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PMID: 1715221 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Analysis at the clonal level of T-cell phenotype and functions in severe aplastic anemia patients.

Blood ·Vol. 78 ·No. 5 ·1991-09-01 ·Pages 1268-74

Viale M, Merli A, Bacigalupo A

Abstract

The aim of this study was to analyze at the clonal level the phenotype and functions of T cells from patients with severe aplastic anemia (SAA). For this purpose we studied 175 T-cell clones obtained from peripheral blood (PB) and bone marrow (BM) of four SAA patients and 97 clones from two healthy controls. The percentage of CD8+ T-cell clones obtained from the patients' PB and BM was higher, but not significantly (P = .07 and P = .14, respectively), than that obtained in controls. A higher proportion of T-cell clones from SAA patients exhibited lectin-dependent cytolytic activity and especially natural killer-like activity when compared with controls (PB: P less than .01, P less than .05; BM: P less than .05, P less than .01, respectively). Lymphokine release was tested before and after mitogen stimulation. A number of patients' clones were able to release interferons (IFNs) spontaneously (PB: 28.6% v 0%, P less than .05; BM: 28.6% v 0%, P less than .10). After mitogen stimulation, patients' BM T-cell clones produced IFNs in greater proportions (90.9% v 46.7%, P less than .01) and in greater quantities (PB: 25.5 arbitrary units [AU]/mL v 5.7 AU/mL, P less than .03; BM: 26 AU/mL v 9.1 AU/mL, P = .011) as compared with controls. Tumor necrosis factor (TNF) activity was not found in supernatants of unprimed T-cell clones. After mitogen stimulation, PB T-cell microcultures produced TNF alpha in greater proportions (97.9% v 72.2%, P less than .01) and, also in this case, in greater quantities (PB: 7.2 AU/mL v 1.5 AU/mL, P = .007; BM: 9.9 AU/mL v 1.5 AU/mL, P = .003) than controls. In conclusion, T-cell clones from SAA patients exhibit predominantly a CD8+ phenotype, a greater cytotoxic activity, and can be shown to produce greater quantities of suppressor lymphokines when compared with controls.

MeSH Terms
Adolescent Adult Anemia, Aplastic/blood Antigens, Differentiation, T-Lymphocyte/analysis Bone Marrow/pathology CD3 Complex CD4 Antigens/analysis CD4-Positive T-Lymphocytes/immunology,physiology CD8 Antigens Cell Separation Clone Cells Female Granulocyte-Macrophage Colony-Stimulating Factor/biosynthesis Humans Immunophenotyping Interferons/biosynthesis Interleukin-3/biosynthesis Male Membrane Glycoproteins/analysis Middle Aged Receptors, Antigen, T-Cell/analysis T-Lymphocytes, Regulatory/immunology,physiology Tumor Necrosis Factor-alpha/biosynthesis
Chemicals
Antigens, Differentiation, T-Lymphocyte CD3 Complex CD4 Antigens CD8 Antigens Interleukin-3 Membrane Glycoproteins Receptors, Antigen, T-Cell Tumor Necrosis Factor-alpha Granulocyte-Macrophage Colony-Stimulating Factor Interferons
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Viale M
Laboratory of Pharmacology, National Institute for Cancer Research (IST), Genova, Italy.
Merli A
Bacigalupo A
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1991-09-01
Pages
1268-74
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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