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重新审视GcMAF免疫疗法——山本信夫研究的批判性综述

Immunotherapy with GcMAF revisited - A critical overview of the research of Nobuto Yamamoto.

作者信息

Albracht Simon Pj

机构信息

Biochemist, retired from the Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Cancer Treat Res Commun. 2022;31:100537. doi: 10.1016/j.ctarc.2022.100537. Epub 2022 Feb 18.

Abstract

This overview describes the research of Nobutu Yamamoto (Philadelphia) concerning immunotherapy with GcMAF for patients with cancer and for patients infected with pathogenic envelope viruses. GcMAF (Group-specific component Macrophage-Activating Factor) is a mammalian protein with an incredible potency to directly activate macrophages. Since the late 1980s Yamamoto's investigations were published in numerous journals but in order to understand the details of his research, a minute survey of many of his patents was required. But even then, regrettably, a precise description of his experiments was sometimes lacking. This overview tries to summarize all of Yamamoto's research on GcMAF, as well as some selected more recent papers from other investigators, who tried to verify and/or reproduce Yamamoto's reports. In my opinion the most important result of the GcMAF research deserves widespread renewed attention: human GcMAF injections (100 ng per week, intramuscular or intravenous) can help to cure patients with a great variety of cancers as well as patients infected with pathogenic envelope viruses like the human immunodeficiency virus 1 (HIV-1), influenza, measles and rubella (and maybe also SARS-CoV-2). From Yamamoto's data it can be calculated that GcMAF is a near-stoichiometric activator of macrophages. Yamamoto monitored the progress of his immunotherapy via the serum level of an enzyme called nagalase (α-N-acetylgalactosaminidase activity at pH 6). I have extensively discussed the properties and potential catalytic site of this enzyme activity in an Appendix entitled: "Search for the potential active site of the latent α-N-acetylgalactosaminidase activity in the glycoproteins of some envelope viruses".

摘要

本综述介绍了山本信人(费城)关于用GcMAF对癌症患者和感染致病性包膜病毒患者进行免疫治疗的研究。GcMAF(群特异性成分巨噬细胞激活因子)是一种哺乳动物蛋白,具有直接激活巨噬细胞的惊人效力。自20世纪80年代末以来,山本的研究成果发表在众多期刊上,但为了了解其研究细节,需要对他的许多专利进行详细调查。但即便如此,遗憾的是,有时仍缺乏对其实验的精确描述。本综述试图总结山本关于GcMAF的所有研究,以及其他研究人员最近发表的一些精选论文,这些研究人员试图验证和/或重现山本的报告。在我看来,GcMAF研究的最重要结果值得广泛重新关注:注射人GcMAF(每周100纳克,肌肉注射或静脉注射)有助于治愈多种癌症患者以及感染致病性包膜病毒的患者,如人类免疫缺陷病毒1型(HIV-1)、流感、麻疹和风疹(也许还有严重急性呼吸综合征冠状病毒2,即SARS-CoV-2)。从山本的数据可以计算出,GcMAF是巨噬细胞的近化学计量激活剂。山本通过一种名为N-乙酰半乳糖胺酶(pH 6时的α-N-乙酰半乳糖胺酶活性)的酶的血清水平来监测其免疫治疗的进展。我在题为“寻找某些包膜病毒糖蛋白中潜在的α-N-乙酰半乳糖胺酶活性的潜在活性位点”的附录中广泛讨论了这种酶活性的性质和潜在催化位点。

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