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B Ristevski

Publications and source records attributed to B Ristevski.

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Lymph, lymphocytes, and lymphatics.

This is a summary of recent developments regarding the role of the lymphatic system in immune responses. Emphasis is on physiological considerations from experiments in sheep. Cell- and tissue-specific lymphocyte traffic patterns measured over several days are considered. Particular attention is given to recent data on the relationship between the central nervous system and the lymphatic system, to cell labeling in situ, and to the entry of immune cells into afferent lymph from the interstitial tissues.

Animals↗

Epinephrine causes a reduction in lymph node cell output in sheep.

The lymphatic system has a critical role in the return of fluids, proteins, and cells to the circulatory system. However, the effects of stress, including exercise, on this system have not been adequately studied. We investigated the effect of a physiological dose (1 mg) of epinephrine (Epi) on lymph flow, cell concentration, and lymphocyte subsets in efferent subcutaneous lymph in sheep. Blood leukocyte numbers, differential, lymphocyte subsets, and blood and lymph pools of lymphocytes were determined simultaneously. A significant acute increase in lymph flow was followed by a post-injection decrease in flow and cellular output. No changes in lymphocyte subsets or pools of lymphocytes were seen in either blood or lymph. The timing of elevated plasma and lymph concentrations of Epi and norepinephrine (NE) corresponded with the increased lymph flow. In conclusion, Epi injection caused no change in lymphocyte subset distribution, leukocyte concentration, or pools of lymphocytes. A decrease in lymph flow and cellularity was documented post-injection, indicating that lymphatic tissue has no role in the leukocytosis seen after Epi injection. Lymphocyte retention by lymph nodes, however, may contribute to post-injection lymphopenia.

Adrenergic alpha-Agonists↗

The traffic of resting lymphocytes through delayed hypersensitivity and chronic inflammatory lesions: a dynamic equilibrium.

This essay is designed as a partial summary of the work of several students and colleagues from our laboratory. For the most part the experimental data have been published and this seminar represents an attempt to summarize, integrate and speculate on this work. In some situations the speculation is rather unrestrained and it is hoped that it will provoke discussion, controversy and better future experiments. Reference is made to the original articles and to recent reviews. In addition, since we have had the advantage of reading the other contributions to this volume, there is considerable reference to other chapters. We and others have argued in other publications that it is imperative to understand the normal physiological traffic of lymphocytes before one can adequately interpret data describing lymphocyte migration through pathological tissues. It has been useful to compare data derived from traffic through lymph nodes because there is considerable information on the individual lymph node with respect to blood-lymphocyte delivery and blood flow, prenodal input via peripheral lymphatics and, particularly in sheep, in the numbers and phenotypic analysis of the lymphocytes exiting lymph nodes in postnodal or efferent lymph (see Young, this volume). We consider the terms prenodal for afferent and post-nodal for efferent to be synonomous. In this volume, a significant contribution has been made by Cahill et al which describes the astonishing degree of lymphocyte traffic which occurs in fetal life prior to antigenic challenge. At the other extreme, in disease states, there is often profound activation of lymphocytes. This is most apparent in viral infections like HIV and SIV (Rosenberg et al, this volume) and also in the various models of diseases such as EAE (Hickey and Kulidjian et al, this volume). It is a central tenet of our paper that resting and activated lymphocyte migration need to be considered separately and that they are very different.

Animals↗