The features of immunological potential in neonates are clarified.
CD4
+ lymphocytes in mature cord blood are naive in terms of phenotypic and functional aspects and they lack the helper function to induce immunoglobulin (Ig) secreting cells. However functional molecules participating in T/B cell interaction in cord blood are capable of being upregulated by the appropriate stimulation the same as for an adult. Meanwhile, T-and B-lymphocytes in premature infants are more susceptible to various activation. Certain cytokines upregulate antigen-presenting capacity of adult blood monocytes, but not of cord blood monocytes. The impaired response of cord blood monocytes may be responsible for their functional immaturity. Moreover, the production of inflammatory cytokines is immature, however, the neonatal T cell is competent to respond to TCR-mediated stimulation and to produce both type 1 and type 2 cytokines. Furthermore neutrophils in cord blood could produce the same level of super oxide as adult neutrophils, however, they are impaired in phagocytizing opsonized
E, coli. In addition, cord blood serum lacks opsonizing activity against
E, coli.
These impaired immune functions in cord blood might play some role in the susceptibility to infection in neonates.
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