Fukue Y, Uchimura H, Kuzuya N, Okano S, Kanaji Y, Takaku F
Endocrinol Jpn. 1986 Jun;33(3):293-302. doi: 10.1507/endocrj1954.33.293.
A bioassay for thyroid stimulating immunoglobulins (TSI) of patients with Graves' disease was developed by porcine thyroid monolayer cells. Thyroid cells were prepared by dispersion using collagenase and trypsin. Aliquots of the cell suspension (2 X 10(6) cells/1.5 ml/dish) in Ham's F-12 medium (pH 7.2) containing 10% calf serum and 1.5 mM Hepes were seeded and cultured in air at 36 C. On day 6 of culture, cells were incubated with test samples (IgG or bTSH) in 1 ml of serum-free, 0.5 mM IMX-included fresh medium for an additional time, and cAMP in the cells was measured by radioimmunoassay. Intracellular cAMP was increased within 5 minutes after the addition of bTSH and the maximal increase was observed after 30 min. Responses of cAMP were in a dose-related manner up to 10 mU/ml of bTSH. With the addition of IgG from untreated Graves' patients, dose-related increases in cAMP were also observed up to 10 mg/ml IgG and the maximal response was seen at 2 hours incubation. Thyroid stimulating activity in IgG's from normal subjects and patients with Graves' disease was tested with a dose of 10 mg/ml and 2 hours incubation and the activity was expressed as a percent of the control (incubated in the same experiment without IgG). One hundred forty one of 145 untreated patients showed higher activity (228 +/- 51.8%, mean +/- SD; 127-393%, range) than normal subjects (103 +/- 13.3%, mean +/- SD, n = 24; 80-129%, range). Sequential changes in TSI activity in 27 patients after initiating thionamide drugs were studied for 24 months. Initially all 27 patients showed positive TSI and 6 months later 15 remained positive. At 6 months after that, 10 of 23, 4 of 16, and 2 of 6 followed patients showed positive TSI. These results indicate that this bioassay is clinically useful for detecting TSI.
采用猪甲状腺单层细胞建立了一种检测格雷夫斯病患者促甲状腺素免疫球蛋白(TSI)的生物测定法。通过胶原酶和胰蛋白酶分散制备甲状腺细胞。将细胞悬液等分试样(2×10⁶个细胞/1.5毫升/培养皿)接种于含10%小牛血清和1.5 mM Hepes的Ham's F - 12培养基(pH 7.2)中,于36℃在空气中培养。在培养第6天,将细胞与测试样品(IgG或bTSH)在1毫升不含血清、含0.5 mM IMX的新鲜培养基中再孵育一段时间,然后通过放射免疫测定法测量细胞内的环磷酸腺苷(cAMP)。加入bTSH后5分钟内细胞内cAMP增加,30分钟后观察到最大增加。cAMP的反应在高达10 mU/ml的bTSH剂量范围内呈剂量相关。加入未经治疗的格雷夫斯病患者的IgG后,在高达10 mg/ml IgG的剂量范围内也观察到cAMP的剂量相关增加,孵育2小时时出现最大反应。用10 mg/ml的剂量和2小时孵育测试正常受试者和格雷夫斯病患者IgG中的促甲状腺活性,活性以对照(在同一实验中不加入IgG孵育)的百分比表示。145例未经治疗的患者中有141例显示出比正常受试者(103±13.3%,平均值±标准差,n = 24;范围80 - 129%)更高的活性(228±51.8%,平均值±标准差;范围127 - 393%)。研究了27例患者开始使用硫酰胺类药物后24个月内TSI活性的连续变化。最初所有27例患者TSI均呈阳性,6个月后15例仍为阳性。此后6个月,随访患者中23例中的10例、16例中的4例和6例中的2例TSI呈阳性。这些结果表明该生物测定法在临床上可用于检测TSI。