| Literature DB >> 35813021 |
Farbod Bahreini1, Markus Niebuhr1, Julia Belde1, Katja Bieber2, Jürgen Westermann1, Kathrin Kalies1.
Abstract
Autoreactive T cells in autoantibody-mediated autoimmune diseases can be divided into two major subsets: (i) follicular T helper cells (Tfh) that provide T cell help in germinal centers (GC) and (ii) effector T (Teff) cells that immigrate into peripheral tissue sites such as the skin and mediate local inflammation. To study the sequence of events leading to the loss of tolerance in autoantibody-mediated autoimmune diseases it is required to investigate both T cell subsets simultaneously. This approach is hampered mainly because the appearance of skin inflammation in mouse models is a random process, which makes it difficult to define the location of inflammation at the right time point. To overcome this problem, we developed a scratching technique for ear skins that leads to the establishment of chronic autoimmune wounds in the mouse model for the pemphigoid-like disease epidermolysis bullosa acquisita. By defining the exact place where the skin wounds should form, this protocol enables a detailed analysis of skin-immigrating Teff cells. Of note, this protocol induces GC in draining lymph nodes in parallel so that Tfh cells in GC can be investigated concurrently. This protocol is not restricted to T cells and can be used for any other skin-immigrating inflammatory cells.Entities:
Keywords: Follicular T helper cells; Germinal centers; Mouse model; Skin immigrating T effector cells; Skin wounds
Year: 2022 PMID: 35813021 PMCID: PMC9183967 DOI: 10.21769/BioProtoc.4414
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325