., MARGARITA, G., HYUN, S.L., JOAQUIN, Q., ERIK, P. and CARIDAD, S. (2016) Induction of protective immunity against experimental Eimeria tenella infection using serum exosomes. Veterinary Parasitology 224: 1-6.Google Scholar
DEL-CACHO, E., MARGARITA, G., HYUN, S.L., JOAQUIN, Q., ERIK, P. and CARIDAD, S. (2012) Induction of Protective Immunity against Eimeria tenella, Eimeria maxima, and Eimeria acervulina Infections Using Dendritic Cell-Derived Exosomes. Infection and Immunity 80: 1909-1916.CrossRefGoogle ScholarPubMed
DEL-CACHO, E., GALLEGO, M., LEE, S., LILLEHOJ, H.S., QUILEZ, J., LILLEHOJ, E. and SÁNCHEZ-ACEDO, C. (2011) Induction of protective immunity against Eimeria tenella infection using Ag-loaded DC (DC) and DC-derived exosomes. Vaccine 29: 3818-3825.Google Scholar
DELCAYRE, A. and LE-PECQ, J.B. (2006) Exosomes as novel therapeutic nanodevices. Current Opinion in Molecular Therapeutics 8: 31-38.Google Scholar
DENZER, K., EIJK, M., KLEIJMEER, M.J., JAKOBSON, E., GROOT, C. and GEUZE, H.J. (2000) Follicular DC carry MHC class II-expressing microvesicles at their surface. Journal of Immunology 165: 1259-1265.Google Scholar
DEXING, M., CHUNLI, M., GAO, M., LI, G., NIU, Z. and XIADON, H. (2012) Induction of Cellular Immune Response by DNA Vaccine Co expressing E. acervulina 3-1E Gene and Mature CHIl-15 Gene. Journal of Parasitology Research: Article ID 654279.Google Scholar
GUERMONPREZ, P., VALLADEAU, J., ZITVOGEL, L., THÉRY, C. and AMIGORENA, S. (2002) Antigen presentation and T cell stimulation by DC. Annual review of immunology 20: 621-667.Google Scholar
IDRIS, M., ABBAS, R.Z., MASOOD, S., REHMAN, T., FAROOQ, U., BABAR, W., HUSSAIN, R., RAZA, A. and RIAZ, U. (2016) The potential of antioxidant rich essential oils against avian coccidiosis. World's Poultry Science Journal 72: 89-104.Google Scholar
KABOUDI, K., UMAR, S. and MUNIR, M.T. (2016) Prevalence of coccidiosis in free-range chicken in Sidi Thabet Tunisia. Scientifica: 1-6: http://dx.doi.org/10.1155/2016/7075195.Google Scholar
KAROLINA, P. and JACQUES, B. (2012) Cancer immunotherapy via DC. Nature Reviews Cancer 12: 265-277.Google Scholar
LIU, K. and NUSSENZWEIG, M.C (2010) Origin and development of dendritic cells. Immunological Reviews 234: 45-54.Google Scholar
LILLEHOJ, H.S., LEE, S.H., JANG, S.I., KIM, D.K. and LEE, K.W. (2011) Recent progress in understanding host mucosal response to avian coccidiosis and development of alternative strategies to mitigate the use of antibiotics in animal production. Korean Journal of Poultry Science 38: 275-284.Google Scholar
MASOOD, U., WANG, L., YAO, Q., GU, Q., ANSARI, M., ZHANG, X., LIU, S. and MASOOD, U. (2017) A Conspectus on the Diagnosis and Treatment of Periprosthetic Joint Infection. Science Letters 5: 53-59.Google Scholar
MAVERAKIS, E., KIM, K., SHIMODA, M., GERSHWIN, M., PATEL, F., WILKEN, R., RAYCHAUDHURI, S., RUHAAK, L.R. and LEBRILLA, C.B. (2015) Glycans in the immune system and The Altered Glycan Theory of Autoimmunity. Journal of Autoimmunity 57: 1-13.Google Scholar
MONICA, , NASIR, F., PAMELA, S., JUAN, Q.L. and LI, J. (2017) Recent understanding of Pathophysiology, Risk factors and treatments of Neonatal Respiratory Distress Syndrome: A review. Science Letters 5: 70-78.Google Scholar
OHGIMOTO, K., OHGIMOTO, S., IHARA, T., MIZUTA, H., ISHIDO, S., AYATA, M., OGURA, H. and HOTTA, H. (2007) Difference in production of infectious wild-type measles and vaccine viruses in monocyte-derived DC. Virus Research 123: 1-8.Google Scholar
REHMAN, Z., SAJID, U., CHUNCHUN, M., ZAFAR, U., FAROOQ, R., SAIF, U.R. and CHAN, D. (2017) Dendritic cell harmonised immunity to poultry pathogens; a review. World's Poultry Science Journal 63: 581-590.Google Scholar
RENAULT, L. (2007) Avian Coccidiosis in France 1969-1970: A Survey of Occurence as Judged by Post-mortem Examinations. World's Poultry Science Journal 28: 406-412.Google Scholar
SHAH, M.A.A. (2013) DNA vaccines as sustainable Coccidiosis control strategies in chickens. Science Letters 1: 1-4.Google Scholar
SHAH, M.A.A., UMAR, S., IQBAL, M.F., REHMAN, F., QADRI, I. and HE, N. (2014) Recent developments in DNA Vaccination approaches against poultry Coccidiosis and its future endeavors. World's Poultry Science Journal 70: 315-328.Google Scholar
SHAH, M.A.A., XU, L., YAN, R., SONG, X. and LI, X. (2010a) Cross immunity of DNA vaccine pVAX1-cSZ2-IL-2 to Eimeria tenella, E. necatrix and E. maxima. Experimental Parasitology 124: 330-333.Google Scholar
SHAH, M.A.A., XU, L., YAN, R., SONG, X. and LI, X. (2010b) The DNA induced protective immunity with chicken interferon gamma against poultry coccidiosis. Parasitology Research 107: 747-750.Google Scholar
SHAH, M.A.A., XU, L., YAN, R., SONG, X. and LI, X. (2011) Construction of DNA vaccines encoding Eimeria acervulina cSZ-2 with chicken IL-2 and IFN-γ and their induced immunity against poultry Coccidiosis . Research in Veterinary Science 90: 72-77.Google Scholar
SIMON, G.S. and OKOTH, E.O. (2016) Species richness and abundance of birds in and around Nimule National Park, South Sudan. Science Letters 4: 92-94 Google Scholar
STEINMAN, R.M. (2007) DC: understanding immunogenicity. European Journal of Immunology 37: 53-60.Google Scholar
VIAUD, S., THÉRY, C., PLOIX, S., TURSZ, T., LAPIERRE, V., LANTZ, O., ZITVOGEL, L. and CHAPUT, N. (2010) Dendritic cell-derived exosomes for cancer immunotherapy: what's next? Cancer Research 70: 1281-1285.Google Scholar
WIEDER, E. (2003) DC: a basic review. International Society for Cellular Therapy: 1-6.Google Scholar
WILLIAMS, R.B. (2002) Anticoccidial vaccines for broiler chickens: pathways to success. Avian Pathology 31: 317-353.Google Scholar
XU, Q., SONG, X., XU, L., YAN, R., SHAH, M.A. and LI, X. (2008) Vaccination of chickens with a chimeric DNA vaccine encoding Eimeria tenella TA4 and chicken IL-2 induces protective immunity against coccidiosis. Veterinary Parasitology 156: 319-323.Google Scholar
YASMIN, A.R., YEAP, S.K., TAN, S.W., HAIR-BEJO, M., FAKURAZI, S., KAISER, P. and OMAR, A.R. (2015) In vitro characterization of chicken bone marrow-derived dendritic cells following infection with very virulent infectious bursal disease virus. Avian Pathology 44: 452-462.Google Scholar