8 research outputs found
Workload-aware Automatic Parallelization for Multi-GPU DNN Training
Deep neural networks (DNNs) have emerged as successful solutions for variety
of artificial intelligence applications, but their very large and deep models
impose high computational requirements during training. Multi-GPU
parallelization is a popular option to accelerate demanding computations in DNN
training, but most state-of-the-art multi-GPU deep learning frameworks not only
require users to have an in-depth understanding of the implementation of the
frameworks themselves, but also apply parallelization in a straight-forward way
without optimizing GPU utilization. In this work, we propose a workload-aware
auto-parallelization framework (WAP) for DNN training, where the work is
automatically distributed to multiple GPUs based on the workload
characteristics. We evaluate WAP using TensorFlow with popular DNN benchmarks
(AlexNet and VGG-16), and show competitive training throughput compared with
the state-of-the-art frameworks, and also demonstrate that WAP automatically
optimizes GPU assignment based on the workload's compute requirements, thereby
improving energy efficiency.Comment: This paper is accepted in ICASSP201
Latent tuberculosis co-infection is associated with heightened levels of humoral, cytokine and acute phase responses in seropositive SARS-CoV-2 infection
OBJECTIVES: : Latent Tuberculosis infection (LTBI) is postulated to modulate immune responses and alter disease severity in SARS-CoV-2 co-infection. However, no data exist on the effect of LTBI on the immune responses in SARS-CoV-2 co-infected individuals. METHODS: : We examined the SARS-CoV-2 specific antibody responses, plasma cytokines, chemokines, acute phase proteins and growth factor levels in LTBI positive and negative individuals with SARS-CoV-2 infection. RESULTS: : Our results demonstrated that individuals with LTBI (LTBI+) and seropositive for SARS-CoV-2 infection were associated with elevated SARS-CoV-2 specific IgM, IgG and IgA antibodies, as well as enhanced neutralization activity compared to those negative for LTBI (LTBI-) individuals. Our results also demonstrate that LTBI+ individuals exhibited significantly higher plasma levels of IFNĪ³, IL-2, TNFĪ±, IL-1Ī±, IL-1Ī², IL-6, IL-12, IL-15, IL-17, IL-3, GM-CSF, IL-10, IL-25, IL-33, CCL3 and CXCL10 compared to LTBI- individuals. Finally, our results show that LTBI+ individuals exhibit significantly higher levels of C-reactive protein, alpha-2 macroglobulin, VEGF and TGFĪ± compared to LTBI- individuals. CONCLUSIONS: : Thus, our data clearly demonstrates that LTBI+ individuals seropositive for SARS-CoV2 infection exhibit heightened levels of humoral, cytokine and acute phase responses compared to LTBI- individuals. Thus, LTBI is associated with modulation of antibody and cytokine responses as well as systemic inflammation in individuals seropositive for SARS-CoV2 infection
BCG vaccination induces enhanced frequencies of dendritic cells and altered plasma levels of type I and type III interferons in elderly individuals
OBJECTIVE: : BCG can improve the response to vaccines directed against viral infections and also BCG vaccination reduces all-cause mortality, most likely by protection against unrelated infections. However, the effect of BCG vaccination on the dendritic cells (DC) subsets is not well characterized. METHODS: : We investigated the impact of BCG vaccination on the frequencies of DC subsets and type I and III interferons (IFNs) using whole blood and plasma samples in a group of elderly individuals (age 60-80 years) at one month post vaccination as part of our clinical study to examine the effect of BCG on COVID-19. RESULTS: : Our results demonstrate that BCG vaccination induced enhanced frequencies of plasmacytoid DC (pDC) and myeloid DC (mDC). BCG vaccination also induced diminished plasma levels of type I IFNs like IFNĪ±Ā and IFNĪ² but increased levels of type III IFNs IL-28A and IL-29. CONCLUSIONS: : Thus, BCG vaccination was associated with enhanced DC subsets as well IL-29 in elderly individuals, suggesting its ability to induce non-specific innate immune responses
BCG vaccination induces enhanced frequencies of memory T cells and altered plasma levels of common Ī³c cytokines in elderly individuals
BCG vaccination is known to induce innate immune memory, which confers protection against heterologous infections. However, the effect of BCG vaccination on the conventional adaptive immune cells subsets is not well characterized. We investigated the impact of BCG vaccination on the frequencies of T cell subsets and common gamma c (Ī³c) cytokines in a group of healthy elderly individuals (age 60ā80 years) at one month post vaccination as part of our clinical study to examine the effect of BCG on COVID-19. Our results demonstrate that BCG vaccination induced enhanced frequencies of central (p<0.0001) and effector memory (p<0.0001) CD4+ T cells and diminished frequencies of naĆÆve (p<0.0001), transitional memory (p<0.0001), stem cell memory (p = 0.0001) CD4+ T cells and regulatory T cells. In addition, BCG vaccination induced enhanced frequencies of central (p = 0.0008), effector (p<0.0001) and terminal effector memory (p<0.0001) CD8+ T cells and diminished frequencies of naĆÆve (p<0.0001), transitional memory (p<0.0001) and stem cell memory (p = 0.0034) CD8+T cells. BCG vaccination also induced enhanced plasma levels of IL-7 (p<0.0001) and IL-15 (p = 0.0020) but diminished levels of IL-2 (p = 0.0033) and IL-21 (p = 0.0020). Thus, BCG vaccination was associated with enhanced memory T cell subsets as well as memory enhancing Ī³c cytokines in elderly individuals, suggesting its ability to induce non-specific adaptive immune responses
Characterization of memory T cell subsets and common Ī³āchain cytokines in convalescent COVID-19 individuals
T cells are thought to be an important correlates of protection against SARSāCoV2 infection. However, the composition of T cell subsets in convalescent individuals of SARSāCoV2 infection has not been well studied. The authors determined the lymphocyte absolute counts, the frequency of memory T cell subsets, and the plasma levels of common Ī³āchain in 7 groups of COVIDā19 individuals, based on days since RTāPCR confirmation of SARSāCoVā2 infection. The data show that both absolute counts and frequencies of lymphocytes as well as, the frequencies of CD4(+) central and effector memory cells increased, and the frequencies of CD4(+) naĆÆve T cells, transitional memory, stem cell memory T cells, and regulatory cells decreased from Days 15ā30 to Days 61ā90 and plateaued thereafter. In addition, the frequencies of CD8(+) central memory, effector, and terminal effector memory T cells increased, and the frequencies of CD8(+) naĆÆve cells, transitional memory, and stem cell memory T cells decreased from Days 15ā30 to Days 61ā90 and plateaued thereafter. The plasma levels of ILā2, ILā7, ILā15, and ILā21ācommon Ī³c cytokines started decreasing from Days 15ā30 till Days 151ā180. Severe COVIDā19 patients exhibit decreased levels of lymphocyte counts and frequencies, higher frequencies of naĆÆve cells, regulatory T cells, lower frequencies of central memory, effector memory, and stem cell memory, and elevated plasma levels of ILā2, ILā7, ILā15, and ILā21. Finally, there was a significant correlation between memory T cell subsets and common Ī³c cytokines. Thus, the study provides evidence of alterations in lymphocyte counts, memory T cell subset frequencies, and common Ī³āchain cytokines in convalescent COVIDā19 individuals