CD30 CELL EXPRESSION AND ABNORMAL SOLUBLE CD30 SERUM ACCUMULATION IN OMENNS SYNDROME - EVIDENCE FOR A T-HELPER 2-MEDIATED CONDITION

Citation
M. Chilosi et al., CD30 CELL EXPRESSION AND ABNORMAL SOLUBLE CD30 SERUM ACCUMULATION IN OMENNS SYNDROME - EVIDENCE FOR A T-HELPER 2-MEDIATED CONDITION, European Journal of Immunology, 26(2), 1996, pp. 329-334
Citations number
28
Categorie Soggetti
Immunology
ISSN journal
00142980
Volume
26
Issue
2
Year of publication
1996
Pages
329 - 334
Database
ISI
SICI code
0014-2980(1996)26:2<329:CCEAAS>2.0.ZU;2-#
Abstract
Omenn's syndrome (OS) is a severe immunodeficiency. characterized by c linical and laboratory features reminiscent of a T helper type-2 (Th2) response. CD30. a member of the tumor necrosis factor receptor superf amily. has been found to be preferentially expressed by human T cell c lones exhibiting a Th2-like profile and function. We investigated whet her there are derangement in CD30 expression in tissues. and/or abnorm alities in soluble CD30 (sCD30) levels in the serum. or both, of three children with OS and one child with maternal engraftment and Omenn's- like syndrome (OLS). Large proportions of tissue-infiltrating T lympho cytes from all four patients expressed CD30. whereas in control tissue s. including peripheral blood. CD30 T lymphocytes were extremely few o r absent. In addition. levels of sCD30 were abnormally increased in al l patients sera. T cell clones were generated from sorted CD30(-) and CD30(-) peripheral blood T cells of the patient with OLS who showed un usually high numbers of circulating CD30(-) T lymphocytes. Most CD4(-) T cell clones derived from CD30(-) cells showed a Th2-like cytokine p rofile. whereas the majority of clones generated from CD30(-) T cells were Th1. These findings support the hypothesis that Th2 cells are inv olved in the pathogenesis of OS. Moreover. they provide evidence that detection of CD30(-) T cells in tissues. increased levels of sCD30 in biological fluids. or both, reflect the presence of immune responses c haracterized by prevalent activation of T cells producing Th2 cytokine s.