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The realization of the protective properties of immunity is related to the functional state of immune cells. The ability of white blood cells to maintain their viability, divide, produce cytokines, and perform other functions largely depends on the degree of cell depletion and aging. It is known that these functional states are determined by the ability of immunocytes to rebuild cellular metabolism. However, the question of how individual metabolic processes of leukocytes change in response to external influences is currently poorly understood.

Intensive metabolic restructuring and an increase in the rate of metabolic processes accompanying the activation, differentiation and proliferation of leukocytes are similar to those in tumor cells. In this sense, tumor cell lines are an excellent model for studying the mechanisms of action of various factors on subpopulations of immunocytes.

The functional state of the cells of the immune system is affected by infections. So, when In HIV infection, immunocompetent cells divide unproductively and cannot increase their numbers sufficiently. This leads to the formation of immunodeficiency, contributes to the development of concomitant diseases and death of patients. Preliminary data suggest that in HIV-infected subjects, the reason for the low productivity of CD4+ T lymphocyte proliferation lies in the depletion of their pool. It has also been shown that, compared with the corresponding cells of healthy individuals, T-helper cells of HIV-positive patients consume more metabolic substrates such as glucose. It is suggested that these substrates are used by cells to divide and perform effector functions, which, however, does not correspond to the realities of empirically observed reality.

Compounds of chemical and biological origin, including pharmacological preparations, can also affect the functional state and metabolism of immune cells. It has been shown that many antiretroviral drugs have a toxic effect on mitochondria, which play the role of central nodes of cellular metabolism. Mitochondrial problems can lead to pathogen-independent disorders of CD4+ proliferative capacity T-lymphocytes of HIV-infected patients. Hormones, analgesics and many drugs, the sale and reception of which often occurs uncontrollably, can also have a significant effect on the functional state of the cells of the immune system. The means of targeted drug delivery , microbial synthesis products, and drug prototypes based on synthetic and biological compounds that are actively being developed today are also not inert and can have both stimulating and inhibitory effects on the immune system.

The causes and mechanisms of changes in the functional state of leukocytes under various influences have not been studied. This prevents the development of new approaches to therapy or modification of health-saving technologies, and hinders the rational use of medicines.

  1. Western blot
  2. Enzyme-linked immunosorbent assay (ELISA)
  3. Real-time PCR (qPCR)
  4. Flow cytometry
  5. Chemiluminescence
  6. Cell and tissue culture
Evgeniya Saidakova 🤝
Head of Laboratory
Maria Nikitina 🤝
Researcher
Violetta Vlasova
Junior researcher
V N Ponomareva
V Ponomareva
Junior researcher

Research directions

Immunometabolism

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The study of immune cell metabolism to study the mechanisms of action of pharmacological substances, determine their safety for immunity, to search for biomarkers of T-lymphocyte division abnormalities, early diagnosis and monitoring of T-cell activity disorders, as well as to develop new diagnostic approaches and optimize therapeutic measures for diseases of the immune system.

Functional studies of T-lymphocytes

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Search for biomarkers of T-lymphocyte abnormalities for early diagnosis and monitoring of T-cell activity disorders. Development of new diagnostic approaches to optimize therapeutic measures for diseases of the immune system.

Discordant immunological response (immunological non-response) for HIV infection therapy

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Discordant immunological response (immunological non-response) for HIV infection therapy
The Russian Federation is one of the world leaders in the growth of HIV incidence. In most regions, the incidence of HIV infection and the prevalence of the population do not tend to decrease. The epidemic has long gone beyond the socially marginalized groups of the population and is actively spreading in the general population. The only method currently available to control the development and spread of HIV infection is antiretroviral therapy (ART). Antiretroviral drugs suppress HIV replication and provide an opportunity to increase the number of CD4+ T lymphocytes, thereby reducing the incidence, disability and mortality of able-bodied citizens. However, in 10-40% of patients receiving ART, a decrease in HIV viral load is not accompanied by CD4+T cell regeneration (the so-called discordant immunological response or immunological non-response). Chronic immunodeficiency prevents such patients, who are immunologically unresponsive– from responding effectively to vaccination, increases the risk of developing cardiovascular disorders, liver and kidney diseases, metabolic syndrome, neurocognitive abnormalities and malignancies; increases the likelihood of developing AIDS and death. The daily increase in the number of HIV-infected patients determines the need to study the mechanisms of impaired regeneration of T-lymphocytes and actualizes the problem of immunological non-response. Laboratory staff are investigating the causes and mechanisms of the discordant immunological response to ART at the molecular and cellular levels.

Publications and patents

Found 

Lab address

Россия, г. Пермь, ул. Голева, д. 13
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