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Potential use of globins and their derivatives of abnormal red blood cells in the treatment of cancer and related immune disorders.

作者信息

Pandit H M

机构信息

D'Youville College, Buffalo, New York 14201.

出版信息

Med Hypotheses. 1993 Jun;40(6):332-4. doi: 10.1016/0306-9877(93)90213-a.

DOI:10.1016/0306-9877(93)90213-a
PMID:8377669
Abstract

One of the most important 'antibodies' that nature has developed for malarial parasites can be used for treating cancer as well as diseases like AIDS. The globins and their derivatives of abnormal red blood cells (sickle cells and thalassemia), have evolved as a selective resistance to malarial infections. Plasmodium species of sporozoa, which parasitize red blood cells and proliferate at their cost are inhibited by these abnormal red blood cells. To test the validity of this hypothesis, the author carried out a preliminary Medline search from 1974 to 1991 to find out if persons suffering from sickle cell or thalassemia diseases are 'immune' to HIV infections and malignancies. Clinical investigations lend support to the hypothesis. A research scheme is suggested for the study of the role of these globulin derivatives as they effect the synthesis of genetic material related to cell proliferation.

摘要

相似文献

1
Potential use of globins and their derivatives of abnormal red blood cells in the treatment of cancer and related immune disorders.
Med Hypotheses. 1993 Jun;40(6):332-4. doi: 10.1016/0306-9877(93)90213-a.
2
Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome.镰状细胞综合征。II. 镰状细胞贫血-α地中海贫血综合征。
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Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes.镰状细胞贫血与α地中海贫血并存。对镰状红细胞病理特性的影响。
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Regulation of hemoglobin synthesis in beta-thalassemia.β地中海贫血中血红蛋白合成的调控
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Molecular pathology of thalassemia syndromes.地中海贫血综合征的分子病理学
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The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.血红蛋白F和α地中海贫血对镰状细胞贫血患者红细胞指数的影响。
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The interaction of alpha-thalassemia and homozygous sickle-cell disease.α地中海贫血与纯合子镰状细胞病的相互作用。
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Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.镰状细胞综合征。I. 血红蛋白SC-α地中海贫血
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Haematologia (Budap). 1989;22(3):175-80.

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