Impact of pre-adapted HIV transmission

被引:79
作者
Carlson, Jonathan M. [1 ]
Du, Victor Y. [2 ]
Pfeifer, Nico [1 ,27 ]
Bansal, Anju [2 ]
Tan, Vincent Y. F. [1 ,28 ,29 ]
Power, Karen [3 ]
Brumme, Chanson J. [4 ]
Kreimer, Anat [1 ,30 ]
DeZiel, Charles E. [1 ]
Fusi, Nicolo [1 ]
Schaefer, Malinda [5 ]
Brockman, Mark A. [4 ,6 ]
Gilmour, Jill [7 ,8 ]
Price, Matt A. [7 ,9 ]
Kilembe, William [10 ]
Haubrich, Richard [11 ]
John, Mina [12 ,13 ]
Mallal, Simon [12 ,14 ]
Shapiro, Roger [15 ]
Frater, John [16 ,17 ,18 ]
Harrigan, P. Richard [4 ,19 ]
Ndung'u, Thumbi [3 ,20 ,21 ,22 ]
Allen, Susan [23 ,24 ]
Heckerman, David [1 ]
Sidney, John [25 ]
Allen, Todd M. [3 ,10 ]
Goulder, Philip J. R. [20 ,26 ]
Brumme, Zabrina L. [4 ,6 ]
Hunter, Eric [5 ,10 ,23 ]
Goepfert, Paul A. [2 ]
机构
[1] Microsoft Res, Redmond, WA USA
[2] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[3] Ragon Inst Massachusetts Gen Hosp Massachusetts I, Cambridge, MA USA
[4] British Columbia Ctr Excellence HIV AIDS, Vancouver, BC, Canada
[5] Emory Univ, Yerkes Natl Primate Res Ctr, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[6] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
[7] Int AIDS Vaccine Initiat, New York, NY USA
[8] Univ London Imperial Coll Sci Technol & Med, London, England
[9] Univ San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94117 USA
[10] Rwanda Zambia HIV Res Grp, Zambia Emory HIV Res Project, Lusaka, Zambia
[11] Gilead Sci Inc, 353 Lakeside Dr, Foster City, CA 94404 USA
[12] Murdoch Univ, Inst Immunol & Infect Dis, Murdoch, WA 6150, Australia
[13] Royal Perth Hosp, Dept Clin Immunol, GPO Box X2213, Perth, WA 6001, Australia
[14] Vanderbilt Univ, Sch Med, Ctr Translat Immunol & Infect Dis, Nashville, TN 37212 USA
[15] Harvard Univ, Harvard TH Chan Sch Publ Hlth, Boston, MA 02115 USA
[16] Univ Oxford, Nuffield Dept Clin Med, Oxford, England
[17] Oxford Biomed Res Ctr, Natl Inst Hlth Res, Oxford, England
[18] Univ Oxford, Oxford Martin Sch, Inst Emerging Infect, Oxford, England
[19] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[20] Univ KwaZulu Natal, Doris Duke Med Res Inst, HIV Pathogenesis Programme, Durban, South Africa
[21] Univ KwaZulu Natal, KwaZulu Natal Res Inst TB & HIV K RITH, Nelson R Mandela Sch Med, Durban, South Africa
[22] Max Planck Inst Infect Biol, Berlin, Germany
[23] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[24] Emory Univ, Rollins Sch Publ Hlth, Dept Global Hlth, Atlanta, GA 30322 USA
[25] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, La Jolla, CA USA
[26] Univ Oxford, Dept Paediat, Oxford, England
[27] Max Planck Inst Informat, Dept Computat Biol & Appl Algorithm, Saarbrucken, Germany
[28] Natl Univ Singapore, Dept Elect & Comp Engn, Singapore 117548, Singapore
[29] Natl Univ Singapore, Dept Math, 10 Kent Ridge Crescent, Singapore 117548, Singapore
[30] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
基金
新加坡国家研究基金会; 英国惠康基金; 加拿大健康研究院;
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; T-CELL RESPONSES; IMMUNE ESCAPE PATHWAYS; REPLICATION CAPACITY; MAXIMUM-LIKELIHOOD; VIRAL-LOAD; LYMPHOCYTE RESPONSE; DISCORDANT COUPLES; TYPE-1; VIREMIA; HLA ALLELES;
D O I
10.1038/nm.4100
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human leukocyte antigen class I (HLA)-restricted CD8(+) T lymphocyte (CTL) responses are crucial to HIV-1 control. Although HIV can evade these responses, the longer-term impact of viral escape mutants remains unclear, as these variants can also reduce intrinsic viral fitness. To address this, we here developed a metric to determine the degree of HIV adaptation to an HLA profile. We demonstrate that transmission of viruses that are pre-adapted to the HLA molecules expressed in the recipient is associated with impaired immunogenicity, elevated viral load and accelerated CD4(+) T cell decline. Furthermore, the extent of pre-adaptation among circulating viruses explains much of the variation in outcomes attributed to the expression of certain HLA alleles. Thus, viral pre-adaptation exploits 'holes' in the immune response. Accounting for these holes may be key for vaccine strategies seeking to elicit functional responses from viral variants, and to HIV cure strategies that require broad CTL responses to achieve successful eradication of HIV reservoirs.
引用
收藏
页码:606 / +
页数:14
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