Constructing α-MnO2/Mn2O3 heterojunction for formaldehyde oxidation.

Constructing heterojunctions with oxygen defect-rich structures and abundant phase interfaces poses an appealing yet challenging task in the development of non-precious metal oxide catalysts for formaldehyde (HCHO) oxidation. Herein, we present a simple and efficient method for fabricating highly active manganese oxide heterojunction catalysts for HCHO oxidation. This method involves the hydrothermal synthesis of a nanostructured α-MnO2/γ-MnOOH composite, followed by mechanical milling-induce phase transformation of γ-MnOOH to Mn2O3. Importantly, mechanical milling not only creates the heterojunction but also imparts oxygen defect-rich structures and an abundant phase interface to the catalyst. The resulting α-MnO2/Mn2O3 heterojunction exhibits outstanding performance in HCHO oxidation, comparable to the best non-precious metal oxide catalysts reported thus far. It achieves a 100% conversion of 100 ppm HCHO under a gas hourly space velocity of 120 L gcat-1 h-1 at 80 °C, corresponding to a mass-specific reaction rate of 8.92 µmol g-1 min-1 and an area-specific reaction rate of 0.18 µmol m-2 min-1. Based on the control experiments using in situ diffuse reflectance infrared Fourier transform spectroscopy combined with online gas chromatography, we gained insights into the mechanism of HCHO oxidation over the α-MnO2/Mn2O3 catalyst and the functional roles played by its component phases.

Cancer cell-intrinsic PD-1: Its role in malignant progression and immunotherapy.

Programmed cell death protein-1 (PD-1), also called CD279, is coded by the PDCD1 gene and is constitutively expressed on the surface of immune cells. As a receptor and immune checkpoint, PD-1 can bind to programmed death ligand-1/programmed death ligand-2 (PD-L1/PD-L2) in tumor cells, leading to tumor immune evasion. Anti-PD-1 and anti-PD-L1 are important components in tumor immune therapy. PD-1 is also expressed as an intrinsic variant (iPD-1) in cancer cells where it plays important roles in malignant progression as proposed by recent studies. However, iPD-1 has received much less attention compared to PD-1 expressed on immune cells although there is an unmet medical need for fully elucidating the mechanisms of actions to achieve the best response in tumor immunotherapy. iPD-1 suppresses tumorigenesis in non-small cell lung cancer (NSCLC) and colon cancer, whereas it promotes tumorigenesis in melanoma, hepatocellular carcinoma (HCC), pancreatic ductal adenocarcinoma (PDAC), thyroid cancer (TC), glioblastoma (GBM), and triple-negative breast cancer (TNBC). In this review, we focus on the role of iPD-1 in tumorigenesis and development and its molecular mechanisms. We also deeply discuss nivolumab-based combined therapy in common tumor therapy. iPD-1 may explain the different therapeutic effects of anti-PD-1 treatment and provide critical information for use in combined anti-tumor approaches.

Influencing factors of knowledge, attitude and behavior in children's palliative care among pediatric healthcare workers: a cross-sectional survey in China.

BACKGROUND: Palliative care has become a key medical field worldwide. Although research relating to adult palliative care is well-established, less is known about children's palliative care (CPC). Therefore, this study investigated the knowledge, attitude and behavior of pediatric healthcare workers (PHWs) regarding CPC and analyzed the influencing factors for the implementation and development of CPC. METHODS: A cross-sectional survey of 407 PHWs was carried out in a Chinese province from November 2021 to April 2022. The questionnaire consisted of two parts: a general information form and questions on the knowledge, attitude and behavior of PHWs about CPC. Data were analyzed using t-test, ANOVA and multiple regression analysis. RESULTS: The total score of the PHWs' knowledge, attitude and behavior about CPC was 69.98, which was at a moderate level. PHWs' CPC knowledge, attitude, and behavior are positively correlated.The most important influencing factors were working years, highest education, professional title, job position, marital status, religion, grade of hospital (I, II or III), type of medical institution, experience of caring for a terminally ill child/kinsfolk and total hours of CPC education and training received. CONCLUSIONS: In this study, PHWs in a Chinese province had the lowest scores on the knowledge dimension of CPC, with moderate attitude and behavior and various influencing factors. In addition to professional title, highest education and working years, it is also worth noting that the type of medical institution and marital status also affected the score. Continuing education and training of PHWs in CPC should be emphasized by the administrators of relevant colleges and medical institutions. Future research should start with the above-mentioned influencing factors and focus on setting up targeted training courses and evaluating the post-training effects.

Trichalcogenasupersumanenes and its concave-convex supramolecular assembly with fullerenes.

Synthesis of buckybowls have stayed highly challenging due to the large structural strain caused by curved π surface. In this paper, we report the synthesis and properties of two trichalcogenasupersumanenes which three chalcogen (sulfur or selenium) atoms and three methylene groups bridge at the bay regions of hexa-peri-hexabenzocoronene. These trichalcogenasupersumanenes are synthesized quickly in three steps using an Aldol cyclotrimerization, a Scholl oxidative cyclization, and a Stille type reaction. X-ray crystallography analysis reveals that they encompass bowl diameters of 11.06 Å and 11.35 Å and bowl depths of 2.29 Å and 2.16 Å for the trithiasupersumanene and triselenosupersumanene, respectively. Furthermore, trithiasupersumanene derivative with methyl chains can form host-guest complexes with C60 or C70, which are driven by concave-convex π ⋯ π interactions and multiple C-H ⋯ π interactions between bowl and fullerenes.

Recyclable TPA-Modified MIL-88-Supported Ionic Pt as a Highly Efficient Catalyst for Alkene Hydrosilylation.

The hydrosilylation reaction driven by a homogeneous catalyst has been widely used in the industrial synthesis of functionalized silicone compounds. However, the homogeneous catalyst for hydrosilylation has the shortcomings of nonrecyclability, undesirable side reactions, and high cost. In this work, a highly efficient heterogeneous catalyst was prepared by loading Pt ions on MIL-88 modified with trimethoxy[3-(phenylamino)propyl]silane. In comparison with previous research studies, the resulting catalyst can exhibit high catalytic activity and excellent stability during the hydrosilylation reaction, which was attributed to the presence of a pyrrolic nitrogen structure between TPA-MIL-88 and the Pt ion. Besides them, 1.2%Pt/TPA-MIL-88 showed the highest catalytic activity and can be reused five times without significant deactivation. Importantly, 1.2%Pt/TPA-MIL-88 also achieved satisfactory results when it was used to catalyze the hydrosilylation reaction for other olefins, implying great potential for application in the silicone industry.

BiVO4-Deposited MIL-101-NH2 for Efficient Photocatalytic Elimination of Cr(VI).

In this study, a flower-like BiVO4/MIL-101-NH2 composite is synthesized by a facile and surfactant-free process. The -COO--Bi3+ ionic bond construction was conductive to enhance the interface affinity between BiVO4 and MIL-101-NH2. Due to the highly efficient light capture and sufficient electron traps induced by oxygen vacancies and the formation of a heterostructure, the improved separation and transportation rates of charge carriers are realized. In addition, the MIL-101-NH2/BiVO4 composite is favorable for Cr(VI) photocatalytic removal (91.2%). Moreover, FNBV-3 (Fe/Bi = 0.25) also exhibited an excellent reusability after five cycles.

Therapeutic significance of tumor microenvironment in cholangiocarcinoma: focus on tumor-infiltrating T lymphocytes.

Cholangiocarcinoma (CCA) is a highly aggressive type of adenocarcinoma distinguished by its invasiveness. Depending on specific anatomical positioning within the biliary tree, CCA can be categorized into intrahepatic CCA (ICCA), perihilar CCA (pCCA) and distal CCA (dCCA). In recent years, there has been a significant increase in the global prevalence of CCA. Unfortunately, many CCA patients are diagnosed at an advanced stage, which makes surgical resection impossible. Although systemic chemotherapy is frequently used as the primary treatment for advanced or recurrent CCA, its effectiveness is relatively low. Therefore, immunotherapy has emerged as a promising avenue for advancing cancer treatment research. CCA exhibits a complex immune environment within the stromal tumor microenvironment (TME), comprising a multifaceted immune landscape and a tumor-reactive stroma. A deeper understanding of this complex TME is indispensable for identifying potential therapeutic targets. Thus, targeting tumor immune microenvironment holds promise as an effective therapeutic strategy.

The Systematic Analyses of RING Finger Gene Signature for Predicting the Prognosis of Patients with Hepatocellular Carcinoma.

RING finger (RNF) proteins are frequently dysregulated in human malignancies and are tightly associated with tumorigenesis. However, the expression profiles of RNF genes in hepatocellular carcinoma (HCC) and their relations with prognosis remain undetermined. Here, we aimed at constructing a prognostic model according to RNF genes for forecasting the outcomes of HCC patients using the data from The Cancer Genome Atlas (TCGA) program. We collected HCC datasets to validate the values of our model in predicting prognosis of HCC patients from International Cancer Genome Consortium (ICGC) platform. Then, functional experiments were carried out to explore the roles of the representative RNF in HCC progression. A total of 107 differentially expressed RNFs were obtained between TCGA-HCC tumor and normal tissues. After comprehensive evaluation, a prognostic signature composed of 11 RNFs (RNF220, RNF25, TRIM25, BMI1, RNF216P1, RNF115, RNF2, TRAIP, RNF157, RNF145, and RNF19B) was constructed based on TCGA cohort. Then, the Kaplan-Meier (KM) curves and the receiver operating characteristic curve (ROC) were employed to evaluate predictive power of the prognostic model in testing cohort (TCGA) and validation cohort (ICGC). The KM and ROC curves illustrated the good predictive power in testing and validation cohort. The areas under the ROC curve are 0.77 and 0.76 in these two cohorts, respectively. Among the prognostic signature genes, BMI1 was selected as a representative for functional study. We found that BMI1 protein level was significantly upregulated in HCC tissues. Moreover, the inhibitor of BMI1, PTC-209, displayed an excellent anti-HCC effect in vitro. Enrichment analysis of BMI1 downstream targets showed that BMI1 might be involved in tumor immunotherapy. Together, our overall analyses revealed that the 11-RNFs prognostic signature might provide us latent chances for evaluating HCC prognosis and developing novel HCC therapy.

Testing a Family Supportive End of Life Care Intervention in a Chinese Neonatal Intensive Care Unit: A Quasi-experimental Study With a Non-randomized Controlled Trial Design.

Background: Neonatal death often occurs in tertiary Neonatal Intensive Care Units (NICUs). In China, end-of-life-care (EOLC) does not always involve parents. Aim: The aim of this study is to evaluate a parent support intervention to integrate parents at the end of life of their infant in the NICU. Methods: A quasi-experimental study using a non-randomized clinical trial design was conducted between May 2020 and September 2021. Participants were infants in an EOLC pathway in the NICU and their parents. Parents were allocated into a family supportive EOLC intervention group or a standard EOLC group based on their wishes. The primary outcomes depression (Edinburgh Postnatal Depression Scale for mothers; Hamilton Depression rating scale for fathers) and Satisfaction with Care were measured 1 week after infants' death. Student t-test for continuous variables and the Chi-square test categorical variables were used in the statistical analysis. Results: In the study period, 62 infants died and 45 infants and 90 parents were enrolled; intervention group 20 infants, standard EOLC group 25 infants. The most common causes of death in both groups were congenital abnormalities (n = 20, 44%). Mean gestational age of infants between the family supportive EOLC group and standard EOLC group was 31.45 vs. 33.8 weeks (p = 0.234). Parents between both groups did not differ in terms of age, delivery of infant, and economic status. In the family support group, higher education levels were observed among mother (p = 0.026) and fathers (p = 0.020). Both mothers and fathers in the family supportive EOLC group had less depression compared to the standard EOLC groups; mothers (mean 6.90 vs. 7.56; p = 0.017) and fathers (mean 20.7 vs. 23.1; p < 0.001). Parents reported higher satisfaction in the family supportive EOLC group (mean 88.9 vs. 86.6; p < 0.001). Conclusions: Supporting parents in EOLC in Chinese NICUs might decreased their depression and increase satisfaction after the death of their infant. Future research needs to focus on long-term effects and expand on larger populations with different cultural backgrounds. Clinical Trial Registration: www.ClinicalTrials.gov, identifier: NCT05270915.

Construction of MIL-125-NH2@BiVO4 Composites for Efficient Photocatalytic Dye Degradation.

The design and construction of a photocatalyst with a heterostructure are a feasible and effective way to enhance the catalytic performance. Herein, a specially designed composite based on MIL-125-NH2 and BiVO4 was prepared and used for wastewater treatment. In the hybrid MIL-125-NH2@BiVO4, MIL-125-NH2 was uniformly dispersed on the BiVO4 surface. There is a high affinity between MIL-125-NH2 and BiVO4 due to the lattice defects. Under visible light irradiation, the catalytic activity of the as-prepared composite was evaluated by the degradation of various dyes such as malachite green, crystal violet, methylene blue, and Congo red. Nearly 98.7, 99.1, and 41.0% of the initial MG, MB and Cr(VI) were respectively removed over the optical sample of BVTN-5, demonstrating that the hybrid holds great promise for practical applications. Moreover, the composites can be recycled and reused with good stability after five consecutive cycles. The mechanism was proposed and discussed in detail. This work will shed light on the construction of MOF-based composites for efficient photocatalysis.

Radiation enhances the efficacy of EGFR-targeted CAR-T cells against triple-negative breast cancer by activating NF-κB/Icam1 signaling.

Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype, with limited treatment options. Epidermal growth factor receptor (EGFR) is reported to be expressed in 50%-75% of TNBC patients, making it a promising target for cancer treatment. Here we show that EGFR-targeted chimeric antigen receptor (CAR) T cell therapy combined with radiotherapy provides enhanced antitumor efficacy in immunocompetent and immunodeficient orthotopic TNBC mice. Intriguingly, this combination therapy resulted in a substantial increase in the number of tumor-infiltrating CAR-T cells. The efficacy of this combination was independent of tumor radiosensitivity and lymphodepleting preconditioning. Cytokine profiling showed that this combination did not increase the risk of cytokine release syndrome (CRS). RNA sequencing (RNA-seq) analysis revealed that EGFR-targeting CAR-T therapy combined with radiotherapy increased the infiltration of CD8+ T and natural killer (NK) cells into tumors. Mechanistically, radiation significantly increased Icam1 expression on TNBC cells via activating nuclear factor κB (NF-κB) signaling, thereby promoting CAR-T cell infiltration and killing. These results suggest that CAR-T therapy combined with radiotherapy may be a promising strategy for TNBC treatment.

Integration of Phosphotungstic Acid into Zeolitic Imidazole Framework-67 for Efficient Methylene Blue Adsorption.

To enhance the dye adsorption capacity of zeolitic imidazolate framework-67 (ZIF-67), phosphotungstic acid (HPW) was integrated into ZIF-67 to prepare composite adsorbents. Characterization results demonstrated that the electronegative HPW was uniformly and tightly deposited on the electropositive ZIF-67. Methylene blue (MB) was selected as a model contaminant to evaluate the adsorption performance of hybrid adsorbents. Results showed that HPW@ZIF-67 had excellent adsorption capacity toward cationic MB. The optimal ZIF-67-0.2 HPW sample with a HPW dosage of 9.9 wt % presented an adsorption capacity of 446.4 mg g-1. ZIF-67-0.2 HPW displayed good reusability, and the adsorption data can be well described by pseudo-second order and Langmuir isotherm models. The adsorption mechanism was ascribed to the preferred electrostatic attraction and π-π stacking between MB and composite adsorbents. This work provides a route to enhance organic dye removal efficiency of ZIF materials through regulation of surface charge property and sheds light on the development of ZIF-based adsorbents.

Long noncoding RNA LINC01234 promotes hepatocellular carcinoma progression through orchestrating aspartate metabolic reprogramming.

Amino acids metabolism, especially aspartate metabolism, is often altered in human cancers including hepatocellular carcinoma (HCC) and this metabolic remodeling is required for supporting cancer cell malignant activities. Argininosuccinate synthase 1 (ASS1), as a crucial rate-limiting enzyme in aspartate metabolism, participates in repressing tumor progression. However, the roles of long noncoding RNAs (lncRNAs) in aspartate metabolism remodeling and the underlying mechanisms remain unclear. Here, we screen LINC01234 as an aspartate metabolism-related lncRNA in HCC. Clinically, LINC01234 was highly expressed in HCC, and a high LINC01234 expression level was correlated with a poor prognosis of patients with HCC. LINC01234 promoted cell proliferation, migration, and drug resistance by orchestrating aspartate metabolic reprogramming in HCC cells. Mechanistically, LINC01234 downregulated the expression of ASS1, leading to am increased aspartate level and activation of the mammalian target of rapamycin pathway. LINC01234 bound to the promoter of ASS1 and inhibited transcriptional activation of ASS1 by transcriptional factors, including p53. Finally, inhibiting LINC01234 dramatically impaired tumor growth in nude mice and sensitized HCC cells to sorafenib. These findings demonstrate that LINC01234 promotes HCC progression by modulating aspartate metabolic reprogramming and might be a prognostic or therapeutic target for HCC.

Hierarchical Nanostructured Co-Mo-B/CoMoO4-x Amorphous Composite for the Alkaline Hydrogen Evolution Reaction.

Transition metal borides (TMBs) are a class of important but less well-explored electrocatalytic materials for water splitting. The lack of an advanced methodology to synthesize complex nanostructured TMBs with tunable surface properties is a major obstacle to the exploration of the full potential of TMBs for electrocatalytic applications. Here, we report the facile fabrication of a cobalt foam (CF)-supported hierarchical nanostructured Co-Mo-B/CoMoO4-x composite using a hydrothermal method, followed by annealing and NaBH4 reduction treatments. Our study found that NaBH4 reduction of CoMoO4 resulted in the concurrent formation of amorphous Co-Mo-B and an O-vacancy-rich CoMoO4-x substrate, which cooperatively catalyzed the hydrogen evolution reaction (HER) in an alkaline electrolyte. The hierarchical nanoporous structure derived from the dehydration and partial reduction reactions of the CoMoO4·nH2O precursor could offer ample accessible active sites, as well as interconnected channels for rapid mass transfer. In addition, the in situ growth of electrically conductive Co-Mo-B nanoparticles on the defective structured CoMoO4-x substrate imparted the electrocatalyst with good electrical conductivity. As a result, the Co-Mo-B/CoMoO4-x/CF catalyst showed impressively high activity and outstanding stability for the alkaline HER, outperforming most reported TMB electrocatalysts. For instance, it required an overpotential of 55 mV to afford 10 mA·cm-2 and showed a fluctuation of only ±8 mV in a 100 h constant-current test at 100 mA·cm-2.

Engineering oxygen vacancies via amorphization in conjunction with W-doping as an approach to boosting catalytic properties of Pt/Fe-W-O for formaldehyde oxidation.

Engineering functional defects in support materials has gained ever-increasing attention as a novel approach to boosting the catalytic performance of oxide-supported catalysts. Herein, we demonstrate the feasibility of engineering oxygen vacancy in iron oxide through amorphization in conjunction with foreign cation doping and elucidate the important role of support functionality in the catalytic oxidation of formaldehyde (HCHO). A supported Pt catalyst on Fe-W-O amorphous nanosheets (denoted as Pt/a-Fe-W-O) was synthesized using a one-step solvothermal method. This simple method allowed us to simultaneously create abundant oxygen vacancies in the substrate and to ensure uniform dispersion of tiny Pt nanoparticles with an average diameter of 1.4 nm on the high-surface-area substrate. This renders an increased possibility of Pt/O-vacancy coexistence in close proximity, which synergistically boosts the formation of active oxygen and surface hydroxyl species. Consequently, the Pt/a-Fe-W-O catalyst with an optimal W/Fe molar ratio of 0.08:1 and a 1.51 wt% Pt loading exhibited a high specific reaction rate of 68.3 µmol gPt-1 s-1 and excellent stability during 24 h continuous test, outperforming most existing HCHO oxidation catalysts. Our study highlights the importance of functional oxygen defects in construction of synergistic active sites for promoting the reactions requiring multiple active species.

A Tandem Adsorption-Catalysis Strategy for the Removal of Copper Ions and Catalytic Reduction of 4-Nitrophenol.

In this work, a consecutive adsorption-catalysis approach to remove Cu2+ ions and catalytic reduction of 4-nitrophenol (4-NP) is proposed. Attapulgite (ATP) nanorods are utilized as adsorbents to enrich Cu2+ ions from contaminated water. Subsequently, the adsorbed ions were in situ reduced to construct Cu-loaded ATP catalysts. The catalytic activities of the composite ATP-Cu catalysts are evaluated by 4-NP reduction in the presence of NaBH4. The optimal ATP-Cu50 sample prepared by putting ATP into a 50 mg L-1 CuSO4 solution could complete the catalytic reaction within 4 min. Moreover, the Cu-deposited ATP nanorods can be integrated into a continuous flow catalytic system, and the 4-NP can be rapidly reduced. This method sheds lights on the fabrication of ATP-based hybrid catalysts and the removal of multiple water pollutants.

Facet- and defect-engineered Pt/Fe2O3 nanocomposite catalyst for catalytic oxidation of airborne formaldehyde under ambient conditions.

Formaldehyde (HCHO) is one of the most infamous indoor pollutants that imposes a great threat to human health. Herein, we report the development of a high-performance Pt/Fe2O3 catalyst for HCHO oxidation employing a facet- and defect-engineering strategy, with special focus on the surface structure effect of α-Fe2O3 on the catalytic properties. A supported Pt nanocatalyst on hollow octadecahedral α-Fe2O3 with exclusively exposed {113} and {104} facets was prepared using a hydrothermal method followed by impregnation-reduction treatment. The high-index facets of α-Fe2O3 render the formation of abundant oxygen vacancies and an improved dispersion of Pt nanoparticles. This led to an increased Pt/O-vacancy coexistence in close proximity, which collaboratively promote the generation of active oxygen and surface OH species. As a consequence, the Pt/Fe2O3-HO catalyst exhibited impressively high and stable activity towards HCHO oxidation at room temperature, which was five-fold higher than that of the supported Pt catalyst on commercial α-Fe2O3.

NiPt Nanoparticles Anchored onto Hierarchical Nanoporous N-Doped Carbon as an Efficient Catalyst for Hydrogen Generation from Hydrazine Monohydrate.

Catalytic decomposition of the hydrogen-rich hydrazine monohydrate (N2H4·H2O) represents a promising hydrogen storage/production technology. A rational design of advanced N2H4·H2O decomposition catalysts requires an overall consideration of intrinsic activity, number, and accessibility of active sites. We herein report the synthesis of a hierarchically nanostructured NiPt/N-doped carbon catalyst using a three-step method that can simultaneously address these issues. The chelation of metal precursors with polydopamine and thermolysis of the resulting complexes under reductive atmosphere resulted in a concurrent formation of N-doped carbon substrate and catalytically active NiPt alloy nanoparticles. Thanks to the usage of a silica nanosphere template and dopamine precursor, the N-doped carbon substrate possesses a hierarchical macroporous-mesoporous architecture. This, together with the uniform dispersion of tiny NiPt nanoparticles on the carbon substrate, offers opportunity for creating abundant and accessible active sites. Benefiting from these favorable attributes, the NiPt/N-doped carbon catalyst enables a complete and rapid hydrogen production from alkaline N2H4·H2O solution with a rate of 1602 h-1 at 50 °C, which outperforms most existing catalysts for N2H4·H2O decomposition.

Monoclonal-Antibody-Templated Gold Nanoclusters for HER2 Receptors Targeted Fluorescence Imaging.

HER2 receptor-specific monoclonal-antibody-templated gold nanoclusters, Herceptin-templated Au NCs (Her-Au NCs), have been successfully obtained via "green" synthesis. This strategy allows the fluorescent gold nanoclusters (Au NCs) formed in the three-dimensional structure of Herceptin without destroying the high specificity and affinity to HER2 receptors. The Her-Au NCs have been found to be superior compared to Cy3-Herceptin in the fluorescence emission (λem = 645 nm) and the photostability under high-intensity UV irradiation or long-time storage. Moreover, Her-Au NCs can achieve receptor-specific imaging without targeted modification owing to the HER2-binding ability of the Herceptin scaffold. For imaging applications, Her-Au NCs can be utilized as effective optical probes for not only fluorescence imaging of HER2-positive cancer cells but also imaging of HER2-positive tumors in vivo.

Combined Adjuvant of Poly I:C Improves Antitumor Effects of CAR-T Cells.

Chimeric antigen receptor modified T cells (CAR-T) therapy is an emerging immunotherapy against malignancies. However, only limited success was obtained in solid tumors. Polyinosinic-polycytidylic acid (poly I:C), ligand of TLR3, mediates innate immune and adaptive immune and shows broad antitumor effect on many types of cancer. In the present study, we combined EGFRvIII-targeted CAR-T cells with poly I:C treatment and evaluated the synergic antitumor effect in vitro and in immunocompetent mice bearing subcutaneous colon or orthotopic breast cancer xenografts. Poly I:C significantly promoted more IL-2 and IFN γ production as well as higher lytic activity of CAR-T cells. Upon systemic administration in vivo, CAR-T cells obviously suppressed tumor growth, and poly I:C significantly enhanced the suppression. Further study showed that poly I:C exerted antitumor effect dependent on type I IFNs. In addition, poly I:C decreased myeloid-derived suppressor cells (MDSC) number in peripheral blood and spleen, and attenuated the immunosuppressive activity of MDSC on proliferation and cytolytic function of CAR-T. Depletion of MDSC with anti-Gr1 Ab further increased the antitumor effect of CAR-T cells plus poly I:C treatment. In conclusion, CAR-T treatment combined with intratumoral delivery of poly I:C resulted in synergistic antitumor activity. We thus provide a rationale to translate this immunotherapeutic strategy to solid tumors.