New insights in cellular immune response in colostrum-deprived pigs after immunization with subunit and commercial vaccines against Glässer's disease

Cellular Immunology

Volumn 277, Issue 1-2, 2012, Pages 74-82

  Frandoloso, R ^a   Martinez Martinez S ^a   Yubero, S ^a   Rodriguez Ferri E F ^a   Gutierrez Martin C B ^a  

^a UNIVERSITY OF LEÓN   (Spain)

Author keywords

Cell response; Gl sser's disease; Haemophilus parasuis; Vaccines

Indexed keywords

CD163 ANTIGEN; CD3 ANTIGEN; CD8 ANTIGEN; NPAPTCP VACCINE; NPAPTM VACCINE; RTBPA VACCINE; SUBUNIT VACCINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANTIGEN EXPRESSION; ARTICLE; B LYMPHOCYTE; CD3+ T LYMPHOCYTE; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CELLULAR IMMUNITY; COLOSTRUM; COMPARATIVE STUDY; CONTROLLED STUDY; EXPERIMENTAL PIG; GLASSER DISEASE; HAEMOPHILUS INFECTION; HAEMOPHILUS PARASUIS; NONHUMAN; OUTCOME ASSESSMENT; PERIPHERAL BLOOD MONONUCLEAR CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEROTYPE; VACCINATION;

ANIMALS; ANTIGENS, CD; B-LYMPHOCYTES; COLOSTRUM; FEMALE; HAEMOPHILUS INFECTIONS; HAEMOPHILUS PARASUIS; HAEMOPHILUS VACCINES; IMMUNITY, CELLULAR; LEUKOCYTES, MONONUCLEAR; PREGNANCY; SWINE; SWINE DISEASES; T-LYMPHOCYTES; VACCINES, SUBUNIT;

ANIMALIA; HAEMOPHILUS PARASUIS; SUIDAE;

EID: 84864292896     PISSN: 00088749     EISSN: 10902163     Source Type: Journal    
DOI: 10.1016/j.cellimm.2012.05.010     Document Type: Article

References (55)

1. Rapp-Gabrielson V.J., Kocur G.J., Muir S.K. Haemophilus parasuis: immunity in swine after vaccination. Veterinary Medicine 1997, 92:83-90.
2. Oliveira S., Pijoan C. Haemophilus parasuis: new trends on diagnosis, epidemiology and control. Veterinary Microbiology 2004, 99:1-12.
3. Kielstein P., Rapp-Gabrielson V.J. Designation of 15 serovars of Haemophilus parasuis on the basis of immunodiffusion using heat-stable antigen extracts. Journal of Clinical Microbiology 1992, 15:1019-1023.
4. Hill C.E., Metcalf D.S., MacInnes J.I. A search for virulence genes of Haemophilus parasuis using differential display RT-PCR. Veterinary Microbiology 2003, 96:189-202.
5. Bak H., Riising H.J. Protection of vaccinated pigs against experimental infections with homologous and heterologous Haemophilus parasuis. Veterinary Record 2002, 151:502-505.
6. Hoffmann C.R., Bilkei G. The effect of a homologous bacterin given to sows prefarrowing on the development of Glässer's disease in postweaning pigs after i.v. challenge with Haemophilus parasuis serotype 5. Deutsch Tierärztl Wochber 2002, 109:271-276.
7. Takahaschi L., Nagai S., Yagihashi T., Idehata T., Nakano Y., Senna K., Maruyama T., Murofushi J. A cross protection experiment in pigs vaccinated with Haemophilus parasuis serovars 2 and 5 bacterins, and evaluation of a bivalent vaccine under laboratory and field conditions. Journal of Veterinary Medicine Science 2001, 63:487-491.
8. Palzer A., Ritzmann M., Hienritzi K. A field trial for early vaccination against Glässer's disease using Porcilis Glässer. Schweiz Arch Tierheilkder 2007, 149:389-394.
9. Zhang M., Guo Y., Zhao J., Hu Q., Hu Y., Zhang A., Chen H., Jin M. Molecular cloning, sequencing and expression of the outer membrane protein A gene from Haemophilus parasuis. Veterinary Microbiology 2009, 136:408-410.
10. Zhou M., Gou Y., Zhao J., Hu Q., Hu Y., Zhang A., Chen H., Jin M. Identification and characterization of novel immunogenic outer membrane proteins of Haemophilus parasuis serovar 5. Vaccine 2009, 27:5271-5277.
11. Hong M., Ahn J., Yoo S., Hong J., Lee E., Yoon I., Jung J.K., Lee H. Identification of novel immunogenic proteins in pathogenic Haemophilus parasuis based on genome sequence analysis. Veterinary Microbiology 2011, 148:89-92.
12. Olvera A., Pina S., Pérez-Simó M., Aragón V., Segalés J., Bensaid A. Immunogenicity and protection against Haemophilus parasuis infection after vaccination with recombinant virulence associated trimeric autotransporters (VtaA). Vaccine 2011, 29:2797-2802.
13. F. Yuan, S. Fu, J. Hu, J. Li, H. Chang, L. Hu, H. Chen, Y. Tian, W. Bei. Evaluation of recombinant proteins of Haemophilus parasuis strain SH0165 as vaccine candidates in a mouse model. Research in Veterinary Science 17 (2001) (Epub ahead of print).
14. S. Fu, F. Yuan, M. Zhang, C. Tan, H. Chen, W. Bei. Cloning, expression and characterization of a cell wall surface protein, 6-phosphogluconate dehydrogenase, of Haemophilus parasuis. Research in Veterinary Science Aug 11 (2011) (Epub ahead of print).
15. Amano H., Shibata M., Takahashi K., Sasaki Y. Effects of endotoxin pathogenicity in pigs with acute septicemia of Haemophilus parasuis infection. Journal of Veterinary Medicine Science 1997, 59:451-455.
16. Müller G., Kohler H., Diller R., Rassbach A., Berndt A., Schimmel D. Influences of naturally occurring and experimentally induced porcine pneumonia on blood parameters. Research in Veterinary Science 2003, 74:23-30.
17. Martín de la Fuente A.J., Gutiérrez-Martín C.B., Rodríguez-Barbosa J.I., Martínez-Martínez S., Frandoloso R., Tejerina F., Rodríguez-Ferri E.F. Blood celular immune response in pigs immunized and challenged with Haemophilus parasuis. Research in Veterinary Science 2009, 86:230-234.
18. Frandoloso R., Martínez S., Rodríguez-Ferri E.F., García-Iglesias M.J., Pérez-Martínez C., Martínez-Fernández B., Gutiérrez-Martín C.B. Development and characterization of protective Haemophilus parasuis subunit vaccines based on native proteins with affinity to porcine transferrin and comparison with other subunit and commercial vaccines. Clinical and Vaccine Immunology 2011, 18:50-58.
19. Solano-Aguilar G.I., Vengroski K.G., Beshah E., Lunney J.K. Isolation and purificaction of lymphocytic subsets from gut-associated lymphoid tissue in neonatal swine. Journal of Immunological Methods 2000, 241:185-199.
20. Yang H., Parkhouse R.M. Phenotypic classification of porcine lymphocyte subpopulations in blood and lymphoid tissues. Immunology 1996, 89:76-83.
21. Solano-Aguilar G.I., Pijoan C., Rapp-Gabrielson V., Collins J., Carvalho L.F., Winkelman N. Protective role of maternal antibodies against Haemophilus parasuis infection. American Journal of Veterinary Research 1999, 60:81-87.
22. Sánchez C., Domenech N., Vázquez J., Alonso F., Ezquerra A., Domínguez J. The porcine 2A10 antigen is homologous to human CD163 and related to macrophage differentiation. Journal of Immunology 1999, 162:5230-5237.
23. + monocytes into functional dendritic cells. Immunobiology 2004, 209:57-65.
24. Frankenberger M., Sternsdorf T., Pechumer H., Pforte A., Ziegler-Heitbrock H.W. Differential cytokine expression in human blood monocyte subpopulations: a polymerase chain reaction analysis. Blood 1996, 87:373-377.
25. Gordon S., Martinez F.O. Alternative activation of macrophages: mechanism and functions. Immunity 2010, 32:593-604.
26. Ondrackova P., Nechvatalova K., Kucerova Z., Leva L., Domínguez J., Faldyna M. Porcine mononuclear phagocyte subpopulations in the lung, blood and bone marrow: dynamics during inflammation induced by Actinobacillus pleuropneumoniae. Veterinary Research 2010, 41:64-77.
27. McHeyzer-Williams M., McHeyzer-Williams L., Panus J., Pogue-Caley R., Bikah G., Driver D., Eisenbraun M. Helper T-cell-regulated B-cell immunity. Microbes. Infection 2003, 5:205-212.
28. Kalia V., Sarkar S., Gourley T.S., Rouse B.T., Ahmed R. Differentiation of memory B and T cells. Current Opinion Immunology 2006, 18:255-264.
29. Faldyna M., Nechvatalova K., Sinkora J., Knotigova P., Leva L., Krejci J., Toman M. Experimental Actinobacillus pleuropneumoniae infection in piglets with different types and levels of specific protection: immunophenotypic analysis of lymphocyte subsets in the circulation and respiratory mucosal lymphoid tissue. Veterinary Immunology and Immunopathology 2005, 107:143-152.
30. Zuckermann F.A., Husmann R.J. Functional and phenotypic analysis of porcine peripheral blood CD4/CD8 double-positive T cells. Immunology 1996, 87:500-512.
31. + extrathymic T lymphocytes. Cell Immunology 1996, 168:291-296.
32. + memory T-helper cells in swine. Journal of Virology 1998, 72:4866-4873.
33. + CTL specific for the mycobacterial major secreted antigen 85A. Journal of Immunology 2000, 165:7088-7095.
34. Salerno-Goncalves R., Sztein M.B. Priming of Salmonella enterica serovar Typhi-specific CD8(+) T cells by suicide dendritic cell cross-presentation in humans. PLoS One 2009, 4:e5879.
35. + cytotoxic T lymphocytes. Experimental Hematology 2005, 33:811-818.
36. Vanier G., Szczotka A., Friedl P., Lacouture S., Jacques M., Gottschalk M. Haemophilus parasuis invades porcine brain microvascular endothelial cells. Microbiology 2006, 152:135-142.
37. Bouchet B., Vanier G., Jacques M., Gottschalk M. Interactions of Haemophilus parasuis and its LOS with porcine brain microvascular endothelial cells. Veterinary Research 2008, 3(9):42.
38. Aragón V., Bouchet B., Gottschalk M. Invasion of endothelial cells by systemic and nasal strains of Haemophilus parasuis. Veterinary Journal 2010, 186:264-267.
39. Bouchet B., Vanier G., Jacques M., Auger E., Gottschalk M. Studies on the interactions of Haemophilus parasuis with porcine epithelial tracheal cells: limited role of LOS in apoptosis and pro-inflammatory cytokine release. Microbial Pathogenesis 2009, 46:108-113.
40. R. Frandoloso, S. Martinez-Martinez, C.B. Gutierrez-Martin, E.F. Rodriguez-Ferri. Haemophilus parasuis serovar 5 Nagasaki strain adheres and invades PK-15 cells. Veterinary Microbiology Jul 28 (2011b) (Epub ahead of print).
41. Paul P.S., van Deusen R.A., Mengeling W.L. Monoclonal precipitating antibodies to porcine immunoglobulin M. Veterinary Immunology and Immunopathology 1985, 8:311-328.
42. Knapp W., Dorken B. Leococyte Typing IV 1989, Oxford University Press, New York.
43. Fischer E., Delibrias C., Kazatchkine M.D. Expression of CR2 (the C3dg/EBV receptor, CD21) on normal human peripheral blood T lymphocytes. Journal of Immunology 1991, 146:865-869.
44. Malherbe L., Mark L., Fazilleau N., McHeyzer-Williams L.J., McHeyzer-Williams M.G. Vaccine adjuvants alter TCR-based selection thresholds. Immunity 2008, 28:698-709.
45. Abbas A.K., Lichtman A.H., Pillai S. Cellular and molecular immunology 2007, Saunders Elsevier, Philadelphia. sixth ed.
46. Lo D.Y., Hung C.N., Lee W.C., Liao J.W., Blacklaws B.A., Chen T.H., Chien M.S., Hsuan S.L. Effect of immunostimulation by detoxified E. coli lipopolysaccharide combined with inactivated Propionibacterium granulosum cells on porcine immunity. Journal of Veterinary Medicine Science 2009, 71:897-903.
47. Appleyard G.D., Furesz S.E., Wilkie B.N. Blood lymphocyte subsets in pigs vaccinated and challenged with Actinobacillus pleuropneumoniae. Veterinary Immunology and Immunopathology 2002, 86:221-228.
48. Sinkora J., Rehakova Z., Sinkora M., Cukrowska B., Tlaskalova-Hogenova H., Bianchi A.T., de Geus B. Expression of CD2 on porcine B lymphocytes. Immunology 1998, 95:443-449.
49. Pescovitz M.D., Book B.K., Aasted B., Domínguez J., Ezquerra A., Trebichavsky I., Novikov B., Valpotic I., Nielsen J., Arn S., Sachs D.H., Lunney J.K., Boyd P.C., Walker J., Lee R., Lackovic G., Kirkham P., Parkhouse R.M., Saalmuller A. Analyses of monoclonal antibodies reacting with porcine CD3: results from the second international swine CD workshop. Veterinary Immunology and Immunopathology 1998, 60:261-268.
50. Pescovitz M.D., Lunney J.K., Sachs J.D.H. Preparation and characterization of monoclonal antibodies reactive with porcine PBL. Veterinary Immunology and Immunopathology 1984, 8:311-328.
51. Binns R.M., Duncan I.A., Powis S.J., Hutchings A., Butcher G.W. Subsets of null and gamma delta T-cell receptor+ T lymphocytes in the blood of young pigs identified by specific monoclonal antibodies. Immunology 1992, 77:219-227.
52. Bullido R., Gómez del Moral M., Doménech N., Alonso F., Ezquerra A., Domínguez J. Monoclonal antibodies to a high molecular weight isoform of porcine CD45: biochemical and tissue distribution analysis. Veterinary Immunology and Immunopathology 1997, 56:151-162.
53. + naïve T cells. Development and Comparative Immunology 2004, 28:239-250.
54. Álvarez B., Sanchez C., Bullido R., Marina A., Lunney J., Alonso F., Ezquerra A., Dominguez J. J. A porcine cell surface receptor identified by monoclonal antibodies to SWC3 is a member of the signal regulatory protein family and associates with protein-tyrosine phosphatase SHP-1. Tissue Antigens 2000, 55:342-351.
55. Saalmüller A., Denham S., Haverson K., Davis B., Domínguez J., Pescovitz M.D., Stokes C.C., Zuckermann F., Lunney J.K. The second international swine CD workshop. Veterinary Immunology and Immunopathology 1996, 54:155-158.