Immune reconstitution inflammatory syndrome: the trouble with immunity when you had none

被引:124
作者
Barber, Daniel L. [1 ]
Andrade, Bruno B. [1 ]
Sereti, Irini [2 ]
Sher, Alan [1 ]
机构
[1] NIAID, Immunobiol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; HIV-INFECTED PATIENTS; PNEUMOCYSTIS-CARINII-PNEUMONIA; CD4(+) T-CELLS; ANTIRETROVIRAL THERAPY; RISK-FACTORS; MYCOBACTERIUM-TUBERCULOSIS; HOMEOSTATIC PROLIFERATION; CRYPTOCOCCAL MENINGITIS; PARADOXICAL RESPONSE;
D O I
10.1038/nrmicro2712
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Some individuals who are infected with HIV rapidly deteriorate shortly after starting antiretroviral therapy, despite effective viral suppression. This reaction, referred to as immune reconstitution inflammatory syndrome ( IRIS), is characterized by tissue-destructive inflammation and arises as CD4(+) T cells re-emerge. It has been proposed that IRIS is caused by a dysregulation of the expanding population of CD4(+) T cells specific for a co-infecting opportunistic pathogen. Here, we argue that IRIS instead results from hyper-responsiveness of the innate immune system to T cell help, a mechanism that may be shared by the many manifestations of IRIS that occur following the reversal of other types of immunosuppression in pathogen-infected hosts.
引用
收藏
页码:150 / 156
页数:7
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