Interferon-gamma secretion and proliferative responses of peripheral blood mononuclear cells after vaccination of pigs against Aujeszky's disease in the presence of maternal immunity.

The development of T-cell responses in pigs vaccinated against Aujeszky's disease in the presence of maternal-derived antibodies (MDA) was examined. The aim of study was to evaluate the influence of MDA on the postvaccinal T-cell responses and optimization vaccination protocols in MDA-positive pigs. Pigs born to immune sows were vaccinated at different ages against Aujeszky's disease virus (ADV). For estimation of T-cell responses the lymphocyte proliferation and interferon (IFN)-gamma and interleukin-4 production were evaluated. High values of stimulation index were noted in groups vaccinated at 8 or 12 weeks of age (in 60% and 100% animals, respectively). In weaners vaccinated at 10 and 14 weeks of age, as well as in those vaccinated at 7 days and revaccinated at 8 or 12 weeks of age, 100% of animals positively responded in the lymphocyte proliferation assay after booster. At 20 weeks of life, only animals vaccinated at 12 weeks of age, 7 days and 12 weeks of age, and 10 and 14 weeks of age showed antigen-specific proliferation. Similar results were observed with IFN-gamma secretion after exposure to live ADV. We demonstrate that early vaccination with a live glycoprotein E-deleted ADV vaccine, in the face of high levels of MDA, could be effective, but the intensity and duration of the anamnestic response depends on the time of booster injection.

[1]  M. Truszczyński,et al.  Bierna i czynna odpornosc przeciw chorobom zakaznym u oseska do okresu okoloodsadzeniowego , 2007 .

[2]  W. Bellini,et al.  Maternal antibody inhibits both cellular and humoral immunity in response to measles vaccination at birth. , 2006, Virology.

[3]  G. Reiner,et al.  Interferon-gamma response of PBMC indicates productive pseudorabies virus (PRV) infection in swine , 2004, Veterinary Immunology and Immunopathology.

[4]  W. Boersma,et al.  Vaccine-induced T cell-mediated immunity plays a critical role in early protection against pseudorabies virus (suid herpes virus type 1) infection in pigs. , 2004, Veterinary immunology and immunopathology.

[5]  J. Casal,et al.  The use of different vaccination schedules for sows to protect piglets against Aujeszky's disease. , 2004, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.

[6]  J. Roth,et al.  Maternal antibody blocks humoral but not T cell responses to BVDV. , 2003, Biologicals : journal of the International Association of Biological Standardization.

[7]  C. Andréoni,et al.  DNA vaccination of neonate piglets in the face of maternal immunity induces humoral memory and protection against a virulent pseudorabies virus challenge. , 2003, Vaccine.

[8]  H. Margolis,et al.  Hepatitis A vaccination of infants: effect of maternal antibody status on antibody persistence and response to a booster dose , 2003, The Pediatric infectious disease journal.

[9]  P. Heinen,et al.  Effect of maternally derived antibodies on the clinical signs and immune response in pigs after primary and secondary infection with an influenza H1N1 virus. , 2003, Veterinary immunology and immunopathology.

[10]  M. D. de Jong,et al.  Influence of maternal antibodies on efficacy of a subunit vaccine: transmission of classical swine fever virus between pigs vaccinated at 2 weeks of age. , 2002, Vaccine.

[11]  J. Roth,et al.  T-cell populations responsive to bovine respiratory syncytial virus in seronegative calves. , 2002, Veterinary immunology and immunopathology.

[12]  C. Siegrist Neonatal and early life vaccinology. , 2001, Vaccine.

[13]  T. Fischer,et al.  T helper 1‐type cytokine transcription in peripheral blood mononuclear cells of pseudorabies virus (Suid herpesvirus 1)‐primed swine indicates efficient immunization , 2000, Immunology.

[14]  R. Dagan,et al.  Immunization against hepatitis A in the first year of life: priming despite the presence of maternal antibody. , 2000, The Pediatric infectious disease journal.

[15]  P. Lambert,et al.  Influence of maternal antibodies on vaccine responses: inhibition of antibody but not T cell responses allows successful early prime‐boost strategies in mice , 1998, European journal of immunology.

[16]  T. Kimman,et al.  Time course of the porcine cellular and humoral immune responses in vivo against pseudorabies virus after inoculation and challenge: significance of in vitro antigenic restimulation. , 1998, Veterinary immunology and immunopathology.

[17]  P. Lambert,et al.  Determinants of infant responses to vaccines in presence of maternal antibodies. , 1998, Vaccine.

[18]  T. Kimman,et al.  The influence of maternal immunity on the development of the in vitro lymphocyte proliferation response against pseudorabies virus in pigs. , 1998, Research in veterinary science.

[19]  M. Eloit,et al.  Effective priming of neonates born to immune dams against the immunogenic pseudorabies virus glycoprotein gD by replication-incompetent adenovirus-mediated gene transfer at birth. , 1997, The Journal of general virology.

[20]  T. Kimman,et al.  Development and antigen specificity of the lymphoproliferation responses of pigs to pseudorabies virus: dichotomy between secondary B- and T-cell responses. , 1995, Immunology.

[21]  M. Pensaert,et al.  Effect of experimental infection with pseudorabies (Aujeszky's disease) virus on pigs with maternal immunity from vaccinated sows. , 1978, American journal of veterinary research.