M MISRA LAB

Human pluripotent stem cells Developmental biology Transplant immunology

McGill University · RI-MUHC · Montréal

Understanding development.
Reimagining transplantation.

We study how human tissues form and how the immune system responds to them, to advance personalized care for people with kidney disease and diabetes.

Explore our research

Better models.
More personal medicine.

Transplantation can transform lives. Our goal is to help that promise go further.

Our research brings together developmental biology, immunology and stem cell bioengineering. By investigating human kidney and pancreas development alongside transplant rejection, we work toward diagnostics and cell therapies that could reduce the burden of lifelong immunosuppression.

Three questions.
One connected program.

01
Immunology

What drives
transplant rejection?

We use stem cell–derived organoids to dissect the molecular mechanisms of allorejection: the immune response against tissue from another individual.

Focus: human organoid models of rejection

02
Personalized medicine

Can we model rejection
for each patient?

We are developing a platform using patient-derived induced pluripotent stem cells to model allorejection in the context of an individual’s biology.

Focus: patient-specific iPSC models

03
Development & cell therapy

How do we build organs
from stem cells?

We investigate how human pluripotent stem cells acquire organ identities, with a focus on pancreas, kidney and thymic progenitors.

Applications: personalized models and cell therapy

Dr. Paraish Misra

Clinician-scientist
Kidney transplantation

Paraish Misra MDCM, PhD, FRCPC

Principal Investigator

Assistant Professor, Division of Nephrology
McGill University

Junior Scientist, RI-MUHC
Metabolic Disorders and Complications Program

Paraish is a nephrologist and clinician-scientist whose work connects stem cell biology with the challenges of kidney transplantation.

He completed his medical degree and internal medicine residency at McGill, followed by nephrology and solid organ transplantation fellowships at the University of Toronto. His doctoral research explored pancreatic islet development and interactions with the immune system.

During postdoctoral training at the McEwen Stem Cell Institute, he investigated reprogramming urinary cells into pluripotent stem cells and their potential for kidney tissue regeneration.

Our team

Rachel Shih

Lab Technician

Stem cells Flow cytometry Molecular biology

C.J. Froese

M.Sc. Student

McGill Graduate Excellence Award

Stem cells Flow cytometry Kidney development and differentiation

Robin Mackenzie White

Medical Undergraduate Research Student

McGill FHMS Summer Research Bursary Award

T cells Flow cytometry Allorejection HLA biology

Jacob Faulkner

M.Sc. Student

T cells Gene editing Endothelial differentiation Allorejection

Edward Wen

Ph.D. Student

Thymic epithelial cells Bioengineering Cell therapies Encapsulation

Sophie Braunstein

Undergraduate Honours Research Student

Thymic epithelial cells Functional maturation Reporter cell lines

Alumni

Felix Chan

Undergraduate Summer Student

Molecular biology Modified RNA

Adele Usmanov

Undergraduate Summer Student

Stem Cell Network Summer Studentship Award

Thymic epithelial cells 3D organoid culture

Carl Korban

Medical Undergraduate Research Student

McGill FHMS Summer Research Bursary Award

Intermediate mesoderm differentiation Neuroectoderm and retinal differentiation Wnt signaling

Nature Communications 2026

Guiding stem cells
toward better islets.

Work led by Paraish during his training at the University of Toronto identified signals that influence whether pancreatic progenitors become islet or enterochromaffin cells—helping improve control over stem cell–derived islet preparations.

Read the research story

Kidney360 2026

Understanding injury
in diabetic kidney disease.

By profiling gene expression in 50 diabetic kidney biopsies and 13 healthy control biopsies, Paraish and collaborators characterized molecular features of kidney injury and disease progression. Expression of genes related to intercalated cell identity was associated with slower progression, pointing to new questions about the biology of diabetic kidney disease.

Read the study

Science starts
with a conversation.

To discuss research collaborations, training opportunities or ways to support the lab, please contact Dr. Misra.

Find usResearch Institute of the
McGill University Health Centre · Glen Site
1001 Boulevard Décarie
Montréal, Québec H4A 3J1
Canada