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Abstract
Autoimmune bullous disease autoantibodies, particularly including bullous pemphigoid (BP)-related anti-BP180-NC16A IgG, have been reported in a small subset of healthy individuals, but information about associated factors is lacking. We hypothesized that an abnormal status of immunomodulatory vitamin D could play a role in anti-BP180-NC16A autoantibody reactivity in healthy persons. In addition, we aimed to evaluate the cytokine profile associated with these autoantibodies. Plasma samples from 34 anti-BP180-NC16A IgG-reactive and 85 anti-BP180-NC16A IgG-negative healthy blood donors were tested for levels of 25-hydroxyvitamin D [25(OH)D] and a wide range of cytokines (IL-2, IL-4, IL-5, IL-6, IL-9, IL-10, IL-13, IL-17A, IL-17F, IL-21, IL-22, IFN-γ, and TNF-α). We observed that anti-BP180-NC16A IgG-reactive healthy subjects had significantly lower plasma 25(OH)D levels and about a two-fold higher rate of vitamin D deficiency (< 20 ng/ml) compared to anti-BP180-NC16A IgG-negative healthy persons. In addition, anti-BP180-NC16A IgG-positive samples were characterized by significantly higher levels of IL-2, IL-5, IL-9, IL-10, and IL-13 which were, however, not significantly associated with the vitamin D levels. Our results indicate that healthy individuals with BP autoantibody reactivity share similarities with BP patients regarding the vitamin D status and cytokine profile (i.e., marked hypovitaminosis D and Th2 predominance), which may have pathophysiologic implications.
Originalsprache | Englisch |
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Zeitschrift | Archives of Dermatological Research |
Jahrgang | 315 |
Ausgabenummer | 10 |
Seiten (von - bis) | 2921-2926 |
Seitenumfang | 6 |
ISSN | 0340-3696 |
DOIs | |
Publikationsstatus | Veröffentlicht - 12.2023 |
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
- Zentren: Center for Research on Inflammation of the Skin (CRIS)
DFG-Fachsystematik
- 204-05 Immunologie
- 205-19 Dermatologie
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SFB 1526, PANTAU: Pathomechanismen Antikörpervermittelter Autoimmunerkrankungen
Sadik, C., Zillikens, D., Scheffold, A., Schmidt, E., Heine, G., Manz, R., Köhl, J., Ludwig, R., Peipp, M., Hammers, M. C., Verschoor, A., Karsten, C., Nimmerjahn, F., Hutloff, A., Ibrahim, S., Wettschureck, N., Bieber, K., Schilf, P., Vaeth, M., Hirose, M., Vaeth, M., Baines, J. F., Bacher, P., Hoffmann, M., Busch, H. S., Höppner, M., Becker, M., Holtsche, M. M., Fähnrich, A., Szymczak, S., Murthy, S. & Lux, A.
01.01.22 → …
Projekt: DFG-Projekte › DFG-Verbundforschung: Sonderforschungsbereiche/ Transregios