Aaron L, Saadoun D, Calatroni I, Launay O, Mémain N, Vincent V, Marchal G, Dupont B, Bouchaud O, Valeyre D, Lortholary O
Service de Maladies Infectieuses et Tropicales, Hôpital Necker-Enfants Malades, Paris, France.
Clin Microbiol Infect. 2004 May;10(5):388-98. doi: 10.1111/j.1469-0691.2004.00758.x.
The incidence of tuberculosis (TB) is currently increasing in HIV-infected patients living in Africa and Asia, where TB endemicity is high, reflecting the susceptibility of this group of patients to mycobacteria belonging to the TB group. In this population, extension of multiple resistance to anti-tuberculous drugs is also a matter of anxiety. HIV-induced immunosuppression modifies the clinical presentation of TB, resulting in atypical signs and symptoms, and more frequent extrapulmonary dissemination. The treatment of TB is also more difficult to manage in HIV-infected patients, particularly with regard to pharmacological interactions secondary to inhibition or induction of cytochrome P450 enzymes by protease inhibitors with rifampicin or rifabutin, respectively. Finally, immune restoration induced by highly active anti-retroviral therapy (HAART) in developed countries may be responsible for a paradoxical worsening of TB manifestations.
在结核病高发的非洲和亚洲,感染艾滋病毒的患者中结核病发病率目前正在上升,这反映出这类患者对结核菌群分枝杆菌易感。在这一人群中,耐多药抗结核药物情况的蔓延也是一个令人担忧的问题。艾滋病毒引起的免疫抑制改变了结核病的临床表现,导致出现非典型体征和症状,肺外播散也更频繁。在感染艾滋病毒的患者中,结核病治疗也更难管理,特别是在蛋白酶抑制剂分别与利福平或利福布汀对细胞色素P450酶产生抑制或诱导作用而引发药物相互作用方面。最后,在发达国家,高效抗逆转录病毒疗法(HAART)诱导的免疫恢复可能会导致结核病表现出现矛盾性恶化。
Clin Microbiol Infect. 2004-5
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