Autologous CD4/CD8 co-culture assay:: A physiologically-relevant composite measure of CD8+ T lymphocyte function in HIV-infected persons

被引:23
作者
Fauce, Steven R.
Yang, Otto O.
Effros, Rita B.
机构
[1] Univ Calif Los Angeles, David Geffen Sch, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USA
关键词
HIV; CD8 T cell; viral inhibition; co-culture;
D O I
10.1016/j.jim.2007.07.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During HIV-1 infection, the CD8(+) T lymphocyte response is critical to controlling the virus; indeed, the development of AIDS results, in large part, from the eventual failure of this response. The ability to measure the composite CD8(+) T lymphocyte anti-viral activity is, therefore, an essential requirement in the evaluation of immune based therapies and potential vaccines. We report here the details of a reproducible assay that measures the ability of CD8(+) T lymphocytes to suppress viral production by infected autologous CD4(+) T lymphocytes. The assay is not limited to persons with any specific HLA type, and the use of bi-specific antibodies for cell expansion makes the assay feasible in situations where cell numbers may be limiting. The measurement of viral production over time provides a global readout of the CD8(+) T lymphocyte overall function against HIV-1, which can be used for longitudinal assessment of individual HIV-infected persons in order to evaluate therapy, immune reconstitution, and new vaccines. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 27 条
[1]   Multiple measures of HIV burden in blood and tissue are correlated with each other but not with clinical parameters in aviremic subjects [J].
Anton, PA ;
Mitsuyasu, RT ;
Deeks, SG ;
Scadden, DT ;
Wagner, B ;
Huang, C ;
Macken, C ;
Richman, DD ;
Christopherson, C ;
Borellini, F ;
Lazar, R ;
Hege, KM .
AIDS, 2003, 17 (01) :53-63
[2]   HIV-specific CD8+ T cells produce antiviral cytokines but are impaired in cytolytic function [J].
Appay, V ;
Nixon, DF ;
Donahoe, SM ;
Gillespie, GMA ;
Dong, T ;
King, A ;
Ogg, GS ;
Spiegel, HML ;
Conlon, C ;
Spina, CA ;
Havlir, DV ;
Richman, DD ;
Waters, A ;
Easterbrook, P ;
McMichael, AJ ;
Rowland-Jones, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (01) :63-75
[3]   Monitoring HIV-specific CD8+T cell responses by intracellular cytokine production [J].
Betts, MR ;
Casazza, JP ;
Koup, RA .
IMMUNOLOGY LETTERS, 2001, 79 (1-2) :117-125
[4]   Resistance to human immunodeficiency virus type 1 in vitro as a surrogate of vaccine-induced protective immunity [J].
Castillo, RC ;
Arango-Jaramillo, S ;
John, R ;
Weinhold, K ;
Kanki, P ;
Carruth, L ;
Schwartz, DH .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (03) :897-903
[5]   Tailoring of immunosuppression in renal and liver allograft recipients displaying donor specific T-suppressor cells [J].
Cortesini, R ;
Renna-Molajoni, E ;
Cinti, P ;
Pretagostini, R ;
Ho, E ;
Rossi, P ;
Cortesini, NSF .
HUMAN IMMUNOLOGY, 2002, 63 (11) :1010-1018
[6]   Control of HIV-1 infection by soluble factors of the immune response [J].
DeVico, AL ;
Gallo, RC .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (05) :401-413
[7]   Shortened telomeres in the expanded CD28- CD8+ cell subset in HIV disease implicate replicative senescence in HIV pathogenesis [J].
Effros, RB ;
Allsopp, R ;
Chiu, CP ;
Hausner, MA ;
Hirji, K ;
Wang, LL ;
Harley, CB ;
Villeponteau, B ;
West, MD ;
Giorgi, JV .
AIDS, 1996, 10 (08) :F17-F22
[8]  
FAUCE S, 2006, AM ASS IMM ANN M ABS, V26, P5
[9]   Clade B-based HIV-1 vaccines elicit cross-clade cytotoxic T lymphocyte reactivities in uninfected volunteers [J].
Ferrari, G ;
Humphrey, W ;
McElrath, MJ ;
Excler, JL ;
Duliege, AM ;
Clements, ML ;
Corey, LC ;
Bolognesi, DP ;
Weinhold, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) :1396-1401
[10]   Late escape from an immunodominant cytotoxic T-lymphocyte response associated with progression to AIDS [J].
Goulder, PJR ;
Phillips, RE ;
Colbert, RA ;
McAdam, S ;
Ogg, G ;
Nowak, MA ;
Giangrande, P ;
Luzzi, G ;
Morgan, B ;
Edwards, A ;
McMichael, AJ ;
RowlandJones, S .
NATURE MEDICINE, 1997, 3 (02) :212-217