Trends Among U.S. High School Seniors in Recent Marijuana Use and Associations With Other Substances: 1976–2013

To describe historical trends in rates of recent substance use, and associations between marijuana and other substances, among United States high school seniors by race and gender

Brainstem morphometric differences in children with autism spectrum disorder, developmental coordination disorder, and those typically developing

Background: The brainstem is a neglected topic in autism research, despite major lines of evidence indicating its active involvement in sensory, motor, affect, arousal, and social regulation (Dadalko & Travers, 2018). It is the substrate of what affective neuroscience identifies as the ‘Core Self’ (Alcaro, Carta, & Panksepp, 2017), and disruption to its growth and function appears to disturb core conscious experience in autism (Delafield-Butt & Trevarthen, 2017; Trevarthen & Delafield-Butt, 2013). Yet, although evidence indicates brainstem growth is disrupted in early childhood (Bosco et al., 2018), how these growth differences compare to closely related neurodevelopmental disorders, such a Developmental Coordination Disorder (DCD), is not yet understood. Objectives: To determine brainstem morphometric differences between children with ASD, DCD, and those typically developing (TD). Methods: Study participants were 87 youths ages 8 to 17 assigned to the ASD (n = 30, 7 female), DCD (n =24, 12 female) or TD (n = 33, 12 female) group. Exclusion criteria for all groups included IQ <80. TD were excluded if they had any neuropsychological or psychopathological disorder. DCD eligibility additionally included performance 16th percentile on the MABC-2 and no concern about an ASD diagnosis. ASD participants had a previous clinical diagnosis confirmed by ADOS-2 and ADI-R. Individuals were excluded if they had another neuropsychological disorder, except attention deficit or anxiety disorder. T1-weighted MPRAGE (1mm isotropic resolution) MRI data were acquired on a 3T MAGNETOM Prisma (Siemens). Brainstem morphology was analysed using SPHARM-MAT (http://lishenlab.com/spharm/), a 3D Fourier surface representation method¬¬¬. A typical surface was calculated for the TD group, and distances from this norm computed for each vertex. Mean distances at each vertex were computed for each group (ASD, DCD, TD) and compared, taking into account age, gender and supratentorial volume as covariates. Results: Significant brainstem morphological differences were identified between all three (TD, ASD and DCD; Figure 1). Significant differences between TD and ASD (p<0.01) were identified in a large region of the anterior-most surface, extending caudally along the right posterior surface. Differences between TD and DCD groups were similar with reduced significance (p0.01), and the pattern diverged with more inclusion of the anterior ventricular surface and less pronouncement at the right anterior border. Finally, significant differences were found between ASD and DCD groups (p<0.01), specifically at the anterior midline either side of the ventricular surface, and especially in two long anteroposterior columns on the left side adjacent and parallel to the fourth ventricle. Conclusions: Surface morphology differences indicate alterations in local nuclei and/or tract growth within the brainstem, especially approaching the anterior surface in ASD and DCD children, and differentially between them at the ventricular surface. The former may relate to specific nerve growth of the pons, and the latter to cerebellar peduncle connectivity differences, superficial nuclei growth such as the hypoglossal, intercalatus, or vagus and associated tracts, or deeper nuclei such as the inferior olivary nucleus. Brainstem structural differences likely disturbs the integrative function of the Core Self. Higher resolution 7T MRI is required to resolve the underlying differential composition

Cytokine Induced Killer cells are effective against sarcoma cancer stem cells spared by chemotherapy and target therapy

Metastatic bone and soft tissue sarcomas often relapse after chemotherapy (CHT) and molecular targeted therapy (mTT), maintaining a severe prognosis. A subset of sarcoma cancer stem cells (sCSC) is hypothesized to resist conventional drugs and sustain disease relapses. We investigated the immunotherapy activity of cytokine induced killer cells (CIK) against autologous sCSC that survived CHT and mTT. The experimental platform included two aggressive bone and soft tissue sarcoma models: osteosarcoma (OS) and undifferentiated-pleomorphic sarcoma (UPS). To visualize putative sCSC we engineered patient-derived sarcoma cultures (2 OS and 3 UPS) with a lentiviral sCSC-detector wherein the promoter of stem-gene Oct4 controls the expression of eGFP. We visualized a fraction of sCSC (mean 24.2 +/- 5.2%) and confirmed their tumorigenicity in vivo. sCSC resulted relatively resistant to both CHT and mTT in vitro. Therapeutic doses of doxorubicin significantly enriched viable eGFP(+)sCSC in both OS (2.6 fold, n = 16) and UPS (2.3 fold, n = 29) compared to untreated controls. Treatment with sorafenib (for OS) and pazopanib (for UPS) also determined enrichment (1.3 fold) of viable eGFP(+)sCSC, even if less intense than what observed after CHT. Sarcoma cells surviving CHT and mTT were efficiently killed in vitro by autologous CIK even at minimal effector/target ratios (40:1 = 82%, 1:4 = 29%, n = 13). CIK immunotherapy did not spare sCSC that were killed as efficiently as whole sarcoma cell population. The relative chemo-resistance of sCSC and sensitivity to CIK immunotherapy was confirmed in vivo. Our findings support CIK as an innovative, clinically explorable, approach to eradicate chemo-resistant sCSC implicated in tumor relapse

Detection of influenza A(H1N1)pdm09 virus in a patient travelling from Shanghai to Italy in July 2018: an uncommon clinical presentation in a non-seasonal period

Influenza is one of the most common infectious diseases in travellers, especially in those returning from subtropical and tropical regions.In late June 2018 an influenza A(H1N1)pdm09 virus infection was diagnosed in a 36-years-old man, returned from a travel in Shanghai and hospitalized at the Ospedale Policlinico San Martino, Genoa, Italy, with a diagnosis of fever and an uncommon clinical presentation characterised by a persistent leukopenia. Phylogenetic analysis revealed a closeness with influenza A(H1N1)pdm09 strains circulating in the US in May-June 2018.Prompt recognition of influenza infection led to a proper case management, demonstrating the crucial role of the continuous influenza surveillance programme

Long-Term Thymic Function and Reconstitution of the T Cell Compartment after T Cell-Replete Haplo-Identical Allografting

INTRODUCTION Post-transplant cyclophosphamide (PTCY) has expanded the application of haploidentical stem cell transplantation (haplo-HSCT). Thymic function may play a pivotal role in long-term clinical outcomes. OBJECTIVES To evaluate the kinetics of long-term immune thymus-dependent reconstitution after PTCY haplo-HSCT. METHODS Twenty-nine patients (median age 53) underwent T-cell replete haplo-HSCT with PTCY. Blood samples were collected before conditioning and at 1, 3, 6, 12, 18, 24 months after transplantation. Analyses of CD4 and CD8 T-cell subsets by flow-cytometry were correlated by generalized linear models with Real-Time PCR quantification of signal joint T-cell receptor excision DNA circles (sjTRECs), specific marker of naive T-cells thymopoiesis. A) Naive; b) central; c) memory; and d) revertant CD4 and CD8 T-cells were defined as follows: a) CD45RA+CD62L+; b) CD45RO+CD62L+; c) CD45RO+CD27-; and d) CD45RA+/45RO+, respectively. SjTRECs real-time PCR was performed on genomic DNA (100 ng) extracted from sorted CD4 and CD8 T-cells. RESULTS Following PTCY induced T-cell depletion, a constant gradual increase in absolute numbers of all CD4 and CD8 T cell subsets and of sjTRECs copies from the first month up to two years post-transplant was observed ( Figure 1 ). Overall, at two years, CD4 and CD8 T-cell levels and sjTRECs levels were however lower than those observed in healthy donors. sjTRECs kinetics was associated with the increase in naive T-cells (overall, p CONCLUSIONS Active thymic function despite age-dependent involution, substantially contributes to T-cell reconstitution after haplo-HSCT. Chronic GVHD and older age are however significantly correlated with lower thymic activity. Overall, lower production of sjTRECs after haplo-HSCT as compared after HLA identical sibling HSCT may partly be due to a higher degree of "mismatching" of MHC molecules during thymic re-education

A year of genomic surveillance reveals how the SARS-CoV-2 pandemic unfolded in Africa.

The progression of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic in Africa has so far been heterogeneous, and the full impact is not yet well understood. In this study, we describe the genomic epidemiology using a dataset of 8746 genomes from 33 African countries and two overseas territories. We show that the epidemics in most countries were initiated by importations predominantly from Europe, which diminished after the early introduction of international travel restrictions. As the pandemic progressed, ongoing transmission in many countries and increasing mobility led to the emergence and spread within the continent of many variants of concern and interest, such as B.1.351, B.1.525, A.23.1, and C.1.1. Although distorted by low sampling numbers and blind spots, the findings highlight that Africa must not be left behind in the global pandemic response, otherwise it could become a source for new variants