CLL lymphocytes gave a low response upon stimulation with PHA or PWM in 3-day cultures. However, after treatment with neuraminidase-galactose oxidase (NGO), in the presence of PWM, CLL lymphocytes transformed into blasts and incorporated 3H-thymidine in 3-day cultures. This response of CLL lymphocytes was similar to that given by normal lymphocytes to PWM in 3-day cultures. The best stimulation of CLL lymphocytes was achieved when conditioned medium (CM) from normal T lymphocytes was present in PWM cultures. Purified B lymphocytes from CLL (T lymphocytes and monocytes removed) did not respond to PHA or PWM. However, after NGO treatment these cells were stimulated by PWM, but only in the presence of CM. PHA failed to stimulate NGO-treated CLL lymphocytes or purified B lymphocytes. This study shows that CLL lymphocytes, which usually fail to respond to mitogens, can be stimulated by PWM to proliferate after treatment with neuraminidase-galactose oxidase (NGO). This technique of B cell stimulation has been found useful in cytogenetic studies of B cell proliferative disorders.

B-Lymphocytes↗

PubMed1980

Inhibition of T-lymphocyte colony formation by inhibitors of mitochondrial protein synthesis.

A double layer technique which requires an underlayer of peripheral blood leucocytes, in addition to phytohaemmagglutinin (PHA) in the overlayer, to obtain good T-lymphocyte colony formation, was used to assess the effect of two inhibitors of mitochondrial protein synthesis, chloramphenicol and ethidium bromide. A significant inhibition of the colony growth of peripheral blood T lymphocytes was observed when either of the drugs was incorporated in the underlayer. The inhibitory effect was always smaller (c. 50%) when the drugs were added to the overlayer. These findings point to the existence of a T-lymphocyte colony stimulating factor(s), released mainly by the leucocyte-rich underlayer and essential for T-colony formation, the production of which is inhibited by these mitochonrial inhibitors.

Chloramphenicol↗

PubMedDate not supplied

Why is it more difficult to transplant children? A perspective in developing countries.

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Adolescent↗