40 Consequently, this study found no evidence for TH2 bias in pregnant sheep, contrary to many previous studies in humans and mice.37 However, as previously mentioned, the TH2 paradigm in pregnancy has been brought into question. A recent study has found no global differences in the production of IFN-γ, IL-4, IL-5, IL-10 or IL-13 production by mitogen-activated PBMC from pre- and post-partum women, concluding that the evidence for a TH2 bias during pregnancy

is certainly debatable and possibly reflective of experimental design.41 This observation is in line with our studies in sheep, and it would therefore appear that other immunological JQ1 in vitro and/or physiological factors (such as placental development) are responsible for the pathogenesis of OEA. For example, we have previously suggested that the placentitis characteristic of OEA originates from the haematomatas in the placentome that create a mechanism for transmission of C. abortus from the maternal blood to the placenta and may not depend on alterations in maternal immune reactivity.21 Consequently, although the TH1/TH2 paradigm provides an attractive explanation

for the pathogenesis of OEA and recrudescence of C. abortus from a peripheral site of latency in mid-gestation, the evidence suggests otherwise and that other factors are involved. Our knowledge of the molecular mechanisms https://www.selleckchem.com/products/r428.html of persistence of C. abortus in ovine cells and of the correlates of immunological protection has greatly advanced our understanding of OEA. Nevertheless, gaps in our knowledge remain that require further investigation if we are developing

more effective control strategies (including vaccination) for this important reproductive disease of sheep and other ruminants. A current area of great interest in vaccine development is the identification of effective delivery strategies that target this website the innate immune system to stimulate an appropriate adaptive host response that confers protection without immunopathology. The particular components of interest in innate immunity are dendritic cells, NK cells, pattern recognition receptors and early cytokine and chemokine production. Several laboratories are actively engaged in the study of these cells and molecules in sheep, with most investing at least some of their effort and resources into the development of immunological tools to define expression and ascribe function. The area of NK cell biology has particular relevance for reproductive biology and definitive moAbs against ovine NK-expressed molecules are expected to become available in the very near future. These probes will help address an unanswered question regarding the relative importance of γδT cells and NK cells in ovine reproduction.