Goal: to to examine the formation of postvaccination immunity and evaluate the therapeutic effect of bacterial vaccines in patients with inflammation diseases of bronchopulmonary system. Objectives of the study: assessment of microbiocenosis mucous membranes of the upper respiratory tract in patients with bronchopulmonary pathology before and after use of bacterial vaccines. Identification of mayor lymphocytes subpopulations in patients in the dynamics of the vaccination process. Study the profile of humoral immune response in patients under different schemes of vaccination. Assessment of the clinic and functional status bronchopulmonary system in the immunized patients.
Methods: 1. Immunoglobulin G (IgG)-antibodies against Streptococcus pneumoniae (S. pneumoniae) - solid-phase enzyme-linked immunoelectrodiffusion essay (ELISA). 2. General levels of Immunoglobulin A (IgA), Immunoglobulin M (IgM), IgG, Immunoglobulin E (IgE) in sera - radial immunodiffusion. 3. Phagocytic activity (granulocytes, monocytes), nitroblue tetrazolium test; T-lymphocytes, T-helpers (cluster of differentiation, CD3+CD4+), cytotoxic T-lymphocytes (СD3+CD8+), B-lymphocytes (CD19+); NK-cells (CD3-CD16+CD56+), NKT-cells (CD3+CD16+CD56+), activated T-cells (human leucocyte antigens, CD3+HLA DR+), CD3-HLA DR+. 4. Microbiological examination of sputum. 5. Determining the clinical effectiveness of vaccination. * the number of exacerbations of chronic bronchopulmonary pathology for the year prior to vaccination and during the first and fourth years after vaccination; * the number of courses of antibiotic therapy a year prior to vaccination and during the first and fourth years after immunization; * the number of hospitalizations for acute exacerbations of chronic bronchopulmonary disease during the year prior to vaccination and during the first and fourth years after immunization. 6. Method of estimating quality of life associated with health in patients with chronic bronchopulmonary pathology (asthma control questionnaire (ACQ-5), COPD assessment test (CAT)). Characteristics of variables (arms 1-8). 1. The age of patients (years): mean (standard deviation) \[min; median; max\] for normally distributed variables; median \[Q25; Q75\] - for variables with distribution different from normal. 2. Gender: male/female. 3. Indicators of immune status * IgG antibodies to S. pneumoniae * IgA, g/l \[0,4-3,5\] * IgM, g/l \[0,7-2,8\] * IgG, g/l \[8-18\] * IgE, IU/ml \[\< 100\] * Phagocytic index (granulocyte), % \[82-90\] * Phagocytic index (monocytes), % \[75-85\] * The participation rate of spontaneous NBT-test (neutrophils), % with intensity of 0.2.e. \[7-14\] * The index of activity induced NBT-test (neutrophils), % if intensity \>of 0.36.e. \[\>28\] * The percentage of NBT-positive cells in spontaneous test, % \[2-19\] * Circulating immune complexes (CEC) cond. units \[0,055-0,11\] * CD3+, % \[55-80\] * CD3+CD4+, % \[31-49\] * CD3+CD8+, % \[12-30\] * CD19+, % \[5-19\] * CD3-CD16+CD56+, % \[6-20\] * CD3+CD16+CD56+, % \[\<10\] * CD3-HLA DR+, % \[5-20\] * CD3+HLA DR+, % \[\<12\] * CD45RO. The reference value = 0,2. 4. Microbiological examination of sputum: frequency of selection of certain microorganisms are presented as absolute number of cases and % in the respective groups. 5. Evaluation of early post-vaccination period * The General condition (satisfactory/unsatisfactory) * Local reactions: pain (n/%), redness (n/%, cm), consolidation (n/%, cm) * General reactions: * Temperature 37,0-37,5 (n/%) * Temperature of 37.6-38,5 (n/%) * A temperature of 38.6 and \> (n/%) * Headache (n/%) * Malaise, fatigue (n/%) * Joint pain (n/%) * Muscle pain (n/%) 6. Health related quality of life (HRQoL): CAT-test (for Chronic obstructive pulmonary disease (COPD) patients), ACQ-5 (for asthma patients).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
219
Conjugate 13 serotype pneumococcal vaccine
Polysaccharide 23-valent pneumococcal vaccine.
Samara State Medical Univercity
Samara, Samara Oblast, Russia
Institute of Sera and Vaccines RAS
Moscow, Russia
Number of Patients Without Exacerbations of the Underlying Disease, Antibiotic Use and Hospitalisation.
Number of patients without exacerbations of the underlying disease, antibiotic use and hospitalisation.
Time frame: Baseline (1 year prior to vaccination), 1 year after vaccination, 4 years after vaccination
The Number of Exacerbations of the Underlying Disease, Antibiotic Use and Hospitalisation
The number of exacerbations of the underlying disease, antibiotic use and hospitalisation. The average number of exacerbations per 1 patient = total exacerbations in the group / number of patients in the group. This is not a mean value.
Time frame: Baseline (1 year prior to vaccination), 1 year after vaccination, 4 years after vaccination
Seeding Frequency S. Pneumoniae From Sputum in Patients With COPD
Seeding frequency S. pneumoniae from sputum in patients with COPD
Time frame: Baseline, after 1 and 4 years after vaccination
Average CAT (COPD) and ACQ-5 (Asthma) Score
CAT - COPD Assessment Test, min. = 0, max. = 40, higher scores mean a worse outcome. ACQ-5 - Asthma control questionnaire, min. = 0, max. = 6, higher scores mean a worse outcome.
Time frame: Baseline, after 1 and 4 years after vaccination
Phagocytic Activity in Patients With COPD at Baseline, 1, 2, and 6 Weeks After PCV13 and PPV13 Vaccination
Phagocytic index (granulocytes), phagocytic index (monocytes), activity of a spontaneous HCT test (neutrophils), activity of an induced HCT test (neutrophils), percentage of HCT-positive white blood cells in a spontaneous test. The phagocytic index was calculated according to the following formula: phagocytic index = (total number of engulfed cells/total number of counted macrophages) × (number of macrophages containing engulfed cells/total number of counted macrophages) × 100 (phagocytic index) The phagocytic index was calculated by counting at least 100 bacteria phagocytized by certain number of phagocytic cells/macrophages and expressed following formula (Mamnur Rashid 1997): Phagocytic index = Total no. of phagocytized bacteria /No of phagocytic cells phagocytizing bacteria. Activation index = % formazan positive cells (FPC) in NBT stimulated / % formazan positive cells (FPC) in NBT Spontaneous.
Time frame: Baseline, 1, 2, 6 weeks after PCV13 and PPV13 vaccination
Immunophenotype of Blood Lymphocytes in Patients With COPD
Immunophenotype of blood lymphocytes in patients with COPD at baseline, 1, 2 and 6 weeks after PCV13 and PPV23 vaccination. It was pre-specified to report data from only the "COPD - Prevenar-13" and the "COPD - Pneumo-23" Arms/Groups for this Outcome Measure". This is due to the fact that we tried to study the effect of PCV13 and PPV23 on immunity values. The study of the immunological effects of vaccination in the early post-vaccination period was carried out in 2 groups of patients: 20 patients with COPD vaccinated with PCV13; 20 patients with COPD vaccinated with PPV23. These patients were selected from patients of the main groups (COPD - Prevenar-13 (1), COPD - Pneumo-23 (3)).
Time frame: Baseline, 1, 2, 6 weeks after PCV13 and PPV13 vaccination
IgA, IgM, IgG, IgE, Circulating Immune Complexes (CIC)
IgA, IgM, IgG, IgE, circulating immune complexes (CIC) in serum at baseline, 1, 2 and 6 weeks after vaccination. It was pre-specified to report data from only the "COPD - Prevenar-13" and the "COPD - Pneumo-23" Arms/Groups for this Outcome Measure". This is due to the fact that we tried to study the effect of PCV13 and PPV23 on immunity values. The study of the immunological effects of vaccination in the early post-vaccination period was carried out in 2 groups of patients: 20 patients with COPD vaccinated with PCV13; 20 patients with COPD vaccinated with PPV23. These patients were selected from patients of the main groups (COPD - Prevenar-13 (1), COPD - Pneumo-23 (3)).
Time frame: Baseline, 1, 2, 6 weeks after PCV13 and PPV13 vaccination in COPD
CD45RO
CD45RO expression on lymphocytes in serum at baseline, 1 and 4 years after vaccination. These patients were selected from patients of the main groups.
Time frame: Baseline, 1 and 4 years after vaccination
Specific IgG Levels in Vaccinated Patients With COPD to S. Pneumoniae Serotypes
Mean specific IgG levels in vaccinated patients with COPD to S. pneumoniae serotypes at baseline, 6 and 12 months after vaccination
Time frame: Baseline, 1 and 12 months after vaccination
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