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Journal article

Multiple T-cell responses are associated with better control of acute HIV-1 infection: An observational study

Abstract:
All rights reserved.Cytotoxic T lymphocyte (CTL) responses play pivotal roles in controlling the replication of human immunodeficiency virus type 1 (HIV-1), but the correlation between CTL responses and the progression of HIV-1 infection are controversial on account of HIV immune escape mutations driven by CTL pressure were reported. The acute HIV-1-infected patients from Beijing were incorporated into our study to investigate the effects of CTL response on the progression of HIV-1 infection. A longitudinal study was performed on acute HIV-1-infected patients to clarify the kinetic of T-cell responses, the dynamic of escape mutations, as well as the correlation between effective T-cell response and the progression of HIV infection. Seven human leukocyte antigen-B51+ (HLA-B51+) individuals were screened from 105 acute HIV-1 infectors. The detailed kinetic of HLA-B51-restricted CTL responses was described through blood sampling time points including seroconversion, 3 and 6 months after HIV-1 infection in the 7 HLA-B51+ individuals, by using 16 known HLA-B51 restricted epitopes. Pol743-751 (LPPVVAKEI, LI9), Pol283-289 (TAFTIPSI, TI8), and Gag327-3459 (NANPDCKTI, NI9) were identified as 3 dominant epitopes, and ranked as starting with LI9, followed by TI8 and NI9 in the ability to induce T-cell responses. The dynamics of escape mutations in the 3 epitopes were also found with the same order as T-cell response, by using sequencing for viral clones on blood sampling at seroconversion, 3 and 6 months after HIV-1 infection. We use solid evidence to demonstrate the correlation between T-cell response and HIV-1 mutation, and postulate that multiple T-cell responses might benefit the control of HIV-1 infection, especially in acute infection phase.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1097/MD.0000000000004429

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM - Investigative Medicine Division
Role:
Author



Publisher:
Lippincott, Williams & Wilkins
Journal:
Medicine More from this journal
Volume:
95
Issue:
30
Publication date:
2016-07-01
Acceptance date:
2016-06-24
DOI:
EISSN:
1536-5964
ISSN:
0025-7974


Language:
English
Keywords:
Pubs id:
pubs:638333
UUID:
uuid:9d761eeb-2502-4fbc-bc1e-96b6eb5f105f
Local pid:
pubs:638333
Source identifiers:
638333
Deposit date:
2016-08-24
ARK identifier:

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