Mechanism for Complement-Mediated, Antibody-Dependent Enhancement of Human Immunodeficiency Virus Type 1 Infection in MT2 Cells Is Enhanced Entry through CD4, CD21, and CXCR4 Chemokine Receptors-Reference-Cited by-同舟云学术

Mechanism for Complement-Mediated, Antibody-Dependent Enhancement of Human Immunodeficiency Virus Type 1 Infection in MT2 Cells Is Enhanced Entry through CD4, CD21, and CXCR4 Chemokine Receptors

Published:2006-09 Issue:3 Volume:19 Page:434-447
ISSN:0882-8245
Container-title:Viral Immunology
language:en
Short-container-title:Viral Immunology

Author:

Robinson W. Edward¹

Affiliation:

1. Departments of Pathology and Laboratory Medicine, Microbiology and Molecular Genetics, and Medicine, University of California, Irvine, CA.

Publisher

Mary Ann Liebert Inc

Subject

Virology,Molecular Medicine,Immunology

Link

https://www.liebertpub.com/doi/pdf/10.1089/vim.2006.19.434

Reference54 articles.

1. Analysis of Neutralizing and Enhancing Antibodies to Human Immunodeficiency Virus Type 1 Primary Isolates in Plasma of Individuals Infected withenvGenetic Subtype B and E Viruses in Thailand

2. A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity

3. Significant decrease of the enhancement/neutralization index in HIV patients during highly active antiretroviral therapy (HAART)

4. Opsonization of HIV-1 by Semen Complement Enhances Infection of Human Epithelial Cells

5. Synthesis and Structure-Activity Relationships of Phenylenebis(methylene)-Linked Bis-Tetraazamacrocycles That Inhibit HIV Replication. Effects of Macrocyclic Ring Size and Substituents on the Aromatic Linker

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