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Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques
Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques
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Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques
Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques

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Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques
Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques
Journal Article

Whole-body immunoPET reveals active SIV dynamics in viremic and antiretroviral therapy–treated macaques

2015
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Overview
ImmunoPET/CT imaging using a labeled SIV-specific antibody can identify sites of viralinfection in SIV-infected macaques without the need for tissue biopsies, even if viral load in the blood is below the detection limit. The detection of viral dynamics and localization in the context of controlled HIV infection remains a challenge and is limited to blood and biopsies. We developed a method to capture total-body simian immunodeficiency virus (SIV) replication using immunoPET (antibody-targeted positron emission tomography). The administration of a poly(ethylene glycol)-modified, 64 Cu-labeled SIV Gp120–specific antibody led to readily detectable signals in the gastrointestinal and respiratory tract, lymphoid tissues and reproductive organs of viremic monkeys. Viral signals were reduced in aviremic antiretroviral-treated monkeys but detectable in colon, select lymph nodes, small bowel, nasal turbinates, the genital tract and lung. In elite controllers, virus was detected primarily in foci in the small bowel, select lymphoid areas and the male reproductive tract, as confirmed by quantitative reverse-transcription PCR (qRT-PCR) and immunohistochemistry. This real-time, in vivo viral imaging method has broad applications to the study of immunodeficiency virus pathogenesis, drug and vaccine development, and the potential for clinical translation.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject

13/1

/ 14/10

/ 59/78

/ 631/1647/245/2092

/ 631/1647/767/1424

/ 631/326/596

/ Adenine - analogs & derivatives

/ Adenine - therapeutic use

/ Animals

/ Anti-Retroviral Agents - therapeutic use

/ Antibodies

/ Antiretroviral agents

/ Antiretroviral drugs

/ Antiretroviral therapy

/ Antiviral agents

/ Bioinformatics

/ Biological Microscopy

/ Biological Techniques

/ Biomedical Engineering/Biotechnology

/ Biopsy

/ Blood

/ Computed tomography

/ Copper Radioisotopes

/ Deoxycytidine - analogs & derivatives

/ Deoxycytidine - therapeutic use

/ Dosage and administration

/ Emissions

/ Emtricitabine

/ Genital tract

/ Glycoprotein gp120

/ Health aspects

/ Immune system

/ Immunohistochemistry

/ In vivo methods and tests

/ Intestine

/ Lentivirus

/ Life Sciences

/ Localization

/ Lymph nodes

/ Lymphoid tissue

/ Macaca

/ Male

/ Medical imaging

/ Membrane Glycoproteins - metabolism

/ Methods

/ Monkeys

/ Monkeys & apes

/ Naphthyridines - therapeutic use

/ Nose

/ Organophosphonates - therapeutic use

/ Pathogenesis

/ Patient outcomes

/ PET imaging

/ Polyethylene glycol

/ Positron emission

/ Positron emission tomography

/ Positron-Emission Tomography - methods

/ Proteomics

/ Real time

/ Reproductive organs

/ Reproductive system

/ Respiratory tract

/ Retroviridae

/ Reverse Transcriptase Polymerase Chain Reaction

/ Sensitivity and Specificity

/ Simian Immunodeficiency Virus

/ Small intestine

/ Tenofovir

/ Tomography

/ Vaccine development

/ Vaccines

/ Viral Envelope Proteins - metabolism

/ Viral infections

/ Viremia

/ Virus Replication

/ Viruses

/ Whole Body Imaging - methods