Korean J Hematol 2003; 38(4):
Published online December 31, 2003
© The Korean Society of Hematology
김명신, 황진미, 임지향, 김용구, 한경자, 이종욱, 민우성, 김춘추
가톨릭대학교 의과대학 임상병리학교실,
가톨릭대학교 의과대학 내과학교실
BACKGROUND :
Immune mediated suppression of hematopoiesis has been regarded as the most important pathogenetic mechanism of idiopathic severe aplastic anemia (AA). However, the immunophenotype of lymphocytes in the bone marrow (BM) of AA has not been compre- hensively studied. We investigated the immunophenotype of lymphocytes in the BM to evaluate immune alteration and the possibility of involvement of lymphocytic lineage in AA.
METHODS : The flow cytometric analysis for 16 cell surface antigens using monoclonal antibodies in 20 patients with AA and 20 healthy persons was performed. The percentage of positive cell population was calculated in the gated region for lymphocytes and compared data between AA and normal controls. And the BM cellularity and lymphocyte population were evaluated by light microscopy.
RESULTS :
The CD34+ cells were significantly decreased in AA (0.79+/-0.76% vs 2.60+/-1.53%) compared to controls. The CD2+, CD8+ and CD4+CD8+ cells were significantly increased in number, but the other T cell antigens were similar to normal control. All the B cell antigens were decreased in AA. The CD56+ cells and CD25+CD56+ cells were significantly increased in AA. The lymphocyte population was negatively correlated to B cell population and positively correlated to CD4+CD8+ cells.
CONCLUSION : The BM lymphocytes populations are significantly altered in AA. The B cells are significantly decreased in AA than normal control whereas, the CD8+ cells, CD4+CD8+cells and CD56+ cells seem to play an important role in destruction of hematopoietic progenitor cells in AA.
Keywords Aplastic anemia, Flow cytometry, Lymphocyte, Immunophenotype
Korean J Hematol 2003; 38(4): 261-266
Published online December 31, 2003
Copyright © The Korean Society of Hematology.
김명신, 황진미, 임지향, 김용구, 한경자, 이종욱, 민우성, 김춘추
가톨릭대학교 의과대학 임상병리학교실,
가톨릭대학교 의과대학 내과학교실
Myung shin Kim, Jinmee Hwang, Jihyang Lim,
Yong goo Kim, Kyungja Han, Jong Wook Lee, Woo Sung Min, Chun Choo Kim
Department of Clinical Pathology, Internal Medicine, The Catholic University of Korea College of Medicine, Seoul, Korea
BACKGROUND :
Immune mediated suppression of hematopoiesis has been regarded as the most important pathogenetic mechanism of idiopathic severe aplastic anemia (AA). However, the immunophenotype of lymphocytes in the bone marrow (BM) of AA has not been compre- hensively studied. We investigated the immunophenotype of lymphocytes in the BM to evaluate immune alteration and the possibility of involvement of lymphocytic lineage in AA.
METHODS : The flow cytometric analysis for 16 cell surface antigens using monoclonal antibodies in 20 patients with AA and 20 healthy persons was performed. The percentage of positive cell population was calculated in the gated region for lymphocytes and compared data between AA and normal controls. And the BM cellularity and lymphocyte population were evaluated by light microscopy.
RESULTS :
The CD34+ cells were significantly decreased in AA (0.79+/-0.76% vs 2.60+/-1.53%) compared to controls. The CD2+, CD8+ and CD4+CD8+ cells were significantly increased in number, but the other T cell antigens were similar to normal control. All the B cell antigens were decreased in AA. The CD56+ cells and CD25+CD56+ cells were significantly increased in AA. The lymphocyte population was negatively correlated to B cell population and positively correlated to CD4+CD8+ cells.
CONCLUSION : The BM lymphocytes populations are significantly altered in AA. The B cells are significantly decreased in AA than normal control whereas, the CD8+ cells, CD4+CD8+cells and CD56+ cells seem to play an important role in destruction of hematopoietic progenitor cells in AA.
Keywords: Aplastic anemia, Flow cytometry, Lymphocyte, Immunophenotype
Yong Goo Kim, Ji Hyang Lim, Myung Shin Kim, Kyung Ja Han, Won IL Kim, Sang In Shim, Dong Wook Kim, Jong Wook Lee, Woo Sung Min, Chun Choo Kim
Korean J Hematol 1999; 34(3): 428-435Eun Jee Oh, Do Hee Kim, Yong Goo Kim, Kyungia Han, Sang In Shim, Ik Joo Jung, Chi Hwa Han, Choon Choo Kim
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