A prospective study of CD45 isoform expression in haemophagocytic lymphohistiocytosis; an abnormal inherited immunophenotype in one family
Open Access
- 1 February 1995
- journal article
- Published by Oxford University Press (OUP) in Clinical and Experimental Immunology
- Vol. 99 (2) , 216-220
- https://doi.org/10.1111/j.1365-2249.1995.tb05535.x
Abstract
SUMMARY: In a prospective study, CD45 isoform expression on T lymphocytes was analysed in seven patients with haemophagocytic lymphohistiocytosis (HLH) and their family members. Six patients, their parents and seven healthy age-matched controls showed the normal pattern of three subpopulations of CD45R expression. In one patient, his mother and one of his healthy brothers only two subpopulations could be identified, which might indicate that the maturation from a CD45RA/RO double-positive to a CD45RO single-positive phenotype does not occur in these individuals. It is not clear if this finding had any impact on the development of HLH in this patient and if the pattern of CD45RA and RO expression observed in this family might represent a predisposition to HLH. In another patient a marked increase of the CD45RO single-positive T cell population was observed during a period of increased disease activity. The clinical relevance of this observation and whether CD45RO expression could serve as a marker for disease activity, or in selected individuals as a susceptibility marker for HLH, remain unknown.Keywords
This publication has 13 references indexed in Scilit:
- Abnormal T-cell phenotype in familial erythrophagocytic lymphohistiocytosisThe Lancet, 1993
- Hypercytokinemia in Hemophagocytic SyndromeJournal of Pediatric Hematology/Oncology, 1993
- Phenotypic comparison of the three populations of human lymphocytes defined by CD45RO and CD45RA expressionCellular Immunology, 1992
- Age-related changes in human blood lymphocyte subpopulationsThe Journal of Pediatrics, 1992
- Variant CD45R expression with autosomal dominant inheritance affects both helper/inducer (CD4 +) and suppressor/cytotoxic (CD8 +) T cell populationsClinical and Experimental Immunology, 1991
- Infection-Associated Hemophagocytic Syndrome: Evidence for Epstein-Barr Virus Gene ExpressionJournal of Pediatric Hematology/Oncology, 1991
- ELEVATED SOLUBLE INTERLEUKIN-2 RECEPTOR IN CHILDHOOD HEMOPHAGOCYTIC HISTIOCYTIC SYNDROMES1989
- Impaired natural killer activity in lymphohistiocytosis syndromeThe Journal of Pediatrics, 1984
- Familial hemophagocytic lymphohistiocytosisEuropean Journal of Pediatrics, 1983
- IMMUNODEFICIENCY IN FAMILIAL ERYTHROPHAGOCYTIC LYMPHOHISTIOCYTOSISThe Lancet, 1978