학술논문

HIV-Specific Cellular Immune Response Is Inversely Correlated with Disease Progression as Defined by Decline of CD4⁺ T Cells in Relation to HIV RNA Load
Document Type
research-article
Source
The Journal of Infectious Diseases, 2004 Apr 01. 189(7), 1199-1208.
Subject
Mononuclear leukocytes
Primate lentiviruses
Infections
GB virus C
Disease progression
RNA
AIDS
Cell mediated immunity
Antigens
Language
English
ISSN
00221899
Abstract
The average time between infection with human immunodeficiency virus (HIV) and development of acquired immune deficiency syndrome is ~8 years. However, progression rates vary widely, depending on several determinants, including HIV-specific immunity, host genetic factors, and virulence of the infecting strain. In untreated HIV-infected patients with different progression rates, we examined HIV-specific T cell responses in combination with host genetic markers, such as chemokine/chemokine-receptor (CCR) polymorphisms and human leukocyte antigen (HLA) genotypes. HIV-specific CD4⁺ T cell responses and, to a lesser extent, HIVspecific CD8⁺ T cell responses were inversely correlated with progression rate. Slower progression was not related to polymorphisms in CCR genes, HLA genotype, or GB virus C coinfection. These data suggest that HIV-specific T cell responses are involved in protecting the host from disease progression.