The secretory glands of many mammals are known to produce large amounts of a gamma-A immunoglobulin (sIgA) which is shed into the external secretions. Immunofluorescent staining of the subepithelial mucosa of many types of secretory glands and tissues (e.g. mammary, lacrimal, salivary, bronchial, and nasal as well as the lamina propria along the whole of the gastrointestinal tract) has shown that the majority of all immunoglobulin-producing cells in these sites are producing IgA (1).In particular, it has been reported (2, 3) that in the rabbit approximately 80% of all immunoglobulin-producing cells in the lamina propria of the small intestine stain specifically for the alpha chain of IgA. In contrast, only 8-10% of all similar cells in the spleen and lymph nodes contain this class of immunoglobulin. The observed predominance of IgA-producing cells in the lamina propria of the intestine suggested to us the possibility that the gut of a normal animal might contain a population of precursor cells which would be capable of proliferating and giving rise to IgA-producing cells.By using a method of analysis developed by Frensdorff et al. (4,5) in which cell transfer and subsequent quantitation of immunocytes by immunofluorescence is used to assess the proliferative and differentiative potential of rabbit lymphoid cells in irradiated allogeneic hosts, we were able to show that the Peyer's patches contain an enriched source of precursors for IgA-producing cells. These cells proliferate both in the spleen and in the intestinal lamina propria and give rise to immunoglobulin-producing cells, most of which make IgA.
Materials and MethodsAnlmal~.--Male rabbits, weighing between 5 and 6 lb., were obtained from B and H Rabbitry (Rockville, Md.). Approximately 96% of the rabbits we have obtained from this rabbitry were homozygous for the b4 allotypic marker, an antigenic marker on the kappa *