PMID- 24012585 OWN - NLM STAT- MEDLINE DCOM- 20140718 LR - 20221207 IS - 1879-1166 (Electronic) IS - 0198-8859 (Linking) VI - 74 IP - 12 DP - 2013 Dec TI - Associations of HLA class I antigen specificities and haplotypes with disease progression in HIV-1-infected Hans in Northern China. PG - 1636-42 LID - S0198-8859(13)00512-0 [pii] LID - 10.1016/j.humimm.2013.08.287 [doi] AB - The human leukocyte antigen (HLA) allele frequencies, which differ among various ethnic populations, may result in population-specific effects on HIV-1 disease progression. No large-scale study has yet been conducted on the Chinese population. In this study, HLA class I antigen specificities were determined in a cohort including 105 long-term non-progressors (LTNPs) and 321 typical progressors (TPs), who were recruited from HIV-1-infected Northern Han Chinese, to determine the associations between certain HLA types and HIV-1 disease progression. The frequencies of HLA class I specificities and haplotypes among the two groups were compared using binary logistic stepwise regression. Results showed that HLA-A( *)30-B( *)13-C( *)06 (OR = 0.387, P = 0.019) and B( *)67 (OR = 0.134, P = 0.005) were associated with a long-term non-progressing condition, and C( *)01 (OR = 2.539, P = 0.050) was overrepresented in TPs after adjusting for non-genetic factors (sex, age, the location of patients, HIV subtype and the route of infection). The influence of HLA homozygosity on HIV disease progression was also analyzed. However, homozygosity at HLA-A, HLA-B or HLA-C conferred no observable disadvantage in our study population (P = 0.730, 0.246 and 0.445, respectively). These findings suggest that the host's genetics make important contributions to HIV viral control and may help to develop peptide-based vaccines for this population. CI - Copyright (c) 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved. FAU - Zhang, Hui AU - Zhang H AD - Key Laboratory of AIDS Immunology of the Ministry of Health, Department of Laboratory Medicine, The First Hospital of China Medical University, Shenyang, China. FAU - Zhao, Bin AU - Zhao B FAU - Han, Xiaoxu AU - Han X FAU - Wang, Zhe AU - Wang Z FAU - Liu, Baogui AU - Liu B FAU - Lu, Chunming AU - Lu C FAU - Zhang, Min AU - Zhang M FAU - Liu, Jing AU - Liu J FAU - Chen, Ou AU - Chen O FAU - Hu, Qinghai AU - Hu Q FAU - Jiang, Fanming AU - Jiang F FAU - Shang, Hong AU - Shang H LA - eng PT - Journal Article DEP - 20130905 PL - United States TA - Hum Immunol JT - Human immunology JID - 8010936 RN - 0 (Histocompatibility Antigens Class I) SB - IM MH - Adult MH - Alleles MH - Asian People/genetics MH - China MH - Disease Progression MH - Female MH - Gene Frequency MH - HIV Infections/*genetics/*immunology/virology MH - HIV-1/genetics/*immunology MH - *Haplotypes MH - Histocompatibility Antigens Class I/*genetics/*immunology MH - Homozygote MH - Humans MH - Male MH - Middle Aged OTO - NOTNLM OT - AIDS OT - CTL OT - HIV-1 OT - HLA OT - KIR OT - LD OT - LTNP OT - NK OT - PBD OT - PCR-SSP OT - RP OT - TP OT - VL OT - acquired immunodeficiency syndrome OT - cytotoxic T lymphocyte OT - human immunodeficiency virus type-1 OT - human leukocyte antigen OT - killer Ig-like receptor OT - linkage disequilibrium OT - long-term non-progressor OT - natural killer OT - paid blood donations OT - polymerase chain reaction sequence-specified primer OT - rapid progressor OT - typical progressor OT - viral load EDAT- 2013/09/10 06:00 MHDA- 2014/07/19 06:00 CRDT- 2013/09/10 06:00 PHST- 2013/05/22 00:00 [received] PHST- 2013/07/17 00:00 [revised] PHST- 2013/08/10 00:00 [accepted] PHST- 2013/09/10 06:00 [entrez] PHST- 2013/09/10 06:00 [pubmed] PHST- 2014/07/19 06:00 [medline] AID - S0198-8859(13)00512-0 [pii] AID - 10.1016/j.humimm.2013.08.287 [doi] PST - ppublish SO - Hum Immunol. 2013 Dec;74(12):1636-42. doi: 10.1016/j.humimm.2013.08.287. Epub 2013 Sep 5.