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. 2022 Mar 10;11(3):371.
doi: 10.3390/antibiotics11030371.

Facing the Increased Prevalence of Antibiotic-Resistant M. tuberculosis: Exploring the Feasibility of Realising Koch's Aspiration of Immunotherapy of Tuberculosis

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Facing the Increased Prevalence of Antibiotic-Resistant M. tuberculosis: Exploring the Feasibility of Realising Koch's Aspiration of Immunotherapy of Tuberculosis

Peter A Bretscher. Antibiotics (Basel). .

Abstract

Koch attempted to treat tuberculosis in the late 1800s by administering an antigenic extract derived from the pathogen to patients. He hoped to bolster the patient's protective immunity. The treatment had diverse results. In some, it improved the patient's condition and in others led to a worsening state and even to death. Koch stopped giving his experimental treatment. I consider here three issues pertinent to realizing Koch's vision. Rational immunotherapy requires a knowledge of what constitutes protective immunity; secondly, how on-going immune responses are regulated, so the patient's immunity can be modulated to become optimally protective; thirdly, a simple methodology by which treatment might be realized. I deliberately cast my account in simple terms to transcend barriers due to specialization. The proposed immunotherapeutic treatment, if realizable, would significantly contribute to overcoming problems of treatment posed by antibiotic resistance of the pathogen.

Keywords: host-targeted therapies; immunotherapy; tuberculosis.

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Conflict of interest statement

The author declares no conflict of interest.

Figures

Figure 1
Figure 1
Dependence of cell-mediated/IgG antibody nature of response on dose of antigen and time after antigen impact.

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References

    1. Nunes-Alves C., Booty M.G., Carpenter S.M., Jayaraman P., Rothchild A.C., Behar S.M. In search of a new paradigm for protective immunity to TB. Nat. Rev. Microbiol. 2014;12:289–299. doi: 10.1038/nrmicro3230. - DOI - PMC - PubMed
    1. Surcel H.M., Troye-Blomberg M., Paulie S., Andersson G., Moreno C., Pasvol G., Ivanyi J. Th1/Th2 profiles in tuberculosis, based on the proliferation and cytokine response of blood lymphocytes to mycobacterial antigens. Immunology. 1994;81:171–176. - PMC - PubMed
    1. Menon J., Hoeppner V.H., Judd A., Power C.A., Bretscher P.A. A hypothesis for the existence of two types of tuberculosis, reflecting two distinct types of immune failure to control the pathogen, based upon prevalence of mycobacterium-specific IgG subclasses. Scand. J. Immunol. 2018;87:e12665. doi: 10.1111/sji.12665. - DOI - PubMed
    1. Lenzini L., Rottoli P., Rottoli L. The spectrum of human tuberculosis. Clin. Exp. Immunol. 1977;27:230–237. - PMC - PubMed
    1. Buddle B.M., de Lisle G.W., Pfeffer A., Aldwell F.E. Immunological responses and protection against Mycobacterium bovis in calves vaccinated with a low dose of BCG. Vaccine. 1995;13:1123–1130. doi: 10.1016/0264-410X(94)00055-R. - DOI - PubMed

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