Bateman E D, Turner-Warwick M, Haslam P L, Adelmann-Grill B C
Thorax. 1983 Feb;38(2):93-101. doi: 10.1136/thx.38.2.93.
Collagen immunofluorescence studies were performed on biopsy specimens from 25 patients with cryptogenic fibrosing alveolitis. We studied the relationship of these results to the clinical, radiological, and physiological assessments of disease activity during six-month periods before and after the lung biopsy; to the appearances on routine histological examination; to the inflammatory cell proportions in bronchoalveolar lavage fluid; and to the response to treatment. Positive associations were observed between the presence of type III collagen and disease activity before (p less than 0.015) and after (p less than 0.02) lung biopsy. These were independent of clinical and routine histological features. The type-III-positive group also contained nine of the 11 responding to treatment. None of the type-III-positive patients had a quiescent or stable course. In contrast, most patients with no type-III-collagen fluorescence had a stable course over the time of this study and did not improve on treatment. It is suggested that collagen typing may be an additional useful method of assessing potentially reversible disease in cryptogenic fibrosing alveolitis.
对25例隐源性纤维性肺泡炎患者的活检标本进行了胶原免疫荧光研究。我们研究了这些结果与肺活检前后六个月期间疾病活动的临床、放射学和生理学评估之间的关系;与常规组织学检查的表现之间的关系;与支气管肺泡灌洗液中炎症细胞比例之间的关系;以及与治疗反应之间的关系。在肺活检前(p<0.015)和肺活检后(p<0.02),Ⅲ型胶原的存在与疾病活动之间观察到正相关。这些与临床和常规组织学特征无关。Ⅲ型阳性组的11例治疗有反应者中,有9例在该组。Ⅲ型阳性患者中没有一例病情静止或稳定。相比之下,在本研究期间,大多数无Ⅲ型胶原荧光的患者病情稳定,治疗后无改善。提示胶原分型可能是评估隐源性纤维性肺泡炎潜在可逆性疾病的另一种有用方法。