scholarly journals Distribution of CCR5 genotypes and HLA Class I B alleles in HIV-1 infected and uninfected injecting drug users from Rio de Janeiro, Brazil

2009 ◽  
Vol 9 (4) ◽  
pp. 638-642 ◽  
Author(s):  
Sylvia Lopes Maia Teixeira ◽  
Francisco Inácio Bastos ◽  
Mariana A. Hacker ◽  
Mariza Gonçalves Morgado
2001 ◽  
Vol 21 (2) ◽  
pp. 143-151 ◽  
Author(s):  
Monick Lindenmeyer Guimarães ◽  
Francisco Inácio Bastos ◽  
Paulo R. Telles ◽  
Bernardo Galvão-Castro ◽  
Ricardo S. Diaz ◽  
...  

2006 ◽  
Vol 81 (4) ◽  
pp. 1619-1631 ◽  
Author(s):  
Xu G. Yu ◽  
Mathias Lichterfeld ◽  
Senica Chetty ◽  
Katie L. Williams ◽  
Stanley K. Mui ◽  
...  

ABSTRACT The relative contributions of HLA alleles and T-cell receptors (TCRs) to the prevention of mutational viral escape are unclear. Here, we examined human immunodeficiency virus type 1 (HIV-1)-specific CD8+ T-cell responses restricted by two closely related HLA class I alleles, B*5701 and B*5703, that differ by two amino acids but are both associated with a dominant response to the same HIV-1 Gag epitope KF11 (KAFSPEVIPMF). When this epitope is presented by HLA-B*5701, it induces a TCR repertoire that is highly conserved among individuals, cross-recognizes viral epitope variants, and is rarely associated with mutational escape. In contrast, KF11 presented by HLA-B*5703 induces an entirely different, more heterogeneous TCR β-chain repertoire that fails to recognize specific KF11 escape variants which frequently arise in clade C-infected HLA-B*5703+ individuals. These data show the influence of HLA allele subtypes on TCR selection and indicate that extensive TCR diversity is not a prerequisite to prevention of allowable viral mutations.


2010 ◽  
Vol 26 (5) ◽  
pp. 605-608 ◽  
Author(s):  
Eric Sanders-Buell ◽  
Meera Bose ◽  
Abdul Nasir ◽  
Catherine S. Todd ◽  
M. Raza Stanekzai ◽  
...  

Author(s):  
H. Syed Iqbal ◽  
Sunil S. Solomon ◽  
Vidya Madhavan ◽  
Suniti Solomon ◽  
P. Balakrishnan

AIDS ◽  
1998 ◽  
Vol 12 (6) ◽  
pp. 635-641 ◽  
Author(s):  
Vladimir V. Lukashov ◽  
Eline L.M. Op de Coul ◽  
Roel A. Coutinho ◽  
Jaap Goudsmit

2011 ◽  
Vol 16 (41) ◽  
Author(s):  
A Hatzakis ◽  
D Paraskevis ◽  
J Kremastinou ◽  
M Malliori

2002 ◽  
Vol 76 (16) ◽  
pp. 8276-8284 ◽  
Author(s):  
Jianming Tang ◽  
Shenghui Tang ◽  
Elena Lobashevsky ◽  
Angela D. Myracle ◽  
Ulgen Fideli ◽  
...  

ABSTRACT The setpoint of viral RNA concentration (viral load [VL]) during chronic human immunodeficiency virus type 1 (HIV-1) infection reflects a virus-host equilibration closely related to CD8+ cytotoxic T-lymphocyte (CTL) responses, which rely heavily on antigen presentation by the human major histocompatibility complex (MHC) (i.e., HLA) class I molecules. Differences in HIV-1 VL among 259 mostly clade C virus-infected individuals (137 females and 122 males) in the Zambia-UAB HIV Research Project (ZUHRP) were associated with several HLA class I alleles and haplotypes. In particular, general linear model analyses revealed lower log10 VL among those with HLA allele B*57 (P = 0.002 [without correction]) previously implicated in favorable response and in those with HLA B*39 and A*30-Cw*03 (P = 0.002 to 0.016); the same analyses also demonstrated higher log10 VL among individuals with A*02-Cw*16, A*23-B*14, and A*23-Cw*07 (P = 0.010 to 0.033). These HLA effects remained strong (P = 0.0002 to 0.075) after adjustment for age, gender, and duration of infection and persisted across three orders of VL categories (P = 0.001 to 0.084). In contrast, neither B*35 (n = 15) nor B*53 (n = 53) showed a clear disadvantage such as that reported elsewhere for these closely related alleles. Other HLA associations with unusually high (A*68, B*41, B*45, and Cw*16) or low (B*13, Cw*12, and Cw*18) VL were either unstable or reflected their tight linkage respecting disequilibria with other class I variants. The three consistently favorable HLA class I variants retained in multivariable models and in alternative analyses were present in 30.9% of subjects with the lowest (<10,000 copies per ml) and 3.1% of those with the highest (>100,000) VL. Clear differential distribution of HLA profiles according to level of viremia suggests important host genetic contribution to the pattern of immune control and escape during HIV-1 infection.


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