Full Length Single Chain Fc Protein (FLSC IgG1) as a Potent Antiviral Therapy Candidate: Implications forIn VivoStudies-Reference-Cited by-同舟云学术

Full Length Single Chain Fc Protein (FLSC IgG1) as a Potent Antiviral Therapy Candidate: Implications forIn VivoStudies

Published:2016-02 Issue:2 Volume:32 Page:178-186
ISSN:0889-2229
Container-title:AIDS Research and Human Retroviruses
language:en
Short-container-title:AIDS Research and Human Retroviruses

Author:

Latinovic Olga S.¹²,Medina-Moreno Sandra¹,Schneider Kate¹,Gohain Neelakshi¹³,Zapata Juan¹,Pazgier Marzena¹³,Reitz Marvin¹⁴,Bryant Joseph¹⁵,Redfield Robert R.¹⁴

Affiliation:

1. Institute of Human Virology, University of Maryland School of Medicine, Baltimore, Maryland.

2. Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland.

3. Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland.

4. School of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.

5. Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland.

Publisher

Mary Ann Liebert Inc

Subject

Infectious Diseases,Virology,Immunology

Link

http://www.liebertpub.com/doi/pdf/10.1089/aid.2015.0020

Reference56 articles.

1. CC CKR5: A RANTES, MIP-1α, MIP-1β Receptor as a Fusion Cofactor for Macrophage-Tropic HIV-1

2. Identification of Determinants on a Dualtropic Human Immunodeficiency Virus Type 1 Envelope Glycoprotein That Confer Usage of CXCR4

3. Two distinct CCR5 domains can mediate coreceptor usage by human immunodeficiency virus type 1

4. Use of (alternative) coreceptors for HIV entry

5. The β-Chemokine Receptors CCR3 and CCR5 Facilitate Infection by Primary HIV-1 Isolates

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