Acute pancreatitis is a common and critical disease in clinical practice, and clinical treatment has formed a multidisciplinary and collaborative model of traditional Chinese and Western medicine. However, its etiology and pathogenesis are complex and varied, and immune response is crucial in the occurrence and development of the disease. Therefore, based on the thinking of the pathological and physiological basis of immune response in the different stages of acute pancreatitis disease progression and related complications, and based on the biological characteristics and laws of the disease, this article summarizes a reasonable and phased implementation of Chinese and Western medicine collaborative management strategy, which is proposed to achieve optimal and precise treatment of the disease.
Rheumatoid arthritis (RA) is one of the most common immune-mediated diseases, and the interaction between the intestinal microbiota and the patient’s immune system may play a role in the occurrence and development of RA. Methotrexate (MTX), as a first-line drug for the treatment of RA, can be directly and indirectly influenced by intestinal microbiota and its enzyme products to affect the bioavailability, clinical efficacy, and toxicity of the drug. Therefore, it is crucial to understand the mechanism by which intestinal microbiota affects RA and the impact of intestinal microbiota on the efficacy of MTX. This article provides a review of the mechanisms by which intestinal microbiota may contribute to the pathogenesis of RA, as well as the role and impact of intestinal microbiota in MTX drug metabolism and treatment response.
ObjectiveTo elucidate the metabolic characteristics of mitochondria in sepsis and review its cellular mechanism, so as to provide new ideas for the treatment of sepsis. MethodThe previous literatures and latest research results about mitochondrial metabolism during sepsis were reviewed. ResultsAt present, the researchers were not only concerned about the inflammatory response of sepsis, but also concerned about the systemic metabolic disorder caused by sepsis. It was believed that the damage of mitochondria caused by sepsis was one of the main reasons for the disorder of cell metabolism. During the sepsis, the patient’s metabolism had changed, for example, enhancement of aerobic glycolysis, lactic acid accumulation, elevated levels of fatty acids and triglycerides in blood, and so on. ConclusionMetabolic change during sepsis is related to mitochondria, which can provide some new methods for treatment of sepsis.
Tuberculosis caused by Mycobacterium tuberculosis is the leading infectious killer posing a major public health threat. The clinical manifestations of ocular tuberculosis are highly heterogeneous. Currently, the diagnosis of ocular tuberculosis still heavily relies on comprehensive clinical judgment and response to anti-tuberculosis therapy. Tuberculosis-specific T-cell detection quantifies the intensity of antigen-specific T-cell responses, providing indirect evidence for the diagnosis of tuberculosis infection. It has become a key auxiliary examination in the diagnosis and management of ocular tuberculosis but must be closely integrated with clinical manifestations and imaging features. A positive result suggests the involvement of a tuberculous immune response but cannot alone confirm a diagnosis of ocular tuberculosis. Future efforts should integrate T-SPOT.TB testing with other diagnostic tools, standardize diagnostic procedures, and explore the mechanisms linking T-cell subset functions with the intraocular immune microenvironment. Further elucidation of the relationship between T-cell responses and ocular tuberculosis phenotypes will help advance personalized treatment.