World's Best Scientists 2026 revealed!

D-Index & Metrics

Immunology

D-Index
63
Citations
15270
World Ranking
3007
National Ranking
1410

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Immune system
  • Internal medicine

Li Wen spends much of his time researching Immunology, NOD mice, Internal medicine, Type 1 diabetes and Endocrinology. His study involves Immune system, Autoantibody, Insulitis, Autoimmunity and Gut flora, a branch of Immunology. His study with NOD mice involves better knowledge in Nod.

His Internal medicine research is multidisciplinary, incorporating perspectives in Autophagy and Aldose reductase. Li Wen works mostly in the field of Type 1 diabetes, limiting it down to topics relating to CD8 and, in certain cases, MHC class II, Cytokine and Molecular biology. His Endocrinology study incorporates themes from Thapsigargin, Acute pancreatitis, Store-operated calcium entry and Pancreatitis.

His most cited work include:

  • Innate immunity and intestinal microbiota in the development of Type 1 diabetes (1479 citations)
  • Identification of an MHC class I-restricted autoantigen in type 1 diabetes by screening an organ-specific cDNA library. (404 citations)
  • Treatment with CD20-specific antibody prevents and reverses autoimmune diabetes in mice (348 citations)

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

Li Wen mainly investigates Immunology, NOD mice, Internal medicine, Type 1 diabetes and Immune system. His research related to Autoimmunity, T cell, Antigen, Gut flora and Autoimmune disease might be considered part of Immunology. His Autoimmunity study combines topics in areas such as Autoantibody and B cell.

His NOD mice research is under the purview of Nod. As part of the same scientific family, he usually focuses on Internal medicine, concentrating on Endocrinology and intersecting with Mitochondrion. In Type 1 diabetes, Li Wen works on issues like Disease, which are connected to Pathogenesis.

He most often published in these fields:

  • Immunology (57.44%)
  • NOD mice (28.51%)
  • Internal medicine (23.55%)

What were the highlights of his more recent work (between 2018-2021)?

  • Acute pancreatitis (19.42%)
  • Pancreatitis (16.53%)
  • Cancer research (12.40%)

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

His primary areas of study are Acute pancreatitis, Pancreatitis, Cancer research, NOD mice and Pancreas. Li Wen combines subjects such as Tumor necrosis factor alpha, Calcineurin, Macrophage polarization, Pharmacology and ORAI1 with his study of Acute pancreatitis. His work on Acinar cell as part of general Pancreatitis research is frequently linked to Trypsinogen activation and Multiple species, bridging the gap between disciplines.

His Cancer research research incorporates elements of Genetically modified mouse, Gene knockdown, Regeneration and Pancreatic islets. The concepts of his NOD mice study are interwoven with issues in Cytotoxic T cell and Gut flora. His study focuses on the intersection of Nod and fields such as Innate immune system with connections in the field of Interleukin 10.

Between 2018 and 2021, his most popular works were:

  • The Orai Ca2+ channel inhibitor CM4620 targets both parenchymal and immune cells to reduce inflammation in experimental acute pancreatitis. (25 citations)
  • The Orai Ca2+ channel inhibitor CM4620 targets both parenchymal and immune cells to reduce inflammation in experimental acute pancreatitis. (25 citations)
  • Dendritic cells license regulatory B cells to produce IL-10 and mediate suppression of antigen-specific CD8 T cells. (16 citations)

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

  • Gene
  • Immune system
  • Internal medicine

Cancer research, NOD mice, Pancreatitis, Acinar cell and Pancreas are his primary areas of study. The study incorporates disciplines such as Cytotoxic T cell, Gut flora, Immune tolerance and CD20 in addition to NOD mice. Immunology covers Li Wen research in Gut flora.

His work deals with themes such as Insulin and Proinsulin, which intersect with Immunology. His studies deal with areas such as Downregulation and upregulation and Acute pancreatitis as well as Acinar cell. As a part of the same scientific family, Li Wen mostly works in the field of Nod, focusing on Immune system and, on occasion, Proinflammatory cytokine and Microbiome.

Best Publications

  • Innate immunity and intestinal microbiota in the development of Type 1 diabetes

    Li Wen;Ruth E. Ley;Ruth E. Ley;Pavel Yu. Volchkov;Peter B. Stranges

  • Identification of an MHC class I-restricted autoantigen in type 1 diabetes by screening an organ-specific cDNA library.

    F. Susan Wong;Jaana Karttunen;Caroline Dumont;Li Wen

  • CD8 T cell clones from young nonobese diabetic (NOD) islets can transfer rapid onset of diabetes in NOD mice in the absence of CD4 cells.

    F. S. Wong;I. Visintin;Li Wen;R. A. Flavell

  • Treatment with CD20-specific antibody prevents and reverses autoimmune diabetes in mice

    Chang-yun Hu;Daniel Rodriguez-Pinto;Wei Du;Anupama Ahuja

  • Factors Influencing the Gut Microbiota, Inflammation, and Type 2 Diabetes

    Li Wen;Andrew Duffy

  • T-cell alpha beta + and gamma delta + deficient mice display abnormal but distinct phenotypes toward a natural, widespread infection of the intestinal epithelium

    S J Roberts;A L Smith;A B West;L Wen

  • The importance of the Non Obese Diabetic (NOD) mouse model in autoimmune diabetes.

    James A. Pearson;F. Susan Wong;Li Wen

  • The role of gut microbiota in the development of type 1, type 2 diabetes mellitus and obesity

    Ningwen Tai;F. Susan Wong;Li Wen

  • Investigation of the role of B-cells in type 1 diabetes in the NOD mouse.

    F. Susan Wong;Li Wen;Michelle Tang;Murugappan Ramanathan

  • Inhibitors of ORAI1 Prevent Cytosolic Calcium-Associated Injury of Human Pancreatic Acinar Cells and Acute Pancreatitis in 3 Mouse Models.

    Li Wen;Svetlana Voronina;Muhammad A. Javed;Muhammad Awais

  • Murine lupus in the absence of alpha beta T cells.

    S. L. Peng;M. P. Madaio;D. P. M. Hughes;I. N. Crispe

  • Immunoglobulin synthesis and generalized autoimmunity in mice congenitally deficient in αβ(+) T cells

    L. Wen;S. J. Roberts;J. L. Viney;F. S. Wong

  • Long term effect of gut microbiota transfer on diabetes development.

    Jian Peng;Sukanya Narasimhan;Julian R. Marchesi;Andrew Benson

  • The gut microbiota and Type 1 Diabetes

    Elke Gülden;F. Susan Wong;Li Wen

  • Microbial antigen mimics activate diabetogenic CD8 T cells in NOD mice

    Ningwen Tai;Jian Peng;Fuqiang Liu;Fuqiang Liu;Elke Gulden

  • The Effect of Innate Immunity on Autoimmune Diabetes and the Expression of Toll-Like Receptors on Pancreatic Islets

    Li Wen;Jian Peng;Zhenjun Li;F. Susan Wong

  • Induction and acceleration of insulitis/diabetes in mice with a viral mimic (polyinosinic-polycytidylic acid) and an insulin self-peptide.

    Hiroaki Moriyama;Li Wen;Norio Abiru;Edwin Liu

  • Germinal center formation, immunoglobulin class switching, and autoantibody production driven by "non alpha/beta" T cells.

    L Wen;W Pao;F S Wong;Q Peng

  • In Vivo Evidence for the Contribution of Human Histocompatibility Leukocyte Antigen (Hla)-Dq Molecules to the Development of Diabetes

    Li Wen;F. Susan Wong;Jie Tang;Ning Yuan Chen

  • Glucose and collagen regulate human platelet activity through aldose reductase induction of thromboxane

    Wai Ho Tang;Jeremiah Stitham;Scott Gleim;Concetta Di Febbo

  • Role of Fas in Autoimmune Diabetes

    Conchi Mora;Li Wen;Ramon Gomis;E. Allison Green

Frequent Co-Authors

F. Susan Wong
F. Susan Wong Cardiff University
Robert Sutton
Robert Sutton University of Liverpool
Richard A. Flavell
Richard A. Flavell Yale University
Alexei V. Tepikin
Alexei V. Tepikin University of Liverpool
Muhammad Awais
Muhammad Awais University of Surrey
Bin Li
Bin Li Shanghai Jiao Tong University
Yun Ma
Yun Ma King's College London
Robert S. Sherwin
Robert S. Sherwin Yale University
Adrian Hayday
Adrian Hayday King's College London
Stephen J. Pandol
Stephen J. Pandol Cedars-Sinai Medical Center

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