HLA-E-restricted Hantaan virus-specific CD8+ T cell responses enhance the control of infection in hemorrhagic fever with renal syndrome
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Boquan Jin | R. Zhuang | K. Tang | Yusi Zhang | Chunmei Zhang | Ying Ma | Yun Zhang | Lihua Chen | Haifeng Hu | X. Jia | Xinyu Li
[1] T. Blicher,et al. Structure‐guided stabilization of pathogen‐derived peptide‐HLA‐E complexes using non‐natural amino acids conserves native TCR recognition , 2022, European journal of immunology.
[2] Weilu Zhang,et al. Spatiotemporal association of rapid urbanization and water-body distribution on hemorrhagic fever with renal syndrome: A case study in the city of Xi’an, China , 2022, PLoS neglected tropical diseases.
[3] B. Charreau,et al. Mapping and Characterization of HCMV-Specific Unconventional HLA-E-Restricted CD8 T Cell Populations and Associated NK and T Cell Responses Using HLA/Peptide Tetramers and Spectral Flow Cytometry , 2021, International journal of molecular sciences.
[4] Simona Baghai Sain,et al. Signature of long-lived memory CD8+ T cells in acute SARS-CoV-2 infection , 2021, Nature.
[5] Jun Yang,et al. The changing epidemiology of hemorrhagic fever with renal syndrome in Southeastern China during 1963–2020: A retrospective analysis of surveillance data , 2021, PLoS Neglected Tropical Diseases.
[6] O. Yang,et al. HLA-E-restricted HIV-1-specific CD8+ T cell responses in natural infection. , 2021, The Journal of clinical investigation.
[7] L. Picker,et al. HLA-E–restricted, Gag-specific CD8+ T cells can suppress HIV-1 infection, offering vaccine opportunities , 2021, Science Immunology.
[8] V. Lange,et al. HLA‐E diversity unfolded: Identification and characterization of 170 novel HLA‐E alleles , 2021, HLA.
[9] V. Lange,et al. HLA-E typing of more than 2.5 million potential hematopoietic stem cell donors: Methods and population-specific allele frequencies. , 2020, Human immunology.
[10] A. Kopitar,et al. Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection , 2020, Frontiers in Cellular and Infection Microbiology.
[11] P. Bi,et al. The impact of climate change on kidney health , 2020, Nature Reviews Nephrology.
[12] T. Ottenhoff,et al. Peptide Binding to HLA-E Molecules in Humans, Nonhuman Primates, and Mice Reveals Unique Binding Peptides but Remarkably Conserved Anchor Residues , 2020, The Journal of Immunology.
[13] L. Picker,et al. Modulation of MHC-E transport by viral decoy ligands is required for RhCMV/SIV vaccine efficacy , 2020, Science.
[14] Trushar R. Patel,et al. Biodefense Implications of New-World Hantaviruses , 2020, Frontiers in Bioengineering and Biotechnology.
[15] C. Szeto,et al. The unconventional role of HLA-E: The road less traveled. , 2020, Molecular immunology.
[16] Zi-yu Liu,et al. Vaccines and Therapeutics Against Hantaviruses , 2020, Frontiers in Microbiology.
[17] T. Ottenhoff,et al. Mobilizing unconventional T cells , 2019, Science.
[18] B. Joseph,et al. Hantavirus Inhibits TRAIL-Mediated Killing of Infected Cells by Downregulating Death Receptor 5. , 2019, Cell reports.
[19] S. Brackenridge,et al. HLA‐E: exploiting pathogen‐host interactions for vaccine development , 2019, Clinical and experimental immunology.
[20] S. Mallal,et al. Dengue-specific CD8+ T cell subsets display specialized transcriptomic and TCR profiles , 2019, The Journal of clinical investigation.
[21] L. Magder,et al. Age-Associated Heterogeneity of Ty21a-Induced T Cell Responses to HLA-E Restricted Salmonella Typhi Antigen Presentation , 2019, Front. Immunol..
[22] H. Ljunggren,et al. Innate and adaptive immune responses against human Puumala virus infection: immunopathogenesis and suggestions for novel treatment strategies for severe hantavirus‐associated syndromes , 2019, Journal of internal medicine.
[23] H. Ljunggren,et al. Orthohantaviruses belonging to three phylogroups all inhibit apoptosis in infected target cells , 2019, Scientific Reports.
[24] A. Cesbron-Gautier,et al. HCMV triggers frequent and persistent UL40-specific unconventional HLA-E-restricted CD8 T-cell responses with potential autologous and allogeneic peptide recognition , 2018, PLoS pathogens.
[25] F. Luciani,et al. Clonally diverse CD38+HLA-DR+CD8+ T cells persist during fatal H7N9 disease , 2018, Nature Communications.
[26] Fang-lin Zhang,et al. Novel Identified HLA-A*0201-Restricted Hantaan Virus Glycoprotein Cytotoxic T-Cell Epitopes Could Effectively Induce Protective Responses in HLA-A2.1/Kb Transgenic Mice May Associate with the Severity of Hemorrhagic Fever with Renal Syndrome , 2017, Front. Immunol..
[27] Yun Zhang,et al. Hantaan Virus Infection Induces Both Th1 and ThGranzyme B+ Cell Immune Responses That Associated with Viral Control and Clinical Outcome in Humans , 2015, PLoS pathogens.
[28] T. Ottenhoff,et al. Human CD8+ T-cells Recognizing Peptides from Mycobacterium tuberculosis (Mtb) Presented by HLA-E Have an Unorthodox Th2-like, Multifunctional, Mtb Inhibitory Phenotype and Represent a Novel Human T-cell Subset , 2015, PLoS pathogens.
[29] R. Lanford,et al. Hepatitis C virus clearance correlates with HLA‐DR expression on proliferating CD8+ T cells in immune‐primed chimpanzees , 2014, Hepatology.
[30] Yun Zhang,et al. Hantaan virus RNA load in patients having hemorrhagic fever with renal syndrome: correlation with disease severity. , 2013, The Journal of infectious diseases.
[31] Yun Zhang,et al. HLA-A2 and B35 Restricted Hantaan Virus Nucleoprotein CD8+ T-Cell Epitope-Specific Immune Response Correlates with Milder Disease in Hemorrhagic Fever with Renal Syndrome , 2013, PLoS neglected tropical diseases.
[32] M. Sztein,et al. Heterogeneity of Multifunctional IL-17A Producing S. Typhi-Specific CD8+ T Cells in Volunteers following Ty21a Typhoid Immunization , 2012, PloS one.
[33] D. Powell,et al. CD27 costimulation augments the survival and antitumor activity of redirected human T cells in vivo. , 2012, Blood.
[34] Boquan Jin,et al. Cellular immune response to Hantaan virus nucleocapsid protein in the acute phase of hemorrhagic fever with renal syndrome: correlation with disease severity. , 2009, The Journal of infectious diseases.
[35] F. Ennis,et al. Human CD8+ T Cell Memory Generation in Puumala Hantavirus Infection Occurs after the Acute Phase and Is Associated with Boosting of EBV-Specific CD8+ Memory T Cells1 , 2007, The Journal of Immunology.
[36] Antonio Lanzavecchia,et al. Central memory and effector memory T cell subsets: function, generation, and maintenance. , 2004, Annual review of immunology.
[37] J. Borst,et al. CD27 Promotes Survival of Activated T Cells and Complements CD28 in Generation and Establishment of the Effector T Cell Pool , 2003, The Journal of experimental medicine.
[38] F. Ennis,et al. Long-lived Memory T Lymphocyte Responses After Hantavirus Infection , 2002, The Journal of experimental medicine.
[39] T. Schumacher,et al. CD27 is required for generation and long-term maintenance of T cell immunity , 2000, Nature Immunology.