scholarly article | Q13442814 |
P50 | author | Fiona Powrie | Q5451098 |
Paul Klenerman | Q7151812 | ||
Philip J. R. Goulder | Q72618990 | ||
Huldrych F Günthard | Q40505165 | ||
Joannah R Fergusson | Q55297936 | ||
Krista Adelmann | Q55297940 | ||
John Frater | Q58309767 | ||
James Ussher | Q63433856 | ||
P2093 | author name string | Peter Simmonds | |
Rodney E Phillips | |||
Ted H Hansen | |||
Ayako Kurioka | |||
Andri Rauch | |||
Brian Gazzard | |||
Kathleen Gärtner | |||
Julie Fox | |||
Nina Khanna | |||
Holm Uhlig | |||
Cormac Cosgrove | |||
Alan Steel | |||
Yu-Hoi Kang | |||
Michael H Hühn | |||
P2860 | cites work | CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract | Q22242965 |
Primary HIV-1 infection is associated with preferential depletion of CD4+ T lymphocytes from effector sites in the gastrointestinal tract | Q22242981 | ||
Microbial translocation is a cause of systemic immune activation in chronic HIV infection | Q22251054 | ||
The non-conventional MHC class I MR1 molecule controls infection by Klebsiella pneumoniae in mice | Q24321872 | ||
Analysis of CD161 expression on human CD8+ T cells defines a distinct functional subset with tissue-homing properties | Q27491282 | ||
Identification of CCR6, the specific receptor for a novel lymphocyte-directed CC chemokine LARC | Q28239561 | ||
Scoring diverse cellular morphologies in image-based screens with iterative feedback and machine learning | Q30485759 | ||
CD4+ T cells mediate abscess formation in intra-abdominal sepsis by an IL-17-dependent mechanism | Q30885696 | ||
Lack of mucosal immune reconstitution during prolonged treatment of acute and early HIV-1 infection | Q33265482 | ||
Stepwise development of MAIT cells in mouse and human | Q33417043 | ||
Human mucosal associated invariant T cells detect bacterially infected cells | Q33627502 | ||
Damaged intestinal epithelial integrity linked to microbial translocation in pathogenic simian immunodeficiency virus infections | Q33680743 | ||
Costimulation of naive CD8(+) lymphocytes induces CD4 expression and allows human immunodeficiency virus type 1 infection. | Q33785363 | ||
Consistent viral evolutionary changes associated with the progression of human immunodeficiency virus type 1 infection | Q33825654 | ||
Simian immunodeficiency virus-induced mucosal interleukin-17 deficiency promotes Salmonella dissemination from the gut. | Q33984007 | ||
Antimicrobial activity of mucosal-associated invariant T cells | Q34022899 | ||
Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity | Q34025875 | ||
Intestinal absorptive capacity, intestinal permeability and jejunal histology in HIV and their relation to diarrhoea | Q34408833 | ||
T-cell subsets that harbor human immunodeficiency virus (HIV) in vivo: implications for HIV pathogenesis | Q35543827 | ||
Colonic epithelial cells are a major site of macrophage inflammatory protein 3alpha (MIP-3alpha) production in normal colon and inflammatory bowel disease | Q35595246 | ||
Mechanisms of gastrointestinal CD4+ T-cell depletion during acute and early human immunodeficiency virus type 1 infection | Q35635026 | ||
Human MAIT and CD8αα cells develop from a pool of type-17 precommitted CD8+ T cells | Q35669203 | ||
CD8+ T cells and risk for bacterial pneumonia and all-cause mortality among HIV-infected women | Q35989605 | ||
IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis | Q36303708 | ||
Severe CD4+ T-cell depletion in gut lymphoid tissue during primary human immunodeficiency virus type 1 infection and substantial delay in restoration following highly active antiretroviral therapy | Q36541079 | ||
Correlates for disease progression and prognosis during concurrent HIV/TB infection | Q36796483 | ||
Early depletion of Mycobacterium tuberculosis-specific T helper 1 cell responses after HIV-1 infection | Q37115595 | ||
Plasma levels of bacterial DNA correlate with immune activation and the magnitude of immune restoration in persons with antiretroviral-treated HIV infection | Q37309633 | ||
IL-23-responsive innate lymphoid cells are increased in inflammatory bowel disease | Q38423061 | ||
Frequent infection of peripheral blood CD8-positive T-lymphocytes with HIV-1. Edinburgh Heterosexual Transmission Study Group | Q71472914 | ||
Trapping and apoptosis of novel subsets of memory T lymphocytes expressing CCR6 in the spleen of HIV-infected patients | Q79466226 | ||
IL-22 is increased in active Crohn's disease and promotes proinflammatory gene expression and intestinal epithelial cell migration | Q82829186 | ||
How soon after infection with HIV does the risk of tuberculosis start to increase? A retrospective cohort study in South African gold miners | Q38475969 | ||
Characterization of human immunodeficiency virus type 1 (HIV-1) diversity and tropism in 145 patients with primary HIV-1 infection | Q39398170 | ||
Decay kinetics of human immunodeficiency virus-specific effector cytotoxic T lymphocytes after combination antiretroviral therapy. | Q39549058 | ||
HIV-related oral disease | Q41111979 | ||
Infection of CD8+ T lymphocytes with HIV. Requirement for interaction with infected CD4+ cells and induction of infectious virus from chronically infected CD8+ cells | Q41690165 | ||
CD161-expressing human T cells. | Q42082102 | ||
A distinct subset of self-renewing human memory CD8+ T cells survives cytotoxic chemotherapy | Q42169041 | ||
CD161 expression on hepatitis C virus-specific CD8+ T cells suggests a distinct pathway of T cell differentiation | Q43047491 | ||
Non-cryptosporidial diarrhoea in human immunodeficiency virus (HIV) infected patients | Q43218956 | ||
Loss of IL-17-producing CD8 T cells during late chronic stage of pathogenic simian immunodeficiency virus infection | Q45370561 | ||
Productive infection of dendritic cells by simian immunodeficiency virus in macaque intestinal tissues. | Q45706697 | ||
Intestinal permeability and function in patients infected with human immunodeficiency virus. A comparison with coeliac disease | Q45776072 | ||
Requirement of interleukin-17A for systemic anti-Candida albicans host defense in mice | Q45876568 | ||
Effective CD4+ T-cell restoration in gut-associated lymphoid tissue of HIV-infected patients is associated with enhanced Th17 cells and polyfunctional HIV-specific T-cell responses | Q46137651 | ||
Impairment of the intestinal barrier is evident in untreated but absent in suppressively treated HIV-infected patients | Q46308412 | ||
Human MAIT cells are xenobiotic-resistant, tissue-targeted, CD161hi IL-17-secreting T cells. | Q51030308 | ||
Loss of mucosal CD4 lymphocytes is an early feature of HIV infection. | Q52062286 | ||
Abnormalities in subset distribution, activation, and differentiation of T cells isolated from large intestine biopsies in HIV infection. The Berlin Diarrhoea/Wasting Syndrome Study Group. | Q53018138 | ||
Quantitation of HIV-1-Specific Cytotoxic T Lymphocytes and Plasma Load of Viral RNA | Q56930699 | ||
IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge | Q58518610 | ||
Selection of evolutionarily conserved mucosal-associated invariant T cells by MR1 | Q59071944 | ||
CD161 is a marker of all human IL-17-producing T-cell subsets and is induced by RORC | Q60452043 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 951-961 | |
P577 | publication date | 2012-12-18 | |
P1433 | published in | Blood | Q885070 |
P1476 | title | Early and nonreversible decrease of CD161++ /MAIT cells in HIV infection | |
P478 | volume | 121 |
Q58699124 | A Low Frequency of IL-17-Producing CD8 T-Cells Is Associated With Persistent Immune Activation in People Living With HIV Despite HAART-Induced Viral Suppression |
Q58580465 | Abnormal T Cell Frequencies, Including Cytomegalovirus-Associated Expansions, Distinguish Seroconverted Subjects at Risk for Type 1 Diabetes |
Q37564579 | Acquisition of innate-like microbial reactivity in mucosal tissues during human fetal MAIT-cell development |
Q90084055 | Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients |
Q37697841 | Activation status of mucosal-associated invariant T cells reflects disease activity and pathology of systemic lupus erythematosus |
Q93186441 | Airway CD8+CD161++TCRvα7.2+ T Cell Depletion During Untreated HIV Infection Targets CD103 Expressing Cells |
Q92846258 | Alcohol Abstinence Does Not Fully Reverse Abnormalities of Mucosal-Associated Invariant T Cells in the Blood of Patients With Alcoholic Hepatitis |
Q35018923 | Altered CD161 bright CD8+ mucosal associated invariant T (MAIT)-like cell dynamics and increased differentiation states among juvenile type 1 diabetics |
Q60920287 | Altered composition and phenotype of mucosal-associated invariant T cells in early untreated rheumatoid arthritis |
Q40263239 | Anaerobic Bacterial Fermentation Products Increase Tuberculosis Risk in Antiretroviral-Drug-Treated HIV Patients. |
Q27680179 | Antigen-loaded MR1 tetramers define T cell receptor heterogeneity in mucosal-associated invariant T cells |
Q35752258 | Arming of MAIT Cell Cytolytic Antimicrobial Activity Is Induced by IL-7 and Defective in HIV-1 Infection |
Q90290433 | Association Between Impaired Vα7.2+CD161++CD8+ (MAIT) and Vα7.2+CD161-CD8+ T-Cell Populations and Gut Dysbiosis in Chronically HIV- and/or HCV-Infected Patients |
Q35494621 | Attrition of TCR Vα7.2+ CD161++ MAIT cells in HIV-tuberculosis co-infection is associated with elevated levels of PD-1 expression |
Q40059465 | CD161 Expression on Mucosa-Associated Invariant T Cells is Reduced in HIV-Infected Subjects Undergoing Antiretroviral Therapy Who Do Not Recover CD4+ T Cells |
Q34450282 | CD161+ MAIT cells are severely reduced in peripheral blood and lymph nodes of HIV-infected individuals independently of disease progression |
Q39098086 | CD161++ CD8+ T cells, including the MAIT cell subset, are specifically activated by IL-12+IL-18 in a TCR-independent manner |
Q92857870 | CD8+ T-Cell Response to HIV Infection in the Era of Antiretroviral Therapy |
Q37739063 | Challenge of Humans with Wild-type Salmonella enterica Serovar Typhi Elicits Changes in the Activation and Homing Characteristics of Mucosal-Associated Invariant T Cells |
Q91432435 | Characterization and Purification of Mouse Mucosal-Associated Invariant T (MAIT) Cells |
Q91432474 | Characterization of Human Mucosal-associated Invariant T (MAIT) Cells |
Q33630962 | Check MAIT. |
Q36536034 | Circulating and tumor-infiltrating mucosal associated invariant T (MAIT) cells in colorectal cancer patients |
Q34075150 | Circulating mucosal associated invariant T cells are activated in Vibrio cholerae O1 infection and associated with lipopolysaccharide antibody responses |
Q37689104 | Clinical relevance of circulating mucosal-associated invariant T cell levels and their anti-cancer activity in patients with mucosal-associated cancer |
Q27694492 | Complex adaptive immunity to enteric fevers in humans: lessons learned and the path forward |
Q52598286 | Contribution of APCs to mucosal-associated invariant T cell activation in infectious disease and cancer. |
Q38747458 | Controlled Human Malaria Infection Leads to Long-Lasting Changes in Innate and Innate-like Lymphocyte Populations. |
Q40163118 | Decrease of CD69 levels on TCR Vα7.2+CD4+ innate-like lymphocytes is associated with impaired cytotoxic functions in chronic hepatitis B virus-infected patients. |
Q50066272 | Development of Asthma in Inner-City Children: Possible Roles of MAIT Cells and Variation in the Home Environment |
Q59304306 | Development of mucosal-associated invariant T cells |
Q40053061 | Differentiating Immune Cell Targets in Gut-Associated Lymphoid Tissue for HIV Cure. |
Q37016414 | Distinct activation thresholds of human conventional and innate-like memory T cells |
Q92642986 | Dynamic MAIT cell response with progressively enhanced innateness during acute HIV-1 infection |
Q36448225 | Dynamic Perturbations of the T-Cell Receptor Repertoire in Chronic HIV Infection and following Antiretroviral Therapy |
Q26800118 | Early innate responses to pathogens: pattern recognition by unconventional human T-cells |
Q37227889 | Enhanced immune response of MAIT cells in tuberculous pleural effusions depends on cytokine signaling |
Q64912367 | Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells. |
Q36077824 | Frequencies of Circulating MAIT Cells Are Diminished in Chronic HCV, HIV and HCV/HIV Co-Infection and Do Not Recover during Therapy |
Q35815577 | Functional Heterogeneity and Antimycobacterial Effects of Mouse Mucosal-Associated Invariant T Cells Specific for Riboflavin Metabolites. |
Q89495082 | Functional MAIT Cells Are Associated With Reduced Simian-Human Immunodeficiency Virus Infection |
Q38852261 | Functional role of mucosal-associated invariant T cells in HIV infection. |
Q36132003 | Gut Mucosal Barrier Dysfunction, Microbial Dysbiosis, and Their Role in HIV-1 Disease Progression |
Q34662270 | HIV infection: epidemiology, pathogenesis, treatment, and prevention |
Q36112685 | HIV-Infected Children Have Lower Frequencies of CD8+ Mucosal-Associated Invariant T (MAIT) Cells that Correlate with Innate, Th17 and Th22 Cell Subsets |
Q38902093 | High expression of CD26 accurately identifies human bacteria-reactive MR1-restricted MAIT cells |
Q50045500 | Human blood MAIT cell subsets defined using MR1 tetramers. |
Q37247617 | Human mucosal-associated invariant T cells contribute to antiviral influenza immunity via IL-18-dependent activation |
Q52608541 | Hyper-Expression of PD-1 Is Associated with the Levels of Exhausted and Dysfunctional Phenotypes of Circulating CD161++TCR iVα7.2+ Mucosal-Associated Invariant T Cells in Chronic Hepatitis B Virus Infection. |
Q40866100 | IL-15 dependent induction of IL-18 secretion as a feedback mechanism controlling human MAIT-cell effector functions |
Q89948602 | IL-17 production by tissue-resident MAIT cells is locally induced in children with pneumonia |
Q37104112 | Immune recovery in HIV-infected patients after Candida esophagitis is impaired despite long-term antiretroviral therapy |
Q55078288 | Impact of Aging on the Frequency, Phenotype, and Function of CD161-Expressing T Cells. |
Q34399419 | Innate mucosal-associated invariant T (MAIT) cells are activated in inflammatory bowel diseases. |
Q52654737 | Innate-like CD8+ T-cells and NK cells: converging functions and phenotypes. |
Q28085321 | Innate-like lymphocytes in intestinal infections |
Q46314074 | Interactions between bile salts, gut microbiota, and hepatic innate immunity. |
Q40093638 | Intra-hepatic Depletion of Mucosal Associated Invariant T cells in Hepatitis C Virus-induced Liver Inflammation |
Q64116658 | Intracellular Pathogens: Host Immunity and Microbial Persistence Strategies |
Q55408012 | Latent Mycobacterium tuberculosis Infection Is Associated With a Higher Frequency of Mucosal-Associated Invariant T and Invariant Natural Killer T Cells. |
Q93047695 | Loss of Circulating CD8+ CD161high T Cells in Primary Progressive Multiple Sclerosis |
Q35082485 | Low levels of peripheral CD161++CD8+ mucosal associated invariant T (MAIT) cells are found in HIV and HIV/TB co-infection |
Q58588189 | Low mucosal-associated invariant T-cell number in peripheral blood of patients with immune thrombocytopenia and their response to prednisolone |
Q40593130 | MAIT be different-persisting dysfunction after DAA-mediated clearance of chronic hepatitis C virus infection |
Q48223629 | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A. |
Q47551345 | MAIT cells and Viruses |
Q38244066 | MAIT cells and pathogen defense |
Q35847725 | MAIT cells are activated and accumulated in the inflamed mucosa of ulcerative colitis |
Q27469032 | MAIT cells are activated during human viral infections |
Q47550378 | MAIT cells are activated in acute Dengue virus infection and after in vitro Zika virus infection |
Q37104082 | MAIT cells are critical for optimal mucosal immune responses during in vivo pulmonary bacterial infection |
Q41687115 | MAIT cells are depleted early but retain functional cytokine expression in HIV infection |
Q34890728 | MAIT cells are licensed through granzyme exchange to kill bacterially sensitized targets. |
Q36338406 | MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications |
Q58568564 | MAIT cells contribute to protection against lethal influenza infection in vivo |
Q58722526 | MAIT cells protect against pulmonary Legionella longbeachae infection |
Q28073095 | MAIT cells: new guardians of the liver |
Q26852490 | MR1-Restricted Mucosal-Associated Invariant T Cells and Their Activation during Infectious Diseases |
Q48137360 | Maximal exercise increases mucosal associated invariant T cell frequency and number in healthy young men. |
Q36153599 | Molecular Analyses Define Vα7.2-Jα33+ MAIT Cell Depletion in HIV Infection: A Case-Control Study |
Q36811942 | Mucosa-Associated Invariant T Cells Are Systemically Depleted in Simian Immunodeficiency Virus-Infected Rhesus Macaques |
Q45071749 | Mucosa-associated invariant T cells link intestinal immunity with antibacterial immune defects in alcoholic liver disease |
Q92058744 | Mucosal Immunity in HIV/SIV Infection: T Cells, B Cells and Beyond |
Q36014529 | Mucosal-Associated Invariant T (MAIT) Cells Are Impaired in Th17 Associated Primary and Secondary Immunodeficiencies |
Q40340158 | Mucosal-Associated Invariant T Cell Deficiency in Chronic Obstructive Pulmonary Disease |
Q49204780 | Mucosal-Associated Invariant T Cell Interactions with Commensal and Pathogenic Bacteria: Potential Role in Antimicrobial Immunity in the Child |
Q54963446 | Mucosal-Associated Invariant T Cells Are Depleted and Exhibit Altered Chemokine Receptor Expression and Elevated Granulocyte Macrophage-Colony Stimulating Factor Production During End-Stage Renal Disease. |
Q55301095 | Mucosal-Associated Invariant T Cells in Autoimmune Diseases. |
Q54268263 | Mucosal-Associated Invariant T Cells in Chronic Inflammatory Liver Disease. |
Q26781518 | Mucosal-Associated Invariant T Cells in Multiple Sclerosis: The Jury is Still Out |
Q47241753 | Mucosal-Associated Invariant T Cells in Regenerative Medicine |
Q96640817 | Mucosal-associated invariant T (MAIT) cells provide B-cell help in vaccinated and subsequently SIV-infected Rhesus Macaques |
Q35408930 | Mucosal-associated invariant T cell alterations in obese and type 2 diabetic patients |
Q35829274 | Mucosal-associated invariant T cell-rich congenic mouse strain allows functional evaluation. |
Q90514963 | Mucosal-associated invariant T cells and Vδ2+ γδ T cells in community acquired pneumonia: association of abundance in sputum with clinical severity and outcome |
Q91904779 | Mucosal-associated invariant T cells and disease |
Q38891491 | Mucosal-associated invariant T cells are numerically and functionally deficient in patients with mycobacterial infection and reflect disease activity |
Q26750384 | Mucosal-associated invariant T cells from induced pluripotent stem cells: A novel approach for modeling human diseases |
Q40100401 | Mucosal-associated invariant T-cell frequency and function in blood and liver of HCV mono- and HCV/HIV co-infected patients with advanced fibrosis. |
Q34305082 | Mucosal-associated invariant T-cells: new players in anti-bacterial immunity |
Q33887115 | Multiple layers of heterogeneity and subset diversity in human MAIT cell responses to distinct microorganisms and to innate cytokines. |
Q27007035 | Nonclassical T cells and their antigens in tuberculosis |
Q40703746 | Nonreversible MAIT cell-dysfunction in chronic hepatitis C virus infection despite successful interferon-free therapy |
Q54256962 | OMIP-046: Characterization of invariant T cell subset activation in humans. |
Q48232467 | Ontogeny of human mucosal-associated invariant T cells and related T cell subsets |
Q50131423 | Pathogenesis of HIV-1 and Mycobacterium tuberculosis co-infection |
Q38892515 | Peripheral loss of CD8(+) CD161(++) TCRVα7·2(+) mucosal-associated invariant T cells in chronic hepatitis C virus-infected patients |
Q35016866 | Persistent changes in circulating and intestinal γδ T cell subsets, invariant natural killer T cells and mucosal-associated invariant T cells in children and adults with coeliac disease. |
Q34851102 | Persistent immune activation in chronic HIV infection: do any interventions work? |
Q59352469 | Preexisting Simian Immunodeficiency Virus Infection Increases Susceptibility to Tuberculosis in Mauritian Cynomolgus Macaques |
Q54214704 | Proteomic definition of human mucosal-associated invariant T cells determines their unique molecular effector phenotype. |
Q27685209 | Recognition of vitamin B metabolites by mucosal-associated invariant T cells |
Q40970092 | Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease |
Q34309058 | Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis. |
Q26797333 | Regulation of Lipid Specific and Vitamin Specific Non-MHC Restricted T Cells by Antigen Presenting Cells and Their Therapeutic Potentials |
Q47589231 | Role of MAIT cells in the immunopathogenesis of inflammatory diseases: New players in old game. |
Q40044893 | Shared and Distinct Phenotypes and Functions of Human CD161++ Vα7.2+ T Cell Subsets. |
Q42250131 | Specific MAIT cell behaviour among innate-like T lymphocytes in critically ill patients with severe infections. |
Q93091820 | Successful direct-acting antiviral therapy in HIV/HCV co-infected patients fails to restore circulating mucosal-associated invariant T cells |
Q90017407 | Sustained IFN-I stimulation impairs MAIT cell responses to bacteria by inducing IL-10 during chronic HIV-1 infection |
Q89972703 | Swimming Against the Current: MAIT Cell Function Is Preserved in the Peritoneum of Advanced Liver Disease Patients |
Q26865650 | T cell recognition of non-peptidic antigens in infectious diseases |
Q37631857 | TLR signaling in human antigen-presenting cells regulates MR1-dependent activation of MAIT cells |
Q93159444 | The CD4-CD8- MAIT cell subpopulation is a functionally distinct subset developmentally related to the main CD8+ MAIT cell pool |
Q37345995 | The Impact of Sex Work Interruption on Blood-Derived T Cells in Sex Workers from Nairobi, Kenya |
Q58697988 | The Role of CD1d and MR1 Restricted T Cells in the Liver |
Q92579050 | The biology and functional importance of MAIT cells |
Q38280290 | The effect of HIV infection on the host response to bacterial sepsis |
Q33808773 | The loss of CCR6+ and CD161+ CD4+ T-cell homeostasis contributes to disease progression in SIV-infected rhesus macaques |
Q96135217 | The role of interleukin-17 in asthma: a protective response? |
Q38955495 | The role of mucosal-associated invariant T cells in infectious diseases |
Q58102795 | Tissue-resident MAIT cell populations in human oral mucosa exhibit an activated profile and produce IL-17 |
Q64100923 | Tumor-infiltrating mucosal-associated invariant T (MAIT) cells retain expression of cytotoxic effector molecules |
Q90989324 | Tuning of human MAIT cell activation by commensal bacteria species and MR1-dependent T-cell presentation |
Q26991896 | Universal immunity to influenza must outwit immune evasion |
Q90044629 | Virus-Mediated Suppression of the Antigen Presentation Molecule MR1 |
Q37732225 | Will loss of your MAITs weaken your HAART [corrected]? |