Cellular Immune Activation in Cerebrospinal Fluid From Ugandans With Cryptococcal Meningitis and Immune Reconstitution Inflammatory Syndrome

被引:54
|
作者
Meya, David B. [1 ,2 ,6 ]
Okurut, Samuel [4 ]
Zziwa, Godfrey [4 ]
Rolfes, Melissa A. [6 ]
Kelsey, Melander [7 ,8 ]
Cose, Steve [2 ,5 ,13 ]
Joloba, Moses [3 ]
Naluyima, Prossy
Palmer, Brent E.
Kambugu, Andrew [1 ]
Mayanja-Kizza, Harriet [2 ]
Bohjanen, Paul R.
Eller, Michael A. [10 ,11 ]
Wahl, Sharon M. [12 ]
Boulware, David R. [6 ]
Manabe, Yuka C. [1 ,9 ]
Janoff, Edward N. [7 ,8 ]
机构
[1] Makerere Univ, Coll Hlth Sci, Infect Dis Inst, Kampala, Uganda
[2] Makerere Univ, Coll Hlth Sci, Sch Med, Kampala, Uganda
[3] Makerere Univ, Dept Microbiol, Sch Biomed Sci, Kampala, Uganda
[4] Makerere Univ Reed Project, Kampala, Uganda
[5] Uganda Virus Res Inst, Med Res Council, Uganda Res Unit AIDS, Entebbe, Uganda
[6] Univ Minnesota, Dept Med, Ctr Infect Dis & Microbiol Translat Res, Minneapolis, MN 55455 USA
[7] Univ Colorado Denver, Mucosal & Vaccine Res Program Colorado, Aurora, CO USA
[8] Denver Vet Affairs Med Ctr, Baltimore, MD USA
[9] Johns Hopkins Univ, Dept Med, Div Infect Dis, Baltimore, MD USA
[10] Walter Reed Army Inst Res, US Mil HIV Res Program, Silver Spring, MD USA
[11] Henry M Jackson Fdn Adv Mil Med, Bethesda, MD USA
[12] Natl Inst Dent & Craniofacial Res, NIH, Bethesda, MD USA
[13] London Sch Hyg & Trop Med, London, England
来源
JOURNAL OF INFECTIOUS DISEASES | 2015年 / 211卷 / 10期
基金
美国国家卫生研究院; 英国惠康基金;
关键词
cryptococcal meningitis; cryptococcus; HIV; cerebrospinal fluid; immune responses; cell activation; CENTRAL-NERVOUS-SYSTEM; CD4(+) T-CELLS; HIV-1-INFECTED PATIENTS; CLINICAL-FEATURES; INFECTED PATIENTS; CHRONIC HIV; TUBERCULOSIS; NEOFORMANS; POLYSACCHARIDE; LYMPHOCYTES;
D O I
10.1093/infdis/jiu664
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Methods.aEuro integral We characterized the lineage and activation status of mononuclear cells in blood and CSF of HIV-infected patients with noncryptococcal meningitis (NCM) (n = 10), those with CM at day 0 (n = 40) or day 14 (n = 21) of antifungal therapy, and those with CM-IRIS (n = 10). Results.aEuro integral At diagnosis, highly activated CD8(+) T cells predominated in CSF in both CM and NCM. CM-IRIS was associated with an increasing frequency of CSF CD4(+) T cells (increased from 2.2% to 23%; P = .06), a shift in monocyte phenotype from classic to an intermediate/proinflammatory, and increased programmed death ligand 1 expression on natural killer cells (increased from 11.9% to 61.6%, P = .03). CSF cellular responses were distinct from responses in peripheral blood. Conclusions.aEuro integral After CM, T cells in CSF tend to evolve with the development of IRIS, with increasing proportions of activated CD4(+) T cells, migration of intermediate monocytes to the CSF, and declining fungal burden. These changes provide insight into IRIS pathogenesis and could be exploited to more effectively treat CM and prevent CM-IRIS.
引用
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页码:1597 / 1606
页数:10
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