Cross-reactive influenza virus-specific CD8+ T cells contribute to lymphoproliferation in Epstein-Barr virus-associated infectious mononucleosis - Wikidata - wikimedia - TriplyDB

Cross-reactive influenza virus-specific CD8+ T cells contribute to lymphoproliferation in Epstein-Barr virus-associated infectious mononucleosis

Cross-reactive influenza virus-specific CD8+ T cells contribute to lymphoproliferation in Epstein-Barr virus-associated infectious mononucleosis

http://www.wikidata.org/entity/Q34147153

about

Immune modulation during latent herpesvirus infection Defining the directionality and quality of influenza virus-specific CD8+ T cell cross-reactivity in individuals infected with hepatitis C virus Infectious Mononucleosis The virome in host health and disease Human memory T cells: generation, compartmentalization and homeostasis Amino Acid Similarity Accounts for T Cell Cross-Reactivity and for “Holes” in the T Cell Repertoire Protective Efficacy of Cross-Reactive CD8+ T Cells Recognising Mutant Viral Epitopes Depends on Peptide-MHC-I Structural Interactions and T Cell Activation Threshold Disparate Epitopes Mediating Protective Heterologous Immunity to Unrelated Viruses Share Peptide-MHC Structural Features Recognized by Cross-Reactive T Cells Lack of heterologous cross-reactivity towards HLA-A*02:01 restricted viral epitopes is underpinned by distinct αβT cell receptor signatures Infectious mononucleosis.Quantitating T cell cross-reactivity for unrelated peptide antigens Structural allele-specific patterns adopted by epitopes in the MHC-I cleft and reconstruction of MHC:peptide complexes to cross-reactivity assessment PC61 (anti-CD25) treatment inhibits influenza A virus-expanded regulatory T cells and severe lung pathology during a subsequent heterologous lymphocytic choriomeningitis virus infection.Anti-IFN-γ and peptide-tolerization therapies inhibit acute lung injury induced by cross-reactive influenza A-specific memory T cells Estimating the diversity, completeness, and cross-reactivity of the T cell repertoire.Epstein-Barr virus but not cytomegalovirus is associated with reduced vaccine antibody responses in Gambian infants Temporal relationship between environmental influenza A and Epstein-Barr viral infections and high multiple sclerosis relapse occurrence.Youth-specific considerations in the development of preexposure prophylaxis, microbicide, and vaccine research trials.Heterologous immunity between viruses Analysis of HLA A*02 association with vaccine efficacy in the RV144 HIV-1 vaccine trial.Relationship between Poor Immunogenicity of HLA-A2-Restricted Peptide Epitopes and Paucity of Naïve CD8(+) T-Cell Precursors in HLA-A2-Transgenic Mice.Heterologous immunity: immunopathology, autoimmunity and protection during viral infections.Bi-specific MHC heterodimers for characterization of cross-reactive T cells Loss of anti-viral immunity by infection with a virus encoding a cross-reactive pathogenic epitope.The identification of HLA class II-restricted T cell epitopes to vaccinia virus membrane proteins.Characterization of cross-reactive CD8+ T-cell recognition of HLA-A2-restricted HIV-Gag (SLYNTVATL) and HCV-NS5b (ALYDVVSKL) epitopes in individuals infected with human immunodeficiency and hepatitis C viruses.Coordinated regulation of NK receptor expression in the maturing human immune system.Vaccination and heterologous immunity: educating the immune system Early virological and immunological events in asymptomatic Epstein-Barr virus infection in African children.Narrowing of human influenza A virus-specific T cell receptor α and β repertoires with increasing age.CD8 T cell cross-reactivity networks mediate heterologous immunity in human EBV and murine vaccinia virus infections.Altered effector functions of virus-specific and virus cross-reactive CD8+ T cells in mice immunized with related flaviviruses.Primary Epstein-Barr virus infection does not erode preexisting CD8⁺ T cell memory in humans.Analysis of the functional WT1-specific T-cell repertoire in healthy donors reveals a discrepancy between CD4(+) and CD8(+) memory formation.A Gene Expression Signature That Correlates with CD8+ T Cell Expansion in Acute EBV Infection Epstein-Barr virus Latent Membrane Protein 2A (LMP2A)-mediated changes in Fas expression and Fas-dependent apoptosis: Role of Lyn/Syk activation.H7N9 T-cell epitopes that mimic human sequences are less immunogenic and may induce Treg-mediated tolerance.Memory of mice and men: CD8+ T-cell cross-reactivity and heterologous immunity.Cross-reactivity of T cells and its role in the immune system Recent advances in the understanding of infectious mononucleosis: are prospects improved for treatment or control?

P2860

Q24624044-5C98527F-E7EA-4A79-B50F-50D7588D8D2C Q24645078-5F972124-357F-4805-A786-F290FE0F4BF7 Q26783692-BA1A3453-3627-42AD-B9A6-2E9BA4853DFE Q26824795-634E4F83-4E29-4EF4-A19C-9EC89C0F069E Q26851748-58194A94-3680-4129-9907-0FA867F10398 Q27485470-37FFB69B-D3F8-443E-820E-96399C082666 Q27664060-1A9C3F35-6597-4146-A517-E17B5AA741C7 Q27680365-DDF1BCD5-99B1-4A49-BFB5-B1913E734A23 Q27728085-0AF7E882-6B3C-4412-BB1C-15DD6365B3A6 Q28084340-7B9736FD-E0BC-4BD8-9C80-3B57C8BE8EC8 Q28750512-4F61B71A-4E92-4E48-AF08-FD9D46DC4A54 Q28752409-514D7A69-9D42-4FC5-B58E-2CF304C89CA6 Q30353758-68AB236B-AB17-4C31-9FFE-58BC07D38E1C Q30427198-F307767F-3700-440B-85E8-99080B127878 Q33357547-65FA2237-1E8E-440D-B28E-18364E76265D Q33754553-87CB3BCA-856D-4E2F-8F9E-3B27BBB625E3 Q33787783-2ABE66B3-9330-4635-B3FF-0DA6EC1ABCAB Q34030735-DB419021-7623-4D39-98FE-163A9FDBD65D Q34051846-EC9A2A28-29EB-4B54-965F-A7A64BA4B5F9 Q34057942-1F4D01B4-7D59-4FC8-9234-8F1BE5A9DD3B Q34105729-1FCD6D99-4CF9-4BC2-AA45-FA55E772D058 Q34159981-0FF24509-ED4D-4968-96A8-6F4EC3C75030 Q34236896-22AE6132-FB7A-4D39-B957-7BFFA5F29165 Q34246886-7D233A6E-699D-4EB7-9041-97F8ACF9F919 Q34288498-784B7F26-B68C-46C5-BACF-457767D5C375 Q34457915-1626C8CC-B1C5-496C-B6F6-C4EA6AA3407B Q34476273-5E5C2912-F350-4EBF-9C54-B51F3B9EAA1E Q35152750-65317294-E74B-4F29-B5AD-0138ED808AD7 Q35223805-965BA668-C4A9-4442-A0FA-A6C04A0098C7 Q35640962-C16B6FC5-94A6-41EB-A1F0-39381AF307A6 Q35660783-1AA38FA2-4AAB-490F-B6C4-03F7B382393D Q35800948-E92545C6-9C73-479E-B891-DCAAB7C1EE79 Q35826013-D42271C5-1C1D-4CF2-BDDC-01746F0DDFE9 Q35889240-2EDF4929-F2A6-41D6-AF7F-56D56347062F Q36176987-6F9E8B9F-4EE5-4F32-8F94-7E1DC3BAF579 Q36199894-7E17C69E-2207-44CE-9677-637FFDE33224 Q36255850-45E189EB-1BC0-403E-BB22-AFF871BE1AD6 Q36528984-67E1F9AF-1DE2-4C1C-8232-665F053E18D9 Q36678774-417A9BF3-312D-4985-A91F-772DDDCE79DC Q36688962-9E973461-8F91-463C-B153-754FFB4BB82E

P2860

Cross-reactive influenza virus-specific CD8+ T cells contribute to lymphoproliferation in Epstein-Barr virus-associated infectious mononucleosis

http://www.wikidata.org/entity/Q34147153

description

2005 nî lūn-bûn

@nan

2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Cross-reactive influenza virus ...... iated infectious mononucleosis

@ast

Cross-reactive influenza virus ...... iated infectious mononucleosis

@en

Cross-reactive influenza virus ...... iated infectious mononucleosis

@nl

type

label

Cross-reactive influenza virus ...... iated infectious mononucleosis

@ast

Cross-reactive influenza virus ...... iated infectious mononucleosis

@en

Cross-reactive influenza virus ...... iated infectious mononucleosis

@nl

prefLabel

Cross-reactive influenza virus ...... iated infectious mononucleosis

@ast

Cross-reactive influenza virus ...... iated infectious mononucleosis

@en

Cross-reactive influenza virus ...... iated infectious mononucleosis

@nl

P1433

Q34147153-F8AC5C1B-07E5-429C-BDF5-CBBA67A57093

P1476

Q34147153-4FA0191B-5FDE-4D11-8CC6-CE790AE1D872

P2093

Q34147153-00D9132B-045D-4AD2-A740-E6568AE72B31

Q34147153-0254EE86-F7AD-4E8B-B48B-FC114B35FD1A

Q34147153-1DDACF6C-D553-43D2-8772-D549EF2F7BD1

Q34147153-3ACD7A5B-D311-4FCF-8DD3-75093064A7F6

Q34147153-4B8B46D2-1D40-4F30-9FE2-9B96D657535C

Q34147153-53CDC812-A609-4B05-90EF-47736EE5179F

Q34147153-7CE02B66-294C-42FF-83AE-41D6E97A7E11

Q34147153-D7C2C544-2702-4B5F-AF49-60C26D04BC4E

P2860

Q34147153-06405D97-DF58-4FEE-868E-A8328989160A

Q34147153-1282E63E-B789-492A-AD71-784730BF034D

Q34147153-12CA98DD-AE71-4167-9BE2-9398E1C9AE71

Q34147153-14009CD9-2095-4478-9322-1AD62079B59A

Q34147153-1DE7EA30-CD2D-43C1-BE7F-EDA5386B4545

Q34147153-25CDD96D-8C06-4C81-9B89-0BDED90BE26C

Q34147153-38680FDD-D5FE-4D10-ACA0-211DA4BE6EEF

Q34147153-3E875EFD-1DB6-41F7-9B91-5E72CED177DB

Q34147153-4A9BCC97-83C7-427E-ADEA-AC6255A2EE11

Q34147153-4D23F2E0-D7E0-472E-BC56-3FE23D796025

P304

Q34147153-65523D67-7355-4646-840D-30C1A8135858

P31

Q34147153-89600A94-D75F-4285-9B10-FFCA97F848F6

P356

Q34147153-D3C94B57-74AF-4468-B8F3-5DFA2CC6033F

P407

Q34147153-2D10023A-B6EB-4C6F-8192-796ED38C8FF5

P433

Q34147153-B4DC6AE3-9707-49E3-91C1-B0F85E01C2A2

P478

Q34147153-0FAD8B85-E193-4179-8959-5EFA79DAAD96

P577

Q34147153-0A8208C0-2BBD-4159-8E53-969530ADF39E

P698

Q34147153-EAC06F8F-48B8-4295-A429-A0034EABAC71

P921

Q34147153-A158B76C-7F96-459A-915C-CCBAAE6F13DF

P932

Q34147153-BF415BA8-D9CA-44D2-BDFD-4B30FCF7E7D4

P356

P1433

Journal of Clinical Investigation

P1476

Cross-reactive influenza virus ...... iated infectious mononucleosis

@en

P2093

John L Sullivan

http://www.w3.org/2001/XMLSchema#string

Katherine Luzuriaga

http://www.w3.org/2001/XMLSchema#string

Levi B Watkin

http://www.w3.org/2001/XMLSchema#string

Liisa K Selin

http://www.w3.org/2001/XMLSchema#string

Markus Cornberg

http://www.w3.org/2001/XMLSchema#string

Raymond M Welsh

http://www.w3.org/2001/XMLSchema#string

Shalyn C Clute

http://www.w3.org/2001/XMLSchema#string

Yuri N Naumov

http://www.w3.org/2001/XMLSchema#string

P2860

Cross-reactivity between hepatitis C virus and Influenza A virus determinant-specific cytotoxic T cells.

Heterologous T cell immunity in severe hepatitis C virus infection

The use of HLA-A*0201-transfected K562 as standard antigen-presenting cells for CD8(+) T lymphocytes in IFN-gamma ELISPOT assays

Epstein-Barr virus: 40 years on

Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever

Immediate early and early lytic cycle proteins are frequent targets of the Epstein-Barr virus-induced cytotoxic T cell response

Immunopathogenesis of Dengue hemorrhagic fever.

Functional heterogeneity and high frequencies of cytomegalovirus-specific CD8(+) T lymphocytes in healthy seropositive donors.

Acyclovir for treatment of infectious mononucleosis: a meta-analysis.

Human peripheral blood T cells, monocytes, and macrophages secrete macrophage inflammatory proteins 1alpha and 1beta following stimulation with heat-inactivated Brucella abortus.

P304

3602-3612

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1172/JCI25078

http://www.w3.org/2001/XMLSchema#string

P407

P433

12

http://www.w3.org/2001/XMLSchema#string

P478

115

http://www.w3.org/2001/XMLSchema#string

P577

2005-11-23T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

16308574

http://www.w3.org/2001/XMLSchema#string

P921

Epstein–Barr virus

P932

1288832

http://www.w3.org/2001/XMLSchema#string