JPS58105922A - Remedy for leukemia - Google Patents
Remedy for leukemiaInfo
- Publication number
- JPS58105922A JPS58105922A JP56204135A JP20413581A JPS58105922A JP S58105922 A JPS58105922 A JP S58105922A JP 56204135 A JP56204135 A JP 56204135A JP 20413581 A JP20413581 A JP 20413581A JP S58105922 A JPS58105922 A JP S58105922A
- Authority
- JP
- Japan
- Prior art keywords
- pantethine
- lysolecithin
- leukemia
- lecithin
- cells
- 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.)
- Granted
Links
Abstract
Description
【発明の詳細な説明】 本発明は白血病治療剤に関するものであり。[Detailed description of the invention] The present invention relates to a therapeutic agent for leukemia.
パンテチン又はパンテチン及びレシチンを有効成分とす
る製剤投与に由来する健常人血液製剤によることを特徴
とするものである。It is characterized in that it is based on a healthy human blood product derived from the administration of a preparation containing pantethine or pantethine and lecithin as active ingredients.
白血病の医学的治療法として、従来化学療法剤あるいは
ステロイドホルモンが使用されているが、いずれも強い
副作用のため長期投与が不可能の場合があり、効果不足
あるいは副作用のため不幸な転帰を招く場合が少くない
。本発明によるパンテチンおよびレシチンはいずれも副
作用がきわめてわずかであり、白血病に対して有効な治
療法(剤)を提供し得るものである。Conventional chemotherapy drugs or steroid hormones have been used as medical treatments for leukemia, but they have strong side effects that sometimes make long-term administration impossible, and sometimes lead to unfortunate outcomes due to lack of efficacy or side effects. There are quite a few. Both pantethine and lecithin according to the present invention have very few side effects and can provide an effective treatment method (agent) for leukemia.
即ち9本発明は生体が腫瘍細胞を排除するに当っては細
胞依存性免疫能が関与していること。In other words, the present invention involves cell-dependent immune ability when a living body eliminates tumor cells.
白血病患者ではこの免疫能が低下していること及び細胞
依存性免疫に於ては免疫能の主役であるリンパ球が白血
病細胞と細胞融合することによって作用を発現すること
等の事実に鑑み9本発明者は健康人血液のリンパ球の細
胞融合性を高めこの血液を用いての白血病の治療に着目
し完成7=るに至ったものであれすなわち本発明者は、
細胞融合を促進する生体の物質であるリゾレシチンの存
在下では健康人血液が白血球細胞を強力に変形破壊する
ことを見出し、この作用を白血病の治療に応用して本発
明を完成したものである。In light of the fact that this immune capacity is reduced in leukemia patients and that in cell-dependent immunity, the effect is expressed by the fusion of lymphocytes, which are the main role of immune capacity, with leukemia cells, etc. The inventor has focused on improving the cell fusion property of lymphocytes in the blood of healthy people and using this blood to treat leukemia.
They discovered that healthy human blood strongly deforms and destroys white blood cells in the presence of lysolecithin, a biological substance that promotes cell fusion, and completed the present invention by applying this effect to the treatment of leukemia.
以下実験例に則して更に詳しく説明する。A more detailed explanation will be given below based on experimental examples.
実験に用いた健康人(52才男性)の血液は。The blood of a healthy person (a 52-year-old man) was used in the experiment.
血液型Bgで白血球数は8800.このうちリンパ球を
80%含むものであり、一方、慢性骨髄性白血病患者(
79才女性)の血液は、血液型B型で、白血球数は25
.700 、このうち白血病細胞が91%を占め、リン
パ球は4%のものである。これ等を用いて次の実験を行
った。Blood type Bg, white blood cell count 8800. Of these, 80% are lymphocytes; on the other hand, patients with chronic myeloid leukemia (
A 79-year-old woman's blood is type B, and her white blood cell count is 25.
.. 700, of which leukemia cells account for 91% and lymphocytes account for 4%. The following experiment was conducted using these.
実験l 白血病患者の血液のみを87℃にて2時間保温
した後に染色し、白血病細胞のうちで変形破壊された細
胞を顕微鏡下で検索したが全く見出されなかった。Experiment 1 Only the blood of a leukemia patient was incubated at 87° C. for 2 hours and then stained. Among the leukemia cells, deformed and destroyed cells were searched under a microscope, but no cells were found.
実験2. 白血病患者の血液にリゾレシチンを25μ9
/−の割合で添加し、87℃にて2時間保温し実験1.
と同様に観測すると白血病細胞のうちで5%が変形破壊
されることが確認された。Experiment 2. 25μ9 of lysolecithin in the blood of leukemia patients
Experiment 1.
When observed in the same manner as above, it was confirmed that 5% of leukemia cells were deformed and destroyed.
実験3 健康人血液と白血病患者の血液を1=1の割合
で混合し87℃にて2時間保温したのち実験1.と同様
に観測し白血病細胞の29%が破壊されていることがl
s紹された。Experiment 3 Blood from a healthy person and blood from a leukemia patient were mixed at a ratio of 1:1 and kept at 87°C for 2 hours. Similarly, it was observed that 29% of leukemia cells were destroyed.
s was introduced.
実験4 健康人血液と白血病患者の血液を1:lの割合
で混じたものにリゾレシチン25μり/−を添加すると
同様な観測の結果、白血病細胞の79%が変形破壊され
ることが確認された。Experiment 4 When 25 μl/- of lysolecithin was added to a mixture of healthy human blood and leukemia patient blood at a ratio of 1:1, similar observations confirmed that 79% of leukemia cells were deformed and destroyed. .
すなわち、実験4の成績は、健康人のリンパ球がリゾレ
シチンの存在下では白血病細胞と効果的に細胞融合し、
白血病細胞を強力に変形破壊し、腫瘍細胞を排除するこ
とを示すものである。しかし、リゾレシチンには強い溶
血作用があるため、そのままでは人に投与することがで
きない。そこで本発明者は、別途に健常人に対するパン
テチンあるいはパンテチンとレシチンの併用投与で生体
内らが生体の許容範囲内でリゾレシチンを増やすことに
注目し、この作用を白血病の治療に応用して成功したも
のである。In other words, the results of Experiment 4 showed that lymphocytes from healthy individuals effectively fused with leukemia cells in the presence of lysolecithin;
This shows that it strongly deforms and destroys leukemia cells and eliminates tumor cells. However, because lysolecithin has a strong hemolytic effect, it cannot be administered directly to humans. Therefore, the present inventor separately focused on the fact that pantethine or a combination of pantethine and lecithin was administered to healthy individuals to increase lysolecithin within the body's tolerance range, and succeeded in applying this effect to the treatment of leukemia. It is something.
以下実施例を挙げて説明する。This will be explained below with reference to examples.
実施例1
健康人にパンテチン1000m9をキシIJ)−ル20
−に溶解して静脈内投与し、2時間後に採血し、この血
液と白血病患者の血液を1:1の割合で混じ、87℃に
て2時間保温した後実験例と同様の観測の結果、白血病
細胞の74%が変形破壊されることを確認した。Example 1 Pantethine 1000m9 was given to a healthy person.
The blood was collected 2 hours later, mixed with the blood of a leukemia patient at a ratio of 1:1, and kept warm at 87°C for 2 hours. As a result of the same observation as in the experimental example, It was confirmed that 74% of leukemia cells were deformed and destroyed.
このことは、パンテチン投与により生体内の酵素である
レシチンコレステロールアシルトランスフェラーゼ活性
が増大し、これにより生体内でリゾレシチンが生成しく
特公昭55−2279)。This means that administration of pantethine increases the activity of lecithin cholesterol acyltransferase, an enzyme in the body, and this results in the production of lysolecithin in the body (Japanese Patent Publication No. 55-2279).
本物質が健康人リンパ球と白血病細胞との融合を促進し
、白血病細胞が変形破壊されたことを示すものである。This substance promotes the fusion of healthy lymphocytes and leukemia cells, indicating that the leukemia cells are deformed and destroyed.
実施例2
健康人にパンテチン静脈内投与と同時にレシチン5gを
経口投与し2時間後に採取した血液と白血病患者の血液
とを1=1の割合で混合し観測の結果、変形破壊された
白血病細胞は89%にも至った。このことは、生体内の
酵素であるレシチンコレステロールアシルトランスフェ
ラーゼ活性が増大し、しかもこの酵素の基質であるレシ
チンが存在するため、より多くのリゾレシチンが生成し
、細胞融合がより強く促進されたことを示すものである
。Example 2 5 g of lecithin was orally administered to a healthy person at the same time as intravenous administration of pantethine, and blood collected 2 hours later was mixed with blood from a leukemia patient at a ratio of 1=1. As a result of observation, leukemia cells that had been deformed and destroyed were It reached 89%. This indicates that lecithin-cholesterol acyltransferase activity, which is an enzyme in the living body, increases, and because lecithin, which is a substrate for this enzyme, is present, more lysolecithin is produced and cell fusion is more strongly promoted. It shows.
以上の成績から、パンテチンを単独投与、またはパンテ
チンとレシチンを併用投与した健康人の血液は、白血病
細胞を強く変形破壊する作用を持ち、したがって、この
健康人血液を白血病患者に輸血することにより白血病の
治療が行えることは確実である。From the above results, the blood of healthy people administered with pantethine alone or in combination with pantethine and lecithin has the effect of strongly deforming and destroying leukemia cells. It is certain that treatment can be performed.
尚、治療に際しての輸装置と頻度は患者の症状によって
も異るが1通常2チ0〜!ioom / 1回成人。In addition, the infusion device and frequency used during treatment vary depending on the patient's symptoms, but usually 1, 2, 0 ~! ioom / Adult once.
数回の投与で効果が期待される。It is expected to be effective after several doses.
本発明の目的遂行のためのパンテチンの投与量は1回1
000■を静脈内投与、およびレシチンは5gを経口投
与したが1個人差もあり。To accomplish the purpose of the present invention, the dosage of pantethine is 1 dose at a time.
000■ was administered intravenously, and 5g of lecithin was administered orally, but there were individual differences.
パンテチンでは1通常、脂質代謝障害の治療に用いられ
ている置から2000■以下程度の投与量で適宜増減さ
れるべきものであり、またレシチンでは9通常、動脈硬
化の治療に用いられている量から7.5g以下程度の蓋
で適宜増減さるべきものであろう。又1両物質とも投与
ルートとしては、経口、注射等特に限定さるべき要因は
なく1通常の薬剤投与と何ら変るところはない。For pantethine, the dosage should be adjusted as appropriate to 2,000 ml or less from the dosage normally used for the treatment of lipid metabolic disorders, and for lecithin, the dosage should be increased or decreased from the dosage usually used for the treatment of arteriosclerosis. The amount should be increased or decreased as appropriate with a lid of around 7.5g or less. In addition, there are no particular limitations on the route of administration for both substances, such as oral or injection routes, and there is no difference from conventional drug administration.
Claims (1)
の健常人血液製剤からなる白血病治療剤(2)血液製剤
が生体由来のリンパ球及びリゾレシチンを有効成分とし
て含有することを特徴とする特許請求の範囲第一項の白
血病治療剤(1) A therapeutic agent for leukemia comprising pantethine or a blood product from a healthy individual after administration of pantethine and lecithin (2) Claim 1, characterized in that the blood product contains biologically derived lymphocytes and lysolecithin as active ingredients Treatment for leukemia
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56204135A JPS58105922A (en) | 1981-12-17 | 1981-12-17 | Remedy for leukemia |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56204135A JPS58105922A (en) | 1981-12-17 | 1981-12-17 | Remedy for leukemia |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58105922A true JPS58105922A (en) | 1983-06-24 |
JPH0149129B2 JPH0149129B2 (en) | 1989-10-23 |
Family
ID=16485410
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56204135A Granted JPS58105922A (en) | 1981-12-17 | 1981-12-17 | Remedy for leukemia |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58105922A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017057643A1 (en) * | 2015-09-29 | 2017-04-06 | 国立大学法人大阪大学 | Leukocyte infiltration promoter and tumor immunoactivator |
-
1981
- 1981-12-17 JP JP56204135A patent/JPS58105922A/en active Granted
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017057643A1 (en) * | 2015-09-29 | 2017-04-06 | 国立大学法人大阪大学 | Leukocyte infiltration promoter and tumor immunoactivator |
CN108136020A (en) * | 2015-09-29 | 2018-06-08 | 国立大学法人大阪大学 | Leukocyte infiltration accelerating agent and tumour immunity activator |
JPWO2017057643A1 (en) * | 2015-09-29 | 2018-08-16 | 国立大学法人大阪大学 | Leukocyte infiltration promoter and tumor immune activator |
AU2016329670B2 (en) * | 2015-09-29 | 2019-12-12 | Osaka University | Leukocyte infiltration promoting agent and antitumor immunostimulatory agent |
JP2020073572A (en) * | 2015-09-29 | 2020-05-14 | 国立大学法人大阪大学 | Leukocyte infiltration promoter and tumor immunoactivator |
US11033559B2 (en) | 2015-09-29 | 2021-06-15 | Osaka University | Leukocyte infiltration promoting agent and antitumor immunostimulatory agent |
Also Published As
Publication number | Publication date |
---|---|
JPH0149129B2 (en) | 1989-10-23 |
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