Page 739 - Veterinary Immunology, 10th Edition
P. 739

capillary endothelium and differentiate into macrophages. In the
  VetBooks.ir  newborn piglet, 75% of particles are removed from the blood by the

               liver and spleen, but by 2 months of age, 75% are removed by the
               lungs. The alveolar macrophages of newborn pigs have poor

               phagocytic activity, but this is effectively acquired by 7 days. These
               alveolar macrophages produce high levels of IL-10 in newborn
               piglets.
                  Newborn calves have fewer NK cells than adults, but these

               respond more strongly to stimulation with IL-2 or IL-15 and are
               more cytotoxic! Age-dependent changes occur in acute-phase
               proteins in newborn calves. Serum amyloid A, lipopolysaccharide-
               binding protein, haptoglobin, and α -acid glycoprotein are present
                                                               1
               in high concentrations immediately after birth but gradually decline
               by 21 days. In developing piglets, IL-8 and tumor necrosis factor-α

               (TNF-α) production by blood monocytes increases significantly
               during the postnatal period, whereas monocyte production of IL-1β
               does not. Absolute numbers of γ/δ T cells increase greatly from
               birth until 20 to 25 weeks of age, and there are progressive changes
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                                                                              −
                                                                −
                                                                                                    +
               in helper cell phenotypes from CD8a , SLA-DR , CD27  to CD8a ,
                                          −
                          +
               SLA-DR , and CD27  during this time.
               Adaptive Immunity

               The early development of the adaptive immune system has been

               well analyzed in newborn foals since some are highly susceptible to
               lethal Rhodococcus equi infection (Box 23.3). Newborn mammals,
               including foals, mount adaptive responses skewed toward type 2
               rather than type 1 responses. Thus they favor antibody responses

               over cell-mediated immunity. This imbalance results from the late
               development of IL-12–producing DC1 cells and the activities of IL-4
               and IL-13 from DC2 cells. Mononuclear cells from newborn foals
               are unable to express IFN-γ. Their Th2 cells rapidly differentiate,

               whereas neonatal Th1 cells are slow to develop. Excess IFN-γ may
               cause placental damage, so this skewing is not accidental. IFN-γ
               production gradually increases through the first 6 months of life to
               reach adult levels within a year, when the acquired responses revert
               to the balanced adult pattern.








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