中华医学杂志
2020年 · 第100卷第32期
中华医学杂志
家族序列相似性13A基因干扰对人气道上皮细胞凋亡和增殖的影响及与慢性阻塞性肺疾病患者小气道重塑的关系
肾功能对老年男性慢性肾脏病患者肌少症的影响
不同体位物理振动排石术治疗结石性肾绞痛的临床观察
经组织病理学检查确诊的结节病葡萄膜炎的临床特征
前庭康复训练对前庭外周性眩晕患者眩晕残障症状的改善作用
濒临破裂腹主动脉瘤诊断中彩色多普勒超声的价值分析
胃黏膜相关淋巴组织淋巴瘤患者68例临床预后分析
stomatin蛋白表达对肺癌细胞增殖和凋亡的影响
补充维生素D辅助治疗肺结核效果和安全性的荟萃分析
大规模检测平台在新型冠状病毒防控中的作用:基于新型数值模型的实证研究
胃肠道惰性T细胞淋巴组织增殖性疾病临床病理特征分析
第513例 黏液脓血便—发热—消瘦
第514例 高血压—低钾血症—肌酶升高—高血糖—中药服用史
胆管混合性腺-神经内分泌癌一例
干细胞与免疫调节在心肌梗死治疗中的研究进展
艾曲泊帕治疗再生障碍性贫血作用机制的研究进展
二甲双胍通过沉默MATE1表达富集在细胞内选择性抑制KRAS突变转移性结肠癌
Colon cancer (CRC) is one of the common cancers, and metastasis is the leading cause of death. Recent studies have found that first-line chemotherapy drugs irinotecan or oxaliplatin combined with epidermal growth factor receptor (EGFR) -targeted drugs can improve the median overall survival of patients with metastatic colorectal cancer (mCRC) by more than 2 years. However, KRAS-mutated colon cancer patients (about 30% to 50%) show resistance to EGFR-targeted drugs. Therefore, EGFR-targeted drugs cannot be used to treat mCRC patients with KRAS mutations. Many previous studies have pointed out that metformin has anti-tumor effects, and taking metformin is closely related to a good prognosis of patients. However, many retrospective studies have found that metformin is not related to the prognosis of cancer patients, and there are still many questions and differences about the therapeutic effect and molecular mechanism of metformin on tumors.
补充维生素D3对HIV感染者预防肺结核及死亡的疗效
To evaluate vitamin D supplementation3Impact on mortality and tuberculosis incidence in HIV-infected individuals initiating antiretroviral therapy (ART) A vitamin D supplementation was administered to HIV-infected individuals with serum 25-hydroxyvitamin D concentrations below 30 ng/ml and initiating ART at four large HIV care and treatment centers in Dar es Salaam, Tanzania3A randomized, double-blind, placebo-controlled trial of. Age of exclusion<18 years of age, pregnant, or participating in any other clinical trial. Subjects were randomly assigned in a 1:1 ratio to oral vitamin D during the first month of ART350 000 U/week, followed by vitamin D supplementation32 000 U/d, the control group was given placebo at the same time interval and frequency. The randomized control list was computer-generated by a non-statistical investigator with a sequence block of 10, ensuring complete assignment concealment, and subjects, field groups, and researchers were assigned in disguise. The trial was followed up for 1 year and the primary outcome measures were death and new tuberculosis in HIV-infected subjects. An intention-to-treat analysis of all-cause mortality was performed, and subjects diagnosed with tuberculosis at the time of randomization, who were receiving antituberculous therapy, or who were suspected of having tuberculosis and were later diagnosed were excluded from the study tuberculosis incidence analysis. Between 24 February 2014 and 24 February 2017, 6 250 ART-initiated adult subjects were screened for serum 25-hydroxyvitamin D, of which 4 000 subjects participated in the trial and were followed for 1 year (all subject follow-ups were completed on 7 March 2018). 2 001 subjects were randomized to vitamin D3Group, 1 999 subjects were randomly assigned to placebo. A total of 415 subjects died, including vitamin D3211 cases in the group and 204 cases in the placebo group were supplemented with vitamin D3There was no statistically significant effect on the risk of death in HIV-infected persons (HR=1.04,95%CI:0.85~1.25)。 Vitamin D3There was no statistically significant difference in the new prevalence of pulmonary tuberculosis between the group and the placebo group (HR=0.78,95%CI:0.54~1.13)。 Vitamin D3There were 3 and 2 cases of hypercalcemia in the group and the placebo group, respectively, and vitamin D supplementation was found3Does not increase the risk of hypercalcemia (RR=1.25,95%CI:0.43~3.66)。 For hospitalization rates, vitamin D3There were 101 cases in the placebo group and 94 cases in the placebo group, and the difference was not statistically significant (IRR=1.06,95%CI:0.80~1.41)。
辅助维生素A和D在肺结核治疗中的应用
In order to understand the effects of vitamin A and D supplementation on symptom relief and sputum smear conversion time in pulmonary tuberculosis patients, a 2×2 factorial design randomized controlled trial was conducted in Qingdao, China. Symptom relief of tuberculosis patients was evaluated by TB-score including cough, expectoration, hemoptysis, dyspnea, chest pain, night hot flashes, night sweats, fatigue, anorexia, fever and body mass index. Between October 2012 and March 2015, a total of 800 patients with pulmonary tuberculosis who received standardized chemotherapy (isoniazid, rifampicin, ethambutol, pyrazinamide for February/isoniazid, rifampicin for April) were randomly assigned 1:1:1:1. 39 patients were withdrawn because they could not complete standard chemotherapy. Finally, 190 patients received standard pulmonary tuberculosis treatment only (control group), 187 patients received vitamin A supplementation (2 000 U/d), 199 patients received vitamin D supplementation (400 U/d), and 185 patients received both vitamin A (2 000 U/d) and vitamin D (400 U/d) combined supplementation were included in the symptom analysis. Finally, 761 patients were included in the tuberculosis symptom analysis. Of the 761 patients with pulmonary tuberculosis, 203 patients had negative sputum smear at baseline, 37 patients had no subsequent sputum smear results, and the remaining 521 patients were included in the sputum smear conversion analysis (128 patients in the vitamin A supplementation group, 145 patients in the vitamin D supplementation, 121 patients in the combined vitamin A and vitamin D supplementation, and 127 patients in the control groupHR=1.021,95%CI: 0.821 to 1.271), vitamin D (HR=0.949,95%CI: 0.760~1.185) had no significant effect on the negative conversion time of sputum smear, and there was no significant interaction between vitamin A and vitamin D supplementation. However, vitamin D supplementation significantly improved the symptoms of tuberculosis patients, and their TB-score decreased at 2 to 4 weeks (MD=-0.2,95%CI:-0.4~0)。
针对Beta冠状病毒的疫苗设计
SARS-CoV-2 is a member of Beta-CoV lineage B and has 75% to 80% homology to the severe acute respiratory syndrome coronavirus (SARS-CoV) genome sequence. Vaccines are an effective measure to control ongoing COVID-19 and previous coronavirus infections such as MERS/SARS. Spike receptor binding domain (RBD) is an ideal target for coronavirus vaccines, but the limited immunogenicity of RBD limits vaccine development against this domain. This study found that a dimeric form of Middle East respiratory syndrome coronavirus (MERS-CoV) RBD can effectively improve RBD immunogenicity. RBD-dimer significantly increased the titer of neutralizing antibodies (NAb) and protected mice from MERS-CoV infection compared to conventional monomeric forms. Crystal structure studies revealed that the RBD-dimer completely exposed the dual receptor binding motif (the primary target of NAbs). Structure-guided design further yielded stable RBD-dimers, i.e. tandem repeating single chains (RBD-SC-dimers), preserving the efficacy of the vaccine. The researchers generalized the strategy to vaccine designs against COVID-19 and SARS, resulting in a 10-to 100-fold increase in NAb titers. The RBD-SC-dimer achieved higher yield in pilot production, which provided a theoretical basis for subsequent clinical development and application. This strategy can be generalized to design vaccines against multiple beta-CoVs, providing safeguards for controlling coronavirus infections such as SARS-CoV-2, MERS, and SARS-CoV.
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