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Quentin J. Sattentau

Quentin J. Sattentau

D-Index & Metrics

Immunology

D-Index
84
Citations
27238
World Ranking
1363
National Ranking
115

Overview

Quentin J. Sattentau is affiliated with the University of Oxford in the United Kingdom. Their research predominantly spans the fields of Medicine and Immunology and Microbiology, with a strong concentration in infectious diseases and viral studies.

Their main fields of study include:

  • Medicine
  • Immunology and Microbiology

Within these fields, their work has involved several subfields such as:

  • Infectious Diseases
  • Virology
  • Radiology, Nuclear Medicine and Imaging
  • Immunology
  • Molecular Biology

The key topics addressed in their research include:

  • HIV Research and Treatment
  • Monoclonal and Polyclonal Antibodies Research
  • SARS-CoV-2 and COVID-19 Research
  • Immune Cell Function and Interaction
  • COVID-19 Clinical Research Studies
  • HIV/AIDS drug development and treatment
  • Glycosylation and Glycoproteins Research

Quentin J. Sattentau has contributed to multiple publication venues. The most frequent outlets for their research include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Oxford Open Immunology
  • npj Vaccines
  • Nature Communications
  • Science Advances

Several recent papers illustrate the breadth of their research:

  • "Vaccine-Associated Enhanced Disease and Pathogenic Human Coronaviruses" (2022), published in Frontiers in Immunology
  • "Disassembly of HIV envelope glycoprotein trimer immunogens is driven by antibodies elicited via immunization" (2021), published in Science Advances
  • "Macrophage Cell-Cell Interactions Promoting HIV-1 Infection" (2020), published in Viruses
  • "Pathogen-sugar interactions revealed by universal saturation transfer analysis" (2022), published in Science
  • "T cell phenotypes in COVID-19 - a living review" (2020), published in Oxford Open Immunology

Their research collaborations include frequent co-authors such as:

  • Lachlan P. Deimel
  • Charles Buchanan
  • Xiaochao Xue
  • James H. Naismith
  • Andrew J. Baldwin

Best Publications

  • A new classification for HIV-1

    E. A. Berger;R. W. Doms;E.-M. Fenyö;B. T. M. Korber

  • Membrane nanotubes physically connect T cells over long distances presenting a novel route for HIV-1 transmission

    Stefanie Sowinski;Clare Jolly;Otto Berninghausen;Marco A. Purbhoo

  • Conformational changes induced in the human immunodeficiency virus envelope glycoprotein by soluble CD4 binding.

    Q J Sattentau;J P Moore

  • Dissociation of gp120 from HIV-1 virions induced by soluble CD4.

    John P. Moore;Jane A. McKeating;Robin A. Weiss;Quentin J. Sattentau

  • HIV-1 cell to cell transfer across an Env-induced, actin-dependent synapse.

    Clare Jolly;Kirk Kashefi;Michael Hollinshead;Quentin J. Sattentau

  • Avoiding the void: cell-to-cell spread of human viruses

    Quentin Sattentau

  • Primary isolates of human immunodeficiency virus type 1 are relatively resistant to neutralization by monoclonal antibodies to gp120, and their neutralization is not predicted by studies with monomeric gp120.

    J. P. Moore;Yunzhen Cao;Limo Qing;Q. J. Sattentau

  • The CD4 antigen: physiological ligand and HIV receptor.

    Quentin J. Sattentau;Robin A. Weiss

  • Identification of the Residues in Human CD4 Critical for the Binding of HIV

    J Arthos;K C Deen;M A Chaikin;J A Fornwald

  • Analysis of Memory B Cell Responses and Isolation of Novel Monoclonal Antibodies with Neutralizing Breadth from HIV-1-Infected Individuals

    Davide Corti;Johannes P. M. Langedijk;Andreas Hinz;Michael S. Seaman

  • Inactivation of human immunodeficiency virus type 1 infectivity with preservation of conformational and functional integrity of virion surface proteins.

    JL Rossio;MT Esser;K Suryanarayana;DK Schneider

  • Epitopes of the CD4 antigen and HIV infection.

    Quentin J. Sattentau;Angus G. Dalgleish;Robin A. Weiss;Peter C. L. Beverley

  • Conformational changes induced in the envelope glycoproteins of the human and simian immunodeficiency viruses by soluble receptor binding.

    Q J Sattentau;J P Moore;F Vignaux;F Traincard

  • Human immunodeficiency virus type 1 neutralization is determined by epitope exposure on the gp120 oligomer.

    Quentin J. Sattentau;John P. Moore

  • Thymic stromal lymphopoietin–elicited basophil responses promote eosinophilic esophagitis

    Mario Noti;Elia D.Tait Wojno;Brian S. Kim;Mark C. Siracusa

  • The neutralizing antibody response to HIV-1: viral evasion and escape from humoral immunity.

    P. W. H. I Parren;J. P Moore;D. R Burton;Q. J Sattentau

  • Selective Interactions of Polyanions with Basic Surfaces on Human Immunodeficiency Virus Type 1 gp120

    Maxime Moulard;Hugues Lortat-Jacob;Isabelle Mondor;Guillaume Roca

  • V3: HIV's switch-hitter.

    Oliver Hartley;Per Johan Klasse;Quentin J. Sattentau;John P. Moore

  • Human Immunodeficiency Virus Type 1 Attachment to HeLa CD4 Cells Is CD4 Independent and gp120 Dependent and Requires Cell Surface Heparans

    Isabelle Mondor;Sophie Ugolini;Quentin J. Sattentau

  • CD4-Induced Conformational Changes in the Human Immunodeficiency Virus Type 1 gp120 Glycoprotein: Consequences for Virus Entry and Neutralization

    Nancy Sullivan;Ying Sun;Quentin Sattentau;Markus Thali

Frequent Co-Authors

John P. Moore
John P. Moore Cornell University
David C. Montefiori
David C. Montefiori Duke University
Dennis R. Burton
Dennis R. Burton Scripps Research Institute
Per Johan Klasse
Per Johan Klasse Cornell University
Joseph Sodroski
Joseph Sodroski Harvard Medical School
Pascal Poignard
Pascal Poignard Grenoble Alpes University
Jonathan L. Heeney
Jonathan L. Heeney University of Cambridge
Robin A. Weiss
Robin A. Weiss University College London
Peter D. Kwong
Peter D. Kwong Columbia University Medical Center

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