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Trypanosoma cruzi , Cancer, and the Cold War. 1. 2. Grigorii Roskin, c1930. 3. The discoverers of “KR” preparation: Nina Kliueva and Grigorii Roskin, 1946. 4. New York Times headlines, 1946. 5. Parin and Soviet oncologists in the US Surgeon General Office. 6. N. Kliueva and G. Roskin
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The discoverers of “KR” preparation: Nina Kliueva and Grigorii Roskin, 1946 4
Parin and Soviet oncologists in the US Surgeon General Office 6
N. Kliueva and G. Roskin Biotherapy of Malignant Tumors 1946 7
Murray J. Shear Theodore S. Hauschka 11
Kliueva and Roskin’s new institute for studies on KR, c1950 9
Lankenau hospital, Philadelphia National Cancer Institute (NCI) Bethesda, MD 12
Murray J. Shear Theodore S. Hauschka 11
H. R. A. Cabral Institute de Biología Celular, Facultad de Ciencias Médicas, Ciudad Universitaria, Córdoba, Argentina The tumoricidal effect of Trypanosoma cruzi: its intracellular cycle and the immune response of the host Medical Hypotheses (2000) 54(1), 1–6 V. D. Kallinikova † , Z. Batmonch, E. G. Kravtsov, L. P. Karpenko, L. V. Pachorukova, and T. A. Ogloblina Department of Invertebrate Zoology, Moscow State University Department of Microbiology, Peoples’ Friendship University of Russia; Antibodies against Trypanosoma cruzi Accompanying the Antitumoral Action of Lysed Epimastigotes in vivo Moscow University Biological Sciences Bulletin, 2008, Vol. 63, No. 2, pp. 72–76.
TRYPANOSOMES AND THE BIOTHERAPY OF TUMORS • Trypanosomes might disorganize themetabolism of the infected organism and, thus, inhibit the development of tumors, which, according to a belief common at that time, required a large and possibly specific supply of materials from the host-organism. • Like malariotherapy, trypanosome infection might stimulate a non-specific immunological reaction that, in turn, could affect implanted tumors. • Trypanosomes might intrude into tumorous cells and directly destroy them. • Either trypanosomes excreted certain toxins that had a directly destructive effect on tumorous cells, or the host-organism produced antibodies against trypanosomes (or their toxins), which, at the same time, appear co-active against tumorous cells. Each one or any combination of the four hypothetical factors might play a role in the inhibition of tumor transplants by trypanosome infection.