Frequency of a mutated CCR-5 allele (Δ32) among Italian healthy donors and individuals at risk of parenteral HIV infection

被引:18
作者
Zamarchi, R
Indraccolo, S
Minuzzo, S
Coppola, V
Gringeri, A
Santagostino, E
Vicenzi, E
De Silvestro, G
Biagiotti, R
Baldassarre, C
Chieco-Bianchi, L
Amadori, A
机构
[1] Univ Padua, Interuniv Ctr Res Canc, Dept Oncol & Surg Sci, I-35128 Padua, Italy
[2] IST Biotechnol Sect, Padua, Italy
[3] Univ Milan, I-20100 Milan, Italy
[4] DIBIT, AIDS Immunopathogensis Unit, Milan, Italy
[5] Azienda Osped, Blood Transfus Unit, Padua, Italy
[6] Univ Florence, Dept Clin Immunol, I-50123 Florence, Italy
[7] ULSS 38, SERT, I-80100 Naples, Italy
[8] Maggiore Hosp, IRCCS, A Bianchi Bonomi Hemophilia & Thrombosis Ctr, I-20100 Milan, Italy
关键词
D O I
10.1089/088922299311303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim of this study was to assess the frequency of a truncated allele of the CCR-5 gene (Delta 32) in Italy, and address its possible role in parenteral HIV transmission, as well as its influence in HIV-associated disease progression. In 371 unrelated seronegative healthy blood donors the Delta 32 allele frequency was 0.047; this figure was significantly different from those reported in northern America and northern Europe populations. However, Delta 32 allele frequency in healthy individuals did not differ significantly from that found in 54 seronegative drug users (0.065), 98 seronegative hemophiliacs (0.051), and 81 seropositive hemophiliacs (0.049). Although in seropositive hemophiliacs the wt/Delta 32 heterozygous genotype was associated with a trend to a slower decline in CD4(+) cell counts, its presence did not seem to influence disease progression, as comparable Delta 32 allele frequency frequencies were found among progressing (0.042) and nonprogressing (0.111) patients. These data do not seem to support a protective role of the Delta 32 allele in preventing HIV infection through the parenteral route, or in influencing the natural history of the disease in this particular risk category, although the Delta 32 heterozygous state was associated with lower plasma viremia levels, On the other hand, the finding of non-syncytium-inducing HIV strains in the majority of Delta 32 heterozygous seropositive patients suggests that its presence could not be a major factor in driving a switch toward more cytopathic, T-tropic HIV strains through selective pressure in coreceptor usage.
引用
收藏
页码:337 / 344
页数:8
相关论文
共 37 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]   GENETIC-CONTROL OF THE CD4/CD8 T-CELL RATIO IN HUMANS [J].
AMADORI, A ;
ZAMARCHI, R ;
DESILVESTRO, G ;
FORZA, G ;
CAVATTON, G ;
DANIELI, GA ;
CLEMENTI, M ;
CHIECOBIANCHI, L .
NATURE MEDICINE, 1995, 1 (12) :1279-1283
[3]  
AMADORI A, 1989, J IMMUNOL, V143, P2146
[4]   Homozygous Delta 32 deletion of the CCR-5 chemokine receptor gene in an HIV-1-infected patient [J].
Balotta, C ;
Bagnarelli, P ;
Violin, M ;
Ridolfo, AL ;
Zhou, D ;
Berlusconi, A ;
Corvasce, S ;
Corbellino, M ;
Clementi, M ;
Clerici, M ;
Moroni, M ;
Galli, M .
AIDS, 1997, 11 (10) :F67-F71
[5]   HIV-1 infection in an individual homozygous for the CCR5 deletion allele [J].
Biti, R ;
French, RF ;
Young, J ;
Bennetts, B ;
Stewart, G ;
Liang, T .
NATURE MEDICINE, 1997, 3 (03) :252-253
[6]  
*CDCP, 1992, MMWR-MORBID MORTAL W, V41, pRR17
[7]   The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates [J].
Choe, H ;
Farzan, M ;
Sun, Y ;
Sullivan, N ;
Rollins, B ;
Ponath, PD ;
Wu, LJ ;
Mackay, CR ;
LaRosa, G ;
Newman, W ;
Gerard, N ;
Gerard, C ;
Sodroski, J .
CELL, 1996, 85 (07) :1135-1148
[8]   IDENTIFICATION OF RANTES, MIP-1-ALPHA, AND MIP-1-BETA AS THE MAJOR HIV-SUPPRESSIVE FACTORS PRODUCED BY CD8(+) T-CELLS [J].
COCCHI, F ;
DEVICO, AL ;
GARZINODEMO, A ;
ARYA, SK ;
GALLO, RC ;
LUSSO, P .
SCIENCE, 1995, 270 (5243) :1811-1815
[9]   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
[10]   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