𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The dependence of tumor neutralization on bone-marrow-derived cells

✍ Scribed by Philip Scuderi; Cornelius Rosse


Publisher
John Wiley and Sons
Year
1981
Tongue
French
Weight
642 KB
Volume
28
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Radiosensitive host cells capable of potentiating tumor neutralization by immunocytes in normal recipients are present only in the bone marrow and not in the spleen or thymus. This was shown by selectively eliminating either the bone marrow, spleen or thymus of groups of mice and then subcutaneously injecting these animals with sensitized splenocytes and tumor cells. Bone marrow ablation was accomplished by the administration of the bone‐seeking radioactive isotope ^88^Sr which did not reduce thymic or splenic cellularity. Sensitized splenocytes completely inhibited the growth of admixed tumor cells in normal, nude, splenectomized, or ^88^Sr‐treated animals, but the sensitized cells were as ineffective in ^89^Sr‐treated recipients as in 900‐rad irradiated mice. Bone marrow cells of normal donors admixed with sensitized splenocytes and the sensitizing tumor cells caused a significant inhibition of tumor growth in 900‐rad and ^89^Sr‐treated mice. Therefore, the radiation‐sensitive host cells that potentiate the tumor‐inhibitory effect of sensitized splenocytes are unique to the marrow and, in the intact animal, apparently emigrate from this organ to interact with sensitized immunocytes at the site of tumor growth.


📜 SIMILAR VOLUMES


Tumor neutralization by immune in vitro-
✍ Philip Scuderi; Cornelius Rosse 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 French ⚖ 569 KB

## Abstract In a Winn assay, the inhibition of methylcholanthrene‐induced sarcoma growth by tumor‐immune, secondarily __in vitro__‐sensitized splenocytes was augmented by normal unsensitized bone‐marrow cells. Bone‐marrow cells augmented the effect of a fixed number of sensitized splenocytes in a d

Antibody-dependent cellular cytotoxicity
✍ Marie-Luise Lohmann-Matthes; Wolfgang Domzig; Hristo Taskov 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 595 KB

## Abstract Mouse bone marrow cells are cultivated in a liquid culture system in the presence of fibroblast conditioned medium. Under these conditions, proliferation of macrophage and granulocyte precursor cells is induced. Cells of a 5‐day‐old culture are shown to act as cytotoxic effector cells a

The therapeutic potential of bone marrow
✍ Eva Mezey 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 873 KB

Since the replacement of the hematopoietic system became feasible through bone marrow (BM) transplantation, the idea of how to replace other organs of the body has been in the forefront of medical research. Scientists have been searching for the ideal stem cell that could be manipulated to different

Problem of tumor cell identification in
✍ Charles P. Emerson; Harvey E. Finkel 📂 Article 📅 1966 🏛 John Wiley and Sons 🌐 English ⚖ 868 KB

The ability to identify cancer cells accurately by the simple technique of bone marrow aspiration is of great potential value, both clinically and in the investigation of many basic aspects of neoplastic disease. Previous workers have reported success in distinguishing exogeneous tumor cells from in

The frequency of tumor cells in the bone
✍ Avery A. Sandberg; George E. Moore; Lois H. Crosswhite; Jean R. Schubarg 📂 Article 📅 1958 🏛 John Wiley and Sons 🌐 English ⚖ 581 KB

T row specimens obtained by needle aspiration of the sternum was described by Reich in 1935.l\* Subsequently, many reports of the finding of tumor cells in the bone marrow have been made. The review by Leitner' in 1949 and the recent papers by Jaimet and Amy5 and Pillers, Marks, and Mitchell9 are pa

miR-223 suppresses differentiation of tu
✍ Qiaofei Liu; Miaomiao Zhang; Xingran Jiang; Zhiqian Zhang; Lingyun Dai; Siping M 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 French ⚖ 856 KB

## Abstract Tumor‐associated factors are related to increased accumulation of CD11b^+^Gr1^+^myeloid‐derived suppressor cells (MDSCs). However, the exact mechanism of how genetic factors control the expansion of MDSCs in tumor‐bearing hosts remains elusive. Herein, we found that tumor‐associated MDS