CD4 + Resident Memory T Cells Mediate Long-Term Local Skin Immune Memory of Contact Hypersensitivity in BALB/c Mice

• Published in: Frontiers in immunology Vol. 11; p. 775
• Main Authors: Murata, Akihiko, Hayashi, Shin-Ichi
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 19.05.2020
• Subjects: Adoptive Transfer; allergic contact dermatitis; Animals; CD4-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - immunology; contact hypersensitivity; Dermatitis, Allergic Contact - immunology; Dermatitis, Contact - immunology; Haptens - immunology; Haptens - pharmacology; helper T cells; Immunologic Memory - immunology; Immunology; Interferon-gamma - metabolism; killer T cells; local skin memory; Mice; Mice, Inbred BALB C; Mice, Nude; Mice, SCID; Mice, Transgenic; Skin - immunology; tissue-resident memory T cells; Tumor Necrosis Factor-alpha - metabolism; local skin memory; allergic contact dermatitis; contact hypersensitivity; tissue-resident memory T cells; helper T cells; killer T cells
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2020.00775

In allergic contact dermatitis (ACD) and contact hypersensitivity (CHS), the healed skin shows greater swelling than the naïve skin in the same individual upon re-exposure to the same hapten. This "local skin memory" (LSM) in healed skin was maintained for a prolonged period of time and mediated by skin CD8 -resident memory T (T ) cells in C57BL/6 mice. However, the number of CD4 T cells is elevated in ACD-healed human skin, and the contribution of CD4 T cells to the formation of LSM currently remains unclear. We herein demonstrated that immediately after CHS subsided, the healed skin in BALB/c mice showed an accumulation of hapten-specific CD4 and CD8 T cells, with a predominance of CD4 T cells. The presence of CD4 or CD8 T cells in the healed skin was sufficient for the induction of a flare-up reaction upon a re-challenge. The CD4 and CD8 T cells both produced interferon-γ and tumor necrosis factor early after the re-challenge. Moreover, while CD8 T cells gradually decreased over time and were eventually lost from the healed skin at 40-51 weeks after the resolution of CHS, the CD4 T cell numbers remained elevated during this period. The present results indicate that the long-term maintenance of LSM is mediated by CD4 T cells, and thus CD4 T cells are an important target for the treatment of recurrent human ACD.