ABSTRACT
We studied the neutrophils and monocytes obtained from 37 patients with various inflammatory diseases such as psoriasis, acute infectious process in the abdominal cavity (acute appendicitis/abscess of the abdominal cavity, and acute cholecystitis), acute pancreatitis, and post-COVID syndrome after mild COVID infection. The number and the morphological structure of neutrophil extracellular traps (NET) as well as the effect of IgG on NET were examined. NET were visualized and counted by fluorescence microscopy with fluorescent dye SYBR Green. All the studied types of inflammation were accompanied by spontaneous formation of NET. After application of IgG, the number of NET doubled, their size increased, and transformation of net-like traps into the cloud forms was observed. The clouds form structure of the network is not capable of capturing pathogens with subsequent retraction, the products of its enzymatic degradation can be the factors of secondary alteration. The study results demonstrate a previously unknown mechanism of infection resistance.
Subject(s)
COVID-19 , Extracellular Traps , Pancreatitis , Humans , Extracellular Traps/metabolism , Acute Disease , Pancreatitis/metabolism , COVID-19/metabolism , Neutrophils/metabolism , Immunoglobulin G/metabolismABSTRACT
AIM: To provide a rationale for choosing the optimal tactics of vaccination against pneumococcal infection in patients with chronic obstructive pulmonary disease (COPD) in the context of evidence-based medicine and on the basis of immunological and clinical data. SUBJECTS AND METHODS: Patients with COPD were examined during a year after vaccination with a 13-valent pneumococcal conjugate (Prevenar-13, PCV13) and a 23-valent pneumococcal polysaccharide (Pnemo-23, PPV23) vaccines. The following vaccination schemes were used: PCV13 monovaccination, PPV23 monovaccination, sequential vaccination with PPV23/PCV13, and sequential vaccination with PCV13/PPV23. RESULTS: Vaccination using all the analyzed schemes in the patients with COPD caused a statistically significant reduction in the frequency of exacerbations, the number of antibiotic cycles, and the number of hospital admissions, as shown by the results of analysis of short-term data. The use of PCV13 was followed by additional effects that were unobserved in the use of PPV23, namely: it promoted the formation of immunological memory to Streptococcus pneumoniae antigens, resulted in the enhanced activity of nonspecific resistance factors, and caused activation of antiviral defense factors. CONCLUSION: If patients with COPD need to be vaccinated against pneumococcal infection, preference should be given to PCV13 monovaccination. Short-term observations have shown that the sequential use of pneumococcal conjugate and polysaccharide vaccines is redundant and gives no additional benefit to patients with COPD. However, the sequential application of both vaccines may have additional advantages in the long term.
Subject(s)
Evidence-Based Medicine/methods , Outcome Assessment, Health Care , Pneumococcal Infections/prevention & control , Pneumococcal Vaccines/pharmacology , Pulmonary Disease, Chronic Obstructive/immunology , Vaccination/methods , Aged , Female , Humans , Male , Middle Aged , Pneumococcal Vaccines/administration & dosageABSTRACT
Relations between hyperventilation, hyperventilation syndrome (HVS) and bronchial asthma (BA) are not finally established. This study modelled HVS in 92 volunteers to investigate HVS effect on external respiration function (ERF), immune status and hormonal and amino regulation. HVS was found to induce significant shifts in regulating systems (adrenergic, cholinergic, serotoninergic, conticosteroids) function and to alter correlations between ERF and blood levels of immune cells carrying various CD- and HLA-DR markers. The HVS model can be used for the study of HV role in immunopathogenesis of BA.
