Studies on the lymphocyte subpopulations and subsets in both peripheral blood and cerebrospinal fluid of various children's viral (the meales, rubella, chickenpox, mumps), bacterial infections, and Kawasaki disease were carried out to examine the change of cell-mediated immunity, using various rosette formation methods and monoclonal antibodies (anti-Leu 1, Leu 2a, Leu 3a, Leu 7) analyzed by fluorescence activated cell sorter III.
1) Both T cells and B cells decreased significantly in the acute phase of the viral infections; the measles, rubella, chickenpox and mumps, and Tγ cells increased in the convalescence. IgM bearing cells increased at first accompanied with IgG or IgD bearing cells l ater.
In whooping cough and Kawasaki disease, both T and B cells didn't decrease in the acute phase. Tμ cells had increased since the 2nd week and the peak of Tγ cells came out later than the peak of viral infections. B cell subsets in bacterial infections had increased significantly after the 2nd week.
2) The lymphocyte subsets of Kawasaki disease changed similar to bacterial infections. Leu 3a and Leu 7 cells decreased significantly in the 1st week of Kawasaki disease. The etiol ogy of Kawasaki disease may be considered as an allergic illness triggered by some b acterial infections.
3) At the onset of encephalitis T, Tμ cells and Leu 1, Leu 3a cells decreased remarkably as compared with non-complicated children. Viral encephalitis may be caused by an abnorma l immunity following viral infections. Considering that Tμ cells induce prekiller cell to killer cell, in encephalitis killer T cells may not been induced and helper T cells impossibly play a part in the recovery from the infections.
Examination of T cell subsets may be beneficial to evaluate prognosis of encephalitis.
4) In CSF of patients with aseptic meningitis and meningoencephalitis an increase in the percentage of T lymphocyte or Leu 2a cell was observed, while a decrease of B lymphoc yte was proven.
The results are likely to suggest that in central nervous system infections there is a strong T cell response in CSF with well preserved proportions of T cell subsets.
5) There were significant good correlations between active E, E rosette forming cells and Leu 1 cells, Tγ cells and Leu 7 cells, while correlations between Tγ cells and Leu 2a cells, Tμ cells and Leu 3a cells are not significant. In viral infections Leu 1 and Leu 3a cells decrease d and Leu 7 cells increased in the acute phase, and Tγ cells increased in the conval escence. In all diseases studied except for varicella-zoster virus, herpes simplex virus and Epstein-Barr virus, Leu 2a cells showed no significant change.
According to the above observations on monocl onal antibody method, Tγ and Tμ cells may have several functional lymphocyte clones. Identifications of Tγ cells and Tμ cells are not enough to know the precise immune state, which is better evaluated by means of monoclonal antibody method.
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