Journal of Diabetes and Cholesterol Metabolism (DCM)

A Proposition of an Auxiliary Treatment for Diabetes Mellitus, Type I

Kimihiko Okazaki1*

1Okazaki Medical Clinic, Ukyoku, Kyoto, Japan

*Corresponding Author: Dr. Kimihiko Okazaki, Okazaki Medical Clinic, Ukyoku, Kyoto, Japan; TEL:0570-046-666 ; FAX:0570-046-666 ;

Citation: Kimihiko Okazaki(2017) A Proposition of an Auxiliary Treatment for Diabetes Mellitus, Type I. Diabetes Cholest metabol 1:106.

Copyright: © 2017 Kimihiko Okazaki, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Received date: June 01, 2017; Accepted date: June 14, 2017; Published date: June 20, 2017.


It is well known that diabetes mellitus, Type-1 is an autoimmune disease. As a matter of course, all of patients of this disease should have anti-pancreatic B cell antibodies on the surface of cytolytic T lymphocytes. Few, if any, contemporary physicians seem to take this fact into consideration presumably because most, if not all, of them take it for granted that most, if not all, antibody molecules rigidly adhere to their receptors on cell-sufaces.

On the other hand, approximately five decades ago, a novel concept of existence of equilibrium state among antibody molecules in the vicinity of their receptors on cell-surfaces has been established [1-3]. It follows that every antibody molecule in the vicinity of its receptors keeps repeating attaching to and detaching from the receptors. The reason why not “receptor” but “receptors” is because each antibody molecule may change receptors. It still follows that these replacements of antibody molecules on a certain receptor keep occurring all the time. Naturally, the traditional concept of rigid adhesions of antibody molecules to the receptors is irrelevant.


In conclusion, progressive destruction of pancreatic B-cells could be terminated if anti-pancreatic B cell antibodies were replaced from the surface of cytolytic T lymphocytes. In order to do so, accumulations of non-specific antibodies in the patients’ bodies are necessary. Still in order to do so, repeated intradermal injections with a non-specific antigen preparation is necessary. An example of the latter preparation is Neurotropin, a product of Nippon Pharmaceutical Company (Osaka), consisting of extracts of rabbit skin inflamed by inoculation of Vaccinia virus.

An alternative proposition might be intra-venous infusions of saline solution of gamma-globulin. However, repeated gamma-globulin infusion are dangerous since anti-gamma-globulin antibodies may be produced in the recipients’ bodies, which may cause an anaphylactic reaction after a large number of infusions.


  1. Andrews P (1965) The gel-filtration behaviour of proteins related to their molecular weights over a wide range. Biochem J 96: 595-606. [crossref]
  2. Rodewald R (1976) pH-dependent binding of immunoglobulins to intestinal cells of the neonatal rat. J Cell Biol 71: 666-669. [crossref]
  3. Neuber T, Frese K, Jaehrling J, Jäger S, Daubert D, et al. (2014) Characterization and screening of IgG binding to the neonatal Fc receptor. MAbs 6: 928-942. [crossref]