Down syndrome, accelerated aging and immunosenescence
- Semin Immunopathol. 2020 Oct;42(5):635-645. doi: 10.1007/s00281-020-00804-1.
- 1. Department of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum, University of Bologna, 40138, Bologna, Italy. [email protected].
- 2. ImmunoConcEpT CNRS UMR 5164, University of Bordeaux, Bordeaux, France. [email protected].
- 3. Department of Internal Medicine and Clinical Immunology, CHU Bordeaux (Groupe Hospitalier Saint-André), 33076, Bordeaux, France. [email protected].
- 4. IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy.
- 5. Department of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum, University of Bologna, 40138, Bologna, Italy.
- 6. Laboratory of Systems Medicine of Healthy Aging and Department of Applied Mathematics, Lobachevsky University, Nizhny Novgorod, 603950, Russia.
- 7. Department of Laboratory Medicine, Clinical Chemistry, Karolinska Institutet, Karolinska University Hospital, 171 76, Stockholm, Sweden.
- 8. Applied Biomedical Research Center (CRBA), Policlinico S. Orsola-Malpighi Polyclinic, 40138, Bologna, Italy.
- 9. CNR Institute of Molecular Genetics "Luigi Luca Cavalli-Sforza," Unit of Bologna, 40136, Bologna, Italy.
Down syndrome is the most common chromosomal disorder, associated with moderate to severe intellectual disability. While life expectancy of Down syndrome population has greatly increased over the last decades, mortality rates are still high and subjects are facing prematurely a phenomenon of atypical and accelerated aging. The presence of an immune impairment in Down syndrome subjects is suggested for a long time by the existence of an increased incidence of infections, the incomplete efficacy of vaccinations, and a high prevalence of autoimmunity. Immunologic abnormalities have been described since many years in this population, both from a numerical and a functional points of view, and these abnormalities can mirror the ones observed during normal aging. In this review, we summarize our knowledge on immunologic disturbances commonly observed in subjects with Down syndrome, and in innate and adaptive immunity, as well as regarding chronic inflammation. We then discuss the role of accelerated aging in these observed abnormalities and finally review the potential age-associated molecular and cellular mechanisms involved.