World's Best Scientists 2026 revealed!

D-Index & Metrics

Immunology

D-Index
59
Citations
18738
World Ranking
3384
National Ranking
1565

Overview

What is he best known for?

The fields of study he is best known for:

  • Immune system
  • Cytokine
  • T cell

His main research concerns Immunology, FOXP3, Immune system, Inflammation and Cytokine. His studies in FOXP3 integrate themes in fields like Interleukin 21, IL-2 receptor and Cell biology. Aldesleukin and Immune tolerance is closely connected to Regulatory T cell in his research, which is encompassed under the umbrella topic of Cell biology.

While the research belongs to areas of Immune system, Daniel J. Campbell spends his time largely on the problem of Homeostasis, intersecting his research to questions surrounding CXCR3, Innate lymphoid cell, Autoimmunity and Autoimmune disease. Daniel J. Campbell integrates Inflammation and Downregulation and upregulation in his studies. His Cytokine research is multidisciplinary, incorporating elements of Immunoglobulin E, Cancer research, Pathogenesis and Atopic dermatitis.

His most cited work include:

  • The transcription factor T-bet controls regulatory T cell homeostasis and function during type 1 inflammation (922 citations)
  • The transcription factor T-bet controls regulatory T cell homeostasis and function during type 1 inflammation (922 citations)
  • Thymic stromal lymphopoietin as a key initiator of allergic airway inflammation in mice. (695 citations)

What are the main themes of his work throughout his whole career to date?

His primary scientific interests are in Immunology, Cell biology, FOXP3, T cell and Immune system. His Immunology and Inflammation, IL-2 receptor, Antigen, Immunity and Autoimmune disease investigations all form part of his Immunology research activities. In general Cell biology study, his work on Effector and Function often relates to the realm of Chemistry, Cellular differentiation and Downregulation and upregulation, thereby connecting several areas of interest.

His FOXP3 research incorporates elements of Proinflammatory cytokine, Immune tolerance, Signal transduction, Regulatory T cell and Interleukin 12. His work investigates the relationship between T cell and topics such as Molecular biology that intersect with problems in C-C chemokine receptor type 6. His work in Immune system addresses subjects such as Cytokine, which are connected to disciplines such as Chemokine.

He most often published in these fields:

  • Immunology (97.86%)
  • Cell biology (55.71%)
  • FOXP3 (50.71%)

What were the highlights of his more recent work (between 2019-2021)?

  • Immunology (97.86%)
  • Immune system (42.86%)
  • Effector (31.43%)

In recent papers he was focusing on the following fields of study:

His primary areas of investigation include Immunology, Immune system, Effector, Cell biology and Antibody. His research on Immunology frequently connects to adjacent areas such as Costimulatory blockade. He has researched Immune system in several fields, including Disease, Disease Presentation, Mass cytometry and Cohort.

His research in Cell biology intersects with topics in Cytokine, Tissue homeostasis, Humanized mouse, Regulatory T cell and FOXP3. His biological study spans a wide range of topics, including PI3K/AKT/mTOR pathway and Chemokine receptor. The various areas that Daniel J. Campbell examines in his Antibody study include Virus and Antigen.

Between 2019 and 2021, his most popular works were:

  • Functional SARS-CoV-2-Specific Immune Memory Persists after Mild COVID-19. (128 citations)
  • Functional SARS-CoV-2-Specific Immune Memory Persists after Mild COVID-19. (128 citations)
  • Functional SARS-CoV-2-specific immune memory persists after mild COVID-19 (34 citations)

In his most recent research, the most cited papers focused on:

  • Immune system
  • Cytokine
  • T cell

Daniel J. Campbell mainly focuses on Antibody, Virus, Antigen, Immunology and Herd immunity. His Antibody research incorporates themes from Acquired immune system, Immunity and Memory T cell. Daniel J. Campbell integrates many fields in his works, including Herd immunity, Immunological memory and Severe acute respiratory syndrome coronavirus 2.

Best Publications

  • The transcription factor T-bet controls regulatory T cell homeostasis and function during type 1 inflammation

    Meghan A Koch;Meghan A Koch;Glady's Tucker-Heard;Nikole R Perdue;Justin R Killebrew;Justin R Killebrew

  • Compartmentalized Control of Skin Immunity by Resident Commensals

    Shruti Naik;Nicolas Bouladoux;Christoph Wilhelm;Michael J. Molloy

  • Thymic stromal lymphopoietin as a key initiator of allergic airway inflammation in mice.

    Baohua Zhou;Michael R Comeau;Thibaut De Smedt;H Denny Liggitt

  • Phenotypical and functional specialization of FOXP3 + regulatory T cells

    Daniel J. Campbell;Meghan A. Koch

  • Subspecialization of Cxcr5+ T Cells: B Helper Activity Is Focused in a Germinal Center–Localized Subset of Cxcr5+ T Cells

    Chang H. Kim;Chang H. Kim;Lusijah S. Rott;Lusijah S. Rott;Ian Clark-Lewis;Daniel J. Campbell;Daniel J. Campbell

  • Regulatory T cells: recommendations to simplify the nomenclature

    Abul K Abbas;Christophe Benoist;Jeffrey A Bluestone;Daniel J Campbell

  • Rapid Acquisition of Tissue-specific Homing Phenotypes by CD4+ T Cells Activated in Cutaneous or Mucosal Lymphoid Tissues

    Daniel J. Campbell;Eugene C. Butcher;Eugene C. Butcher

  • Spontaneous atopic dermatitis in mice expressing an inducible thymic stromal lymphopoietin transgene specifically in the skin

    Jane Yoo;Miyuki Omori;Dora Gyarmati;Baohua Zhou

  • Functional SARS-CoV-2-Specific Immune Memory Persists after Mild COVID-19.

    Lauren B. Rodda;Jason Netland;Laila Shehata;Kurt B. Pruner

  • Altering the distribution of Foxp3(+) regulatory T cells results in tissue-specific inflammatory disease.

    Blythe D. Sather;Piper R. Treuting;Nikole R. Perdue;Mike Miazgowicz

  • Functionally distinct subsets of human FOXP3+ Treg cells that phenotypically mirror effector Th cells.

    Thomas Duhen;Thomas Duhen;Rebekka Duhen;Rebekka Duhen;Antonio Lanzavecchia;Federica Sallusto

  • CCR7 provides localized access to IL-2 and defines homeostatically distinct regulatory T cell subsets

    Kate S. Smigiel;Elizabeth Richards;Shivani Srivastava;Shivani Srivastava;Kerri R. Thomas

  • Chemokines in the systemic organization of immunity.

    Daniel J. Campbell;Chang H. Kim;Eugene C. Butcher;Eugene C. Butcher

  • Recirculating Intestinal IgA-Producing Cells Regulate Neuroinflammation via IL-10

    Olga L. Rojas;Anne-Katrin Pröbstel;Elisa A. Porfilio;Angela A. Wang

  • FOXP3 modifies the phenotypic and functional properties of regulatory T cells.

    Daniel J. Campbell;Steven F. Ziegler

  • T-bet+ Treg Cells Undergo Abortive Th1 Cell Differentiation due to Impaired Expression of IL-12 Receptor β2

    Meghan A. Koch;Kerri R. Thomas;Nikole R. Perdue;Kate S. Smigiel;Kate S. Smigiel

  • Human CD4+CD103+ cutaneous resident memory T cells are found in the circulation of healthy individuals

    Maria M. Klicznik;Peter A. Morawski;Barbara Höllbacher;Barbara Höllbacher;Suraj R. Varkhande

  • Chemokines in Lymphocyte Trafficking and Intestinal Immunity

    Eric J. Kunkel;Daniel J. Campbell;Eugene C. Butcher

  • Control of Regulatory T Cell Migration, Function, and Homeostasis.

    Daniel J. Campbell

  • Foxp3+ regulatory T cells maintain immune homeostasis in the skin

    Jan C. Dudda;Nikole Perdue;Eva Bachtanian;Daniel J. Campbell;Daniel J. Campbell

Frequent Co-Authors

Steven F. Ziegler
Steven F. Ziegler Virginia Mason Medical Center
Alexander Y. Rudensky
Alexander Y. Rudensky Memorial Sloan Kettering Cancer Center
Jane H. Buckner
Jane H. Buckner Virginia Mason Medical Center
Leonidas Stamatatos
Leonidas Stamatatos Fred Hutchinson Cancer Research Center
Eugene C. Butcher
Eugene C. Butcher Stanford University
Laurence A. Turka
Laurence A. Turka Harvard University
Shimon Sakaguchi
Shimon Sakaguchi Osaka University
Michael Gale
Michael Gale University of Washington
David J. Rawlings
David J. Rawlings Seattle Children's Hospital
David G. Brooks
David G. Brooks University of Toronto

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