Hostname: page-component-848d4c4894-2pzkn Total loading time: 0 Render date: 2024-05-28T02:33:28.269Z Has data issue: false hasContentIssue false

Vaccinating against zoonotic parasitic diseases: myth or reality?

Published online by Cambridge University Press:  28 February 2007

Dante S. Zarlenga*
Affiliation:
US Department of Agriculture ARS, ANRI, Immunology and Disease Resistance Laboratory, Beltsville, MD, USA
*
US Department of Agriculture, ARS, ANRI, Immunology and Disease Resistance Laboratory, Bldg 1180 BARCEast, Beltsville, Maryland 20705, USA E-mail: Zarlenga@anri.barc.usda.gov

Abstract

The largely unanticipated difficulties of parasite vaccine development have led us to a renewed awareness of the survival strategies evolutionarily embedded within parasites over hundreds of millions of years. We have grown to appreciate that efforts to disrupt parasite–host relationships are substantially compounded by our incomplete understanding of the complex immune responses that occur in the naturally infected host. Given the inability to transfer laboratory successes to field trials, research is leading us to conclude that genetically defined animal models may not be good predictors of the unique and disparate protective immune responses one can expect from the genetically heterogeneous populations of animals that represent the parasite's natural environment. This is further compounded by the abundance of mechanisms parasites have created for themselves to defend against immune intervention. Thus, in the never-ending saga of vaccine development, it is only appropriate that pitfalls and advancements be critiqued as they apply across parasite groups, with a look towards promising technologies that may propel this field to the level of scientific achievement once envisaged.

Type
Research Article
Copyright
Copyright © CAB International 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aboobaker, AA and Blaxter, ML (2003). Use of RNA interference to investigate gene function in the human filarial nematode parasite Brugia malayi. Molecular and Biochemical Parasitology 129: 4151.CrossRefGoogle ScholarPubMed
Ashrafi, K, Chang, FY, Watts, JL, Fraser, AG, Kamath, RS, Ahringer, J and Ruvkun, G (2003). Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes. Nature 421: 268272.CrossRefGoogle ScholarPubMed
Canals, A, Zarlenga, DS, Almeria, S and Gasbarre, LC (1997). Cytokine profile induced by a primary infection with Ostertagia ostertagi in cattle. Veterinary Immunology and Immunopathology 58: 6375.CrossRefGoogle ScholarPubMed
Caplen, NJ (2003). RNAi as a gene therapy approach. Expert Opinion on Biological Therapy 3: 575586.CrossRefGoogle ScholarPubMed
Dame, JB, Williams, JL, McCutchan, TF, Weber, JL, Wirtz, RA, Hockmeyer, WT, Maloy, WL, Haynes, JD, Schneider, I, Roberts, D, Sanders, SG, Reddy, P, Diggs, CL and Miller, LH (1984). Structure of the gene encoding the immunodominant surface antigen on the sporozoite of the human malaria parasite Plasmodium falciparum. Science 225: 593599.CrossRefGoogle ScholarPubMed
Ellis, J, Ozaki, LS, Gwadz, RW, Cochrane, AH, Nussenzweig, V, Nussenzweig, RS and Godson, GN (1983). Cloning and expression in E. coli of the malarial sporozoite surface antigen gene from Plasmodium knowlesi. Nature 302: 536538.CrossRefGoogle Scholar
Enea, V, Ellis, J, Zavala, F, Arnot, DE, Asavanich, A, Masuda, A, Quakyi, I and Nussenzweig, RS (1984). DNA cloning of Plasmodium falciparum circumsporozoite gene: amino acid sequence of repetitive epitope. Science 225: 628630.CrossRefGoogle ScholarPubMed
Fire, A, Xu, S, Montgomery, MK, Kostas, SA, Driver, SE and Mello, CC (1998). Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391: 806811.CrossRefGoogle ScholarPubMed
Gomez-Escobar, N, Lewis, E and Maizels, RM (1998). A novel member of the transforming growth factor-beta (TGF-beta) superfamily from the filarial nematodes Brugia malayi and B. pahangi. Experimental Parasitology 88: 200209.CrossRefGoogle ScholarPubMed
Gomez-Escobar, N, Gregory, WF and Maizels, RM (2000). Identification of tgh-2, a filarial nematode homolog of Caenorhabditis elegans daf-7 and human transforming growth factor beta, expressed in microfilarial and adult stages of Brugia malayi. Infection and Immunity 68: 64026410.CrossRefGoogle ScholarPubMed
Graves, P and Gelband, H (2003). Vaccines for preventing malaria. Cochrane Database of Systematic Reviews 1: CD000129.Google Scholar
Hoberg, EP, Alkire, NL, de Queiroz, A and Jones, A (2001). Out of Africa: origins of the Taenia tapeworms in humans. Proceedings of the Royal Society of London, Series B. Biological Sciences 268: 781787.CrossRefGoogle ScholarPubMed
Kamath, RS, Fraser, AG, Dong, Y, Poulin, G, Durbin, R, Gotta, M, Kanapin, A, Le Bot, N, Moreno, S, Sohrmann, M, Welchman, DP, Zipperlen, P and Ahringer, J (2003). Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 421: 231237.CrossRefGoogle ScholarPubMed
Lawrence, SB, Heath, DD, Harrison, GBL, Robinson, CM, Dempster, RP, Lightowlers, MW and Rickard, MD (1996). Pilot field trial of a recombinant Taenia ovis vaccine in lambs exposed to natural infection. New Zealand Veterinary Journal 44: 155157.CrossRefGoogle ScholarPubMed
Lightowlers, MW, Rolfe, R and Gauci, CG (1996). Taenia saginata: vaccination against cysticercosis in cattle with recombinant oncosphere antigens. Experimental Parasitology 84: 330338.CrossRefGoogle ScholarPubMed
Maeda, I, Kohara, Y, Yamamoto, M and Sugimoto, A (2001). Large-scale analysis of gene function in Caenorhabditis elegans by high-throughput RNAi. Current Biol 11: 171176.CrossRefGoogle ScholarPubMed
McRobert, L and McConkey, GA (2002). RNA interference (RNAi) inhibits growth of Plasmodium falciparum. Molecular and Biochemical Parasitology 119: 273278.CrossRefGoogle ScholarPubMed
Newfeld, SJ, Wisotzkey, RG and Kumar, S (1999). Molecular evolution of a developmental pathway: phylogenetic analyses of transforming growth factor-beta family ligands, receptors and Smad signal transducers. Genetics 152: 783795.CrossRefGoogle ScholarPubMed
Plancarte, A, Flisser, A, Gauci, CG and Lightowlers, MW (1999). Vaccination against Taenia solium cysticercosis in pigs using native and recombinant oncosphere antigens. International Journal of Parasitology 29: 643647.CrossRefGoogle ScholarPubMed
Patterson, GI and Padgett, RW (2000). TGF beta-related pathways. Roles in Caenorhabditis elegans development. Trends in Genetics 16: 2733.CrossRefGoogle ScholarPubMed
Pozio, E (2001). New patterns of Trichinella infection. Veterinary Parasitology 98: 133148.CrossRefGoogle ScholarPubMed
Solano-Aguilar, GI, Zarlenga, D, Beshah, E, Vengroski, K, Gasbarre, L, Junker, D, Cochran, M, Weston, C, Valencia, D, Chiang, C, Dawson, H, Urban, JF and Lunney, JK (2002). Limited effect of recombinant porcine interleukin-12 on porcine lymphocytes due to a low level of IL-12 beta2 receptor. Veterinary Immunology and Immunopathology 89: 133148.CrossRefGoogle ScholarPubMed
Waldvogel, AS, Hediger-Weithaler, BM, Eicher, R, Zakher, A, Zarlenga, DS, Gasbarre, LC and Heussler, VT (2000). Interferon-gamma and interleukin-4 mRNA expression by peripheral blood mononuclear cells from pregnant and non-pregnant cattle seropositive for bovine viral diarrhea virus. Veterinary Immunology and Immunopathology 77: 201212.CrossRefGoogle ScholarPubMed