Knutsen A P, Slavin R G, Roodman S T, Mueller K R, Marino N L
Department of Pediatrics, St. Louis University Medical Center, Mo.
Int Arch Allergy Appl Immunol. 1988;85(2):208-12. doi: 10.1159/000234504.
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.
对囊性纤维化(CF)患者的T细胞免疫功能进行了进一步评估。CF患者,无论肺部疾病的严重程度如何或是否被铜绿假单胞菌定植,其辅助性T细胞的百分比均较低(p<0.01),并且辅助性T细胞功能降低,这表现为对对照B细胞美洲商陆有丝分裂原刺激的IgG(p<0.01)和IgM(p<0.01)合成的辅助作用减弱。通过与对照B细胞和T细胞共培养测量,仅25%的CF患者出现抑制性T细胞功能增强。与正常对照相比,CF患者的T细胞表现出同种异体T细胞细胞毒性降低(p<0.01)。这项研究扩展了先前的研究,这些研究表明CF患者的T细胞功能降低,并表明辅助性T细胞功能有特异性降低。