The Opposing Roles of the Transcription Factor E2A and its Antagonist Id3 that Orchestrate and Enforce the Naive Fate of T Cells Here researchers demonstrate that Id3 expression was higher beyond the precursor to the T cell antigen receptor checkpoint, remained high in naive T cells and showed a bimodal pattern in the effector-memory population. [Nat Immunol] CD8+ Cellular Immunity Mediates rAd5 Vaccine Protection Against Ebola Virus Infection of Nonhuman Primates The findings indicate that CD8+ cells have a major role in recombinant adenovirus virus serotype 5-glycoprotein–induced immune protection against Ebola virus infection in nonhuman primates. [Nat Med] Genome-Wide Analyses of Transcription Factor GATA3-Mediated Gene Regulation in Distinct T Cell Types To understand GATA3-mediated gene regulation, investigators identified genome-wide GATA3 binding sites in ten well-defined developmental and effector T lymphocyte lineages. [Immunity] CD8α+ Dendritic Cells Are the Critical Source of Interleukin-12 that Controls Acute Infection by Toxoplasma gondii Tachyzoites Researchers examined Toxoplasma gondii infection of Batf3-/- mice, which selectively lack only lymphoid-resident CD8α+ dendritic cells (DCs) and related peripheral CD103+ DCs. [Immunity] CD8α+ Dendritic Cells Are an Obligate Cellular Entry Point for Productive Infection by Listeria monocytogenes Although the loss of CD8α+ dendritic cells (DCs) in Batf3-/- mice increases their susceptibility to several pathogens, researchers observed that Batf3-/- mice exhibited enhanced resistance to the intracellular bacterium Listeria monocytogenes. [Immunity] Interleukin 37 Expression Protects Mice from Colitis In the present study, investigators examined a role for IL-37 during experimental colitis. [Proc Natl Acad Sci USA] Long-Term Persistence of a Polyclonal T Cell Repertoire After Gene Therapy for X-Linked Severe Combined Immunodeficiency Gene therapy for X-linked severe combined immunodeficiency without myelosuppressive conditioning effectively restored T cell immunity and was associated with high survival rates for up to 9 years. [Sci Transl Med] Hematopoietic Stem Cell Gene Therapy for Adenosine Deaminase–Deficient Severe Combined Immunodeficiency Leads to Long-Term Immunological Recovery and Metabolic Correction Gene therapy for adenosine deaminase severe combined immunodeficiency is safe, with effective immunological and metabolic correction, and may offer a viable alternative to conventional unrelated donor hematopoietic stem cell transplantation. [Sci Transl Med] |