Crothers K, Huang L
Division of Pulmonary and Critical Care Medicine, San Francisco General Hospital, University of California, San Francisco, CA 94110, USA.
HIV Med. 2003 Oct;4(4):346-9. doi: 10.1046/j.1468-1293.2003.00170.x.
Although several studies have reported that it is safe to discontinue secondary Pneumocystis carinii pneumonia (PCP) prophylaxis in patients infected with HIV who experience a sustained immune response as a result of antiretroviral therapy, we describe a patient who developed recurrent PCP <3 months after discontinuing trimethoprim-sulfamethoxazole prophylaxis. He developed disease despite a sustained CD4 T-cell count above 200 cells/microL for more than 3 years while on antiretroviral therapy, as well as an apparent immune reconstitution against disseminated Mycobacterium avium complex (MAC) and Histoplasma capsulatum, for which he also discontinued therapy but without adverse effects. Thus, although increasing evidence continues to indicate that HIV-infected patients receiving combinations of antiretroviral therapies may regain specific immunity against opportunistic infections, our patient's experience suggests that this immune recovery may be selective and incomplete.
尽管有多项研究报告称,对于因抗逆转录病毒疗法而产生持续免疫反应的HIV感染患者,停用继发性卡氏肺孢子虫肺炎(PCP)预防措施是安全的,但我们描述了一名患者,他在停用甲氧苄啶-磺胺甲恶唑预防措施后不到3个月就出现了复发性PCP。尽管在接受抗逆转录病毒治疗期间,他的CD4 T细胞计数持续高于200个/微升超过3年,并且对播散性鸟分枝杆菌复合体(MAC)和荚膜组织胞浆菌有明显的免疫重建,他也因此停用了治疗但未出现不良反应,但他仍患上了PCP。因此,尽管越来越多的证据继续表明,接受抗逆转录病毒疗法联合治疗的HIV感染患者可能恢复针对机会性感染的特异性免疫,但我们这位患者的经历表明,这种免疫恢复可能是选择性的且不完全的。