Familial Occurrence of impaired interleukin-2 activity and increased peripheral blood B cells actively secreting immunoglobulins in systemic lupus erythematosus☆
Abstract
purpose: We tested the hypothesis that some abnormalities of immune functions are genetically controlled in patients with systemic lupus erythematosus (SLE).
subjects and methods: We used a phytohemaglutinin-induced interleukin-2 (IL2) activity assay and a spontaneous plaque-forming cell assay to evaluate T-cell and B-cell function, respectively, in 34 clinically healthy family members of six SLE probands.
results: Impaired IL-2 activity was found in 15 of the 29 consanguineous relatives. There was no relation between the household relatives and the nonhousehold relatives; none of the five nonconsanguineous household persons had abnormal results. Results for the B-cell assay were abnormal in 22 of the 29 consanguineous relatives. The B-cell abnormalities were more commonly observed in the consanguineous household relatives; four of the five nonconsanguineous household relatives also had abnormal assay results.
conclusion: The findings indicate that the impaired IL-2 activity in relatives appears to strongly correlate with a genetic relationship. Although the evidence favors in genetic basis for the B-cell abnormalties, environmental effects may also contribute to the familial occurrence of these abnormalities.
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☆ This work was supported in part by a 1988 grant-in-aid for scientific research (project number 63480191) from the Ministry of Education, Science, and Culture of Japan, and by a 1988 research grant from the Autoimmune Disease Research Committee of Japan, Ministry of Welfare, Tokyo, Japan.
PII: 0002-9343(89)90334-3
doi:10.1016/0002-9343(89)90334-3
© 1989 Published by Elsevier Inc.

