Immune response to HIV

被引:45
作者
Perreau, Matthieu [1 ]
Levy, Yves [3 ]
Pantaleo, Giuseppe [1 ,2 ]
机构
[1] Univ Lausanne, CHU Vaudois, Div Immunol & Allergy, Lausanne, Switzerland
[2] Univ Lausanne, CHU Vaudois, Swiss Vaccine Res Inst, Lausanne, Switzerland
[3] Univ Paris Est Creteil, INSERM U955, Grp Henri Mondor Albert Chenevier, Fac Med,Immunol Clin,Vaccine Res Inst, Creteil, France
关键词
antibodies; HIV; immune response; T cells; HUMAN-IMMUNODEFICIENCY-VIRUS; T-CELL RESPONSES; PLASMACYTOID DENDRITIC CELLS; PROXIMAL EXTERNAL REGION; NEUTRALIZING MONOCLONAL-ANTIBODIES; TYPE-1; INFECTION; DC-SIGN; HLA-B; UNINFECTED INDIVIDUALS; PRODUCTIVE INFECTION;
D O I
10.1097/COH.0b013e328361faf4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of reviewMajor advances have been made in the delineation of HIV-specific immune response and in the mechanisms of virus escape. The kinetics of the immunological and virological events occurring during primary HIV infection indicate that the establishment of the latent HIV reservoir, the major obstacle to HIV eradication likely occurs during the very early stages of primary infection, that is, the eclipse phase', prior to the development of the HIV-specific immune response which has limited efficacy in the control of the early events of infection. Therefore, the window of opportunity to develop effective interventions either to clear HIV during primary infection or to prevent rebound of HIV in patients successfully treated who stop antiretroviral therapy is very narrow.Recent findingsGenetic factors most strongly associated with nonprogressive infection are human leukocyte antigen (HLA) class I alleles and particularly HLA-B5701. CD4 and CD8 T-cell responses with polyfunctional profile are associated with nonprogressive infection. Broader neutralizing antibodies are detected 3-4 years after infection, generated only in 20% of individuals but show no efficacy in the control of HIV replication.SummaryIn the present review, we shall discuss the different components of the HIV-specific immune response elicited by the infection, the kinetics of these responses during primary infection and the changes following transition to the chronic phase of infection, and the functional profile of effective' versus noneffective' HIV-specific immune responses.
引用
收藏
页码:333 / 340
页数:8
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