RU95109221A - Method of interferon therapy - Google Patents

Method of interferon therapy

Info

Publication number
RU95109221A
RU95109221A RU95109221/14A RU95109221A RU95109221A RU 95109221 A RU95109221 A RU 95109221A RU 95109221/14 A RU95109221/14 A RU 95109221/14A RU 95109221 A RU95109221 A RU 95109221A RU 95109221 A RU95109221 A RU 95109221A
Authority
RU
Russia
Prior art keywords
ifn
interferon
initial dose
dose
treatment
Prior art date
Application number
RU95109221/14A
Other languages
Russian (ru)
Other versions
RU2105566C1 (en
Inventor
Ю.А. Севрук
Original Assignee
Ю.А. Севрук
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ю.А. Севрук filed Critical Ю.А. Севрук
Priority to RU95109221A priority Critical patent/RU2105566C1/en
Publication of RU95109221A publication Critical patent/RU95109221A/en
Application granted granted Critical
Publication of RU2105566C1 publication Critical patent/RU2105566C1/en

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

FIELD: medicine, therapy. SUBSTANCE: method involves intramuscular administration to patient recombinant interferon, for example, α--interferon, γ--interferon or their mixture at initial dose providing increase of body temperature by 1.9 ± 0.5 C after 5.2 + 1.2 h. Among α--interferon preparations reaferon, realdiron, intron A, roferon A can be used; among γ--interferon - imukin and others. Initial dose of the indicated preparations is 1 mln IU. Administration of interferon is repeated once per 24 h at increasing gradient to obtain pyrogenic effect of each the next dose, up to its disappearance after administration of a single dose, 10-50-fold to initial dose. Repeated course can be carried out 2 months (not early) after termination of preliminary treatment course. Method can be used for treatment viral, allergic, rheumatological, oncological and other diseases. EFFECT: enhanced effectiveness. 12 cl, 6 tbl, 7 ex

Claims (1)

Использование: в области медицины, а именно в терапии для лечения различных заболеваний иммунного генеза, в том числе вирусных, аллергических, ревматологических, онкологических и прочих заболеваний. Задача: создание способа, обеспечивающего формирование нового динамического стереотипа взаимосвязи иммунной системы и ЦНС, имитирующего ответ организма на воздействие фактора, явившегося причиной развития иммунодефицитного состояния у данного конкретного больного, который обуславливает возможность нейрогуморальной регуляции работы иммунной системы, за счет создания условий для функционирования работоспособных звеньев иммунной системы в режиме дублирования функций дефектных звеньев. Сущность изобретения: больному вводят внутримышечно препарат рекомбинантного интерферона, например, α--ИФН, γ--ИФН или их смесь в начальной дозе, обеспечивающей повышение по сравнению с нормой температуры тела у данного конкретного больного через 5,2±1,2 ч после введения препарата на 1,9±0,5oС. В качестве препаратов α--ИФН используют, например, реаферон, реальдирон, интрон А, роферон А; в качестве препаратов γ--ИФН - имукин и т. п. При этом начальная доза указанных препаратов составляет, как правило, 1 млн МЕ. Повторяют введение препарата ИФН 1 раз в сут в повышающемся градиенте разовых доз, таким образом, чтобы каждая последующая доза обеспечивала у данного конкретного больного вышеуказанный пирогенный эффект, до его исчезновения при введении разовой дозы, 10-50-кратной начальной дозе. По показаниям проводят повторный курс лечения с ранее неиспользованным препаратом ИФН, но не ранее, чем через 2 месяца после окончания предыдущего курса лечения.Usage: in the field of medicine, namely in therapy for the treatment of various diseases of the immune genesis, including viral, allergic, rheumatological, oncological and other diseases. Objective: to create a method that provides the formation of a new dynamic stereotype of the relationship between the immune system and the central nervous system that mimics the body’s response to the influence of a factor that caused the development of an immunodeficiency state in this particular patient, which determines the possibility of neurohumoral regulation of the immune system, by creating conditions for the functioning of functional units the immune system in the mode of duplication of the functions of defective links. The essence of the invention: the patient is injected intramuscularly with a preparation of recombinant interferon, for example, α-IFN, γ-IFN or their mixture in an initial dose, which provides an increase compared to normal body temperature in this particular patient 5.2 ± 1.2 hours after the introduction of the drug at 1.9 ± 0.5 o C. As drugs α - IFN use, for example, reaferon, realdiron, intron A, roferon A; as preparations of γ - IFN - imukin, etc. Moreover, the initial dose of these drugs is, as a rule, 1 million IU. The administration of IFN preparation is repeated once a day in an increasing gradient of single doses, so that each subsequent dose provides the aforementioned pyrogenic effect for this particular patient, until it disappears with a single dose, 10-50 times the initial dose. According to indications, a repeated course of treatment is carried out with a previously unused IFN preparation, but not earlier than 2 months after the end of the previous course of treatment.
RU95109221A 1995-06-06 1995-06-06 Method for carrying out interferon therapy RU2105566C1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU95109221A RU2105566C1 (en) 1995-06-06 1995-06-06 Method for carrying out interferon therapy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU95109221A RU2105566C1 (en) 1995-06-06 1995-06-06 Method for carrying out interferon therapy

Publications (2)

Publication Number Publication Date
RU95109221A true RU95109221A (en) 1997-06-10
RU2105566C1 RU2105566C1 (en) 1998-02-27

Family

ID=20168505

Family Applications (1)

Application Number Title Priority Date Filing Date
RU95109221A RU2105566C1 (en) 1995-06-06 1995-06-06 Method for carrying out interferon therapy

Country Status (1)

Country Link
RU (1) RU2105566C1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2449770C2 (en) * 2010-08-03 2012-05-10 Федеральное государственное учреждение "Ростовский научно-исследовательский онкологический институт Федерального агентства по высокотехнологичной медицинской помощи" Method of immunotherapy of rhenal cell carcinoma
RU2427373C1 (en) 2010-11-08 2011-08-27 Виктор Вениаминович Тец Method for endogenous interferon induction
RU2596792C1 (en) * 2015-05-22 2016-09-10 Федеральное государственное бюджетное учреждение "Научно-исследовательский институт детских инфекций Федерального медико-биологическое агентства" Method of treating multiple sclerosis in children

Also Published As

Publication number Publication date
RU2105566C1 (en) 1998-02-27

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