Juan J. Lafaille
· ProfessorNew York University · Cell Biology
Active 1984–2026
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About
Juan J. Lafaille, PhD, is a professor in the Department of Cell Biology and the Department of Pathology at NYU Grossman School of Medicine. His research focuses on the molecular pathogenesis of autoimmune and allergic diseases, cancer, and immunology. His laboratory uses transgenic and knockout mice to study the molecular mechanisms responsible for the normal control of T-lymphocyte reactivity and the changes that occur when T-lymphocytes become either aggressive against self antigens or inappropriately reactive against environmental substances. Currently, his work includes examining the development of experimental autoimmune encephalomyelitis (EAE), an animal model for multiple sclerosis, in transgenic mice bearing anti-myelin basic protein (MBP) T-lymphocytes, and investigating factors controlling the synthesis of interleukins involved in asthma, such as IL-4 and IL-5, and the increased production of immunoglobulin E.
Research topics
- Biology
- Medicine
- Immunology
- Biochemistry
- Microbiology
- Internal medicine
- Endocrinology
- Cell biology
Selected publications
Regulatory T Cells License Macrophage Pro-Resolving Functions During Atherosclerosis Regression
Circulation Research · 2020 · 253 citations
RATIONALE: Regression of atherosclerosis is an important clinical goal; however, the pathways that mediate the resolution of atherosclerotic inflammation and reversal of plaques are poorly understood. Regulatory T cells (Tregs) have been shown to be atheroprotective, yet the numbers of these immunosuppressive cells decrease with disease progression, and whether they contribute to atherosclerosis regression is not known. OBJECTIVE: We investigated the roles of Tregs in the resolution of atheroscl…
Vasculature-associated fat macrophages readily adapt to inflammatory and metabolic challenges
The Journal of Experimental Medicine · 2019-03-12 · 152 citations
articleOpen accessSenior authorTissue-resident macrophages are the most abundant immune cell population in healthy adipose tissue. Adipose tissue macrophages (ATMs) change during metabolic stress and are thought to contribute to metabolic syndrome. Here, we studied ATM subpopulations in steady state and in response to nutritional and infectious challenges. We found that tissue-resident macrophages from healthy epididymal white adipose tissue (eWAT) tightly associate with blood vessels, displaying very high endocytic capacity.…
Immunometabolism · 2019-07-01 · 113 citations
articleOpen accessObesity can lead to type 2 diabetes and is an epidemic. A major contributor to its adverse effects is inflammation of the visceral adipose tissue (VAT). Life-long caloric restriction (CR), in contrast, results in extended lifespan, enhanced glucose tolerance/insulin sensitivity, and other favorable phenotypes. The effects of CR following obesity are incompletely established, but studies show multiple benefits. Many leukocyte types, macrophages predominantly, reside in VAT in homeostatic and path…
Niche-Selective Inhibition of Pathogenic Th17 Cells by Targeting Metabolic Redundancy
Cell · 2020 · 110 citations
Cell Metabolism · 2021 · 97 citations
Recent grants
NIH · $1.5M · 2006
NIH · $423k · 2011
NIH · $821k · 2011
Frequent coauthors
- 283 shared
Susumu Tonegawa
Massachusetts Institute of Technology
- 232 shared
Shigeyoshi Itohara
RIKEN Center for Brain Science
- 226 shared
Marc Bonneville
Institut Mérieux (France)
- 222 shared
Yohtaroh Takagaki
University of Washington
- 218 shared
Andrew G. Farr
University of Washington
- 215 shared
Peter Mombaerts
Max Planck Research Unit for Neurogenetics
- 202 shared
Ralph T. Kubo
University of Occupational and Environmental Health Japan
- 201 shared
Charles A. Janeway
St. John’s Health Sciences Centre
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