Fuhrman C, Parrot A, Wislez M, Prigent H, Boussaud V, Bernaudin J F, Mayaud C, Cadranel J
Service de Pneumologie et de Réanimation Respiratoire, Hôpital Tenon, AP-HP, Paris, France.
Am J Respir Crit Care Med. 2001 Oct 1;164(7):1186-91. doi: 10.1164/ajrccm.164.7.2010120.
The present study was conducted to confirm the presence of severe lymphocytic alveolitis and to determine the factors responsible for the very different alveolar CD4 to CD8 T-cell ratios (CD4/ CD8) described in methotrexate-induced pneumonitis (MTX-pneumonitis). Clinical and radiologic findings, as well as bronchoalveolar lavage (BAL) data, including CD4 and CD8 subset analysis, were retrospectively reviewed for patients hospitalized between 1985 and 2000 for MTX-pneumonitis. BAL cell counts from patients with MTX-pneumonitis (cases) were compared with those from patients receiving MTX but who did not have evidence of MTX toxicity (MTX-exposed patients) and those from healthy subjects (control subjects). Nineteen BAL were performed in 14 consecutive cases of MTX-pneumonitis. MTX was given for various underlying diseases. All cases presented a subacute diffuse interstitial pneumonitis that recovered, with MTX discontinuation and/or initiation of adjunctive steroid therapy. At the time of diagnosis, BAL cell counts in MTX-pneumonitis indicated severe lymphocytic alveolitis when compared with MTX-exposed patients and control subjects and moderate neutrophil alveolitis compared with control subjects. The lymphocytic alveolitis resulted from an increase in both CD4 and CD8 lymphocyte cell counts. Nevertheless, alveolar CD4/ CD8 T-cell ratios ranged from 0.4 to 9.6. CD4/CD8 values correlated positively with lymphocyte counts but negatively with time elapsed between last MTX administration and BAL and with steroid cumulative dose received by the patients. Severe lymphocytic alveolitis was confirmed in our series of MTX-pneumonitis. The between-patient variation in CD4/CD8 T-cell ratios may reflect the large range of time intervals between last MTX administration and BAL evaluation and the use of adjunctive steroid therapy.
本研究旨在证实严重淋巴细胞性肺泡炎的存在,并确定导致甲氨蝶呤诱发肺炎(MTX肺炎)中所描述的肺泡CD4与CD8 T细胞比例(CD4/CD8)差异极大的因素。对1985年至2000年间因MTX肺炎住院患者的临床和放射学检查结果以及支气管肺泡灌洗(BAL)数据(包括CD4和CD8亚群分析)进行了回顾性研究。将MTX肺炎患者(病例组)的BAL细胞计数与接受MTX但无MTX毒性证据的患者(MTX暴露患者)以及健康受试者(对照组)的BAL细胞计数进行比较。对14例连续的MTX肺炎患者进行了19次BAL检查。MTX用于治疗各种基础疾病。所有病例均表现为亚急性弥漫性间质性肺炎,在停用MTX和/或开始辅助性类固醇治疗后病情恢复。诊断时,与MTX暴露患者和对照组相比,MTX肺炎患者的BAL细胞计数显示存在严重淋巴细胞性肺泡炎,与对照组相比存在中度中性粒细胞性肺泡炎。淋巴细胞性肺泡炎是由CD4和CD8淋巴细胞计数均增加所致。然而,肺泡CD4/CD8 T细胞比例范围为0.4至9.6。CD4/CD8值与淋巴细胞计数呈正相关,但与最后一次MTX给药至BAL的时间间隔以及患者接受的类固醇累积剂量呈负相关。在我们的MTX肺炎系列研究中证实了严重淋巴细胞性肺泡炎的存在。患者之间CD4/CD8 T细胞比例的差异可能反映了最后一次MTX给药至BAL评估的时间间隔范围较大以及辅助性类固醇治疗的使用情况。