PARSA LAB • BIOHUB RESEARCH INSTITUTE • NEW YORK CITY
Our mission is to decode how tissue-derived signals dictate the migration, fate, and function of immune cells across diverse disease states.
Our research is dedicated to unraveling the mechanisms underlying T cell tissue adaptation and residency. We aim to decode the tissue-derived signals that instruct T cell residency and to explore whether circulating cells carry genetic information reflecting the tissues they have interacted with throughout their lifespan. Our work provides crucial insights into how tissue-specific environments shape T cell responses, offering the potential for more targeted therapies for cancer and autoimmune conditions.
T cells are extremely heterogeneous and have an important role in orchestrating immune responses and eliminating pathogens and cancer cells. A core part of our research is to understand the various immune states of T cells and describe their functions with a focus on early disease states. This knowledge can reveal novel therapeutic targets, enabling precise modulation of T cell activity for improved treatment of diseases like cancer and autoimmunity.
Autoimmune diseases occur when T cells mistakenly target the body's own cells. Our goal is to identify these self-reactive T cells, understand their distribution and clonal characteristics, and investigate the reactivity of their T cell receptors (TCRs) towards self-proteins.
Published in Nature Immunology. This study introduces TRACK mice to reveal that distinct tissue environments drive organ-specific differentiation and clonal selection of CD4⁺ T cells during influenza infection, shaping both effector and memory T cell responses.
Published in Immunity. This study identifies a protective population of Ly6A+CCR9+CD4+ intraepithelial T cells that are recruited during enteric viral infection and control adenovirus through IFN-γ-dependent antiviral activity.
Published in Immunity. This review summarizes how the intestinal immune system mounts antiviral defenses against enteric viruses while maintaining tissue homeostasis, and discusses how these insights can guide the development of effective oral vaccines.
Published in Nature Immunology. This study shows that TGF-β signaling is essential for the functional integration of monocyte-derived macrophages into the CNS, as its loss drives inflammatory macrophage activation and fatal demyelinating disease.
Published in Glia. This study shows that TGF-β signaling in monocyte-derived dendritic cells is required to suppress chronic neuroinflammation and demyelination during EAE by limiting an IL-12–IFN-γ–ROS inflammatory loop linked to MS severity.
Published in Journal of Experimental Medicin. This study shows that emergency granulopoiesis enhances humoral immunity by promoting neutrophil recruitment to lymph nodes, where neutrophils accelerate plasma cell formation and antigen-specific antibody production.
Published in Diabetes. This study demonstrates that adoptive transfer of IL-4/IL-10/TGF-β–induced immunosuppressive macrophages protects against autoimmune type 1 diabetes by suppressing inflammation, inhibiting T cell responses, and promoting pancreatic β-cell survival.
A simple R app that allows you to summarize TCR output from IMGT HighV-Quest output data. Diversity index, Morisita-Horn overlap across samples, overlap across samples, and clonal counts. Unpaired TCR analysis, i.e. only alpha or beta chain.
We are located at the Biohub in New York City. We welcome inquiries about open positions and collaborative opportunities.