T-CELLS AND CD45R EXPRESSION IN B-CHRONIC LYMPHOCYTIC-LEUKEMIA

被引:21
作者
BRIGGS, PG
KRAFT, N
ATKINS, RC
机构
[1] Department of Nephrology, Monash Medical Centre, Melbourne, 3004, Prnc. Henry's Hospital Campus, St Kilda Rd.
关键词
B-chronic lymphocytic leukemia; CD45R phenotype; monocytes; Rai staging; T cells;
D O I
10.1016/0145-2126(90)90044-A
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A major secondary immunodeficiency exists in B cell derived chronic lymphocytic leukemia (B-CLL) which involves both humoral and cellular immunity and is largely unexplained. Several T cell subset redistributions have been noted in B-CLL. We therefore examined in more detail the immunophenotype of T cells by assessing CD45R expression using a two-colour immunofluorescence technique. The proportion of CD45R+ cells among CD3+, CD4+ and CD8+ cells in B-CLL was significantly (p < 0.001) higher than in corresponding normal cell populations. We also sought relationships between major T cell subsets and progress of disease and found strongly positive correlations between the total leukocyte count in B-CLL and numbers of CD3+, CD4+, CD8+ cells and monocytes. Further, in patients with clinically more advanced disease, CD3+ and CD4+ cells were present in higher numbers than in patients with less advanced disease (p < 0.05). CD8+ cells, CD4 CD8 ratio, monocytes and total leukocyte count were not significantly different when comparing the less advanced and more advanced disease patients. An excess of CD45R+ suppressor-inducer T cells has implications for both B and T cell dysfunction and for disease progression. © 1990.
引用
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页码:155 / 159
页数:5
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