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Literally, reproductive immunology was born in bovine on-farm reproduction where seminal experiments intended for developing methods for embryo transfer in cattle were performed. Actually, these experiments led to two of major concepts and fundamental principles of reproductive immunology using the bovine species as a model for biomedical research, namely the concept of acquired immunological tolerance and the paradox of the semiallogeneic bovine foetus whereby such organism can develop within an immunologically competent host. Peter Medawar, a scientist who together with Frank Macfarlande Burnet shared the 1960 Nobel Prize in physiology or medicine for discovery of acquired immunological tolerance, while studying dizygotic cattle twins, thereby giving birth to reproductive immunology. Also, these findings significantly influenced development of organ transplants and showed that using farm animals as models for studying transplantation immunology had general relevance for mammalian biology and health including those of humans. However, the interest for further research of the fascinating maternal immune influences on pregnancy and perinatal outcomes and of the prevention and treatment of immunologically mediated reproductive disorders in viviparous mammals of veterinary relevance by veterinary immunologists and reproductive clinicians have been very scarce regarding the application of nonspecific immunomodulatory agents for prevention and treatment of subfertility and infertility in pigs and cattle, but still broadening knowledge in this area and hold great potential for improving such therapy in the future. The aim of the current overview is to provide up-to-date information and explaining/translating relevant immunology phenomena into veterinary practice for specialists and scientists/clinicians in reproduction of animals.

The ban on dietary antibiotic growth promoters (AGP) in swine production has focused increasing research efforts on the development of alternative feed supplements. One such alternative to AGP is the dietary zeolite clinoptilolite (CPL). The aims of this study were to evaluate, in weaned pigs, the effects of CPL on: (a) growth performance, (b) gut health (reduction of harmful bacteria and, incidence/severity of diarrhoea) and (c) circulating or ileal mucosal subsets of lymphoid immune cells, over the course of five weeks post weaning. The non-treated pigs received standard Phase 1 diet from Day 0 to 21 and Phase 2 diet from Day 22 to 35, whereas both diets of experimental pigs were supplemented with 0.5% CPL. The pigs receiving diet supplemented with CPL had significantly higher average daily gain at Day 28 but significantly lower daily gain at Day 35 of the experiment (P < 0.05). The CPL group exhibited non-significantly improved feed conversion ratio (1.83 vs. 2.17) for the total duration of the experiment (Day 0 to Day 35). Although shedding of haemolytic/enterotoxigenic E. coli was more frequent in the CPL group, the sum of their diarrhoea severity score was 12.96% lower (47 vs 54) than that of the non-treated controls. The proportions of circulating lymphoid cell subsets tested (CD45+, CD4+, CD21+), were significantly (P < 0.05 to P < 0.01) higher in CPL-treated pigs between Day 21 and Day 35 of the experiment. Immunohistology/morphometry of ileal segments revealed an increased recruitment of CD45RA+ cells in interfollicular (P < 0.05), but not in follicular areas of ileal PP of CPL-treated pigs at Day 35. In conclusion, CPL did not improve growth in weaned pigs, and generally it failed to improve their feed conversion efficiency. Further, it did not suppress faecal shedding of enterotoxigenic E. coli; however, it was shown to be effective as an immunomodulatory agent by promoting the recruitment of circulating and intestinal immune cell subsets.