Natural killer-cell activity and the response to interferons α, β, and γ in patients with primary biliary cirrhosis
Primary biliary cirrhosis (PBC) is a chronic, life-threatening disorder that is believed to be immunologically mediated. Abnormal immunologic findings have been detected in T suppressor cell activity, B cell responsiveness, and natural kill (NK)-cell function. NK-cell function has been described as...
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Published in | Journal of allergy and clinical immunology Vol. 84; no. 2; pp. 214 - 218 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.08.1989
Elsevier Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0091-6749 1097-6825 |
DOI | 10.1016/0091-6749(89)90327-8 |
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Summary: | Primary biliary cirrhosis (PBC) is a chronic, life-threatening disorder that is believed to be immunologically mediated. Abnormal immunologic findings have been detected in T suppressor cell activity, B cell responsiveness, and natural kill (NK)-cell function. NK-cell function has been described as low and to be poorly responsive to high concentrations of interferon (IFN). The present study was initiated to determine the response of NK-cell function of patients with PBC to all forms of IFN (α, β, and γ) at low concentrations. Ten patients were assessed on two occasions approximately 5 months apart. There was a significant decrease in the NK-cell function in a 4-hour assay but only one patient had low NK-cell function after an 18-hour assay. The augmentation of NK-cell activity secondary to 10 and 50 U/ml of IFN-α, β, and γ was equivalent in the patients and in the control subjects. The relative increase induced by IFN was higher during the 4-hour assay than in the 18-hour assay. Hence, there may be a kinetic impairment of NK-cell function in patients with PBC, but the ultimate lytic activity, and response to the various forms of IFN, are normal. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
ISSN: | 0091-6749 1097-6825 |
DOI: | 10.1016/0091-6749(89)90327-8 |