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Immunology

D-Index
66
Citations
16203
World Ranking
2757
National Ranking
1313

Overview

David V. Serreze is affiliated with The Jackson Laboratory in the United States. Their research focuses on immunology, microbiology, medicine, and biochemistry, genetics, and molecular biology, with prominent subfields including immunology, genetics, oncology, surgery, and endocrinology, diabetes, and metabolism.

Their work covers several main topics such as diabetes and associated disorders, immune cell function and interaction, T-cell and B-cell immunology, pancreatic function and diabetes, diabetes management and research, CAR-T cell therapy research, and cancer immunotherapy and biomarkers.

Recent publications by David V. Serreze include:

  • "Aberrant type 1 immunity drives susceptibility to mucosal fungal infections," 2021, Science
  • "Decreased pancreatic acinar cell number in type 1 diabetes," 2020, Diabetologia
  • "CD226 Deletion Reduces Type 1 Diabetes in the NOD Mouse by Impairing Thymocyte Development and Peripheral T Cell Activation," 2020, Frontiers in Immunology
  • "Toll-Like Receptor 7 Is Required for Lacrimal Gland Autoimmunity and Type 1 Diabetes Development in Male Nonobese Diabetic Mice," 2020, International Journal of Molecular Sciences
  • "The CD137 Ligand Is Important for Type 1 Diabetes Development but Dispensable for the Homeostasis of Disease-Suppressive CD137+ FOXP3+ Regulatory CD4 T Cells," 2020, The Journal of Immunology

Frequent co-authors collaborating with Serreze include Jeremy J. Racine, Aron M. Geurts, Yi-Guang Chen, Harold D. Chapman, and Jennifer R. Dwyer.

The scientist regularly publishes in venues such as:

  • Faculty Opinions - Post-Publication Peer Review of the Biomedical Literature
  • The Journal of Immunology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Science
  • Frontiers in Immunology

In addition to research articles, David V. Serreze has contributed to book publications, including a 2022 work titled Genetic Basis of Tolerance Induction Defects Underlying the Development of Autoimmune Pathologies, published by Frontiers Media.

Best Publications

  • Single domain antibodies: promising experimental and therapeutic tools in infection and immunity.

    Janusz Wesolowski;Vanina Alzogaray;Jan Reyelt;Mandy Unger

  • B lymphocytes are essential for the initiation of T cell-mediated autoimmune diabetes: analysis of a new "speed congenic" stock of NOD.Ig mu null mice.

    D V Serreze;H D Chapman;D S Varnum;M S Hanson

  • Interleukin 4 reverses T cell proliferative unresponsiveness and prevents the onset of diabetes in nonobese diabetic mice.

    M J Rapoport;A Jaramillo;D Zipris;A H Lazarus

  • B Lymphocytes Are Critical Antigen-Presenting Cells for the Initiation of T Cell-Mediated Autoimmune Diabetes in Nonobese Diabetic Mice

    David V. Serreze;Sara A. Fleming;Harold D. Chapman;Scott D. Richard

  • Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice

    Rulang Jiang;Yu Lan;Harry D. Chapman;Carrie Shawber

  • Identification of the β cell antigen targeted by a prevalent population of pathogenic CD8+ T cells in autoimmune diabetes

    Scott M. Lieberman;Anne M. Evans;Bingye Han;Toshiyuki Takaki

  • Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity

    Jun Yamanouchi;Dan Rainbow;Pau Serra;Sarah Howlett

  • TRPV1+ sensory neurons control beta cell stress and islet inflammation in autoimmune diabetes.

    Rozita Razavi;Yin Chan;F. Nikoo Afifiyan;Xue Jun Liu

  • Three recessive loci required for insulin-dependent diabetes in nonobese diabetic mice.

    Michal Prochazka;Edward H. Leiter;David V. Serreze;Douglas L. Coleman

  • Major Histocompatibility Complex Class I-Deficient NOD-B2mnull Mice are Diabetes and Insulitis Resistant

    David V Serreze;Edward H Leiter;Gregory J Christianson;Dale Greiner

  • Defects in the differentiation and function of antigen presenting cells in NOD/Lt mice.

    D V Serreze;H R Gaskins;E H Leiter

  • Major histocompatibility complex class I-restricted T cells are required for all but the end stages of diabetes development in nonobese diabetic mice and use a prevalent T cell receptor α chain gene rearrangement

    Teresa P. DiLorenzo;Robert T. Graser;Toshiro Ono;Toshiro Ono;Gregory J. Christianson

  • Defective activation of T suppressor cell function in nonobese diabetic mice. Potential relation to cytokine deficiencies.

    D V Serreze;E H Leiter

  • Acceleration of type 1 diabetes by a coxsackievirus infection requires a preexisting critical mass of autoreactive T-cells in pancreatic islets.

    David V. Serreze;Eric W. Ottendorfer;Tamir M. Ellis;Charles J. Gauntt

  • Mouse models for the study of autoimmune type 1 diabetes: a NOD to similarities and differences to human disease.

    John P. Driver;David V. Serreze;Yi-Guang Chen

  • Immunostimulation circumvents diabetes in NOD/Lt mice.

    David V. Serreze;Kazuyuki Hamaguchi;Edward H. Leiter

  • Hematopoietic stem-cell defects underlying abnormal macrophage development and maturation in NOD/Lt mice: defective regulation of cytokine receptors and protein kinase C

    David V. Serreze;Jens W. Gaedeke;Edward H. Leiter

  • The preferential ability of B lymphocytes to act as diabetogenic APC in NOD mice depends on expression of self-antigen-specific immunoglobulin receptors.

    Pablo A. Silveira;Ellis Johnson;Harold D. Chapman;Thi Bui

  • Use of recombinant congenic and congenic strains of NOD mice to identify a new insulin-dependent diabetes resistance gene.

    D V Serreze;M Prochazka;P C Reifsnyder;M M Bridgett

  • Identification of a CD8 T Cell That Can Independently Mediate Autoimmune Diabetes Development in the Complete Absence of CD4 T Cell Helper Functions

    Robert T. Graser;Teresa P. DiLorenzo;Fuming Wang;Gregory J. Christianson

  • Th1 to Th2 Cytokine Shifts in Nonobese Diabetic Mice: Sometimes an Outcome, Rather Than the Cause, of Diabetes Resistance Elicited by Immunostimulation

    David V. Serreze;Harold D. Chapman;Cristina M. Post;Ellis A. Johnson

Frequent Co-Authors

Edward H. Leiter
Edward H. Leiter The Jackson Laboratory
Dale L. Greiner
Dale L. Greiner University of Massachusetts Chan Medical School
Mark A. Atkinson
Mark A. Atkinson University of Florida
Leonard D. Shultz
Leonard D. Shultz Jackson Laboratory
Derry C. Roopenian
Derry C. Roopenian The Jackson Laboratory
Laurence B. Peterson
Laurence B. Peterson Roche (Switzerland)
Aldo A. Rossini
Aldo A. Rossini University of Massachusetts Chan Medical School
Pere Santamaria
Pere Santamaria University of Calgary
Linda S. Wicker
Linda S. Wicker University of Oxford
John P. Mordes
John P. Mordes University of Massachusetts Chan Medical School

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