Role of CD4 and CCR5 levels in the susceptibility of primary macrophages to infection by CCR5-dependent HIV type 1 isolates

被引:22
作者
Pesenti, E
Pastore, C
Lillo, F
Siccardi, AG
Vercelli, D
Lopalco, L
机构
[1] San Raffaele Sci Inst, Mol Immunoregulat Unit, I-20132 Milan, Italy
[2] San Raffaele Sci Inst, Immunobiol HIV Unit, I-20132 Milan, Italy
[3] San Raffaele Sci Inst, Virol Lab, I-20132 Milan, Italy
[4] Univ Milan, Dipartimento Biol Genet Sci Med, I-20100 Milan, Italy
关键词
D O I
10.1089/088922299310494
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages are a preferred target for sexually transmitted human immunodeficiency virus type 1 (HIV-1) isolates that use CCR5 as a coreceptor in combination with CD4, To assess whether the susceptibility of MDMs to infection by an R5 isolate was influenced by CD4 and/or CCR5 expression, levels of membrane CD4 or CCR5 transcripts at the time of infection and ID50 values 15 days postinfection were measured in cultures of primary macrophages infected with HIV-1(10005). To analyze the data, subjects were divided so as to maximize differences in the levels of CD4 or CCR5 expression between groups. Indeed, the difference in CD4 expression between the CD4(high) (MFI, 16.7 +/- 2.2) and CD4(low) (MFI, 6.7 +/- 0.7) groups attained high significance (p < 0.005). Of note, susceptibility to infection of MDMs isolated from CD4(high) donors was strikingly enhanced as compared with CD4(low) subjects, as shown by a fourfold increase in ID50 titers at day 15 postinfection (p < 0.002). In contrast, no significant difference in ID50 was apparent when the subjects were grouped according to the levels of CCR5 transcripts, even though CCR5 expression in the two groups differed significantly (p = 0.01). These results suggest that, regardless of variations among individuals, the intensity of CD4 expression in macrophages is such that CCR5 levels are above the threshold required for efficient HIV-1 infection. Consistent with this hypothesis, macrophages from three additional donors selected for high CD4 expression and low CCR5 transcripts were found to be highly susceptible to HIV-1 infection.
引用
收藏
页码:983 / 987
页数:5
相关论文
共 30 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]   SUSCEPTIBILITY TO INFECTION BY THE HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) CORRELATES WITH T4 EXPRESSION IN A PARENTAL MONOCYTOID CELL-LINE AND ITS SUBCLONES [J].
ASJO, B ;
IVHED, I ;
GIDLUND, M ;
FUERSTENBERG, S ;
FENYO, EM ;
NILSSON, K ;
WIGZELL, H .
VIROLOGY, 1987, 157 (02) :359-365
[3]   Infectious cellular load in human immunodeficiency virus type 1 (HIV-1)-infected individuals and susceptibility of peripheral blood mononuclear cells from their exposed partners to non-syncytium-inducing HIV-1 as major determinants for HIV-1 transmission in homosexual couples [J].
Blaak, H ;
vantWout, AB ;
Brouwer, M ;
Cornelissen, M ;
Kootstra, NA ;
AlbrechtvanLent, N ;
Keet, RPM ;
Goudsmit, J ;
Coutinho, RA ;
Schuitemaker, H .
JOURNAL OF VIROLOGY, 1998, 72 (01) :218-224
[4]  
CHOE H, 1996, CELL, V85, P135
[5]   MACROPHAGE-TROPIC STRAINS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 UTILIZE THE CD4 RECEPTOR [J].
COLLMAN, R ;
GODFREY, B ;
CUTILLI, J ;
RHODES, A ;
HASSAN, NF ;
SWEET, R ;
DOUGLAS, SD ;
FRIEDMAN, H ;
NATHANSON, N ;
GONZALEZSCARANO, F .
JOURNAL OF VIROLOGY, 1990, 64 (09) :4468-4476
[6]   Macrophages and CD4(+) T lymphocytes from two multiply exposed, uninfected individuals resist infection with primary non-syncytium-inducing isolates of human immunodeficiency virus type 1 [J].
Connor, RI ;
Paxton, WA ;
Sheridan, KE ;
Koup, RA .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8758-8764
[7]   Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene [J].
Dean, M ;
Carrington, M ;
Winkler, C ;
Huttley, GA ;
Smith, MW ;
Allikmets, R ;
Goedert, JJ ;
Buchbinder, SP ;
Vittinghoff, E ;
Gomperts, E ;
Donfield, S ;
Vlahov, D ;
Kaslow, R ;
Saah, A ;
Rinaldo, C ;
Detels, R ;
OBrien, SJ .
SCIENCE, 1996, 273 (5283) :1856-1862
[8]   Identification of a major co-receptor for primary isolates of HIV-1 [J].
Deng, HK ;
Liu, R ;
Ellmeier, W ;
Choe, S ;
Unutmaz, D ;
Burkhart, M ;
DiMarzio, P ;
Marmon, S ;
Sutton, RE ;
Hill, CM ;
Davis, CB ;
Peiper, SC ;
Schall, TJ ;
Littman, DR ;
Landau, NR .
NATURE, 1996, 381 (6584) :661-666
[9]  
Di Marzio P, 1998, AIDS RES HUM RETROV, V14, P129, DOI 10.1089/aid.1998.14.129
[10]   A dual-tropic primary HIV-1 isolate that uses fusin and the beta-chemokine receptors CKR-5, CKR-3, and CKR-2b as fusion cofactors [J].
Doranz, BJ ;
Rucker, J ;
Yi, YJ ;
Smyth, RJ ;
Samson, M ;
Peiper, SC ;
Parmentier, M ;
Collman, RG ;
Doms, RW .
CELL, 1996, 85 (07) :1149-1158