Flow-cytometric analysis of peripheral blood lymphocytes in patients with chronic idiopathic neutropenia of adults
- PMID: 9368479
- DOI: 10.1007/s002770050322
Flow-cytometric analysis of peripheral blood lymphocytes in patients with chronic idiopathic neutropenia of adults
Abstract
Flow-cytometric analysis of peripheral blood lymphocytes was performed in 96 patients with chronic idiopathic neutropenia of adults (CINA) and in 36 age- and sex-matched healthy volunteers (controls) using a panel of monoclonal antibodies. Patients were classified arbitrarily into group A (68 patients with 2500-1500 neutrophils/microliter) and group B (28 patients with neutrophil counts below 1500/microliter). We found that CINA patients displayed low numbers of peripheral blood lymphocytes compared with the controls, which correlated with the numbers of circulating neutrophils. This decrease was due mainly to the reduction of T lymphocytes and, to lesser degree, to the decline of NK cells. Both CD4+ and CD8+ T cells decreased, so that the CD4+/CD8+ cell ratio remained within normal range. Moreover, decrease of T lymphocytes was due essentially to the diminution of CD45RO+ T-cell subsets (CD4+/CD45RO+ and CD8+/CD45RO+), while CD45RA+ T cells did not change. A highly significant positive correlation was found between the numbers of CD45RO+ T cells and the numbers of circulating neutrophils. All these alterations were more pronounced in the patients of group B than in those of group A. NK cells were found to be significantly reduced in the patients of group B, but not in those of group A. The numbers of both CD16+ and CD56+ cells correlated with the numbers of circulating neutrophils. Patients of group B had also low numbers of CD57+ cells, probably due to the reduction of T cells and NK cells. B cells did not change significantly. No significant changes were found also in the numbers of lymphocytes carrying activation-related cell surface markers. We concluded that lymphocyte reduction in CINA patients is due mainly to the diminution of CD45RO+ cells, and we postulated that the most probable explanation for this abnormality is an increased extravasation of these cells, which pass into the tissues following an accelerated adhesion to endothelial cells. This hypothesis and its relationship with the underlying neutropenia in CINA patients remain to be clarified.
Similar articles
-
Selective loss of peripheral blood CD45RO+ T lymphocytes correlates with increased levels of serum cytokines and endothelial cell-derived soluble cell adhesion molecules in patients with chronic idiopathic neutropenia of adults.Ann Hematol. 1998 Oct;77(4):153-9. doi: 10.1007/s002770050433. Ann Hematol. 1998. PMID: 9829846
-
Defective natural killer cell activity of peripheral blood lymphocytes correlates with the degree of neutropenia in patients with chronic idiopathic neutropenia of adults.Ann Hematol. 1998 Mar-Apr;76(3-4):127-34. doi: 10.1007/s002770050376. Ann Hematol. 1998. PMID: 9619729
-
Reference ranges of lymphocyte subsets in healthy adults and adolescents with special mention of T cell maturation subsets in adults of South Florida.Immunobiology. 2014 Jul;219(7):487-96. doi: 10.1016/j.imbio.2014.02.010. Epub 2014 Mar 2. Immunobiology. 2014. PMID: 24661720
-
T and NK Cell Phenotypic Abnormalities in Systemic Sclerosis: a Cohort Study and a Comprehensive Literature Review.Clin Rev Allergy Immunol. 2015 Dec;49(3):347-69. doi: 10.1007/s12016-015-8505-8. Clin Rev Allergy Immunol. 2015. PMID: 26445774 Review.
-
Surface engineering for lymphocyte programming.Adv Drug Deliv Rev. 2017 May 15;114:102-115. doi: 10.1016/j.addr.2017.05.005. Epub 2017 May 10. Adv Drug Deliv Rev. 2017. PMID: 28501510 Free PMC article. Review.
Cited by
-
Reduced CD43 expression on the neutrophils of MDS patients correlates with an activated phenotype of these cells.Int J Hematol. 2001 Jun;73(4):483-491. doi: 10.1007/BF02994011. Int J Hematol. 2001. PMID: 11503963
-
Genetic Landscape of Non-Remitting Neutropenia in Children and Chronic Idiopathic Neutropenia in Adults.Int J Mol Sci. 2025 Jul 18;26(14):6929. doi: 10.3390/ijms26146929. Int J Mol Sci. 2025. PMID: 40725177 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Research Materials