Immune Cell Crisis and Excess Histopathological Features During the Development and Progression of Infection in the Gastric Mucosa.

Objective: To investigate immune cell crisis and excess histopathological features during the development and progression of infection in the gastric mucosa.

Methods: One thousand two hundred and seventy-six cases of infection were examined by endoscopic biopsy and endoscopic submucosal dissection (ESD) resection. The relationship between epithelial cells and immune cells and the pathological features of immune cell dysfunction and excess tissue were observed. The 1276 cases of mucosal biopsy of infection and ESD resection were included. Among them, 39 were ESD excision and 1237 were gastric mucosal biopsy specimens. Among them, there were 896 cases of antrum infection, 274 cases of stomach body infection, and 106 cases of infection in antrum and body of stomach. Three to five pieces of mucosal tissue were extracted from each site. There were 789 males (61.8%) and 454 females (35.6%). There were 724 cases (56.7%) with age ≤60 and 552 cases (43.3%) with age >60.

Results: During the occurrence and development of infection, there were not only spider-like vacuolar degeneration of surface epithelial cells, compensatory cervical mucous cell proliferation, proliferation disorder of stem cells in proliferating areas, and neoplastic proliferation of gastric mucosal epithelial cells, but also morphological changes of immune cells in the process of occurrence and development of infection. First, neutrophils that rapidly respond and attack the infection; however, neutrophils quickly display functional deficiencies, forming mucosal erosion and micro-abscesses. Then, it enters a phase of immune cell crisis. The immune defense is adjusted. The rapid proliferation of lymphocytes leads to the formation of lymphocyte immunity and the formation of lymphocyte follicle-like structures. In this stage, the lesions are wide and deep, the duration is long, and the number of patients is large. Persistent can result in abnormal proliferation and transformation of gastric mucosal epithelial cells and immune cells and gastric adenocarcinoma and MALT lymphoma.

Conclusion: Understanding the immune cell crisis and excess histopathological features during the occurrence and development of infection is important for controlling the occurrence and development of gastric cancer and lymphoid system tumors via immune intervention.