The immunological synapse.

Journal article

The adaptive immune response is initiated by the interaction of T cell antigen receptors with major histocompatibility complex molecule-peptide complexes in the nanometer scale gap between a T cell and an antigen-presenting cell, referred to as an immunological synapse. In this review we focus on the concept of immunological synapse formation as it relates to membrane structure, T cell polarity, signaling pathways, and the antigen-presenting cell. Membrane domains provide an organizational principle for compartmentalization within the immunological synapse. T cell polarization by chemokines increases T cell sensitivity to antigen. The current model is that signaling and formation of the immunological synapse are tightly interwoven in mature T cells. We also extend this model to natural killer cell activation, where the inhibitory NK synapse provides a striking example in which inhibition of signaling leaves the synapse in its nascent, inverted state. The APC may also play an active role in immunological synapse formation, particularly for activation of naïve T cells.

Authors: Bromley, S; Burack, W; Johnson, K; Somersalo, K; Sims, T

• Journal: Annual review of immunology
• Volume: 19
• Pages: 375-396
• Publication date: 2001-01-01
• DOI: 10.1146/annurev.immunol.19.1.375
• EISSN: 1545-3278
• ISSN: 0732-0582
• Language: English
• Keywords: Receptors, Immunologic; Cell Adhesion; Cell Membrane; T-Lymphocyte Subsets; Antigen Presentation; Immunologic Capping; Chemokines; Membrane Microdomains; Killer Cells, Natural; Cell Adhesion Molecules; Cell Polarity; Models, Immunological; Receptors, Antigen, T-Cell; Cell Communication; Cholera Toxin; Animals; Receptor-CD3 Complex, Antigen, T-Cell; Lymphocyte Activation; Signal Transduction; Receptors, Chemokine; Mice