By George Klein, Sidney Weinhouse, Alexander Haddow (Eds.)
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Additional resources for Advances in Cancer Research, Vol. 13
At the start of the experiment the average diameter of the tumors ranged from 8 to 10 mm, and on the graph the dimensions were adjusted to the same starting point. Tumors that had been biopsied only had all attained a relative diameter of 200 mm by 15 days. The reason why foreign immunoblasts can be used against tumors in vivo is that they have the capacity to extravasate rapidly and this enables these cells to avoid destruction by the reticuloendathelial system (RES) the recipient. Small lymphocytes do not have the same facility of passing vascular barriers and penetrating into intercellular spaces, and they are, in fact, found almost entirely in the RES following intravenous injection into a foreign host.
The transient increase in the percentage of immunoblasts in thoracic duct lymph of rats following the implantation of viable syngeneic sarcomata into the hindquarter region. Once the growing tumors became established the percentage of immunoblasts fell to near normal levels but increased as soon as the tumors had been excised. ( 0 )Expt. 1 ; (0) Expt. 2. 9. The increase in the percentage of immunoblasts in the thoracic duct lymph of rats following the excision of their primary tumors. Each point on the graph represents the mean of results obtained from at least 3 rats.
ALEXANDER AND J. G. HALL early stages of tumor growth, antigen is released and is carried via the afferent lymphatics to the regional node and a normal immune response is induced so that specifically reactive immunoblasts are discharged into the lymph and ultimately the blood. However, if tumor growth is not halted a t this stage, more and more antigenic material impinges on the draining node. We speculate that the antigen reacts with newly formed immunoblasts in the node and immobilizes them so that, instead of being released into the efferent lymph, they settle down in the medulla of the node and transform into plasma cells.
Advances in Cancer Research, Vol. 13 by George Klein, Sidney Weinhouse, Alexander Haddow (Eds.)