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Mucosal-associated invariant T (MAIT) cells are semi-invariant Vα7.2 CD161CD4 T cells that recognize microbial riboflavin precursor derivatives such as 5-OP-RU presented by MR1. Human MAIT cells are abundant in adult blood, but there are very few in cord blood. We longitudinally studied Vα7.2 CD161 T cell and related subset levels in infancy and after cord blood transplantation. We show that Vα7.2 and Vα7.2 CD161 T cells are generated early during gestation and likely share a common prenatal developmental program. Among cord blood Vα7.2 CD161 T cells, the minority recognizing MR1:5-OP-RU display a TRAV/TRBV repertoire very similar to adult MAIT cells. Within a few weeks of life, only the MR1:5-OP-RU reactive Vα7.2 CD161 T cells acquire a memory phenotype. Only these cells expand to form the adult MAIT pool, diluting out other Vα7.2 CD161 and Vα7.2 CD161 populations, in a process requiring at least 6 years to reach adult levels. Thus, the high clonal size of adult MAIT cells is antigen-driven and likely due to the fine specificity of the TCRαβ chains recognizing MR1-restricted microbial antigens.
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http://dx.doi.org/10.1084/jem.20171739 | DOI Listing |
Front Immunol
September 2025
Department of Ophthalmology, The Second Hospital of Jilin University, Changchun, China.
Human C-type lectin-like molecule CD161 is a type II transmembrane protein expressed on the surface of various lymphocytes within both the innate and adaptive immune systems. CD161 serves as a marker for innate-like T cells and IL-17-producing cells. However, the meaning of these T cells expressing CD161 has not yet been fully determined.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Department of Hematology, Third Xiangya Hospital, Central South University, Changsha, Hunan Province, 410013, China.
Immune checkpoint inhibitors (ICIs) have transformed the treatment of many solid tumors. Still, their effectiveness in multiple myeloma (MM) remains underwhelming, highlighting the need to explore alternative approaches beyond conventional ICIs. Here, CD161 is identified as a novel inhibitory receptor on bone marrow (BM) tissue resident memory CD8 T cells (CD8 TRM), known for their sustained presence and vital role in local immune surveillance in MM BM tumor microenvironments.
View Article and Find Full Text PDFExp Neurol
August 2025
Laboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland.
Epilepsy frequently develops as a result of a brain insult, for example, brain injury or stroke. Currently, no tools are allowing us to predict which trauma patients will eventually develop epilepsy. There is evidence that microRNA levels are altered in the blood, making them attractive candidates for peripheral biomarkers of epilepsy.
View Article and Find Full Text PDFNat Commun
August 2025
Precision Research Center for Refractory Diseases, Shanghai Jiao Tong University Pioneer Research Institute for Molecular and Cell Therapies, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Interleukin (IL)-23 is the master pathogenic cytokine in psoriasis and neutralization of IL-23 alleviates psoriasis. Psoriasis relapses after the withdrawal of anti-IL-23 antibodies, and the persistence of IL-23-producing cells potentially contributes to such recurrence, but the cellular source of IL-23 is unclear. Here we show that IL4I1CD200CCR7 dendritic cells (CCR7 DC) are the main producer of IL-23 by concomitantly expressing the IL-23A and IL-12B subunits in human psoriatic skin.
View Article and Find Full Text PDFAm J Transplant
August 2025
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA; Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA; Immunology Graduate Program, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
T cell-mediated rejection (TCMR) affects ∼50% of pediatric liver transplant recipients within 5 years, and late TCMR is associated with graft failure due to ineffective treatment. Although CD8 T cells promote late TCMR, their clonal expansion, intragraft persistence, localization, and gene expression remain largely undefined. Here, single-cell RNA sequencing and immune repertoire profiling of 30 cryopreserved liver biopsies from rejecting and nonrejecting pediatric patients identified expanded intragraft CD8 T cell clonotypes (CD8) and their gene expression profiles.
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