High-Sequence Diversity and Rapid Virus Turnover Contribute to Higher Rates of Coreceptor Switching in Treatment-Experienced Subjects with HIV-1 Viremia-Reference-Cited by-同舟云学术

High-Sequence Diversity and Rapid Virus Turnover Contribute to Higher Rates of Coreceptor Switching in Treatment-Experienced Subjects with HIV-1 Viremia

Published:2017-03 Issue:3 Volume:33 Page:234-245
ISSN:0889-2229
Container-title:AIDS Research and Human Retroviruses
language:en
Short-container-title:AIDS Research and Human Retroviruses

Author:

Nedellec Rebecca¹,Herbeck Joshua T.²,Hunt Peter W.³,Deeks Steven G.³,Mullins James I.⁴,Anton Elizabeth D.⁵,Reeves Jacqueline D.⁵,Mosier Donald E.¹

Affiliation:

1. Department of Immunology and Microbial Science, IMM-7, The Scripps Research Institute, La Jolla, California.

2. International Clinical Research Center, Department of Global Health, University of Washington, Seattle, Washington.

3. Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California San Francisco, San Francisco, California.

4. Department of Microbiology, University of Washington, Seattle, Washington.

5. Monogram Biosciences, Laboratory Corporation of America® Holding, Virology Research and Development, South San Francisco, California.

Publisher

Mary Ann Liebert Inc

Subject

Infectious Diseases,Virology,Immunology

Link

http://www.liebertpub.com/doi/pdf/10.1089/aid.2016.0153

Reference91 articles.

1. CHEMOKINE RECEPTORS AS HIV-1 CORECEPTORS: Roles in Viral Entry, Tropism, and Disease

2. Consistent Viral Evolutionary Changes Associated with the Progression of Human Immunodeficiency Virus Type 1 Infection

3. Evolution of CCR5 Use before and during Coreceptor Switching

4. The V3 domain of the HIV–1 gp120 envelope glycoprotein is critical for chemokine–mediated blockade of infection

5. Identification of the Envelope V3 Loop as the Primary Determinant of Cell Tropism in HIV-1

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