Journal
NATURE
Volume 610, Issue 7933, Pages 752-+Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41586-022-05309-5
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Funding
- NCI Cancer Center Support Grant (CCSG) [P30 CA08748]
- Parker Institute for Cancer Immunotherapy
- Ludwig Center at Memorial Sloan Kettering, NCI Cancer Center Support Grant [P30 CA08748]
- NCI [U54 CA209975]
- NIAID [R01AI034206]
- Hilton-Ludwig Cancer Prevention Initiative (Conrad N. Hilton Foundation)
- MSTP grant from NIGMS of the NIH [T32GM007739]
- NIAID F30 Predoctoral Fellowship [F30AI154660-01]
- Barbara and Wilfried Mohr foundation
- French Ministry of Research
- Wellcome Trust Fellowship [WT201483/Z/16/Z]
- Parker Institute for Cancer Immunotherapy Senior Fellowship
- Hilton-Ludwig Cancer Prevention Initiative (Ludwig Cancer Research)
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This study identifies a class of antigen-presenting cells called Thetis cells that play a crucial role in peripheral T-reg cell differentiation. Thetis cells express AIRE and promote self-tolerance, while Thetis cells lacking AIRE expression are enriched for molecules required for pT(reg) generation. Loss of MHCII or ITGB8 in Thetis cells impairs intestinal pT(reg) differentiation and leads to colitis.
Establishing and maintaining tolerance to self-antigens or innocuous foreign antigens is vital for the preservation of organismal health. Within the thymus, medullary thymic epithelial cells (mTECs) expressing autoimmune regulator (AIRE) have a critical role in self-tolerance through deletion of autoreactive T cells and promotion of thymic regulatory T (T-reg) cell development(1-4). Within weeks of birth, a separate wave of T-reg cell differentiation occurs in the periphery upon exposure to antigens derived from the diet and commensal microbiota(5-8), yet the cell types responsible for the generation of peripheral T-reg (pT(reg)) cells have not been identified. Here we describe the identification of a class of ROR gamma t(+) antigen-presenting cells called Thetis cells, with transcriptional features of both mTECs and dendritic cells, comprising four major sub-groups (TC I-TC IV). We uncover a developmental wave of Thetis cells within intestinal lymph nodes during a critical window in early life, coinciding with the wave of pT(reg) cell differentiation. Whereas TC I and TC III expressed the signature mTEC nuclear factor AIRE, TC IV lacked AIRE expression and was enriched for molecules required for pT(reg) generation, including the TGF-beta-activating integrin alpha v beta 8. Loss of either major histocompatibility complex class II (MHCII) or ITGB8 by Thetis cells led to a profound impairment in intestinal pT(reg) differentiation, with ensuing colitis. By contrast, MHCII expression by ROR gamma t(+) group 3 innate lymphoid cells (ILC3) and classical dendritic cells was neither sufficient nor required for pT(reg) generation, further implicating TC IV as the tolerogenic ROR gamma t(+) antigen-presenting cell with an essential function in early life. Our studies reveal parallel pathways for the establishment of tolerance to self and foreign antigens in the thymus and periphery, respectively, marked by the involvement of shared cellular and transcriptional programmes.
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