Results 81 to 90 of about 406 (129)

Herpes simplex virus type 1 impairs mucosal-associated invariant T cells

open access: yesmBio
Herpes simplex virus type 1 (HSV-1) is a highly successful pathogen that infects mucosal sites and adopts an arsenal of strategies to manipulate host immunity.
Lauren Stern   +11 more
doaj   +1 more source

The emerging relationship between mucosal-associated invariant T cell populations and the onset and progression of type 1 diabetes

open access: yesFrontiers in Immunology
Type 1 diabetes (T1D) is a chronic autoimmune disorder characterized by autoreactive CD8+ T cells that destroy insulin-producing pancreatic β-cells. CD8+ T cells are unlikely to be the only cells involved in diabetes.
Devin R. Fraser   +3 more
doaj   +1 more source

Regulation and heterogeneity of human mucosal-associated invariant T (MAIT) cells in blood and liver

open access: yes, 2020
Mucosal-associated invariant T (MAIT) cells are an abundant population of innate-like, effector memory T cells, that secrete proinflammatory cytokines and exhibit direct cytotoxic activity. Given their semi-invariant T cell receptor (TCR) and characteristic phenotype, MAIT cells appear as a homogeneous population.
openaire   +2 more sources

Circulating MAIT cells in multiple sclerosis and amyotrophic lateral sclerosis

open access: yesFrontiers in Immunology
Neurological disorders, including multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS), may be associated with alterations in blood cell composition and phenotype.
Davide De Federicis   +18 more
doaj   +1 more source

Diversity and hallmarks of metabolites surveyed by MR1

open access: yesImmunobiology
Mucosal-associated invariant T (MAIT) cells are one of the innate T cell subset. They are known to contribute to anti-bacterial response by recognizing bacterial components with invariant TCRs which are presented on a monomorphic antigen presenting ...
Emi Ito, Sho Yamasaki
doaj   +1 more source

Engineering CAR-Mucosal-Associated Invariant T (MAIT) cells for cancer therapy

open access: yes
The advent of chimeric antigen receptor (CAR) technology has revolutionized cancer immunotherapy by empowering T cells to recognize and eliminate tumour cells in a highly specific and efficient manner. In recent years, there has been a heightened interest in harnessing unconventional T cell subsets as potential candidates for CAR-based therapies ...
openaire   +2 more sources

Human neonatal MR1T cells have more diverse TCR repertoires but reduced bacterial recognition than adult MR1T cells

open access: yesNature Communications
Bacterial sepsis is a leading cause of neonatal mortality. Pro-inflammatory MR1-restricted T (MR1T) cells may help protect from sepsis by recognizing bacterial pathogens producing the canonical MR1 antigen 5-OP-RU.
Dylan Kain   +13 more
doaj   +1 more source

Implication of MAIT (Mucosal Associated Invariant T) cells in rheumatoid arthritis

open access: yes
Mucosal-associated invariant T (MAIT) cells are unconventional T lymphocytes capable of producing inflammatory cytokines and cytotoxic molecules. A decrease in their frequency and phenotypic alterations have been reported in several autoimmune diseases.
openaire   +1 more source

Human MAIT cells inhibit alloreactive T cell responses and protect against acute graft-versus-host disease

open access: yesJCI Insight
Adoptive transfer of immunoregulatory cells can prevent or ameliorate graft-versus-host disease (GVHD), which remains the main cause of nonrelapse mortality after allogeneic hematopoietic stem cell transplantation.
Nana Talvard-Balland   +12 more
doaj   +1 more source

Mucosal-Associated Invariant T (MAIT) Cells Are Highly Activated and Functionally Impaired in COVID-19 Patients [PDF]

open access: yesViruses, 2021
Coronavirus disease 2019 (COVID-19), caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), comprises mild courses of disease as well as progression to severe disease, characterised by lung and other organ failure.
Johanna Erber   +2 more
exaly   +6 more sources

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