Shellito J, Suzara V V, Blumenfeld W, Beck J M, Steger H J, Ermak T H
Section of Respiratory Care, Veterans Administration AIDS Research Center, San Francisco, California.
J Clin Invest. 1990 May;85(5):1686-93. doi: 10.1172/JCI114621.
Pulmonary infections with Pneumocystis carinii are an important cause of morbidity and mortality in patients with AIDS. P. carinii infections are seen in patients with decreased numbers of helper T lymphocytes, suggesting that these cells are important in preventing infection. To test this hypothesis, we sought to establish experimental infection with P. carinii in mice selectively depleted of helper T lymphocytes. Weekly injections of a monoclonal anti-CD4 antibody produced sustained depletion of helper T lymphocytes from blood and lymphoid organs. To establish pulmonary infection, lymphocyte-depleted mice were then given intratracheal inoculations of P. carinii organisms derived from the lungs of chronically infected athymic mice. Pulmonary infection with P. carinii was demonstrable in the antibody-treated mice and was centered around the conducting airways. Infection was persistent for up to 3 mo with continued antibody treatments, and yet could be cleared from the lungs if antibody treatments were discontinued. This experimental model of P. carinii infection permits the study of infection associated with a specific immune defect and implicates the helper T lymphocyte as a critical cell in host defense against this pathogen.
卡氏肺孢子虫肺部感染是艾滋病患者发病和死亡的重要原因。在辅助性T淋巴细胞数量减少的患者中可见卡氏肺孢子虫感染,这表明这些细胞在预防感染中很重要。为了验证这一假设,我们试图在选择性清除辅助性T淋巴细胞的小鼠中建立卡氏肺孢子虫实验性感染。每周注射一次单克隆抗CD4抗体可使血液和淋巴器官中的辅助性T淋巴细胞持续减少。为了建立肺部感染,然后给淋巴细胞减少的小鼠进行气管内接种来自慢性感染无胸腺小鼠肺部的卡氏肺孢子虫。在抗体治疗的小鼠中可证实有卡氏肺孢子虫肺部感染,且感染集中在传导气道周围。在持续抗体治疗的情况下,感染可持续长达3个月,但如果停止抗体治疗,感染可从肺部清除。这种卡氏肺孢子虫感染的实验模型允许研究与特定免疫缺陷相关的感染,并表明辅助性T淋巴细胞是宿主抵御这种病原体的关键细胞。