Different Proliferative Potential and Migratory Characteristics of Human CD4+ Regulatory T Cells That Express either CD45RA or CD45RO

• Published in: The Journal of immunology (1950) 2010-04, Vol.184 (8), p.4317-4326
• Main Authors: Booth, Nicola J, McQuaid, Arthur J, Sobande, Toni, Kissane, Steve, Agius, Elaine, Jackson, Sarah E, Salmon, Mike, Falciani, Francesco, Yong, Kwee, Rustin, Malcolm H, Akbar, Arne N, Vukmanovic-Stejic, Milica
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Cell Differentiation - immunology; Cell Movement - immunology; Cell Proliferation; Cells, Cultured; Forkhead Transcription Factors - biosynthesis; Humans; Immunophenotyping; Isoenzymes - biosynthesis; Isoenzymes - genetics; Leukocyte Common Antigens - biosynthesis; Leukocyte Common Antigens - genetics; Middle Aged; Organ Specificity - immunology; T-Lymphocytes, Regulatory - cytology; T-Lymphocytes, Regulatory - immunology; T-Lymphocytes, Regulatory - metabolism; Thymus Gland - cytology; Thymus Gland - enzymology; Thymus Gland - immunology; Young Adult
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.0903781

Although human naturally occurring regulatory T cells (Tregs) may express either CD45RA or CD45RO, we find in agreement with previous reports that the ( approximately 80%) majority of natural Tregs in adults are CD45RO(+). The proportion of CD45RA(+) Tregs decreases, whereas CD45RO(+) Tregs increase significantly with age. Nevertheless, a small proportion of CD45RA(+) Tregs are found even in old (>80 y) adults and a proportion of these express CD31, a marker for recent thymic emigrants. We found that CD45RO(+) Tregs were highly proliferative compared with their CD45RA(+) counterparts. This was due in part to the conversion of CD45RA Tregs to CD45RO expression after activation. Another difference between these two Treg populations was their preferential migration to different tissues in vivo. Whereas CD45RA(+) Tregs were preferentially located in the bone marrow, associated with increased CXCR4 expression, CD45RO(+) Tregs were preferentially located in the skin, and this was associated with their increased expression of CLA and CCR4. Our studies therefore show that proliferation features strongly in maintenance of the adult Treg pool in humans and that the thymus may make a minor contribution to the maintenance of the peripheral pool of these cells, even in older adults. Furthermore, the different tissue compartmentalization of these cells suggests that different Treg niches exist in vivo, which may have important roles for their maturation and function.