DE10045621A1 - Treating hepatitis B and C comprises administration of prothymosin alpha - Google Patents

Treating hepatitis B and C comprises administration of prothymosin alpha

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Publication number
DE10045621A1
DE10045621A1 DE10045621A DE10045621A DE10045621A1 DE 10045621 A1 DE10045621 A1 DE 10045621A1 DE 10045621 A DE10045621 A DE 10045621A DE 10045621 A DE10045621 A DE 10045621A DE 10045621 A1 DE10045621 A1 DE 10045621A1
Authority
DE
Germany
Prior art keywords
prothymosin
hepatitis
comprises administration
treating hepatitis
prothymosin alpha
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
DE10045621A
Other languages
German (de)
Inventor
Milan C Pesic
Jan Czarnecki
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Individual
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Individual
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 Individual filed Critical Individual
Priority to DE10045621A priority Critical patent/DE10045621A1/en
Publication of DE10045621A1 publication Critical patent/DE10045621A1/en
Withdrawn legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22Hormones
    • A61K38/2292Thymosin; Related peptides

Abstract

Prothymosin alpha or one of its salts is used for the treatment of hepatitis B and/or hepatitis C.

Description

Die Erfindung betrifft die Behandlung von Hepatitis in den Formen B oder C.The invention relates to the treatment of hepatitis in forms B or C.

Die medikamentöse Therapie von Lebererkrankungen, wie Hepatitis B oder C, ist bisher nur in bescheidenem Umfang möglich. Die früher vorgeschlagenen Be­ handlungen mit hohen Vitamindosen oder sogenannten Lipotropenstoffen, wie z. B. Cholin oder Methionin, können Lebererkrankungen nur dann günstig beein­ flussen, wenn diese Stoffe nicht in ausreichender Menge mit der Nahrung zuge­ führt werden, was aber nur selten zutrifft. Die Wirkung zahlreicher pflanzlicher Kombinationspräparate ist nicht belegt und umstritten. In schweren Fällen des Krankheitsverlaufs wird eine kurzfristige, hoch dosierte Gabe von Glucocorticoi­ den, vorgenommen, die jedoch erhebliche Nebenwirkungen mit sich bringt. Zu­ meist werden gleichzeitig auch Immunsuppressiva (insbesondere Azathioprin) gegeben. Drug therapy for liver diseases such as hepatitis B or C is so far only possible on a modest scale. The previously proposed Be acts with high doses of vitamins or so-called lipotropic substances, such as z. B. choline or methionine, can only affect liver diseases favorably flow when these substances are not in sufficient quantities with the food are carried out, which is rarely the case. The effect of numerous herbal Combination drugs have not been proven and are controversial. In severe cases of The course of the disease is a short-term, high-dose administration of Glucocorticoi which, however, has significant side effects. to mostly immunosuppressive drugs (especially azathioprine) given.  

Es besteht daher ein erheblicher Bedarf an einer medikamentösen Behandlung von Hepatitis B oder C mit Wirkstoffen, die die Bekämpfung der die Hepatitis auslösenden Viren B und C ermöglichen.There is therefore a significant need for drug treatment of hepatitis B or C with active ingredients that fight the hepatitis enable triggering viruses B and C.

Erfindungsgemäß wurde gefunden, das Prothymosin α eine erfolgreiche medika­ mentöse Therapie für Hepatitis B und C ermöglicht.According to the invention, the prothymosin α was found to be a successful medication mental therapy for hepatitis B and C enables.

Prothymosin α ist ein biologisches Polypeptidhormon, das etwa 107 bis 113 Aminosäurereste aufweist und in US 4,659,694 und US 4,716,148 ausführlich beschrieben ist. Prothymosin α ist als immunpotenzierender Wirkstoff bekannt.Prothymosin α is a biological polypeptide hormone that is approximately 107 to 113 Has amino acid residues and in detail in US 4,659,694 and US 4,716,148 is described. Prothymosin α is known as an immunopotentiating agent.

Überraschend ist gefunden worden, dass Prothymosin α zur Bekämpfung von Hepatitis B und C geeignet ist, wobei die Wirkung von Prothymosin α nicht auf einer Immunverstärkung beruht, die bei Hepatitiserkrankungen regelmäßig auch gar nicht angestrebt wird (vgl. die Verabreichung von Immunsuppressiva), son­ dern auf einer direkten Beeinflussung der infizierten Hepatocyten beruht. Diese Wirkung von Prothymosin α ist überraschend und war nicht vorhersehbar.Surprisingly, it has been found that prothymosin α is used to combat Hepatitis B and C is suitable, but the effect of prothymosin α is not an immune boost that is also regular in hepatitis diseases is not at all desired (cf. the administration of immunosuppressants), son which is based on a direct influence on the infected hepatocytes. This The effect of prothymosin α is surprising and was not predictable.

In einem in vitro Test lässt sich eine direkt durch Prothymosin α verursachte signifikante Abnahme der Replikation der Viren B und C in den infizierten Hepa­ tocyten feststellen. Der Test konnte des Weiteren bei einer potenzierenden Do­ sierung von Prothymosin α die Reduktion bzw. Eliminierung der Hepatitisviren in der Zellkultur nachweisen.In an in vitro test, one can be caused directly by prothymosin α significant decrease in replication of viruses B and C in the infected Hepa detect tocytes. The test was also successful in a potentiating Do sation of prothymosin α the reduction or elimination of the hepatitis viruses in detect the cell culture.

Nachfolgend sind zwei Behandlungsbeispiele aufgeführt:Two treatment examples are listed below:

Beispiel 1example 1

Patientin, 49 Jahre, seit 1½ Jahren an Hepatitis B erkrankt. Nach langer und systematischer potenzierender Behandlung von 2× wöchentlich 5 bis 20 mg Pro­ thymosin α zeigte sich innerhalb von 6 Monaten Therapiedauer eine eindeutige Verringerung der Viren bis hin zur Nachweisbarkeitsgrenze sowie eine Serum­ konversion. Patient, 49 years old, had hepatitis B for 1½ years. After a long and systematic potentiating treatment of 5 to 20 mg Pro twice a week thymosin α was clearly evident within 6 months of therapy Reduction of viruses up to the detectability limit as well as a serum conversion.  

Beispiel 2Example 2

Patientin, 74 Jahre, seit 2½ Jahren an Hepatitis C erkrankt. Nach einjähriger potenzierender Behandlung mit 2× wöchentlich 5 bis 20 mg Prothymosin α wur­ de eine Serumkonversion festgestellt und der Hepatitisvirus C war reduziert bzw. konnte nicht mehr nachgewiesen werden.Patient, 74 years old, had hepatitis C for 2½ years. After one year potentiating treatment with twice a week 5 to 20 mg prothymosin α wur en a serum conversion was found and the hepatitis virus C was reduced or could no longer be proven.

Die Bekämpfung der Hepatitisviren B und C durch Prothymosin α, wie sie im in vitro Test festgestellt wurde, konnte somit durch klinische Erfahrungen bestätigt werden.The fight against hepatitis viruses B and C by prothymosin α, as in vitro test was determined, could thus be confirmed by clinical experience become.

Claims (2)

1. Verwendung von Prothymosin α oder eines pharmazeutisch verwendbaren Salzes hiervon zur spezifischen Behandlung von Hepatitis B und/oder He­ patitis C.1. Use of prothymosin α or a pharmaceutically usable Salt thereof for the specific treatment of hepatitis B and / or He patitis C. 2. Verwendung von Prothymosin α nach Anspruch 1 in einer Dosierung von 5 bis 20 mg Prothymosin α 2× wöchentlich.2. Use of prothymosin α according to claim 1 in a dosage of 5 up to 20 mg prothymosin α twice a week.
DE10045621A 2000-09-15 2000-09-15 Treating hepatitis B and C comprises administration of prothymosin alpha Withdrawn DE10045621A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE10045621A DE10045621A1 (en) 2000-09-15 2000-09-15 Treating hepatitis B and C comprises administration of prothymosin alpha

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE10045621A DE10045621A1 (en) 2000-09-15 2000-09-15 Treating hepatitis B and C comprises administration of prothymosin alpha

Publications (1)

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DE10045621A1 true DE10045621A1 (en) 2002-04-04

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DE10045621A Withdrawn DE10045621A1 (en) 2000-09-15 2000-09-15 Treating hepatitis B and C comprises administration of prothymosin alpha

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DE (1) DE10045621A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7754687B2 (en) * 2005-02-24 2010-07-13 Mount Sinai School Of Medicine Methods of inhibiting viral infection

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4716148A (en) * 1984-08-13 1987-12-29 Hoffman-La Roche Inc. Prothymosin alpha
US6106868A (en) * 1990-08-24 2000-08-22 The Board Of Governors Of Wayne State University Method for the treatment of hepatitis

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4716148A (en) * 1984-08-13 1987-12-29 Hoffman-La Roche Inc. Prothymosin alpha
US6106868A (en) * 1990-08-24 2000-08-22 The Board Of Governors Of Wayne State University Method for the treatment of hepatitis

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7754687B2 (en) * 2005-02-24 2010-07-13 Mount Sinai School Of Medicine Methods of inhibiting viral infection

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Free format text: DER 1. ANMELDER IST ZU AENDERN IN: PESIC, MILAN C., DR.MED., 38667 BAD HARZBURG, DE

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