Page 727 - Veterinary Immunology, 10th Edition
P. 727

VetBooks.ir  Development of the Immune System





               The development of the immune system in the mammalian fetus
               follows a consistent pattern. The thymus is the first lymphoid organ

               to develop, followed by the secondary lymphoid organs. B cells
               appear soon after the development of the spleen and lymph nodes,
               but antibodies are not usually detectable until late in fetal life. The
               ability of the fetus to respond to antigens develops very rapidly
               once the lymphoid organs appear, but all antigens are not equally

               capable of stimulating fetal lymphoid tissue. The immune system
               develops in a series of steps, with each step permitting the fetus to
               respond to more antigens. These steps are driven by a gradual

               increase in the use of gene conversion or somatic mutation to
               increase antibody diversity. The ability to mount cell-mediated
               immune responses develops at the same time as antibody
               production. T cell receptor (TCR) diversity is also limited in the
               fetus and neonate, and their cytokine production may be low. This

               may simply be due to their lack of exposure to foreign or microbial
               antigens.



               Specific Animal Immune Systems


               Foal

               The gestation period of the mare is about 340 days. Lymphocytes
               are seen first in the thymus at about 60 to 80 days post-conception.
               They are found in the mesenteric lymph node and intestinal lamina

               propria at 90 days and in the spleen at 175 days. Blood lymphocytes
               appear at about 120 days. A few plasma cells may be seen at 240
               days. Graft-versus-host disease, a cell-mediated response, has
               developed in immunodeficient foals transplanted with tissues from
               a 79-day-old fetus. The equine fetus can respond to coliphage T2 at

               200 days post-conception and to Venezuelan equine encephalitis
               virus at 230 days. VDJ sequence diversity increases as the fetus
               develops and as the foal develops into an adult. Newborn foals
               have detectable quantities of IgM and IgG and occasionally IgG3 in

               their serum, but IgE production in the horse does not begin until
               foals are 9 to 11 months of age. Like other large herbivores, the foal




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