<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Herrmann M</submitter><funding>Deutsches Zentrum fÃ¼r Infektionsforschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><pubmed_abstract>Coronavirus disease 2019 (COVID-19) which is caused by the novel SARS-CoV-2 virus is a severe flu-like illness which is associated with hyperinflammation and immune dysfunction. The virus induces a strong T and B cell response but little is known about the immune pathology of this viral infection. Acute &lt;i>Plasmodium falciparum&lt;/i> malaria also causes acute clinical illness and is characterized by hyperinflammation due to the strong production of pro-inflammatory cytokines and a massive activation of T cells. In malaria, T cells express a variety of co-inhibitory receptors which might be a consequence of their activation but also might limit their overwhelming function. Thus, T cells are implicated in protection as well as in pathology. The outcome of malaria is thought to be a consequence</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1870</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7479337</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analysis of Co-inhibitory Receptor Expression in COVID-19 Infection Compared to Acute &lt;i>Plasmodium falciparum&lt;/i> Malaria: LAG-3 and TIM-3 Correlate With T Cell Activation and Course of Disease.</pubmed_title><pmcid>PMC7479337</pmcid><pubmed_authors>Herrmann M</pubmed_authors><pubmed_authors>Woost R</pubmed_authors><pubmed_authors>Wildner NH</pubmed_authors><pubmed_authors>Jacobs T</pubmed_authors><pubmed_authors>Schulze Zur Wiesch J</pubmed_authors><pubmed_authors>Schulte S</pubmed_authors><pubmed_authors>Lohse AW</pubmed_authors><pubmed_authors>Wittner M</pubmed_authors><pubmed_authors>Ramharter M</pubmed_authors><pubmed_authors>Brehm TT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of Co-inhibitory Receptor Expression in COVID-19 Infection Compared to Acute &lt;i>Plasmodium falciparum&lt;/i> Malaria: LAG-3 and TIM-3 Correlate With T Cell Activation and Course of Disease.</name><description>Coronavirus disease 2019 (COVID-19) which is caused by the novel SARS-CoV-2 virus is a severe flu-like illness which is associated with hyperinflammation and immune dysfunction. The virus induces a strong T and B cell response but little is known about the immune pathology of this viral infection. Acute &lt;i>Plasmodium falciparum&lt;/i> malaria also causes acute clinical illness and is characterized by hyperinflammation due to the strong production of pro-inflammatory cytokines and a massive activation of T cells. In malaria, T cells express a variety of co-inhibitory receptors which might be a consequence of their activation but also might limit their overwhelming function. Thus, T cells are implicated in protection as well as in pathology. The outcome of malaria is thought to be a consequence</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-07-16T04:38:32.785Z</modification><creation>2026-07-09T10:36:35.616Z</creation></dates><accession>S-EPMC7479337</accession><cross_references><pubmed>32983106</pubmed><doi>10.3389/fimmu.2020.01870</doi></cross_references></HashMap>