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Decreased T helper cell function in patients with cystic fibrosis.

作者信息

Knutsen A P, Slavin R G, Roodman S T, Mueller K R, Marino N L

机构信息

Department of Pediatrics, St. Louis University Medical Center, Mo.

出版信息

Int Arch Allergy Appl Immunol. 1988;85(2):208-12. doi: 10.1159/000234504.

Abstract

T cell immune function was further evaluated in cystic fibrosis (CF) patients. CF patients, regardless of severity of pulmonary disease or colonization with Pseudomonas aeruginosa, had lower percentages of T helper cells (p less than 0.01) and decreased T helper function as demonstrated by diminished T help for control B cell pokeweed mitogen-stimulated IgG (p less than 0.01) and IgM (p less than 0.01) synthesis. Increased T suppressor function, measured by co-culture with control B and T cells, was noted in only 25% of CF patients. CF patients' T cells exhibited decreased allogeneic T cell cytotoxicity compared to normal controls (p less than 0.01). This study extends previous studies demonstrating decreased T cell functions in CF patients and indicates a specific decrease in T helper function.

摘要

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