Autoimmune diseases and drugs for their treatment

Human bone marrow promotes the production of lymphocytes. After entering the bloodstream, they become immature. The first place where their maturation occurs is the thymus, the second is the lymph node. The localization of the thymus is the upper part of the chest, and the lymph nodes are the neck, groin, and armpit. T-lymphocytes are called cells after the maturation process in the thymus, and B-lymphocytes mature in the lymph node. These two types of lymphocytes produce antibodies that fight foreign tissue and infections. The antibody response is directed only at the antigen that matches it. For example, a child who has had mumps will not develop immunity against measles.

The essence of vaccination is to familiarize the immune system with a certain type of disease. Administration of a vaccine means that a small dose of the pathogen penetrates the body, which is needed for the further destructive effect of antibodies on antigens. However, there are situations when lymphocytes begin to attack the tissues of their own body. This is how autoimmune diseases begin to develop. They occur in approximately 10 percent of the world's population. Medical practice shows that rare autoimmune diseases affect men less often than women. There are ten main causes of death. These causes include autoimmune and immunodeficiency diseases.

Every person’s body has immunity, which begins its development from the moment of birth. It consists of special organs and cells that protect against negative microbial and viral effects. The immune system is based on a mechanism that can distinguish between self and foreign tissue. Various damage provokes dysfunction of the immune system, as a result of which it ceases to distinguish its own cells from foreign ones. This phenomenon activates the production of autoantibodies that mistakenly attack healthy cells. As a result, the regulatory work of t-lymphocytes disappears, and severe autoimmune diseases appear that affect the internal organs and systems of the body.

A list of autoimmune diseases should be considered. The first type is a disorder that appears when the histohematological barrier is disrupted. The second type of disease appears after the body’s tissue is transformed from physical, chemical, or viral effects. Deep metamorphotic processes occur in healthy cells, and as a result, they are perceived by others. There are cases where antigenic or exoantigenic concentration occurs. The body will react by damaging the cell on the membrane of which the antigenic complex is preserved. Sometimes contact with a virus provokes the formation of an antigen that has a hybrid property. It can affect the central nervous system.

The third group includes diseases of the autoimmune system, in which coalescence of tissue with an exoantigen occurs. As a result, a natural reaction is activated, aimed at the affected areas. The fourth group includes ailments caused by a genetic deviation or the influence of an unfavorable external factor. This entails a rapid mutation of immune cells, which manifests itself as lupus erythematosus.

The development of an autoimmune disease can develop at any age. Despite this, there is a group of people who are more susceptible to autoimmune diseases. Namely:

  • A person who is exposed to negative influences from external factors. Specialists in autoimmune diseases in Moscow highlight the influence of sunlight, chemicals, viral or bacterial infections, which cause pathological processes in the immune system.
  • A woman of childbearing age. Autoimmune diseases occur more often in women than in men.
  • Certain races and ethnic groups. Signs of an autoimmune disease are more likely to occur in people with white skin. For example, African Americans and Hispanics have a hard time with systemic lupus erythematosus.
  • Hereditary factor. It should be remembered that autoimmune diseases are inherited from close relatives. Medical practice shows that a family history can reveal different types of immune disorders.

Why do they appear?

Medical research identifies internal and external reasons why autoimmune diseases occur. One of the internal reasons when aggression and uncontrolled proliferation of lymphocytes occurs is a gene mutation of the first type. At the same time, recognition of healthy cells by lymphocytes disappears. A person inherits such an immune disorder from a close relative. Considering the mutation process in a specific organ or system, thyroiditis and goiter may develop.

Another internal cause is a type 2 gene mutation, in which uncontrolled proliferation of nurse lymphocytes occurs. As a result, immune and autoimmune diseases appear, which are mainly inherited. Among the external causes of autoimmune disease are a severe, protracted infectious disease, after which inadequate behavior of immune cells occurs, as well as the negative impact of environmental factors (radiation, ultraviolet rays). The occurrence of a malfunction of the immune system occurs due to the cunning of the cell that causes the disease. They are able to pretend to be similar to their own, but pathogenic cells. As a result, lymphocytes lose the ability to recognize foreign organisms and begin to fight both.

Systemic autoimmune diseases appear when the integrity of the blood barrier that separates a certain organ or tissue from the blood is disrupted. The norm is the absence of penetration of cellular antigens into the bloodstream. This means that T-lymphocytes do not develop tolerance to them. The barrier cells include brain cells, thyroid cells, and cells that produce insulin. In the presence of such a mechanism, chronic autoimmune prostatitis develops. This means that sperm-producing cells are separated from the blood by the blood-testis barrier. Infection, inflammation, trauma can cause a violation of its integrity, as a result of which auto-aggression begins, directed at the prostate tissue.

What types of autoimmune diseases exist?

Speaking about the classification of disorders, there are three groups of autoimmune diseases. The first group includes organ-specific pathologies, characterized by the direction of antibodies and lymphocytes to the autoantigen of one or more organs. This includes a barrier antigen, to which there is no innate tolerance. The second group includes organ-nonspecific diseases, when autoantibodies and lymphocytes interact with autoantigens of a tissue or organ. The pathological process develops when tolerance already exists. The third group consists of the above mechanisms.

If a person is faced with an immune disorder, he will be interested in which doctor deals with autoimmune diseases. In case of organ-specific autoimmune disease, you must consult a specialized doctor. With a mixed or systemic illness, qualified assistance from many doctors is required. This is a neurologist, hematologist, rheumatologist, endocrinologist, cardiologist, pulmonologist, dermatologist, nephrologist.

What are systemic autoimmune diseases?

The appearance of lupus erythematosus is associated with a violation of the autoimmune process, when all internal organs are involved. The disease affects two to three people out of a thousand. Lupus erythematosus occurs when abnormal antibodies are formed in the body due to the influence of a genetic factor. Confirmation is the presence of a relationship between pathology and a lack of hereditary components of immunity. In addition, a toxic substance, a virus, or uncontrolled use of medications can provoke the appearance of an immune disorder.

The systemic disorder occurs without symptoms for a long time, manifests itself as a skin rash, and the musculoskeletal system is disrupted. However, at this time, the intensity of immune imbalance in the body increases, which can cause an inflammatory process in any internal organ. Lupus erythematosus is characterized by damage to the connective tissue present in organs and systems. As a result, skin rashes appear on the face and chest, and the skin becomes sensitive to ultraviolet radiation (redness, rash, spots). A distinctive feature is the appearance on the body of a disc-shaped element, which has a red edge and a pale middle.

With this autoimmune disease, the symptoms are as follows:

  • The appearance of lupus arthritis is characterized by sharp or aching pain, swelling, and redness of the joints that are involved in the pathological process. After limited movement of the affected limb, complete immobilization of the bone joint occurs.
  • Damaged outer serous membranes of internal organs cause coughing attacks and pain when inhaling and exhaling. The doctor will hear a moist wheeze in the lower lobe of the lung.
  • Damage to the heart and blood vessels occurs, aching pain appears, and the rhythm of heart contractions is disrupted.
  • Due to pathological vascular changes, the feet and hands turn blue, and the extremities become cold.
  • The appearance of visual and auditory hallucinations, a state of delirium.
  • With abdominal syndrome, abdominal pain, diarrhea, and anorexia appear.

If the question arises of how to identify an autoimmune disease, a comprehensive examination should be used, which includes clinical, laboratory, immunological, and histological methods. The doctor will prescribe a blood test, an electrocardiogram, an x-ray, an ultrasound of the abdominal cavity, and kidneys. With timely treatment of an autoimmune disease, the patient's chances of avoiding pathological changes in an internal organ or system increase. Therapeutic measures consist of taking anti-inflammatory and immune suppressing drugs, as well as corticosteroids.

Inflammatory myopathy

This includes a group of diseases that are caused by muscle inflammation and weakness. The presence of polymyositis and dermatomyositis is often diagnosed in women. Inflammatory myopathy causes slowly progressive weakness of the muscles that control movement on both sides of the body. Dermatomyositis is characterized by a skin rash accompanied by muscle weakness. A person gets tired after a long walk or standing. Frequent stumbling, falling, difficulty swallowing food or water, or inhaling or exhaling air are noted.

Presence of myasthenia gravis

This is an autoimmune disease, how to diagnose and treat it, they will tell you at the Moscow clinic. Characterized by an immune attack on the nerves and muscles that are present throughout the body. A person with myasthenia gravis has double vision, difficulty focusing their eyes and lowering their eyelids. Difficulty swallowing, frequent belching, and choking occur. In addition, there are:

  • The onset of paralysis, weakness.
  • It's hard to hold your head up.
  • It’s hard to go down or up stairs or lift things.
  • Intelligible speech disappears.

Psoriasis lesion

With this disease, there is an excessive and rapid appearance of new skin cells, the accumulation of which is found on the skin. A sick person notices the appearance of dense red spots that are covered with scales. The areas where such spots are present include the head, elbows, and knees. Itching and pain also appear, which negatively affect performance and impair sleep.

Psoriasis can be accompanied by a form of arthritis that affects the joints and phalanges of the fingers of the upper and lower extremities. When the spine is affected, pain appears in the back area. A person can seek treatment for an autoimmune disease in Moscow.

For Sjögren's syndrome

The list of autoimmune diseases in humans is supplemented by Sjögren's syndrome, which is characterized by an attack of the lacrimal and salivary glands. With this syndrome, the patient has the following symptoms:

  • Dry eyes.
  • The appearance of severe dental caries.
  • Presence of dry mouth.
  • Blurred vision.
  • Difficulty swallowing food and drinks.
  • Joints become swollen and painful.
  • Swelling of the tonsils is detected.
  • Fever due to autoimmune disease.
  • A person loses his sense of taste.
  • The voice becomes hoarse.
  • The appearance of excessive fatigue.

Presence of scleroderma

An immune disorder in which abnormal development of connective tissue appears in the skin and blood vessels. The signs of scleroderma are as follows:

  • The appearance of shortness of breath.
  • The skin thickens.
  • Whitening, redness or blue discoloration of the fingers of the upper and lower extremities is visible.
  • Body weight decreases sharply.
  • Frequent diarrhea or constipation appears.
  • The skin of the hands and forearms becomes shiny.
  • Painful sensations, swelling of the fingers.
  • The skin on the face becomes stretched, looking like a mask.
  • Difficulty swallowing.
  • Wounds appear on the fingers.

Detection of rheumatoid arthritis

When listing what belongs to autoimmune diseases, rheumatoid arthritis should be highlighted, in which the joints and surrounding tissue become inflamed. It can appear at any age. Research to cure this type of autoimmune disease involves taking a blood test for the presence of rheumatoid factor and magnetic resonance imaging of the affected joint.

Presence of diabetes mellitus

When determining what autoimmune diseases are, type 1 diabetes mellitus, in which the metabolism of carbohydrates and water is disrupted, should be included. As a result, the functioning of the pancreas, which produces insulin, is disrupted. It helps process sugar. The disease can be acquired or inherited. Lack of insulin provokes the occurrence of pustular lesions of the skin. Teeth begin to crumble, a feeling of angina pectoris appears, blood pressure jumps, the functioning of the kidneys and nervous system is disrupted, and there is a sharp deterioration in visual function.

Symptoms are gradual. The onset of diabetes mellitus is accompanied by the following symptoms:

  • Wounds heal slowly.
  • The presence of constant dryness in the oral cavity.
  • There is an increased tendency to form a purulent process on the skin and tissues.
  • Profuse sweating.
  • Weakness in all muscles.
  • A thirst appears that is difficult to quench. As a result, the patient has to drink several liters per day.
  • The skin begins to itch due to excessive dryness.
  • Frequent urge to urinate.

The presence of one of the above symptoms is a reason to donate blood to determine the glucose level. If the autoimmune disease is not treated, other signs appear:

  • The smell of acetone is heard from the mouth.
  • Dysfunction of the visual organ.
  • Consciousness is lost.
  • Constant headache.
  • The face and legs swell.
  • Painful sensations in the heart.
  • The liver is enlarged.
  • My legs become numb and sore, which prevents me from walking fully.
  • The skin on the feet loses sensitivity.
  • Blood pressure rises sharply.

A person who is faced with diabetes mellitus is interested in whether it is possible to get rid of this type of autoimmune disease, which doctor to see, how long the treatment will last. After the examination, the doctor prescribes a drug that stimulates the pancreas to produce more insulin. As well as medications that can increase cellular sensitivity to insulin, inhibitors and agonists. To get rid of diabetes, you should follow a diet that is low in carbohydrates, do not self-medicate, and go to the gym to increase physical activity. There are times when it is necessary to inject insulin to normalize glucose levels.

Detection of sarcoidosis

Refers to a rare chronic inflammatory disease that affects four out of one hundred thousand people. Lung damage occurs. Rarely occurs in children and the elderly. Sarcoidosis is characterized by difficulty breathing during physical activity, a sharp decrease in body weight, loss of appetite, and excessive fatigue. Apathy, muscle weakness, and coughing attacks may occur. Signs of sarcoidosis include coughing up blood, shortness of breath, and chest pain. In advanced forms, respiratory function decreases due to the inflammatory process in the lungs. There may be a disturbance in the eyeball, joints, and skin. If autoimmune diseases are not treated with immunoglobulins, the risk of complete loss of vision increases.

Sarcoidosis can appear due to contact with beryllium or zirconium, a strong reaction of the body to fungal exposure, pine pollen, atypical microbacteria, as well as genetic predisposition. To determine the pathology, X-rays and Kveim Silzbach skin testing are done. If you have a question about how to treat this type of autoimmune disease, you should visit a qualified doctor. He determines the causative agent of the disease, how long the illness lasts, and prescribes medications, the use of which will help avoid damage to vital organs. Without timely initiation of therapy, the prognosis for an autoimmune disease of this type is not comforting. The person may go blind and have respiratory failure.

“There are two directions in which the pathology of the immune system can develop:

  • Immunodeficiency is the inability of one or more components of the immune system to respond to a pathogen through a defense mechanism
  • Autoimmune disease is an erroneous response to the structures of the host body, or, one might say, a loss of immune tolerance to them

Traditionally, autoimmune diseases have been considered rare and, according to epidemiological studies, occur in 3-5% of people, with the most common being chronic autoimmune thyroiditis (targeting the thyroid gland) and type 1 diabetes mellitus.
There are approximately 100 different autoimmune diseases, both locally affecting a target organ (for example, autoimmune hepatitis) and systemic in nature with multiple lesions (a typical variant is systemic lupus erythematosus). A clear increase in the risk of developing autoimmune diseases has been described in the presence of such in first-degree relatives, as well as in monozygotic twins. In general, almost all such diseases are more common in women (in a ratio of 1:1 to 10:1), with the exception of one of the inflammatory bowel diseases - Crohn's disease, which is approximately 1.2 times more common in men. Data also varies by geographic region. Thus, the autoimmune disease of the central nervous system - multiple sclerosis - is registered tens of times more often in Asia than in Europe, and type 1 diabetes mellitus is most common in the USA and is practically not observed in China. Until now, the causative factor in the occurrence of autoimmune diseases is known only in isolated cases. The most actively discussed roles are the intestinal microbiota, infectious agents, combustion products of tobacco, drugs, hormones, exposure to ultraviolet radiation, heavy metals, and collagen/silicone implants. A classic example is the long-known phenomenon of molecular mimicry (imitation of the antigenic structure of the cell’s own component) of the M-protein of streptococcus pyogenes (a common causative agent of acute tonsillitis) and “human” lysoganglioside and myosin, resulting in the appearance of cardiotoxic T-lymphocytes.

Today, despite the fact that for most autoimmune diseases the key trigger causative factor has not been established, we know through which parts of the immune system the mechanism of progression of the immune attack against one’s own body (pathogenesis) is realized. Basically, this process does not involve any single component of the immune system, but a group of such components, and for each specific disease (or at least a “subclass” of diseases), the mechanism may differ. This aspect determines the exceptional importance of correct diagnosis verification at the earliest possible stage. At the very least, it is necessary to understand the general nature of the pathogenesis that underlies the totality of the patient’s symptoms, and to begin a universal treatment that acts on the key “points” of the disease mechanism.

The process of confirming the diagnosis of an autoimmune disease in modern realities is an assessment of the patient’s combination of clinical symptoms, laboratory changes (including the determination of autoimmune antibodies of various types), comparing them with data from a morphological study of biopsy material (the most important diagnostic step in many autoimmune clinical situations) and with the results of the trial treatment, if any. Next, this complex information is compared with sets of diagnostic criteria that have been developed by expert communities for almost every disease, and if the number of necessary criteria is reached, this makes it possible to confirm (verify) the exact diagnosis. Verification of the diagnosis, in turn, already makes it possible to use therapy that targets the incorrectly functioning parts of the immune system.

In recent decades, thanks to the successes of pharmacology in the treatment of autoimmune diseases, without unnecessary exaggeration one can claim a breakthrough associated with the emergence of so-called genetically engineered biological drugs. Unlike traditional synthetic drugs, such drugs are biological substances (mainly antibodies), the purpose of which is to “point” block exactly those components of the immune system that are most involved in the mechanism of development of a particular disease. Thus, firstly, several lines of immune defense do not “switch off” at once and high efficiency of treatment is ensured with a significantly lower frequency of specific and nonspecific adverse events, although, of course, they are present in the form of nuances for such medicinal agents. It is also worth noting that currently genetic engineering biological therapy is successfully used in oncology, oncohematology, allergology, cardiology, and even in the treatment of infectious diseases (here, in fact, we should mention effective approaches to blocking the cytokine storm in severe cases of coronavirus infection using antibodies to interleukin-6, one of the main mediators of immunity that triggers systemic inflammation).

To summarize, it should be said that autoimmune diseases remain one of the most complex areas of internal medicine, and working with them requires the doctor to pay exceptional attention to the individuality of each patient, carefully analyze and synthesize the diagnostic concept, apply the principles of evidence-based medicine and deep factual knowledge, constantly updated therapeutic approaches to the treatment of such diseases."

Major systemic and “localized” autoimmune diseases

  • Vessels and blood system: local leukocytoclastic vasculitis, idiopathic thrombocytopenic purpura, antiphospholipid syndrome
  • Skin: psoriasis, vitiligo, pemphigus
  • Pancreas: type 1 diabetes mellitus, autoimmune pancreatitis
  • Nervous system: acute disseminated encephalomyelitis, acute and chronic inflammatory demyelinating polyneuropathy, multiple sclerosis, myasthenia gravis
  • Thyroid and parathyroid glands: Graves' disease, autoimmune hypoparathyroidism, autoimmune Hashimoto's thyroiditis
  • Hearing organ: autoimmune inner ear disease
  • Heart: rheumatic fever
  • Liver: autoimmune hepatitis, primary sclerosing cholangitis, primary biliary cholangitis (primary biliary cirrhosis)
  • Gastrointestinal tract: ulcerative colitis, Crohn's disease, celiac disease, autoimmune atrophic gastritis
  • Adrenal glands: Addison's disease
  • Reproductive system: autoimmune orchitis and oophoritis
  • Connective tissue and joints: rheumatoid arthritis, systemic lupus erythematosus, Sjogren's disease, systemic scleroderma, mixed connective tissue diseases, ankylosing spondylitis, psoriatic arthritis, dermato- and polymyositis

What is the prevention of autoimmune diseases?

To reduce the risk of immune pathology, viral infections and acute respiratory diseases should be completely treated. A person’s diet should include foods that contain vitamins and microelements. As well as fresh vegetables, fruits, whole grains, low-fat dairy products, a lean source of protein. Eliminate saturated fats, cholesterol, salt, refined sugar. The number of meals is two to four times.

Minimize stressful situations and nervous tension, since disturbances in the central nervous system increase the sensitivity of the immune system to the negative effects of external and internal factors. Start meditating, reading books, choosing a hobby. Also, a person should get proper rest. Poor sleep provokes a disruption in hormonal production. Do moderate physical activity and yoga. It is necessary to increase the load only after consulting a doctor. By following preventive rules, a person will reduce the likelihood of an immune disorder.

Diagnosis of reactive arthritis

In patients suffering from reactive arthritis, during a comprehensive examination, doctors find the following changes in laboratory parameters;

  • Anemia (decreased number of red blood cells);
  • Moderate neutrophilic leukocytosis (increase in the number of leukocytes due to neutrophils);
  • Increased erythrocyte sedimentation rate, increased ESR, C-reactive protein level;
  • Proteinuria (the appearance of protein in the urine);
  • Leukocyturia (leukocytes in urine);
  • Microhematuria (red blood cells in the urine).

Rheumatoid factors and antinuclear factor are not detected. When examining synovial fluid, nonspecific signs of inflammation are determined: low viscosity, loose mucin clot, high number of leukocytes with a predominance of neutrophils. To identify trigger infectious agents, doctors at the Yusupov Hospital use microbiological, immunological and molecular biological research methods.

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