Judith Mandl

Academic title(s): 

Associate Member, Department of Microbiology and Immunology

Associate Professor, Department of Physiology

Judith Mandl
Contact Information
Address: 

Life Sciences Complex (Bellini Pavilion), Rm 364
3649 Promenade Sir William Osler
Montreal, QC H3G 0B1


jmandl.lab.mcgill.ca

Phone: 
514-398-3149
Email address: 
judith.mandl [at] mcgill.ca
Division: 
Associate Members
Branch: 
Immunology
Location: 
McGill Life Sciences Complex, Bellini Pavillion
Graduate supervision: 

ACCEPTING GRADUATE STUDENTS AND POST-DOCTORAL FELLOWS.

Please email your CV, letter of interest, and transcript. I will consider outstanding applications.

Biography: 

Bachelor of Science (Hons), University of Warwick, Coventry, United Kingdom. 1999 - 2002.

Field: Computational Biology

PhD, Emory University, Atlanta, United States. 2002 - 2008. Field: Population Biology, Ecology, and Evolution; Immunology.

Supervisor: Mark B. Feinberg, M.D., Ph.D.

Postdoctorate, NIAID, National Institutes of Health, Bethesda, United States. 2008 – 2014.

Field: Immunology, Systems Biology; Supervisor: Ronald N. Germain, M.D., Ph.D.

Awards, honours, and fellowships: 

Tier 2, Canada Research Chair in Immune Cell Dynamics (2021 - 2025)

Current research: 

T cells are a major effector arm of the adaptive immune system. We study two fascinating properties of T cells: they are highly motile cells able to migrate all around the body, and each T cell is subtly different. Both the continuous motion and the diversity of a T cell population are critical to mounting effective T cell responses. We investigate how T cells move through complex tissue, through what mechanisms T cell collectives avoid crowding issues, and how the interactions made during migration impact T cell heterogeneity. We take a systems approach to study T cell immunity at the organism level (responses to infection, homeostasis), at the tissue level (T cell trafficking, localization, adaptation to distinct tissue environments), at the cell level (migration, navigation strategies through tissue-imposed obstacles), and at the within cell level (cytoskeletal processes, gene expression and T cell receptor sequences), illustrated in Figure.

 

 

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