Staphylococcus aureus Leukotoxin ED Targets the Chemokine Receptors CXCR1 and CXCR2 to Kill Leukocytes and Promote Infection The authors identified the chemokine receptors CXCR1 and CXCR2 as the targets of Staphylococcus aureus leukotoxin ED (LukED) on neutrophils. The LukE subunit binds neutrophils in a specific and saturable manner, and this interaction is inhibited by CXCL8, the high-affinity endogenous ligand of CXCR1 and CXCR2. [Cell Host Microbe] Abstract | Graphical Abstract | Press Release Perpetual Expression of PAMPs Necessary for Optimal Immune Control and Clearance of a Persistent Pathogen Using the protozoan parasite Trypanosoma cruzi, which is deficient in strong pathogen-associated molecular patterns (PAMPs), researchers demonstrated a requirement for the continuous expression of PAMPs for optimal anti-pathogen immunity. [Nat Commun] Abstract Cytomegalovirus-Seropositive Children Show Inhibition of In Vitro EBV Infection that Is Associated with CD8+CD57+ T Cell Enrichment and IFN-γ Scientists used mononuclear cells from cord blood and from 2- and 5-year-old EBV-naive children for in vitro EBV infection. They showed that the degree of EBV-induced B cell activation and expansion differs between age groups and in particular in relationship to IFN-γ production capacity. [J Immunol] Abstract Co-Expression of S. Typhi GroEL and IL-22 Gene Augments Immune Responses against Salmonella Infection The immunomodulatory effect of Interleukin 22 (IL-22) as an adjuvant was studied by DNA vaccination with S. Typhi Heat shock protein 60 (HSP60/GroEL) in mice. DNA construct of IL-22 gene fused with GroEL was developed and immunization studies were carried out in mice. [Immunol Cell Biol] Abstract HIV CD36-Specific Antibodies Block Release of HIV-1 from Infected Primary Macrophages and Its Transmission to T Cells The authors showed that upon HIV-1 infection of primary human macrophages, Gag is recruited to preexisting compartments containing the scavenger receptor CD36, which then become virus-containing compartments. Silencing of CD36 in HIV-1-infected macrophages decreases the amount of virions released. [J Exp Med] Abstract Recognition of Synthetic Glycopeptides by HIV-1 Broadly Neutralizing Antibodies and Their Unmutated Ancestors Researchers report that synthetic, homogeneously glycosylated peptides that bind avidly to variable loop 1/2 (V1V2) broadly neutralizing antibodies PG9 and CH01 bind minimally to strain-specific neutralizing V2 antibodies that are targeted to the same envelope polypeptide site. [Proc Natl Acad Sci USA] Abstract | Press Release Regulatory T Cells Prevent Liver Fibrosis during Human Immunodeficiency Virus Type 1 Infection in a Humanized Mouse Model Investigators report that regulatory T (Treg) cells prevent liver immunopathogenesis during HIV-1 infection using a humanized mouse model. In the absence of Treg cells, HIV-1 infection induced liver fibrosis associated with hepatic stellate cell activation, hepatitis and liver injury. [J Infect Dis] Abstract Both HLA-B*57 and Plasma HIV RNA Levels Contribute to the HIV-Specific CD8+ T Cell Response in HIV Controllers The authors performed an extensive study in 101 HIV controllers (HIC) to determine the impact of HLA-B*57 on the HIV-specific CD8+ response. HLA-B*57-restricted response displayed better qualitative features such as higher functional avidity, higher proliferation capacity, higher cytokine production than responses not restricted by HLA-B*57. [J Virol] Abstract Lower HIV Provirus Levels Are Associated with More APOBEC3G Protein in Blood Resting Memory CD4+ T Lymphocytes of Controllers In Vivo Provirus levels in resting memory cells that can serve as latent reservoirs of HIV in blood were compared between controllers and antiretroviral therapy-suppressed non-controllers. APOBEC3G, a cellular factor that blocks provirus formation at multiple steps if not antagonized by HIV virion infectivity factor, was also studied. [PLoS One] Full Article | Press Release |