Multi-objective optimisation of process parameters for laser-based directed energy deposition of a mixture of H13 and M2 steel powders on 4Cr5Mo2SiV1 steel

In present paper, a universal method for multi-objective parameter optimisation of additive manufacturing processes was proposed and successfully applied to laser-based directed energy deposition (DED) experiments with mixtures of H13 and M2 steel powders that were deposited on 4Cr5Mo2SiV1 hot work die steel. The DED experiments were designed and completed based on the response surface method with 13 groups of laser parameters. The microstructure of the deposited alloy steel was observed and its mechanical properties were tested. The deposited steel alloy achieved an ultimate tensile strength (UTS) of 1821 ± 30 MPa with a reasonable elongation of approximately 4.5%, and the bond strength specimens achieved a bond toughness of ∼10.66% with a moderate UTS (1329 ± 28 MPa). A multi-objective optimisation method was proposed based on response surfaces which were established according to microstructural characteristics and mechanical properties data. It provided a basis for achieving high strength or high toughness DED-fabricated steel alloys.</p

Multifaceted Pt Nanoclusters for Targeting Recognition, Cellular Uptake, and Therapy In Vivo and In Vitro in Chronic Myeloid Leukemia Cells

In the past few years, platinum nanomaterials (Pt NMs) have gained attraction owing to their ability to address the drawbacks of classical Pt-based chemotherapy drugs including drug resistance and clinical side effects, which have been preliminarily used in lung cancer, liver cancer, gynecological cancer, etc. In order to investigate the effect of Pt NMs on hematopoietic tumors, ultra-small Pt nanoclusters (Pt NCs) were employed to clarify their targeting recognition, cellular uptake, and effective therapy in vivo for chronic myeloid leukemia (CML) cells. Through the facile surface modification of Pt NCs with anti-CD19 to form the anti-CD19-Pt NC composite, the specific aggregation in BV173 cells could be realized based on their high protein expression of CD19 in comparison to that in CD19-negative K562 cells. Furthermore, the endocytic pathways of Pt NCs in K562 and BV173 cells were investigated by qualitative and quantitative analyses via inductively coupled plasma-optical emission spectroscopy and flow cytometry. It was observed that Pt NCs entered into the K562 cells mainly through the caveolin-dependent endocytic pathway and in BV173 cells primarily via phagocytosis and micropinocytosis. Moreover, these Pt NCs exerted an excellent inhibitory effect on proliferation, migration, and invasion of hematopoietic tumor cells and tended to gather the acidic organelles (lysosomes or endosomes), resulting in the proliferation inhibition of tumor cells by the generation of corrosive Pt. Notably, Pt NCs were significantly aggregated at the site of tumor inoculation in mice and exhibited satisfactory in vivo inhibition of the increase in tumor weight and its size under the premise of not damaging the liver and spleen. Thus, the merits of versatile Pt NCs included facile target recognition, explicit cellular uptake behavior, and therapeutic efficacy in vivo, thereby hinting at their promising prospects for the clinical diagnosis and treatment of hematological malignancies

Clinical characteristics of HFMD patients.

<p>WBC, white blood cells.</p>a<p>, P values were analyzed via <i>X</i>² test; the rest P values were analyzed by Student's <i>t</i>-test.</p>b<p>, fever duration refers to the total duration after hospitalization until the fever had settled.</p

The Cytokine and Chemokine Profiles in Patients with Hand, Foot and Mouth Disease of Different Severities in Shanghai, China, 2010

<div><p>Background and purpose</p><p>Systemic upregulation of inflammatory cytokines is characteristic of critical severe hand, foot, and mouth disease (HFMD) with pulmonary edema. Thus, immunomodulatory medicines such as steroids, including methylprednisolone, have been proposed to treat patients with severe HFMD in China, because it is postulated that inflammatory cytokines play a role in the development of severe complications. This study is to further investigate the inflammatory response in the relatively mild HFMD patients, and whether steroid treatment has a beneficial effect on the suppression of inflammation in HFMD patients.</p><p>Method</p><p>We measured the levels of 50 kinds of chemokines, cytokines, growth factors and soluble receptors in serum samples from control patients without HFMD and the HFMD patients with or without prior treatment of intravenous methylprednisolone.</p><p>Results</p><p>Our present study found that even relatively mild HFMD patients without central nervous system (CNS) complications had elevated serum levels of inflammatory cytokines, including interleukin (IL)-3, IL-6, IL-12p40, and tumor necrosis factor (TNF)-α, which suggested systemic inflammation. In contrast, these patients also have decreased levels of other serum biomarkers, including IL-1Ra, IL-8, IL-16, soluble ICAM-1, CXCL-1, and CCL27. The dysregulation of cytokine and chemokine expression may be involved in CNS complications and unbalanced circulating leukocytes in HFMD patients. Surprisingly, patients treated with methylprednisolone had no difference in the expression levels of HFMD-associated biomarkers instead had slightly increased levels of IL-17A, which was not associated with the occurrence of HFMD.</p><p>Conclusion</p><p>Whether steroid treatment has any beneficial effect on the prognosis of HFMD patients requires to be further investigated.</p></div

The effect of methylprednisolone (MP) treatment on serum levels of IL-17A.

<p>(A) IL-17A levels in serum samples obtained from control (Ctrl, n = 20) and HFMD patients (HFMD, n = 40). (B) IL-17A levels in serum samples obtained from untreated (n = 27) or MP-treated HFMD patients (n = 13). (C) IL-17A levels in serum samples obtained from untreated (n = 7) or MP-treated CNS-complicated HFMD patients (n = 13). Numbers above square brackets indicate P values for the corresponding comparisons.</p

Immune biomarkers whose levels in serum samples of HFMD patients were significantly different from those of control patients.

*<p>Significance was analyzed via Student's <i>t</i>-test and P values were further adjusted with the Benjamini-Hochberg procedure.</p

The correlation between host biomarkers and disease prognosis.

<p>Levels of CCL27 (A), CXCL1 (B), and soluble VCAM-1 (C) in serum samples obtained from control patients (Ctrl, n = 20) and HFMD patients with or without CNS complications (n = 20, respectively). The line represents the average value. (D) Plots of soluble VCAM-1 concentrations in sera of HFMD patients against their maximal fever temperatures. Numbers above square brackets indicate P values for the corresponding comparisons.</p

TLR3 Signaling in Macrophages Is Indispensable for the Protective Immunity of Invariant Natural Killer T Cells against Enterovirus 71 Infection

<div><p>Enterovirus 71 (EV71) is the most virulent pathogen among enteroviruses that cause hand, foot and mouth disease in children but rarely in adults. The mechanisms that determine the age-dependent susceptibility remain largely unclear. Here, we found that the paucity of invariant natural killer T (iNKT) cells together with immaturity of the immune system was related to the susceptibility of neonatal mice to EV71 infection. iNKT cells were crucial antiviral effector cells to protect young mice from EV71 infection before their adaptive immune systems were fully mature. EV71 infection led to activation of iNKT cells depending on signaling through TLR3 but not other TLRs. Surprisingly, iNKT cell activation during EV71 infection required TLR3 signaling in macrophages, but not in dendritic cells (DCs). Mechanistically, interleukin (IL)-12 and endogenous CD1d-restricted antigens were both required for full activation of iNKT cells. Furthermore, CD1d-deficiency led to dramatically increased viral loads in central nervous system and more severe disease in EV71-infected mice. Altogether, our results suggest that iNKT cells may be involved in controlling EV71 infection in children when their adaptive immune systems are not fully developed, and also imply that iNKT cells might be an intervention target for treating EV71-infected patients.</p></div

Age-dependent susceptibility of suckling mice to EV71 infection correlates with the immaturity of their immune system.

<p>(A) Cytopathic effects in human RD cells and murine L929 cells after infected with the parental human isolate EV71H and mouse-adaptive EV71M. (B) Replication kinetics of EV71H and EV71M in RD and L929 cells. (C) The survival rates of 1-, 3-, 7-, and 14-day-old ICR mice (n = 8, per group) after being infected with 2×10⁶ PFU of EV71M. (D) The proportions of NKT and T cells in the thymus or spleen of young mice aged 3, 7 and 14 days. Splenocytes were stained with TCRβ, DX5 and DAPI. TCRβ versus DX5 profiles are shown for live cells (n = 4–8). Data are representative of three (A, B, C) or two (D) independent experiments.</p

EV71 infection activates iNKT cells through triggering macrophages.

<p>(A) Increase of IFN-γ-producing cells among splenocytes after EV71M infection. Splenocytes from 6–8-week-old C57BL/6 mice (n = 3) were infected with 10 MOIs of EV71M for 18 hours and then stained with TCRβ, CD1d tetramer, NK1.1 and IFN-γ. CD1d-tetramer, TCRβ versus NK1.1 profiles are shown for IFN-γ-positive cells. (B) Splenocytes from RAG1-knockout (RAG1^-/-) mice upon EV71M infection produced little IFN-γ. Splenocytes from WT (n = 3) and RAG1^-/- (n = 3) mice were cultured in the presence of EV71M for 24 hours. The supernatants were examined for IFN-γ with an ELISA assay. (C) The CD69 and CD25 expression levels of iNKT cells in the spleens (Sp) and intrahepatic leukocytes (IHL) of EV71M-infected mice (n = 3). Splenocytes of control (PBS) or EV71M-infected C57BL/6 mice were stained with TCRβ, CD1d tetramer, CD69 or CD25 and DAPI. (D) EV71M-infected macrophages, but not DCs, induced IFN-γ production by iNKT cells. Purified DCs and macrophages were cultured with EV71M for 24 hours and then co-cultured with purified NK or iNKT cells for a further 18 hours. Cytokine concentrations were determined by ELISA. Data are represented of five (A), three (mean ± SD in D) or two (B, C) independent experiments.</p