Microbial translocation is associated with sustained failure in CD4+ T-cell reconstitution in HIV-infected patients on long-term highly active antiretroviral therapy

被引:241
作者
Marchetti, Giulia [1 ]
Bellistri, Giusi M. [1 ]
Borghi, Elisa [2 ]
Tincati, Camilla [1 ]
Ferramosca, Stefania [3 ]
La Francesca, Maria [2 ]
Morace, Giulia [2 ]
Gori, Andrea [4 ]
Monforte, Antonella d'Arminio [1 ]
机构
[1] Univ Milan, San Paolo Hosp, Clin Infect Dis, Dept Med Surg & Dent, I-20142 Milan, Italy
[2] Univ Milan, Dept Publ Hlth, I-20142 Milan, Italy
[3] Univ Milan, Luigi Sacco Hosp, Chair Infect Dis & Trop Med, Dept Clin Sci, I-20142 Milan, Italy
[4] San Gerardo Hosp, Div Infect Dis, Monza, Italy
关键词
D O I
10.1097/QAD.0b013e3283112d29
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with inefficient (CD4+ T-cell recovery on virogically suppressive highly active antiretroviral therapy constitute a major clinical hurdle given the threat of HIV/AIDS disease progression. We show heightened circulating lipopolysaccharide associated with plasma enterobacterial DNA and highly activated Ki67+CD4+CD8+ in 24 immunologic-nonresponders (CD4+ T-cell <= 200; HIV-RNA <= 50) compared with 11 full responders (CD4+ T-cell >= 400; HIV-RNA <= 50). These data provide novel insight into INRs pathogenesis, since they correlate augmented systemic translocation of microbial bioproducts with T-cell hyperactivation.
引用
收藏
页码:2035 / 2038
页数:4
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