Frontiers in Immunology

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The Chimeric Antigen Receptor Detection Toolkit
Frontiers in Immunology - Tập 11
Yifei Hu, Jun Huang
Eosinophils in Autoimmune Diseases
Frontiers in Immunology - Tập 8
Nicola L. Diny, Noel R. Rose, Daniela Čiháková
B Cell Subsets as Severity-Associated Signatures in COVID-19 Patients
Frontiers in Immunology - Tập 11
Víctor A. Sosa‐Hernández, Jiram Torres-Ruíz, Rodrigo Cervantes‐Díaz, Sandra Romero‐Ramírez, José C. Páez-Franco, David Eduardo Meza-Sánchez, Guillermo Juárez‐Vega, Alfredo Pérez‐Fragoso, Vianney Ortiz‐Navarrete, Alfredo Ponce‐de‐León, Luis Enrique Montiel Llorente, Laura Berrón-Ruíz, Nancy R. Mejía‐Domínguez, Diana Gómez‐Martín, José Luis Maravillas‐Montero
BackgroundSARS-CoV-2 infection represents a global health problem that has affected millions of people. The fine host immune response and its association with the disease course have not yet been fully elucidated. Consequently, we analyze circulating B cell subsets and their possible relationship with COVID-19 features and severity.MethodsUsing a multiparametric flow cytometric approach, we determined B cell subsets frequencies from 52 COVID-19 patients, grouped them by hierarchical cluster analysis, and correlated their values with clinical data.ResultsThe frequency of CD19+ B cells is increased in severe COVID-19 compared to mild cases. Specific subset frequencies such as transitional B cell subsets increase in mild/moderate cases but decrease with the severity of the disease. Memory B compartment decreased in severe and critical cases, and antibody-secreting cells are increased according to the severity of the disease. Other non-typical subsets such as double-negative B cells also showed significant changes according to disease severity. Globally, these differences allow us to identify severity-associated patient clusters with specific altered subsets. Finally, respiratory parameters, biomarkers of inflammation, and clinical scores exhibited correlations with some of these subpopulations.ConclusionsThe severity of COVID-19 is accompanied by changes in the B cell subpopulations, either immature or terminally differentiated. Furthermore, the existing relationship of B cell subset frequencies with clinical and laboratory parameters suggest that these lymphocytes could serve as potential biomarkers and even active participants in the adaptive antiviral response mounted against SARS-CoV-2.
Platelets in Viral Infections – Brave Soldiers or Trojan Horses
Frontiers in Immunology - Tập 13
Waltraud C. Schrottmaier, Anna Schmuckenschlager, Anita Pirabe, Alice Assinger
Viral infections are often associated with platelet activation and haemostatic complications. In line, low platelet counts represent a hallmark for poor prognosis in many infectious diseases. The underlying cause of platelet dysfunction in viral infections is multifaceted and complex. While some viruses directly interact with platelets and/or megakaryocytes to modulate their function, also immune and inflammatory responses directly and indirectly favour platelet activation. Platelet activation results in increased platelet consumption and degradation, which contributes to thrombocytopenia in these patients. The role of platelets is often bi-phasic. Initial platelet hyper-activation is followed by a state of platelet exhaustion and/or hypo-responsiveness, which together with low platelet counts promotes bleeding events. Thereby infectious diseases not only increase the thrombotic but also the bleeding risk or both, which represents a most dreaded clinical complication. Treatment options in these patients are limited and new therapeutic strategies are urgently needed to prevent adverse outcome. This review summarizes the current literature on platelet-virus interactions and their impact on viral pathologies and discusses potential intervention strategies. As pandemics and concomitant haemostatic dysregulations will remain a recurrent threat, understanding the role of platelets in viral infections represents a timely and pivotal challenge.
Extracellular Acidification Inhibits the ROS-Dependent Formation of Neutrophil Extracellular Traps
Frontiers in Immunology - Tập 8
Martina Behnen, Sonja Möller, Antonia Brozek, Matthias Klinger, Tamás Laskay
Intrinsic Expression of Immune Checkpoint Molecule TIGIT Could Help Tumor Growth in vivo by Suppressing the Function of NK and CD8+ T Cells
Frontiers in Immunology - Tập 9
Xiuman Zhou, Wanqiong Li, Yahong Wu, Lu Han, Xiaoqin Cao, Xuanming Yang, Hongfei Wang, Wenshan Zhao, Wenjie Zhai, Yuanming Qi, Yanfeng Gao
Mucosal-Associated Invariant T Cells Improve Nonalcoholic Fatty Liver Disease Through Regulating Macrophage Polarization
Frontiers in Immunology - Tập 9
Yanmei Li, Bingyuan Huang, Xiang Jiang, Weihua Chen, Jun Zhang, Yiran Wei, Yong Chen, Min Lian, Zhaolian Bian, Qi Miao, Yanshen Peng, Jing‐Yuan Fang, Qixia Wang, Ruqi Tang, M. Eric Gershwin, Xiong Ma
Gut Microbiota and the Paradox of Cancer Immunotherapy
Frontiers in Immunology - Tập 5
Theofilos Poutahidis, Markus Kleinewietfeld, Susan E. Erdman
Tổng số: 104   
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