JPS58116422A - Antitumor agent - Google Patents

Antitumor agent

Info

Publication number
JPS58116422A
JPS58116422A JP21143681A JP21143681A JPS58116422A JP S58116422 A JPS58116422 A JP S58116422A JP 21143681 A JP21143681 A JP 21143681A JP 21143681 A JP21143681 A JP 21143681A JP S58116422 A JPS58116422 A JP S58116422A
Authority
JP
Japan
Prior art keywords
virus
live vaccine
mice
antitumor agent
cancer
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.)
Pending
Application number
JP21143681A
Other languages
Japanese (ja)
Inventor
Yoshiomi Okuno
奥野 良臣
Takuji Doi
土居 卓治
Hirobumi Arimura
有村 博文
Ryoichi Naito
内藤 良一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Tanabe Pharma Corp
Original Assignee
Green Cross Corp Japan
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 Green Cross Corp Japan filed Critical Green Cross Corp Japan
Priority to JP21143681A priority Critical patent/JPS58116422A/en
Publication of JPS58116422A publication Critical patent/JPS58116422A/en
Pending legal-status Critical Current

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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

PURPOSE:An antitumor agent, containing a live vaccine of a virus belonging to the genus Paramyxovirus as an active constituent, and capable of exhibiting the antitumor effect on mammals. CONSTITUTION:An antitumor agent containing a live vaccine of a virus belonging to the genus Paramyxovirus, e.g. parainfluenza 1, 2 or 3 or mumps virus, as a principal constituent. The mumps virus is particularly preferred. The live vaccine of the virus is obtained by the subculture and attenuation of the virus in a grown hen's egg, yalk sac or amniotic cavity, and the attenuated viral live vaccine is if desired subjected to the purification, germ-free filtration, etc. and in general orally, preferably parenterally, administered. In experiments on ddy mice, BDF1 mice, etc., the viral live vaccine is observed to have the antitumor effect on the Ehrlich's cancer and leukemia L1210 cancer.

Description

【発明の詳細な説明】 本発明は、抗腫瘍剤に関する。さらに詳しくは、バラミ
クソウィルス属のウィルスの生ワクチンを主成分とする
抗腫瘍剤に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to antitumor agents. More specifically, the present invention relates to an antitumor agent containing a live vaccine of a virus of the genus Balamyxovirus as a main ingredient.

バラミクソウィルス(Paramyxovi rus 
)は1オルソミクソウイルスと形態的に似ているところ
からこの名がある。このウィルスのグイリオンは直径1
50〜600 nmの球形で、エングエロープの内側に
らせん形ヌクレオキャップを含み、核酸は分子量4〜8
XlOの一本領で蛋白合成の鋳型にならない0このウィ
ルスはヒトや動物の呼吸器疾患をおこすものが多い。
Paramyxovirus (Paramyxovirus)
) is so named because of its morphological resemblance to 1 orthomyxovirus. The diameter of this virus is 1
It has a spherical shape of 50 to 600 nm, contains a helical nucleocap inside the engrape, and the nucleic acid has a molecular weight of 4 to 8.
This virus, which has a single domain of XlO and does not serve as a template for protein synthesis, often causes respiratory diseases in humans and animals.

本発明者らは、このようなバラミクソウィルス属のウィ
ルスの生ワクチンが、鴫乳動物(ヒト、ウマ、マウス、
ラット、イヌ、ウシなど)に対して抗lI蕩作用を有し
ていることを見い出し、本発明を完成したのである。
The present inventors have demonstrated that a live vaccine for a virus of the genus Balamyxovirus can be used in mammals (humans, horses, mice,
They discovered that it has anti-II activity against rats, dogs, cows, etc., and completed the present invention.

本発明社、バラミクソウィルスのウィルスの生ワクチン
を主成分とする抗腫瘍剤からなる。
This product consists of an anti-tumor agent whose main ingredient is a live vaccine of Varamyxovirus.

本発明で使用されるバラミクソウィルスとして轄、バラ
インフルエンザ1!、2型及び3型、ニューキャッスル
病ウィルス、ムンプスウィルス、はしかウィルス、ジス
テンパーウィルス、センダイウィルスなどがあけられ、
特に好ましいものとしてはムンプスウィルスがあげられ
る。
As the rose myxovirus used in the present invention, rose influenza 1! , types 2 and 3, Newcastle disease virus, mumps virus, measles virus, distemper virus, Sendai virus, etc.
Particularly preferred is mumps virus.

かかるウィルスの生ワクチンは自体既知の操作にて製造
され、たとえtffi該ウィルつ七発育鶏卵、卵黄ツク
、羊小脂等にて継代培養、弱毒化する方法などによって
得られる。
Live vaccines of such viruses are produced by procedures known per se, such as by subculturing the virus in embryonated chicken eggs, egg yolks, sheep fat, etc., and attenuating the virus.

弱毒化されたウィルス生ワクチンは、医療用に供するた
めに所望によりn襞、除菌ろ過等の処理に付される。
The attenuated live virus vaccine may be subjected to treatments such as n-folding and sterilization filtration, if desired, in order to be used for medical purposes.

本発明の抗mm剤は、一般に経口または好ましくは非経
口投与され、その剤型としては計知の生ワクチンの剤型
、特に凍結乾燥製剤が好ましい。
The anti-mm agent of the present invention is generally administered orally or preferably parenterally, and its dosage form is preferably a live vaccine, particularly a freeze-dried preparation.

凍結乾燥製剤にはアルブミン、ゼラチン等の安定化剤を
添加しても構わない。また、凍結乾燥製剤は通常アンプ
ルに充填して片時溶解して注射薬として用いられるが、
lアンプル当シの充填貴社通常5〜1100IIである
。本発明に関して、生ワクチンの投与量は症状、投与ル
ート、体重その他によって異なるが、当該生ワクチンを
従来用途に投与する場合の投与量に準じて投与される。
Stabilizers such as albumin and gelatin may be added to the lyophilized preparation. In addition, lyophilized preparations are usually filled into ampoules and temporarily dissolved to be used as injections.
The filling per ampoule is usually 5 to 1100 II. Regarding the present invention, the dose of the live vaccine varies depending on symptoms, route of administration, body weight, etc., but is administered in accordance with the dose when administering the live vaccine for conventional purposes.

次に、本発明抗#!蕩剤の主成分たる生ワクチンの抗S
本作用を確認するための実験例を示す。
Next, the invention anti-#! Live vaccine anti-S, which is the main component of the antiseptic
An experimental example is shown to confirm this effect.

実験例1 実験動物としてddYマウス(体重約2011ニ一群2
0匹)とBDF1マウス(体重約18.fニ一群20匹
)をもちい、それぞれddYマウスにはエールリッヒ鳩
細胞20 X I O@個、BDFl−fウスにはロイ
コミアL1210癌細胞2×lθ″個接種し、接種彼我
1に示した投与方法に従ってHVJウィルス(センダイ
ウィルス)の生ワクチン(HVJウィルス全利用したの
は、マウスに対して選択的感受性をもつから)i15,
0OOHA価にワトリ赤血球凝集反応試験に基づく値〕
にて!ウス腹腔に投与してマウスの生存日数を観察し勧
その結果は、表1に示す通シであった。
Experimental Example 1 Experimental animals were ddY mice (body weight approx. 2011cm/group 2).
0 mice) and BDF1 mice (body weight approximately 18.f, group of 20 mice) were used, and ddY mice were injected with 20 x IO cells of Ehrlich pigeon cells, and BDFl-f mice were injected with 2 x lθ'' of Leukomia L1210 cancer cells. Live vaccine of HVJ virus (Sendai virus) (the whole HVJ virus was used because it has selective susceptibility to mice) according to the administration method shown in 1.
0OOHA value based on Watori hemagglutination test]
At! The drug was administered intraperitoneally to mice, and the survival days of the mice were observed. The results were as shown in Table 1.

(以下余白) カくシてHVJウィルスの生ワクチンは、驚異的な抗肺
瘍効果を有するものであることが確認でき九〇この結果
から、他のバラミキソウィルス属の生ワクチンが抗腟瘍
性を有すること、就中ムンプスウィルス(人に感受性が
高く、マウスの)IVJウィルスに相応する人のウィル
ス)の生ワクチンも人趣瘍に対して同様の効果のあるこ
とがわかる。
(Blank below) It has been confirmed that the HVJ virus live vaccine has an amazing anti-lung cancer effect.90 From these results, other live vaccines of the genus Varamyxovirus have an anti-vaginal effect. Live vaccines against mumps virus (human virus, which is highly susceptible to humans and corresponds to mouse IVJ virus) have been shown to have similar effects on human ulcers.

実IIA例1 ムンプスウィルス(MLV)の生ワクチンを生理食塩水
100mで2 X I O’p、 f、 u、 /dの
濃度に調整し、これにアルブミン596(w/マン、ゼ
ラチンO,s%(v/マ)量會添加し、除菌ろ過を行っ
た◇このろ液【分注し、凍結乾燥した。得られた凍結乾
燥MLV生ワクチンは、asxlfp、 f、 ile
 /)  であり、1ケ月−1θ℃保存後も6.8XI
Op、f、u、/)  の活性を保持した。
Practical IIA Example 1 A live vaccine of mumps virus (MLV) was adjusted to a concentration of 2×I O'p, f, u, /d in 100 m of physiological saline, and albumin 596 (w/man, gelatin O, s) was added to this. % (v/ma) amount was added and filtered for sterilization.◇This filtrate was dispensed and lyophilized.The obtained lyophilized live MLV vaccine was asxlfp, f, ile.
/) and 6.8XI even after storage for 1 month at -1θ℃
Op, f, u, /) activities were retained.

CP−f、 ile  (Plaque formin
g t*nit )  :国立予防衛生研究所学友会−
「ウィルス実験学、各論」丸善(1967)) 実施例2 HVJウィルスの生ワクチンをアルブミン5%(w/v
)に懸濁して60.000 HA/sljに調製し除菌
ろ過を行った。このろ液を分注し、−80℃に凍結した
。得らカ、た凍結品は5力年保存においても60,00
0HA/d ”t’、!、−flJ解り、7’j場合で
も4℃保存において、2週間経過後60,000HA/
sl 、3〜4週間経過後ao、ooo〜6゜000 
HA/dであった。
CP-f, ile (Plaque formin
g t * nit ): National Institute of Preventive Health Alumni Association
"Virus Experiments, Specifics" Maruzen (1967)) Example 2 HVJ virus live vaccine was added to albumin 5% (w/v)
) and adjusted to 60,000 HA/slj, followed by sterilization filtration. This filtrate was divided into portions and frozen at -80°C. The obtained frozen product retains 60,000 yen even after being stored for 5 years.
0HA/d ``t',!, -flJ understood, even in the case of 7'j, 60,000HA/d after 2 weeks when stored at 4℃
sl, ao, ooo~6°000 after 3-4 weeks
It was HA/d.

手続補正書(自発ン 特許庁長官      殿 1、事件の表示 昭和56年特 許 1第211436号3、 補正をす
る者 事件との関係    特許出願人 (1)  明細書第1頁下から第9行及び最終行並びに
第2頁第5行及び第7行に「パラミクソ」とあるt「パ
ラミキソ」に訂正する。
Procedural amendment (volunteer to the Commissioner of the Japan Patent Office1, Indication of the case 1982 Patent No. 1 No. 2114363, Person making the amendment Relationship to the case Patent applicant (1) Line 9 from the bottom of page 1 of the specification In the last line and in the 5th and 7th lines of page 2, the text ``paramyxo'' is corrected to ``paramyxo''.

(2)回書第1頁下から第8行に「オルソミクン」トす
るを「オルソミキソ」に訂正する。
(2) In the 8th line from the bottom of page 1 of the circular, the word ``orthomicun'' is corrected to ``orthomixo.''

(3)同書第3頁下から第3行に「ロイデミア」とある
t「ロイケミア」に訂正する。
(3) In the third line from the bottom of page 3 of the same book, the word "leudemia" has been corrected to "leukemia."

(4)同書第6頁第15行及び第16行に「ダ」とらる
を「−」に訂正する。
(4) In the same book, page 6, lines 15 and 16, "da" toraru is corrected to "-".

(5)同書第6頁第16行にrlO’Jとある會「10
」に訂正する。
(5) On page 6, line 16 of the same book, there is a meeting called rlO'J "10
” is corrected.

Claims (1)

【特許請求の範囲】[Claims] パラミキソウイルス属のウィルスの生ワクチンを活性成
分とする抗腫瘍剤。
An antitumor agent containing a live vaccine of a virus of the genus Paramyxovirus as an active ingredient.
JP21143681A 1981-12-28 1981-12-28 Antitumor agent Pending JPS58116422A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21143681A JPS58116422A (en) 1981-12-28 1981-12-28 Antitumor agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21143681A JPS58116422A (en) 1981-12-28 1981-12-28 Antitumor agent

Publications (1)

Publication Number Publication Date
JPS58116422A true JPS58116422A (en) 1983-07-11

Family

ID=16605915

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21143681A Pending JPS58116422A (en) 1981-12-28 1981-12-28 Antitumor agent

Country Status (1)

Country Link
JP (1) JPS58116422A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986000811A1 (en) * 1984-07-30 1986-02-13 Csatary Laszlo Therapeutic preparations for treatment of certain viral and other diseases and the preparation of the same
WO1997042335A1 (en) * 1996-05-02 1997-11-13 GESELLSCHAFT FüR BIOTECHNOLOGISCHE FORSCHUNG MBH (GBF) Polycistronic expression plasmid for tumor-rejection
EP1267626A4 (en) * 2000-03-21 2003-06-18 Aviron Inc Recombinant parainfluenza virus expression systems and vaccines
US7056689B1 (en) 1993-04-30 2006-06-06 Wellstat Biologics Corporation Methods of treating and detecting cancer using viruses
US7470426B1 (en) 1997-10-09 2008-12-30 Wellstat Biologics Corporation Treatment of neoplasms with viruses
US7682619B2 (en) 2006-04-06 2010-03-23 Cornell Research Foundation, Inc. Canine influenza virus
US7780962B2 (en) 1997-10-09 2010-08-24 Wellstat Biologics Corporation Treatment of neoplasms with RNA viruses
US8043612B2 (en) 1997-10-09 2011-10-25 Wellstat Biologics Corporation Infection and treatment of neoplasms with vesicular stomatitis virus
US8105578B2 (en) 1997-10-09 2012-01-31 Wellstat Biologics Corporation Treatment of neoplasms with viruses
US8147822B1 (en) 1999-09-17 2012-04-03 Wellstat Biologics Corporation Oncolytic virus

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986000811A1 (en) * 1984-07-30 1986-02-13 Csatary Laszlo Therapeutic preparations for treatment of certain viral and other diseases and the preparation of the same
US7736640B2 (en) 1993-04-30 2010-06-15 Wellstat Biologics Corporation Methods of treating and detecting cancer using viruses
US7056689B1 (en) 1993-04-30 2006-06-06 Wellstat Biologics Corporation Methods of treating and detecting cancer using viruses
WO1997042335A1 (en) * 1996-05-02 1997-11-13 GESELLSCHAFT FüR BIOTECHNOLOGISCHE FORSCHUNG MBH (GBF) Polycistronic expression plasmid for tumor-rejection
US7780962B2 (en) 1997-10-09 2010-08-24 Wellstat Biologics Corporation Treatment of neoplasms with RNA viruses
US7470426B1 (en) 1997-10-09 2008-12-30 Wellstat Biologics Corporation Treatment of neoplasms with viruses
US8043612B2 (en) 1997-10-09 2011-10-25 Wellstat Biologics Corporation Infection and treatment of neoplasms with vesicular stomatitis virus
US8105578B2 (en) 1997-10-09 2012-01-31 Wellstat Biologics Corporation Treatment of neoplasms with viruses
US8147822B1 (en) 1999-09-17 2012-04-03 Wellstat Biologics Corporation Oncolytic virus
US7678376B2 (en) 2000-03-21 2010-03-16 Medimmune, Llc Recombinant parainfluenza virus expression systems and vaccines
US7238481B2 (en) 2000-03-21 2007-07-03 Medimmune Vaccines, Inc. Recombinant parainfluenza virus expression systems and vaccines
EP1267626A4 (en) * 2000-03-21 2003-06-18 Aviron Inc Recombinant parainfluenza virus expression systems and vaccines
US8084037B2 (en) 2000-03-21 2011-12-27 Medimmune, Llc Recombinant parainfluenza virus expression systems and vaccines
US7682619B2 (en) 2006-04-06 2010-03-23 Cornell Research Foundation, Inc. Canine influenza virus

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