1 Thymus-activated cell phenotypes confirmed the T - lymphocyte activation after a 48-h culture period.
2 The present study was undertaken to examine the T - lymphocyte activation in IgA nephropathy.
3 HIV load and CD4 T - lymphocyte counts in serum were determined at each visit.
4 Serum HIV load was associated with relapse, whereas CD4 T - lymphocyte counts were not.
5 T - lymphocyte activation increases the number of MVBs that contain FasL.
6 T - lymphocytes play an important role in the pathogenesis of asthma.
7 Tumor responses, T-lymphocyte and subset counts, and toxicity were monitored.
8 Additionally, these primary cells could suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli.
9 CD4+ T-lymphocytes are increased in number, express activation markers and cluster around RS cells.
10 There was no difference between the curves of CD4 T - lymphocytes raise of coinfected and monoinfected groups.
11 The influence of potentially suppressing monocytes and positive regulatory T-lymphocytes was eliminated using purified B-cell cultures.
12 T - lymphocytes , B-lymphocytes and macrophages were identified and counted.
13 T - lymphocyte activation markers and serum interleukins were measured.
14 Quantification of the T - lymphocyte subpopulations in peripheral blood did not indicate the presence of metastatic disease.
15 Improvements in migration response with thymosin alpha 1 appeared to be independent of levels of various T-lymphocyte subpopulations.
16 The expression of CD95 on naive T-lymphocyte subsets was increased whereas that on memory T-lymphocyte subsets was decreased.
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