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This article examines the role of CD147, a protein found on certain immune cells, in the development and recurrence of psoriasis. The study discovered that high levels of CD147 on CD4+ T cells were associated with the effectiveness of IL-17A inhibitor treatment and the likelihood of psoriasis returning. The researchers developed two models that accurately predicted treatment outcomes and long-term effectiveness based on CD147 levels. Additionally, the study found that a lack of CD147 on CD4+ T cells worsened psoriasis and increased the chances of it coming back. These findings provide valuable insights into the causes of psoriasis and could inform personalized treatment approaches. [Extracted from the article]

This paper presents an experimental investigation into the flexural and cracking behavior of corroded reinforced concrete continuous beams with 11‐month wet–dry cycles strengthened by anodic polarized carbon‐fabric‐reinforced cementitious matrix (C‐FRCM) plates. The failure modes and flexural bearing capacities were discussed. The influences of the layer of carbon fabric mesh and complete carbon fiber‐reinforced polymer (CFRP) wrapping as end anchorage on the strengthening effectiveness were explored. The complete crack development patterns were captured by a digital image correlation system, and the results showed that the C‐FRCM system can provide satisfactory crack width control, as proved by the reduced crack spacing and the maximum crack width. The flexural capacities of the strengthened beams were effectively enhanced and the debonding failure can be eliminated through complete CFRP wrappings. Moreover, the design recommendations were proposed based on the estimation of the crack development as per related design guidelines. [ABSTRACT FROM AUTHOR]

Regimens based on Bruton's tyrosine kinase inhibitors (BTKi) have been increasingly used to treat mantle cell lymphoma (MCL). A real‐world multicenter study was conducted to characterize treatment patterns and outcomes in patients with newly diagnosed MCL by Chinese Hematologist and Oncologist Innovation Cooperation of the Excellent (CHOICE). The final analysis included 1261 patients. Immunochemotherapy was the most common first‐line treatment, including R‐CHOP in 34%, cytarabine‐containing regimens in 21% and BR in 3% of the patients. Eleven percent (n = 145) of the patients received BTKi‐based frontline therapy. Seventeen percent of the patients received maintenance rituximab. Autologous hematopoietic stem cell transplantation (AHCT) was conducted in 12% of the younger (<65 years) patients. In younger patients, propensity score matching analysis did not show significant difference in 2‐year progression‐free survival and 5‐year overall survival rate in patients receiving standard high‐dose immunochemotherapy followed by AHCT than induction therapy with BTKi‐based regimens without subsequent AHCT (72% vs 70%, P =.476 and 91% vs 84%, P =.255). In older patients, BTKi combined with bendamustine plus rituximab (BR) was associated with the lowest POD24 rate (17%) compared with BR and other BTKi‐containing regimens. In patients with resolved hepatitis B at the baseline, HBV reactivation rate was 2.3% vs 5.3% in those receiving anti‐HBV prophylaxis vs not; BTKi treatment was not associated with higher risk of HBV reactivation. In conclusion, non‐HD‐AraC chemotherapy combined with BTKi may be a viable therapeutic strategy for younger patients. Anti‐HBV prophylaxis should be implemented in patients with resolved hepatitis B. [ABSTRACT FROM AUTHOR]

Background: Although abnormal metabolism plays a critical role in the pathogenesis of psoriasis, the details are unclear. Objectives: Here, we identified to explore the role and mechanism of lysophosphatidylcholine (LPC) on the pathogenesis of psoriasis. Methods: The level of LPC in plasma and skin lesions and the expression of G2A on skin lesions of psoriasis patients were detected by enzyme‐linked immunosorbent assay, liquid chromatography–tandem mass spectrometry, or immunohistochemistry, respectively. The glycolysis in the skin lesions of imiquimod (IMQ)‐induced psoriasis‐like mouse model was detected by extracellular acidification rate. LPC was subcutaneously injected into IMQ‐treated mouse ears, and the phenotype as well as the glycolysis were evaluated. Exploring the effects and mechanism of LPC on keratinocytes and CD4+ T cells by culturing primary keratinocytes and CD4+ T in vitro. Results: We found that LPC was significantly increased both in the plasma and skin lesions of psoriatic patients, while G2A, exerting an essential role in LPC‐inducing biological functions, was increased in psoriatic lesions. The abundance of LPC was positively correlated with glycolytic activity in the psoriasis‐like mouse model. LPC treatment facilitated psoriasis‐like inflammation and glycolytic activity in skin lesions. Mechanistically, the LPC/G2A axis significantly triggered glycolytic activity and produced inflammatory factors in keratinocytes, and blockade of glycolysis abrogated LPC‐induced expression of inflammatory mediators in keratinocytes. LPC activated STAT1, resulting in recognition and binding to the promoters of GCK and PKLR, which are glycolytic rate‐limiting enzymes. Furthermore, the LPC/G2A axis directly benefited Th1 differentiation, which was dependent on LPC‐induced glycolytic activity. Notably, LPC indirectly facilitated Th17 differentiation by inducing the secretion of IL‐1β in keratinocytes‐T cells coculture system. Conclusions: Taken together, our findings revealed the role of the LPC/G2A axis in the pathogenesis of psoriasis; targeting LPC/G2A is a potential strategy for psoriasis therapy. [ABSTRACT FROM AUTHOR]

Extensive use of thermal energy in daily life is ideal for reducing carbon emissions to achieve carbon neutrality; however, the effective collection of thermal energy is a major hurdle. Thermoelectric (TE) conversion technology based on the Seebeck effect and thermal energy storage technology based on phase change materials (PCMs) represent smart, feasible, and research‐worthy approaches to overcome this hurdle. However, the integration of multiple thermal energy sources freely existing in the environment for storage and output of thermal and electrical energy simultaneously still remains a huge challenge. Herein, three‐dimensional (3D) nanostructured metal–organic frameworks (MOFs) are in situ nucleated and grown onto carbon nanotubes (CNTs) via coordination bonding. After calcination, the prepared core–shell structural CNTs@MOFs are transformed into tightened 1D/3D carbon heterostructure loading Co nanoparticles for efficient solar–thermoelectric energy harvesting. Surprisingly, the corresponding composite PCMs show a record‐breaking solar–thermal conversion efficiency of 98.1% due to the tightened carbon heterostructure and the local surface plasmon resonance effect of Co nanoparticles. Moreover, our designed all‐in‐one composite PCMs are also capable of creating an electrical potential of 0.5 mV based on the Seebeck effect without a TE generator. This promising approach can store thermal and electrical energy simultaneously, providing a new direction in the design of advanced all‐in‐one multifunctional PCMs for thermal energy storage and utilization. [ABSTRACT FROM AUTHOR]

Ischemia/hypoxia (I/H)‐induced myocardial injury has a large burden worldwide. Hesperetin (HSP) has a cardioprotective effect, but the molecular mechanism underlying this is not clearly established. Here, we focused on the protective mechanisms of HSP against I/H‐induced myocardium injury. H9c2 cardiomyocytes were challenged with CoCl2 for 22 h to imitate hypoxia after treatment groups received HSP for 4 h. The viability of H9c2 cardiomyocytes was evaluated, and cardiac function indices, reactive oxygen species, apoptosis, mitochondrial membrane potential (MMP), and intracellular Ca2+ concentration ([Ca2+]i) were measured. L‐type Ca2+ current (ICa‐L), myocardial contraction, and Ca2+ transients in isolated ventricular myocytes were also recorded. We found that HSP significantly increased the cell viability, and MMP while significantly decreasing cardiac impairment, oxidative stress, apoptosis, and [Ca2+]i caused by CoCl2. Furthermore, HSP markedly attenuated ICa‐L, myocardial contraction, and Ca2+ transients in a concentration‐dependent manner. Our findings suggest a protective mechanism of HSP on I/H‐induced myocardium injury by restoring oxidative balance, inhibiting apoptosis, improving mitochondrial function, and reducing Ca2+ influx via L‐type Ca2+ channels (LTCCs). These data provide a new direction for HSP applied research as a LTCC inhibitor against I/H‐induced myocardium injury. [ABSTRACT FROM AUTHOR]

Background: Ibrutinib has revolutionized the treatment of mantle cell lymphoma (MCL). Both ibrutinib monotherapy and ibrutinib‐based combination therapy are important salvage options for patients with relapsed/refractory (R/R) MCL. The real‐world efficacy and safety profile of the two strategies in Chinese patients with R/R MCL remain unclarified. Methods: In the present study, data of 121 R/R MCL patients who received either ibrutinib monotherapy (N = 68) or ibrutinib combination therapy (N = 53) in 13 medical centers in China were retrospectively reviewed. Results: With a median follow‐up of 20.5 months, the overall response rate was 60.3% versus 84.9% (p = 0.003), complete remission rate was 16.2% versus 43.4% (p < 0.001), and median progression‐free survival (PFS) was 18.5 months (95% confidence interval [CI], 12.1–21.8) vs. 30.8 months (95% CI, 23.5‐NR) (hazard ratio, 0.53 [95% CI, 0.30–0.93]; p = 0.025), with ibrutinib monotherapy and ibrutinib‐based combination therapy, respectively. Subgroup analysis showed that patients with male gender, no refractory disease, Ki67 <30%, previous line of therapy = 1, non‐blastoid subtype, and the number of extranodal sites involved <2 might benefits more from the combination therapy. Treatment‐emergent adverse events were similar, except for a higher incidence of all grade neutropenia in the ibrutinib combination group (12.7% vs. 32.0%, p = 0.017). Conclusions: Ibrutinib combination therapy demonstrated potentially superior efficacy and comparable tolerability to ibrutinib monotherapy. Ibrutinib‐based combination therapy could be one of the prominent treatment options for R/R MCL patients. [ABSTRACT FROM AUTHOR]

BACKGROUND: Floral and sweet odors are two typical characteristic aromas of Congou black tea, but their aroma‐active compounds are still unclear. Characterizing the key aroma‐active compounds can provide a theoretical foundation for the practical aroma quality evaluation of Congou black tea and directional processing technology of high‐quality black tea with floral or sweet odors. Gas chromatography–olfactometry (GC‐O) combined with odor activity value (OAV) is often used to screen key aroma‐active substances, but the interaction between aroma components and their impact on the overall sensory quality is ignored. Therefore, in this study, OAV combined with variable importance in projection (VIP) and Spearman correlation analysis (SCA) were used to characterize the aroma‐active components of Congou black teas with floral and sweet odors. RESULTS: Eighty‐five volatiles were identified in these samples using gas chromatography–mass spectrometry (GC‐MS). Twenty‐three compounds were identified as potential markers for the floral and sweet odors of Congou black teas from orthogonal partial least squares discriminant analysis (OPLS‐DA). Eighteen compounds were selected as candidate aroma compounds based on GC‐O analysis and OAV calculations. In addition, 26 compounds were screened as crucial aroma compounds based on SCA. Finally, 19 compounds were evaluated as key aroma compounds by the comprehensive evaluation of VIP, OAV, and SCA. Terpenoids are the main active compounds that contribute to the floral odor of Congou black tea, whereas aldehydes are the key compounds for the sweet odor. CONCLUSION: The proposed method can effectively screen the aroma‐active compounds and can be used for comprehensive quality control of products. © 2022 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

TEMPO‐oxidized nanofibrillated cellulose (ONFC) with charged carboxyl groups is introduced for the efficient exfoliation of two‐dimensional (2D) MoS2/graphene composites. As an effective dispersant agent, ONFC can be easily absorbed between the adjacent layers, so as to prevent the accumulation of the exfoliated nanosheets. With the assistance of charged ONFC, the exfoliated MoS2/graphene is gradually increased in the aqueous dispersions with the elongated sonication time. After dewatering, self‐standing MoS2/Graphene/ONFC/CNTs composite films are rationally constructed using ONFC as flexible fibrous skeleton, and CNTs/graphene as 1D/2D interpenetrating electrical networks. Ultrathin MoS2 nanosheets anchored on the 1D/2D heterogeneous networks is directly acted as an ideal paper‐anode for lithium‐ion batteries (LIBs) without using traditional metallic current collector. The self‐standing flexible electrode materials based on natural cellulose will promote the future green electronics with high flexibility, miniaturization, and increased portability. [ABSTRACT FROM AUTHOR]