Skip to Main Content

Ann Haberman, PhD

Associate Professor of Immunobiology; Director, In Vivo Imaging Facility; Director, Flow Cytometry Research Facility, Laboratory Medicine - Education

Contact Information

Ann Haberman, PhD

Lab Location

Office Location

Mailing Addresses

  • PO Box 208011

    300 Cedar Street

    New Haven, CT 06510-8011

    United States

  • 1 Gilbert St

    New Haven, CT 06519

    United States

Research Summary

I am interested in understanding the factors that influence the proliferation, migration and differentiation of germinal center B lymphocytes. A particular interest of mine is the behavior of activated B cells and their interaction with other cell types within the context of tissue architecture. I use a combination of histology, flow cytometry and intravital multiphoton microscopy to study the factors that regulate B cell subset activation and their movements in vivo. A related area of interest includes the cellular interactions of B cell lymphomas with other cell types within lymphoma microenvironments that may influence lymphoma resistance to therapeutic treatments.

Extensive Research Description

My research has focused on the cellular and molecular interactions regulating the form and function of an inducible lymphoid tissue structure called germinal centers. Germinal centers (GC) develop in the center of B cell follicles in spleen and lymph nodes about one week after initial immunization. GCs are sites of extreme metabolism, with very high proliferation and death rates, and evolve over time to form structures with phenotypically distinct zones. GC development requires intricate interactions of B cells with multiple other cell types to achieve both the affinity maturation of immunoglobulin and the generation of memory B cells that are key to long-term immune protection.

Several lymphoma subtypes derive from germinal centers, including diffuse large B cell lymphomas, follicular lymphomas and angioImmunoblastic T cell lymphomas. The regional composition of other cell types can vary tremendously and can include CD4+ T cell subsets, dendritic cells and activated macrophages. Defining the impact of interactions with other adjacent cell types will be an essential component of advances in this field. My current research aims to tease apart the role that each may play in the cascade of events regulating the pathological variants of germinal centers.


Research Interests

Antibody Formation; Immunity, Cellular; Lymphocyte Activation; Lymphoid Tissue; Lymphoma, Follicular; Lymphoma, B-Cell; Germinal Center; Dendritic Cells, Follicular; Immunological Synapses

Public Health Interests


Research Images

Selected Publications