Experience with 13-valent conjugated pneumococcal vaccine in HIV-infected patients


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Abstract

Aim. Evaluate the effect of PCV13 vaccination on the composition of the microflora of the upper respiratory tract and the immune system in HIV-infected patients.

Materials and methods. 100 patients with HIV-infection were included in the study. The patients underwent immunological examination and the collection of biomaterial from the posterior pharyngeal wall for microbiological examination. After obtaining the results of the examinations, PCV13 was intramuscularly administered. 7 days after the introduction of the vaccine, an assessment of adverse events was carried out, after 3 months, microbiological and immunological examinations were repeated.

Results. Immediately after the administration of PCV13, 5% of patients felt pain during the administration. Local reactions were reported in 6 patients. One participant showed a rise in temperature to 38.3°C over 2 days. Before vaccination, 16 strains of S. pneumoniae were seeded in patients. 3 months after the administration of PCV13, pneumococcus was isolated in 8 patients. 3 months after immunization, the median level of populations and subpopulations of lymphocytes became higher than the pre-vaccination.

Discussion. Our results show high risk of pneumococcal infections in HIV-positive patients. A tendency towards a decrease in the level of S. pneumoniae carriage was revealed 3 months after the administration of PCV13. The high level of enterobacteria carriage in HIV-positive patients is noteworthy. There is a pronounced positive effect from the use of PCV13 in HIV-positive patients on cellular factors of the immune system.

Conclusion. The use of PCV13 is a safe and effective method for the prevention of S. pneumoniae infections.

About the authors

A. V. Zhestkov

Samara State Medical University

Author for correspondence.
Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0002-3960-830X

д.м.н, проф., зав. каф. общей и клинической микробиологии, иммунологии и аллергологии

Russian Federation, Samara

M. O. Zolotov

Samara State Medical University

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0002-4806-050X

очный аспирант каф. общей и клинической микробиологии, иммунологии и аллергологии

Russian Federation, Samara

A. V. Lyamin

Samara State Medical University

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0002-5905-1895

к.м.н., доц. каф. общей и клинической микробиологии, иммунологии и аллергологии

Russian Federation, Samara

O. V. Borisova

Samara State Medical University

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0003-1430-6708

д.м.н., проф. каф. детских инфекций

Russian Federation, Samara

O. E. Chernova

Samara Regional Clinical Center for AIDS Prevention and Control

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0003-4600-0738

к.м.н., глав. врач

Russian Federation, Samara

L. V. Limareva

Samara State Medical University

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0003-4529-5896

д.б.н, проф. каф. общей и клинической микробиологии, иммунологии и аллергологии, дир.

Russian Federation, Samara

D. D. Ismatullin

Samara State Medical University

Email: m.o.zolotov@gmail.com
ORCID iD: 0000-0002-4283-907X

ассистент каф. общей и клинической микробиологии, иммунологии и аллергологии

Russian Federation, Samara

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Supplementary files

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2. Figure: 1. The proportion of seeding of various representatives of microflora in HIV-infected patients from the total number of isolated strains before vaccination (%).

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3. Figure: 2. The proportion of seeding of various representatives of microflora in HIV-infected patients from the total number of isolated strains 3 months after vaccination (%).

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4. Figure: 3. Comparison of the seeding frequency of various microflora representatives in HIV-infected patients from the total number of isolated strains before vaccination and 3 months after (%).

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5. Figure: 4. Comparison of the median level of subpopulations of lymphocytes before vaccination and 3 months after immunization.

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