TY - JOUR
T1 - Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children
AU - Pignata, Claudio
AU - Alessio, M.
AU - Ramenghi, U.
AU - Bonissoni, S.
AU - Difranco, D.
AU - Brusco, A.
AU - Matrecano, E.
AU - Franzese, A.
AU - Dianzani, I.
AU - Dianzani, U.
PY - 2000
Y1 - 2000
N2 - To ascertain whether alterations of lymphocyte switching off may be associated with clustering of autoimmune diseases in children, Fas- and C2- ceramide-induced cell death was evaluated on T cell lines derived from three patients affected by clustering of autoimmune disorders. Three patterns were found: patient 3 was resistant to Fas- and C2-ceramide, patient 1 was resistant to Fas, but sensitive to C2-ceramide, patient 2 was resistant to C2-ceramide, but sensitive to Fas. By contrast, Fas- and C2-ceramide-induced cell death was normal in five children with systemic juvenile rheumatoid arthritis, five children with insulin-dependent diabetes and 10 age-matched healthy controls. Surface expression of Fas was low in patient 1, but normal in patients 2 and 3. Together with normal Fas transcripts, patients 2 and 3 displayed a transcript 152 bp longer than the normal one retaining intron 5. Our data indicate that polyreactive autoimmune syndromes may be associated with heterogeneous alteration of the immune response switching-off system.
AB - To ascertain whether alterations of lymphocyte switching off may be associated with clustering of autoimmune diseases in children, Fas- and C2- ceramide-induced cell death was evaluated on T cell lines derived from three patients affected by clustering of autoimmune disorders. Three patterns were found: patient 3 was resistant to Fas- and C2-ceramide, patient 1 was resistant to Fas, but sensitive to C2-ceramide, patient 2 was resistant to C2-ceramide, but sensitive to Fas. By contrast, Fas- and C2-ceramide-induced cell death was normal in five children with systemic juvenile rheumatoid arthritis, five children with insulin-dependent diabetes and 10 age-matched healthy controls. Surface expression of Fas was low in patient 1, but normal in patients 2 and 3. Together with normal Fas transcripts, patients 2 and 3 displayed a transcript 152 bp longer than the normal one retaining intron 5. Our data indicate that polyreactive autoimmune syndromes may be associated with heterogeneous alteration of the immune response switching-off system.
KW - Cell apoptosis
KW - Fas
KW - Polyreactive autoimmune diseases
UR - http://www.scopus.com/inward/record.url?scp=0033921089&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2249.2000.01275.x
DO - 10.1046/j.1365-2249.2000.01275.x
M3 - Article
SN - 0009-9104
VL - 121
SP - 53
EP - 58
JO - Clinical and Experimental Immunology
JF - Clinical and Experimental Immunology
IS - 1
ER -