Humoral and cell-mediated immune responses of foxes (Vulpes vulpes) after experimental primary and secondary oral vaccination using SAG(2) and V-RG vaccines
M. Lambot et al., Humoral and cell-mediated immune responses of foxes (Vulpes vulpes) after experimental primary and secondary oral vaccination using SAG(2) and V-RG vaccines, VACCINE, 19(13-14), 2001, pp. 1827-1835
Humeral and cell-mediated immune responses of 36 captive foxes to two oral
vaccines against rabies currently used for foxes in Europe were studied. Th
e Street Alabama Dufferin (SAD) mutant Gif (SAG,) vaccine has been selected
by double mutation from the SAD virus. The vaccinia recombinant virus (V-R
G) expresses the rabies glycoprotein. Both vaccines induce similar humoral
and cell-mediated responses after primary and secondary oral administration
. We observed a typical anamnestic response, although of a limited duration
, after the booster vaccination. Therefore, our results suggested that two
successive oral vaccination campaigns should not significantly improve the
immunisation of foxes. Lymphocyte in vitro proliferative response to the SA
D antigen highlighted the presence in blood of a T-cell specific memory 6 m
onths after vaccination. The synthesis of several vulpine cytokines was det
ected in peripheral blood mononuclear cells (PBMC) stimulated by SAD antige
n via reverse transcription polymerase chain amplification. The data showed
a concomitant expression of interleukin (IL)-4 and interferon-gamma in PBM
C of vaccinated foxes. No change was detected in the level of IL-2, IL-10 a
nd IL-12 synthesis, whereas the pro-inflammatory cytokine tumour necrosis f
actor-alpha seemed involved in the activation of naive T lymphocytes. (C) 2
001 Elsevier Science Ltd. All rights reserved.