Cycloferon is a means of increasing nonspecific resistance in respiratory diseases in children

Cycloferon (table) is widely used for the treatment and prevention of colds, flu and other acute respiratory viral infections in children over 4 years of age.

Why do doctors use Cycloferon in children?

  1. Cycloferon has a direct antiviral effect, helping to block the activity of influenza and ARVI viruses. Has a wide spectrum of antiviral activity.
  2. Increases the body's resistance to infectious diseases caused by influenza and ARVI viruses, as it stimulates the activity of the child's innate antiviral immunity cells.
  3. It has a precise selective effect, that is, it acts on the virus directly in the areas affected by the virus.
  4. Reduces the frequency, severity and duration of viral infections, including colds and flu.
  5. Cycloferon is not metabolized by the liver (that is, it does not put additional stress on the liver) and is almost completely eliminated from the body within a day.
  6. Does not reduce the therapeutic effect even with frequent use.
  7. It is used not only for treatment, but also for emergency prevention of colds and flu (after contact with a patient).
  8. Compatible with various products to relieve flu and cold symptoms.
  9. Within 2-3 hours from the moment of administration, the maximum concentration of the active substance in the patient’s blood is observed and processes are launched aimed at providing an antiviral effect.

Cycloferon tablets are coated with a special enteric coating designed to transport the active substance (meglumine acridone acetate) through the stomach to the intestines, where the active substance is absorbed and subsequently distributed to areas affected by the viral infection.

Given this feature, Cycloferon tablets should be swallowed whole. It is not recommended to crush, chew, divide, or cut them, as this disrupts the enteric coating and reduces the therapeutic effect of the drug.

Cycloferon tablets are not used in children under 4 years of age. The limitation is due to the fact that in children under this age the swallowing reflex is not fully formed, and therefore most children cannot swallow the tablet whole.

Dosage of Cycloferon (table) in children

One of the advantages of the drug Cycloferon is the standard dosage of the active substance in one tablet. This allows you to select an individual dosage of medication for the patient, which is determined by the number of tablets per dose and depends on the age and weight of the child. This makes it possible to use the drug for the treatment of influenza and acute respiratory viral infections both for children from 4 years of age and for adults.

One tablet of Cycloferon contains 150 mg of the active substance (meglumine acridone acetate).

  1. Children aged 4 to 6 years are prescribed 1 tablet (150 mg) per dose, a course of treatment of 5 tablets.
  2. Children 7-11 years old are recommended to take 2-3 tablets (up to 450 mg) per dose (depending on the child’s weight, use our calculator).
  3. Children over 12 years of age are advised to take 3-4 tablets (up to 600 mg) per dose (depending on the child’s weight, use a calculator for a more accurate calculation).

Method of use of Cycloferon in children

Cycloferon tablets should be taken at once, without chewing, in an age-appropriate dosage, half an hour before meals, with ½ glass of water. It is advisable to take the medication in the morning.

Emergency prevention

Emergency prevention is the use of a drug to avoid illness in case of contact with a sick person, as well as during an epidemic or when the threshold for the incidence of influenza or ARVI in the region is exceeded.

For emergency prevention of influenza and acute respiratory diseases (in direct contact with patients with influenza or acute respiratory infections of another etiology, during an influenza epidemic), Cycloferon is taken on days 1, 2, 4, 6, 8. At the beginning of prophylaxis, the tablets are taken for two days in a row (days 1, 2), after which it is necessary to take a break for one day and continue taking the drug on the fourth day. Next, Cycloferon is taken every other day (days 6 and 8 of treatment), without changing the dosage. Then they take a break of 72 hours (three days) and continue the course for 11, 14, 17, 20, 23 days. The general course is from 5 to 10 doses.

Treatment of influenza and ARVI (colds)

At the beginning of treatment, the tablets are taken for two days in a row (days 1, 2), after which it is necessary to take a break for one day and continue taking the drug on the fourth day of treatment. Next, Cycloferon is taken every other day (days 6 and 8 of treatment), without changing the dosage. This scheme fully corresponds to the biochemical rhythms in the child’s body and ranges from 5 to 10 doses of the drug.

Experience with the use of cycloferon in the treatment of human papillomavirus infection

Isakov V.A., Ermolenko D.K., Goncharov S.B., Ermolenko K.D.

Lesions of the skin and mucous membranes caused by human papillomaviruses (HPV) have been known to mankind for a long time. More than 130 types of HPV are distinguished based on the nucleotide sequence and antigenic properties of capsids. The HPV genome contains DNA. HPVs are species and tissue specific. They are capable of infecting squamous epithelial cells and exhibiting replicative activity within them; they are found on the skin, mucous membranes of the oral cavity, conjunctiva, esophagus, bronchi, larynx, rectum, and genitals [14].

At the end of the twentieth century. An unprecedented spread of HPV infection has been noted: it is believed that approximately three quarters of sexually active adults worldwide are infected with HPV at different stages of their lives. In general, at the moment, HPV infection in people of biologically active age is 20–60% [14]. The infection is transmitted primarily through sexual contact, during medical procedures (infection of medical personnel is possible), vertically, during pregnancy and childbirth. The incubation period is 1–6 months, the maximum content of the virus in the affected tissues is detected in the 6th month. Often the result of infection is diseases of the anogenital area: cancer of the cervix, vulva, vagina, perianal area and genital warts. Cervical cancer is the second most common malignant disease in women: more than 500 thousand cases are registered annually in the world. According to WHO forecasts, the number of deaths from cervical cancer will increase to 320 thousand in 2015 and to 435 thousand in 2030 [12]. The average age of patients with carcinoma in situ is 29 years, i.e. It takes approximately 10 years from the time of initial infection to the appearance of severe neoplasia. Invasive cancer is registered at the age of 49 years, when additional changes in immunity occur, leading to invasion and metastasis [14,15]. Papillomaviruses are the only group of viruses that have been proven to induce tumor formation in humans under natural conditions. The combined persistence of HPV with herpes simplex virus-2, cytomegalovirus, Epstein-Barr virus, human immunodeficiency virus, chlamydia and mycoplasma is unfavorable.

Up to 20 million American citizens suffer from genital warts, and HPV is 3 times more common than genital herpes and no less common than gonorrhea [5]. According to the Ministry of Health of the Russian Federation (2001), the frequency of the most common clinical form of HPV - genital warts - is 26 per 100 thousand population, in the USA - 100 per 100 thousand population.

An essential feature of HPV is its ability to switch from a non-productive type of infection to a productive type of infection and vice versa. In the first case, the virus replicates synchronously with the cell and does not harm it. In the second case, it quickly multiplies and lyses the cell, releasing a mass of new virions that can infect other cells [14]. It has been shown that HPV can have different effects on the mucosa. Thus, the manifestation of a productive effect is papillomas and condylomas, and the result of a transforming effect can be intraepithelial lesions (dysplasia, invasive cancer). Thus, the conditions for the formation of irreversible neoplasia are [9]: active expression of the E6 and E7 HPV genes; induction of metabolic mechanisms for the conversion of estradiol into 16a-hydroxysterone, which belongs to the category of “aggressive hormones” that cause a long-term effect; induction of multiple chromosomal DNA damage in the infected cell, which completes the process of degeneration.

HPV-1 – HPV-4 types were isolated from stratified squamous epithelium. They are associated with the development of vulgar and flat warts of the hands, as well as plantar warts. In most cases, HPV types 6, 11, 13, and 30 are associated with the development of verrucous laryngitis (juvenile laryngeal papillomatosis). The disease is diagnosed more often in children under 5 years of age who are infected perinatally, and is characterized by the appearance of papillomatous growths on the vocal cords, which leads to speech difficulties and air circulation problems in the upper respiratory tract. HPVs have also been isolated from the mucous membranes of the oral cavity. Cases of laryngeal papillomatosis have been described in children born by cesarean section, so cesarean section should not be performed for the sole purpose of preventing HPV infection of the newborn.

As shown above, HPV-6, 11 can cause cancer of the larynx and pharynx, while the role of other types of HPV in malignant degeneration of the oral mucosa has not been sufficiently studied. Rare cases of the development of oropharyngeal warts caused by “genital” serotypes HPV-16, 18 have been noted. The presence of the same types of viruses in different localizations of mucosal lesions suggests a single source of infection and the ability of viruses to interact with various receptors on the epithelium of the oral cavity and urogenital tract.

We examined 40 women of childbearing age practicing commercial oral-genital sex. Material was collected (scrapings from altered areas of the mucous membranes) from patients with clinical manifestations of HPV infection. Subsequently, all samples were subjected to genetic analysis using polymerase chain reaction (PCR) with primers aimed at identifying the following types of HPV: 16, 18, 31, 33, 50, 59 [3]. HPV-16 was isolated in 52.5%, and HPV-18 – in 27.5% of cases. HPV-31, 50, 59 were detected much less frequently (7.5%) in the samples. HPV-33 was detected in only two women. It should be noted that in 6 patients several serotypes of the virus were recorded simultaneously. Thus, in 2 samples HPV-16 and 18 were isolated, in 3 samples - HPV-16 and 50, in 1 sample - HPV-16, 31 and 39. The studies conducted indicate the significant role of oral-genital contacts in the spread of human papillomavirus infection, including viruses of high oncogenic risk, and may also indirectly indicate an increased risk of developing malignant diseases of the oral cavity and larynx in women who use oral-genital contact [3].

According to Kozlova V.I. et al. (2003) [10], the urogenital tract is most often affected by HPV-6, 11, 16, 18, 31, 35. Based on the ability of HPV to induce neoplastic processes, they are usually divided into low-grade types (types 3, 6, 11, 13, 32 , 34, 40, 41, 42, 43, 44, 51, 61, 72, 73), medium (30, 35, 45, 52, 53, 56, 58) and high (16, 18, 31, 33, 39 , 50, 59, 64, 68, 70) cancer risk [9,10]. Recently, about 20 types of HPV have been associated with cervical cancer (95%). Among them, HPV-16 (50%) and HPV-18 (10%) are most often detected, and therefore women with confirmed HPV infection should undergo an annual examination by a gynecologist with colposcopy, cytological examination of cervical smears, virological and immunological examination. It is believed that in 50% of cases of human papillomavirus infection (PVI), the virus is cleared from a woman’s body within 1 year, and in 85% of cases – within 4 years. In St. Petersburg from 1999 to 2004, from 28 to 34% of the female population aged 20 to 60 years were infected with HPV and high-risk (HPV types 16 and 18) cancer [11]. HPV contributes to the development of cervical cancer in 99.7%, cancer of the vulva, vagina, penis, prostate, testicle - in 10-30%, cancer of the larynx and oral cavity - in 10-30% of cases.

In addition to HPV, a number of concomitant factors play a decisive role in the development of oncogenic transformation. First of all, it is necessary to highlight concomitant infectious diseases of the anogenital area, the causative agents of which are often isolated in patients with HPV infection: chlamydia - 62.1%, gonococci - 23.3%, ureaplasma - 16.2%, herpes viruses - 16%, trichomonas - 14.8%. The combination of HPV infection with two infections was detected in 23.3%, with three – in 16.2%, with four – in 8.1% of cases [2,8]. Of great importance in the development of cancer against the background of PVI are social status and living conditions, hormonal levels corresponding to age, gynecological history (risk factors: early onset of sexual activity, frequent change of sexual partners, cervical canal injuries, number of pregnancies and births, anogenital contacts). An important feature of HPV infection is polymorphism, multifocality of damage to the skin and mucous membranes of the genital tract in the form of clinical, subclinical and latent forms [2,6,7].

In St. Petersburg, a system of preventive measures has been proposed aimed at reducing the incidence of virus-related malignant neoplasms in the population. A comprehensive examination program includes cytological methods, testing for viruses (HPV, CMV, EBV, viral hepatitis B and C). Detection of high cancer risk viruses (HPV-16, 18 types) requires the examination to be supplemented with clarifying diagnostic methods: determination of the level of prolactin, prolactin/TSH in the blood, HPV gene testing (ratio of E2-E6 genes), drawing up a patient’s genetic risk map, which will allow us to offer an individual model of strategy and tactics for treatment and monitoring of the patient, as well as to form risk groups for virus-related tumors [11].

Principles of complex treatment of HPV infection. With PVI, as with other chronic diseases with long-term persistence of the virus, immunodeficiency states (IDS) develop due to insufficiency of various parts of the immune system: there is a decrease in T-cell immunity, immunoregulatory index (CD4/CD8), the number of Langerhans cells and immune response of cervical lymphocytes. The functional activity of natural killer (NK) cells and the level of basic serum immunoglobulins are reduced. The content of CEC in the peripheral blood is increased, which correlates with the prevalence and severity of the process [7,12,13].

Due to the imbalance of the immune system, for more successful treatment in the regimen of infection caused by HPV, it is necessary to include, in addition to antiviral (systemic and local), immunocorrective drugs, as well as pathogenetic agents (systemic enzyme therapy, antioxidants, pro- and prebiotics), which alleviate the patient's condition and contribute to more effective use of the drugs used. When PVI is combined with other pathogens, complex treatment is carried out using etiotropic drugs against specific pathogens in standard dosages. It has been shown that modern treatment does not avoid recurrence of PVI in 20–30% of cases [1,2].

It is assumed that the sensitivity of HPV to certain chemotherapy drugs is primarily due to genetically programmed features of the immune response in this pathology. In the process of evolution, a mechanism has emerged in which a viral infection is protected at the molecular level from the systemic effects of the host immunity. In some cases, the reason for the failure of therapy for infection caused by HPV is the use of interferon drugs (IFN), since the E7 oncoprotein causes resistance of infected cells to IFN drugs during treatment [1,12].

Thus, the treatment of PVI remains a rather difficult task, despite a significant arsenal of drugs and treatment methods. Since complete cure is currently impossible to achieve, it is believed that the goal of the treatment procedures should not be to eliminate the pathogen, but to transfer the infection to a stage of stable remission (clinical recovery). In this regard, the following tactics for managing patients with HPV infection are proposed: 1) destruction of papillomatous foci; 2) stimulation of antiviral immunity, i.e. correction of general and local immunity; 3) a combination of these approaches, eliminating factors contributing to relapse of the disease [7,12,13].

Local destruction of foci during the clinical and subclinical course of HPV infection (aimed at removing the surface layer of the epidermis without sanitizing the cells of the basal layer) makes it possible to cure only the area of ​​the epithelium where the infection manifested itself. In the surrounding tissues, a reservoir of HPV remains in an inactive state or an undiagnosed subclinical form, which can cause relapses of the disease. During a five-year observation of patients with cervical infections caused by HPV, progression of the latent stage of papillomavirus infection into a clinical or subclinical form was noted in 21.4% of cases. Moreover, the clinical manifestation of infection occurs in women with persistent HPV against the background of an imbalance in immunity parameters. Adequate immunotherapy helps suppress the activity of HPV and its complete elimination, reducing the frequency of relapses and the risk of developing precancerous diseases and cervical cancer in patients with latent HPV infection [4,6,12]. For genital warts, both sexual partners are treated. It is recommended to abstain from sexual intercourse while taking medications and use barrier contraception for 6 months. after completion of therapy.

Experience with the use of Cycloferon in the treatment of HPV infection. Currently, in the treatment of patients with HPV infection, an alternative approach to the treatment of PVI is very promising. With this technique, IFNs have a protective effect, i.e. Interferon inducers (II) are used, among which the domestic drug Cycloferon deserves special attention (NTTF POLYSAN LLC, St. Petersburg). Cycloferon belongs to low-molecular interferon inducers, the acridone class. When Cycloferon is administered, endogenous IFN is formed, which is not antigenic or pyrogenic; the activity of induced IFN is controlled by special regulatory mechanisms, which ensures the absence of side effects inherent in recombinant IFN drugs as a result of their cumulation; Cycloferon also does not have mutagenic, teratogenic, embryotoxic, or carcinogenic effects; Cycloferon does not induce autoimmune processes. The drug has no described side effects, it goes well with traditional therapeutic treatments (antibiotics, vitamins, immunotropic drugs, etc.).

Advantages of using Cycloferon: rapid penetration into the blood, low level of binding to serum proteins, high bioavailability in organs, tissues, biological fluids of the body; the predominant method of elimination from the body is through the kidneys (99% of the administered drug) unchanged, within 24 hours [4,5]. After the administration of Cycloferon, a high level of synthesis of IFN-a in tissues and organs containing lymphoid elements is observed for at least 72 hours, while in the blood serum of a normal person, high levels of IFN remain for 48 hours.

Mechanisms of action of Cycloferon. One of the key parameters when introducing interferon-inducing drugs into the body, which determine the effectiveness of the immune response, is the profile of cytokines - factors that activate the proliferation and differentiation of body cells, controlling the processes of regeneration, angiogenesis and metabolism. The existence of different cytokine profiles provided by Th cells has been established, with the Th1 type of immune response associated with the production of IFN-g, IL-2 and TNF; the Th2 type is characterized by increased production of IL-4,5,6,10 and leads to increased humoral and suppression of cellular immunity [4,5]. Currently, the direct and indirect immunotropic effects of CP are well described.

The influence of Cycloferon on nonspecific immune cells: Cycloferon increases the formation of reactive oxygen species by phagocytes, which promotes completed phagocytosis with the elimination of captured pathogens; causes an increase in the level of NK cells in the peripheral blood.

The influence of Cycloferon on specific immune cells: 1) an increase in the level of CD4+ and a decrease in CD8+ T-lymphocytes, normalization of the immunoregulatory index even with a single use of Cycloferon; 2) the use of Cycloferon leads to a decrease in the level of B-lymphocytes in the peripheral blood and to an increase in the production of high-affinity antibodies, which reflects its effect on switching the synthesis of immunoglobulin classes in B-cells; induces the synthesis of IFN-α in B cells, macrophages and neutrophils. These secondary effects of Cycloferon can be partially explained by the induction of the synthesis of interleukins (IL-2, IL-1), IFN-α, IFN-γ by various cells of the immune and other body systems, as well as the suppression of the synthesis of IL-8, TNF-a ( shown using ELISA, RT–PCR). Other immunocorrective effects of Cycloferon include experimentally discovered radioprotective and anti-inflammatory effects, stimulation of reparative osteogenesis (in the area of ​​​​a long bone fracture in animals).

In addition, the direct antiviral effect of Cycloferon has been shown, which manifests itself at the stage of virus assembly, leading to the formation of defect-interfering particles (DI-particles), which are a kind of autovaccine in the body. DI particles interfere with the normal replication of viruses, which leads to the suppression of their cytocidal effect. At the same time, DI particles retain their IFN-inducing properties, stimulating nonspecific immunity.

Thus, Cycloferon, as an IFN inducer, has a bifunctional effect - it is able to suppress the reproduction of a wide range of viruses (orthamyxoviruses, paramyxoviruses, adenoviruses, coronaviruses, herpes viruses, HPV, HIV, etc.) and at the same time has a pronounced immunocorrective effect, normalizing disorders immune systems (secondary immunodeficiencies), so characteristic of viral infections. A dose- and interval-dependent effect of the drug has been established, which must be taken into account when using Cycloferon [4,5,13].

Release forms of Cycloferon. The drug is available in the form of a solution for intramuscular and intravenous administration of 125 mg/ml in ampoules of 2 ml; tablets of 0.15 g, enteric-coated and liniment 5% for external use in tubes of 5 and 30 ml. Liniment Cycloferon 5% 30 ml contains in one package five disposable applicators for intravaginal administration of liniment, which allows patients to use the drug at home.

Clinical effectiveness of Cycloferon drugs. Taking into account the antiviral, interferon-inducing and immunomodulatory effects of Cycloferon, it is actively used for systemic and local use in the treatment of viral infections, incl. papillomavirus diseases of the skin and mucous membranes [2,4,7,13]. Cycloferon is effective against cytomegalovirus, HIV-1, HSV, human papillomavirus and other viruses. Cycloferon is used as monotherapy or in combination with other antiviral and immunotropic drugs. Thus, patients with filamentous warts were prescribed bemitil 1 tablet 4 times a day. for 14 days followed by electrocoagulation. Intramuscular injections of Cycloferon solution 125 mg/ml, 1 ampoule every other day, were additionally prescribed to patients in case of a large number of warts or in the development of relapses after local destructive treatment. The course of treatment with Cycloferon was repeated after 10 days. Cycloferon liniment (lCF) was prescribed for vulgar warts, alternating with tebrofen ointment for 4–6 weeks (with pre-treatment with keratolytic agents). If there was no effect, local destructive treatment was performed.

PVI is often combined with urogenital chlamydia. When examining such patients, we identified dysbiosis of the vagina and intestines. Appropriate comprehensive treatment was carried out. Often small papillomas decrease in size and HPV activity decreases. If the clinical picture of HPV infection remained unchanged, then destructive treatment of the main condylomas was carried out and a course of Cycloferon was prescribed intramuscularly: 10 injections of 2 ml according to the basic regimen. Applications of 5% lCF were used locally, as a result of which normalization of local immunity parameters and restoration of vaginal endoecology were observed. Normalization of vaginal microbiocenosis from the point of view of eliminating the infectious agent (antibacterial, antiviral, antifungicidal effects) is based primarily on the distinct immunocorrective effect of lCF. This effect consists of an impact on the local immunity of the mucous membranes of the lower part of the female genital area and consists of increasing the permeability of the vaginal histohematic barrier (VHB) and compensation for the initially reduced local synthesis of IgG, at the beginning of therapy - due to increased diffusion of immunoglobulins from the bloodstream, and subsequently by normalizing and increasing the degree of local synthesis of immunoglobulins.

It is known that high doses of Cycloferon (500 mg) promote the active synthesis of IFN-γ, which has immunoregulatory and antiproliferative properties, and also ensures the induction of a Th1-type immune response.

Cycloferon in the treatment of PVI of the anogenital area. We observed 100 patients of both sexes with PVI of the anogenital area aged from 19 to 50 years. Diagnosis was carried out on the basis of characteristic clinical manifestations of the disease, cytological examination of smears and PCR. In 20 patients, HPV was not detected or not identified. In 80 patients, when determining the HPV type, the following results were obtained: 40% (32 people) – HPV-11, 7% (6 people) – HPV-16, 4% (3 people) – HPV-6, 4% ( 3 people) – HPV-18. 45% (36 people) – HPV-2, 7, 31 and 33 were identified. Clinically, forms of PVI were more often recorded – genital warts, papillomas and flat warts. Laboratory examination: immunogram (CD4+ and NK cells, interferon status, transferrin (TF), ceruloplasmin (CP). To assess non-enzymatic antioxidant activity, the coefficient K was determined, obtained as the quotient of dividing the values ​​of TF to CP (TF/CP).

PVI therapy regimen. Treatment was carried out in 2 stages. First, papillomatous elements were removed using chemical destructive therapy: Solcoderm 2 sessions, with an interval of 4–5 days. The second stage was an anti-relapse course with Cycloferon (systemic and local) in 50 patients (36 women and 14 men). Cycloferon solution 125 mg/ml was prescribed intramuscularly according to the following regimen: 2 ml on the first and second days, and from the third day, 2 ml every 48 hours, course of 8–10 injections. At the same time, 5% lCF was applied to the sites of former lesions daily for 10 days. 50 patients in the control group (35 women and 15 men) were prescribed rectal suppositories of recombinant a2-interferon (3 million IU) according to the standard regimen: 1 st. 2 times/day. – 10 days, then every other day No. 10.

During therapy with Cycloferon, positive clinical dynamics were observed faster (resolution of elements of HPV infection, etc.), and indicators of nonspecific resistance of the body (level of CD4+, NK–cells, transferrin, synthesis of endogenous IFN) significantly increased. HPV was detected significantly less frequently by PCR after completion of the course of treatment (Table 1). The use of Cycloferon in the complex therapy of PVI made it possible to reduce the recurrence rate of PVI from 48 to 15% within 6 months. after a course of therapy.

It has been shown that the use of liquid 5% lCF for local treatment of diseases of the urogenital tract can solve many problems that arise in the treatment of STIs. A pronounced antiviral, antibacterial and antichlamydial effect of the drug due to activation of the immune system, as well as anti-inflammatory and antiproliferative effects of CP, have been established. The effectiveness of lCF in the complex treatment of acute and chronic bacterial and viral infections (chlamydia, bacterial and fungal infections of the genitourinary tract, genital herpes, human papillomavirus infection) has been shown.

It is believed that HPV-5, HPV-6 and HPV-11 types cause the development of genital warts (AC). 28 adult patients with OK received two-stage treatment. First, the OC was removed by cryodestruction with liquid nitrogen, then 17 patients were prescribed intravaginal and intraurethral instillations of 5% lCF once a day. No. 10 every other day to prevent relapse of the disease. 11 patients in the control group were treated only by cryodestruction. Within 10–24 hours, swelling and hyperemia developed at the cryoapplication site, followed by the formation of blisters and erosions. Bubbles and erosions were treated with a fucorcin solution, the affected area was washed with a solution of chlorhexidine bigluconate for 2 weeks (to prevent secondary infection). Complete rejection of neoplasms and epithelization were observed on days 10–14 [13]. As a result of treatment in patients of the main and control groups, relapses in the first days after cryodestruction were observed in 3 (17.6%) and 2 (18%) patients, respectively. During the first month after surgery, relapses of OK were observed in 4 (23.5%) patients of the main and 3 (27.2%) control groups. During the second month, relapses were observed in 1 (5.8%) and 3 (27.7%) patients, respectively. Assessing the results obtained, it should be noted the effectiveness of local application of lCF. Thus, already during the second month after cryodestruction, the frequency of OK relapses was significantly higher in the control group compared to the main group of patients (27.2 and 5.8%, respectively, p <0.05). The final examination showed that combined OC therapy using cryodestruction and instillation of 5% lCF significantly reduced the incidence of disease recurrence in the first 3 months. after surgery: 49.9% in the main group and 72.7% in the control group (p<0.05).

lCF has no side effects that limit its use during intravaginal/intraurethral administration and is recommended in the complex treatment of urogenital infections, including those caused by HPV. The use of lCF is effective in women both as monotherapy for urogenital infections and as a combination treatment. The drug combines well with various official intravaginal drugs (vaginal tablets, suppositories) and with medicinal mixtures prepared ex tempore. The effectiveness of lCF in women has also been proven for the following types of pathologies: nonspecific bacterial vaginitis, bacterial vaginosis, candidal vaginitis, nonspecific urethritis.

Regimen for the treatment of lCF urogenital infections can be variable depending on the severity of the disease, its nosological form and the nature of local changes.

Schemes for using Cycloferon liniment

For genital herpes, recurrent genital warts - intravaginal (intraurethral) instillations 1 time per day. 5 ml daily, 10–15 days. It is possible to combine lCF with other antiviral agents (both systemic and local) in the form of ointment (gel) applications to the lesion. When treating candidal vaginitis, nonspecific vaginitis (endocervicitis) and bacterial vaginosis, the drug can be used both as monotherapy and as part of complex treatment. Use intravaginal instillations of the drug, 5–10 ml daily for 10–15 days. To prevent free evacuation of the drug, the entrance to the vagina is tamponed with a small cotton swab for 2–3 hours. In parallel, in the case of combined damage to the mucous membranes of the vagina and urethra (human papillomavirus infection, etc.), it is advisable to use a combination of intravaginal and intraurethral instillations (in a volume of 5 ml daily, 10– 14 days). Considering the wide range of effects of 5% lCF, we can say that it has not only taken its place in the treatment of urogenital infections, but has also supplanted traditional drugs used in the treatment of STIs.

Thus, the safety and high clinical effectiveness of the use of Cycloferon in the treatment of patients with recurrent HPV infection has been demonstrated. Cycloferon has antiviral and immunomodulatory effects, is combined with basic dosage forms, is well tolerated by patients, is highly effective when used locally and systemically as monotherapy and in combination with antiviral chemotherapy drugs, enhancing and prolonging the therapeutic effect.

Literature

1. Van Krogh D., Lacey S.D., Gross D., Baracco R., Schneider A. European guidelines for anogenital warts // STI. 2002. No. 3. P.29–37.

2. Dmitriev G.A., Bitkina O.A. Human papillomavirus infection. M.: Medical book, 2006. 76 p.

3. Ermolenko D.K., Ermolenko K.D., Isakov V.A. Frequency of occurrence of human papillomaviruses of high oncogenic risk in the oral cavity in women practicing commercial oral-genital sex / 3rd Interregional Scientific and Practical. conf. "Benign neoplasms and infections in urology and gynecology." St. Petersburg, 2008. pp. 20–21.

4. Ershov F.I., Kiselev O.I. Interferons and their inducers (from molecules to drugs). M.: GEOTAR-Media, 2005.

5. Ershov F.I., Romantsov M.G. Medicines used for viral diseases. Guide for doctors. M.: GEOTAR-Media, 2007.

6. Ershov V.A., Narvskaya O.V. Background processes and neoplasia of the cervical epithelium. St. Petersburg: Chelovek, 2007. 79 p.

7. Isakov V.A., Ermolenko D.K., Ermolenko E.I. Herpesvirus and human papillomavirus infections. / Chapter in the book: “Sexually transmitted infections.” / Ed. V.A. Akovbyana, V.I. Prokhorenkova, E.V. Sokolovsky. A textbook for the system of postgraduate professional education of doctors. M.: Media Sphere, 2007. pp. 448–513.

8. Isakov V.A., Ermolenko D.K., Kutueva F.R., Ermolenko E.I., Moskvin I.I. The use of cycloferon in the treatment of human papillomavirus infection. Recommendations for doctors. St. Petersburg–V.Novgorod: Taktik–Studio, 2007. 64 p.

9. Kiselev V.I. Human papillomaviruses in the development of cervical cancer. M.: Dimitrade Graphic Group Company, 2004. 180 p.

10. Kozlova V.I., Puhner A.F. Viral, chlamydial and mycoplasma diseases of the genitals. A guide for doctors. M.: Publishing house “Triada-X”, 2003. 439 p.

11. Safronnikova N.R. Preventive gynecological oncology. SPb.: COSTA, 2007. 207 p.

12. Semenov D.M., Zanko S.N., Dmitrachenko T.I. Human papillomavirus infection (clinical and pathogenetic features, treatment, prevention). Educational and methodological manual. St. Petersburg: Dialect, 2008. 83 p.

13. Fedotov V.P., Rybalkin S.B., Romantsov M.G. Essays on immunocorrection in dermatovenerology. A manual for doctors. St. Petersburg, 2005.

14. Ludicke F., Stalberg A., Vassilokos P. et al. High and intermediate risk human papillomavirus infection in sexually active adolescent females. //J. Pediatr. Adolesc. Gynecol.–2001. Vol. 14. N4. P.171–174.

Injections for herpes: answers to patient questions

What are the best injections for herpes?

Currently, the most powerful antiviral drugs are Cycloferon, Allokin-Alpha, Alloferon.

What injections can you buy that completely kill herpes?

Today, no drugs have been found that can completely destroy the herpes virus.

However, there are drugs that can effectively suppress the symptoms of the virus and increase the protective functions of the immune system, reducing the risk of relapse of the disease.

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